diff --git a/releases/EDAM.owl b/releases/EDAM.owl
index 27b617d..d517bfc 100644
--- a/releases/EDAM.owl
+++ b/releases/EDAM.owl
@@ -32,15 +32,15 @@
EDAM is an ontology of well established, familiar concepts that are prevalent within bioinformatics, including types of data and data identifiers, data formats, operations and topics. EDAM is a simple ontology - essentially a set of terms with synonyms and definitions - organised into an intuitive hierarchy for convenient use by curators, software developers and end-users. EDAM is suitable for large-scale semantic annotations and categorization of diverse bioinformatics resources. EDAM is also suitable for diverse application including for example within workbenches and workflow-management systems, software distributions, and resource registries.
Hervé Ménager
topics "EDAM topics"
- 14:11:2014 09:26
+ 17:11:2014 23:35
EDAM_format http://edamontology.org/format_ "EDAM data formats"
Jon Ison, Matus Kalas, Herve Menager
Matúš Kalaš
- 3429
1.5
Jon Ison
concept_properties "EDAM concept properties"
EDAM_data http://edamontology.org/data_ "EDAM types of data"
+ 3442
application/rdf+xml
EDAM http://edamontology.org/ "EDAM relations and concept properties"
operations "EDAM operations"
@@ -379,17 +379,17 @@
- OBO_REL:bearer_of
- Is defined anywhere? Not in the 'unknown' version of RO. 'OBO_REL:bearer_of' is narrower in the sense that it only relates ontological categories (concepts) that are an 'independent_continuant' (snap:IndependentContinuant) with ontological categories that are a 'specifically_dependent_continuant' (snap:SpecificallyDependentContinuant), and broader in the sense that it relates with any borne objects not just functions of the subject.
-
-
-
-
true
In very unusual cases.
+
+ Is defined anywhere? Not in the 'unknown' version of RO. 'OBO_REL:bearer_of' is narrower in the sense that it only relates ontological categories (concepts) that are an 'independent_continuant' (snap:IndependentContinuant) with ontological categories that are a 'specifically_dependent_continuant' (snap:SpecificallyDependentContinuant), and broader in the sense that it relates with any borne objects not just functions of the subject.
+ OBO_REL:bearer_of
+
+
+
@@ -434,8 +434,14 @@
- 'OBO_REL:has_participant' is narrower in the sense that it only relates ontological categories (concepts) that are a 'process' (span:Process) with ontological categories that are a 'continuant' (snap:Continuant), and broader in the sense that it relates with any participating objects not just inputs or input arguments of the subject.
+ In very unusual cases.
+ true
+
+
+
+
OBO_REL:has_participant
+ 'OBO_REL:has_participant' is narrower in the sense that it only relates ontological categories (concepts) that are a 'process' (span:Process) with ontological categories that are a 'continuant' (snap:Continuant), and broader in the sense that it relates with any participating objects not just inputs or input arguments of the subject.
@@ -445,12 +451,6 @@
-
- In very unusual cases.
- true
-
-
-
@@ -475,18 +475,18 @@
- 'OBI:has_specified_output' only relates subjects that are a 'planned process' (http://purl.obolibrary.org/obo/OBI_0000011) with objects that are a 'continuant' (snap:Continuant).
-
-
-
-
-
OBO_REL:has_participant
'OBO_REL:has_participant' is narrower in the sense that it only relates ontological categories (concepts) that are a 'process' (span:Process) with ontological categories that are a 'continuant' (snap:Continuant), and broader in the sense that it relates with any participating objects not just outputs or output arguments of the subject. It is also not clear whether an output (result) actually participates in the process that generates it.
+ 'OBI:has_specified_output' only relates subjects that are a 'planned process' (http://purl.obolibrary.org/obo/OBI_0000011) with objects that are a 'continuant' (snap:Continuant).
+
+
+
+
+
true
In very unusual cases.
@@ -524,12 +524,6 @@
- true
- In very unusual cases.
-
-
-
-
'is about' is narrower in the sense that it only relates subjects that are information artifacts and the relation is not necessarily the one of having a topic. It is broader in the sense that it relates with any object.
@@ -547,6 +541,12 @@
+
+ In very unusual cases.
+ true
+
+
+
@@ -601,18 +601,18 @@
- OBO_REL:inheres_in
- Is defined anywhere? Not in the 'unknown' version of RO. 'OBO_REL:inheres_in' is narrower in the sense that it only relates ontological categories (concepts) that are a 'specifically_dependent_continuant' (snap:SpecificallyDependentContinuant) with ontological categories that are an 'independent_continuant' (snap:IndependentContinuant), and broader in the sense that it relates any borne subjects not just functions.
-
-
-
-
In very unusual cases.
true
+ OBO_REL:inheres_in
+ Is defined anywhere? Not in the 'unknown' version of RO. 'OBO_REL:inheres_in' is narrower in the sense that it only relates ontological categories (concepts) that are a 'specifically_dependent_continuant' (snap:SpecificallyDependentContinuant) with ontological categories that are an 'independent_continuant' (snap:IndependentContinuant), and broader in the sense that it relates any borne subjects not just functions.
+
+
+
+
Is defined anywhere? Not in the 'unknown' version of RO. 'OBO_REL:function_of' only relates subjects that are a 'function' (snap:Function) with objects that are an 'independent_continuant' (snap:IndependentContinuant), so for example no processes. It does not define explicitly that the subject is a function of the object.
OBO_REL:function_of
@@ -664,23 +664,23 @@
- true
In very unusual cases.
+ true
- OBO_REL:participates_in
- 'OBO_REL:participates_in' is narrower in the sense that it only relates ontological categories (concepts) that are a 'continuant' (snap:Continuant) with ontological categories that are a 'process' (span:Process), and broader in the sense that it relates any participating subjects not just inputs or input arguments.
-
-
-
-
'OBI:is_specified_input_of' only relates subjects that are a 'continuant' (snap:Continuant) with objects that are a 'planned process' (http://purl.obolibrary.org/obo/OBI_0000011).
+
+ OBO_REL:participates_in
+ 'OBO_REL:participates_in' is narrower in the sense that it only relates ontological categories (concepts) that are a 'continuant' (snap:Continuant) with ontological categories that are a 'process' (span:Process), and broader in the sense that it relates any participating subjects not just inputs or input arguments.
+
+
+
@@ -718,8 +718,8 @@
- OBO_REL:participates_in
'OBO_REL:participates_in' is narrower in the sense that it only relates ontological categories (concepts) that are a 'continuant' (snap:Continuant) with ontological categories that are a 'process' (span:Process), and broader in the sense that it relates any participating subjects not just outputs or output arguments. It is also not clear whether an output (result) actually participates in the process that generates it.
+ OBO_REL:participates_in
@@ -820,16 +820,22 @@
- Data record
- EDAM does not distinguish a data record (a tool-understandable information artefact) from data or datum (its content, the tool-understandable encoding of an information).
+ Data does theoretically not need to have a purpose, but in all regular cases it does. Remark: EDAM Data sub-ontology focuses on scientific data (SIO_000472), in particular the bioinformatics (SIO_010065) and biological (SIO_010019).
-
+
+
- Data does theoretically not need to have a purpose, but in all regular cases it does. Remark: EDAM Data sub-ontology focuses on scientific data (SIO_000472), in particular the bioinformatics (SIO_010065) and biological (SIO_010019).
+ GFO 'Perpetuant' is in general broader than data, but it may be seen narrower in the sense of being a concrete individual.
-
+
+
+
+ Data set
+ EDAM does not distinguish the multiplicity of data, such as one data item (datum) versus a collection of data (data set).
+
+
IAO 'data item' is a closely related ontological category (concept) broader in the sense of being any type of data in any role, and narrower in the sense of being limited to a 'generically_dependent_continuant' (snap:GenericallyDependentContinuant), standing in relation of aboutness to some entity (http://purl.obolibrary.org/obo/IAO_0000030), and to data that is intended to be a truthful statement about something.
@@ -838,6 +844,12 @@
+ EDAM does not distinguish a data record (a tool-understandable information artefact) from data or datum (its content, the tool-understandable encoding of an information).
+ Data record
+
+
+
+
IAO 'information content entity' is a closely related ontological category (concept) broader in the sense of covering any type of data in any role, and narrower in the sense of being limited to a 'generically_dependent_continuant' (snap:GenericallyDependentContinuant) and standing in relation of aboutness to some entity.
@@ -850,20 +862,8 @@
- Data set
EDAM does not distinguish the multiplicity of data, such as one data item (datum) versus a collection of data (data set).
-
-
-
-
- GFO 'Perpetuant' is in general broader than data, but it may be seen narrower in the sense of being a concrete individual.
-
-
-
-
-
Datum
- EDAM does not distinguish the multiplicity of data, such as one data item (datum) versus a collection of data (data set).
@@ -921,7 +921,7 @@
- DEP_Directory metadata
+ Directory metadata
true
beta12orEarlier
@@ -1133,7 +1133,7 @@
- DEP_Sequence mask character
+ Sequence mask character
A character used to replace (mask) other characters in a molecular sequence.
1.5
@@ -1142,13 +1142,11 @@
-
-
- DEP_Sequence mask type
+ Sequence mask type
true
1.5
@@ -1181,7 +1179,7 @@
- DEP_Sequence length specification
+ Sequence length specification
1.5
beta12orEarlier
@@ -1196,7 +1194,7 @@
- DEP_Sequence metadata
+ Sequence metadata
true
1.5
@@ -1292,7 +1290,7 @@
- DEP_Sequence alignment (words)
+ Sequence alignment (words)
Alignment of exact matches between subsequences (words) within two or more molecular sequences.
Sequence word alignment
@@ -1345,7 +1343,7 @@
- DEP_Sequence alignment parameter
+ Sequence alignment parameter
beta12orEarlier
1.5
@@ -1374,7 +1372,7 @@
- DEP_Sequence alignment metadata
+ Sequence alignment metadata
1.5
true
@@ -1790,7 +1788,7 @@
- DEP_Sequence-3D profile alignment
+ Sequence-3D profile alignment
true
beta12orEarlier
@@ -1918,7 +1916,7 @@
- DEP_Protein domain classification
+ Protein domain classification
beta12orEarlier
1.5
@@ -2676,7 +2674,7 @@
- DEP_Data resource definition
+ Data resource definition
A definition of a data resource serving one or more types of data, including metadata and links to the resource or data proper.
1.5
@@ -2740,7 +2738,7 @@
- DEP_EMBOSS database resource definition
+ EMBOSS database resource definition
1.5
true
@@ -2755,7 +2753,7 @@
- DEP_Version information
+ Version information
true
Information on a version of software or data, for example name, version number and release date.
@@ -2865,7 +2863,7 @@
- DEP_Job metadata
+ Job metadata
Textual metadata on a submitted or completed job.
Moby:PDGJOB
@@ -3222,7 +3220,7 @@
- DEP_Molecule type
+ Molecule type
Protein|DNA|RNA
A label (text token) describing the type a molecule.
@@ -3721,7 +3719,7 @@
- DEP_Sequence position specification
+ Sequence position specification
true
beta12orEarlier
@@ -5126,7 +5124,7 @@
- DEP_Sequence type
+ Sequence type
beta12orEarlier
true
@@ -5374,7 +5372,7 @@
- DEP_EMBOSS listfile
+ EMBOSS listfile
beta12orEarlier
true
@@ -5538,7 +5536,7 @@
- DEP_Sequence alignment type
+ Sequence alignment type
A label (text token) describing the type of a sequence alignment.
Possible values include for example the EMBOSS alignment types, BLAST alignment types and so on.
@@ -5569,7 +5567,7 @@
- DEP_Phylogenetic tree type
+ Phylogenetic tree type
nj|upgmp
1.5
@@ -5616,7 +5614,7 @@
- DEP_Comparison matrix type
+ Comparison matrix type
For example 'blosum', 'pam', 'gonnet', 'id' etc. Comparison matrix type may be required where a series of matrices of a certain type are used.
Substitution matrix type
@@ -7104,7 +7102,7 @@
- DEP_Word size
+ Word size
beta12orEarlier
true
@@ -7121,7 +7119,7 @@
- DEP_Window size
+ Window size
Size of a sequence window.
beta12orEarlier
@@ -7137,7 +7135,7 @@
- DEP_Sequence length range
+ Sequence length range
1.5
beta12orEarlier
@@ -7730,7 +7728,7 @@
- DEP_Sequence features (repeats)
+ Sequence features (repeats)
Location of short repetitive subsequences (repeat sequences) in (typically nucleotide) sequences.
The report might include derived data map such as classification, annotation, organization, periodicity etc.
@@ -7748,7 +7746,7 @@
- DEP_Gene and transcript structure (report)
+ Gene and transcript structure (report)
true
A report on predicted or actual gene structure, regions which make an RNA product and features such as promoters, coding regions, splice sites etc.
@@ -7798,7 +7796,7 @@
- DEP_Nucleic acid features (quadruplexes)
+ Nucleic acid features (quadruplexes)
beta12orEarlier
A report on quadruplex-forming motifs in a nucleotide sequence.
@@ -7906,7 +7904,7 @@
- DEP_Nucleic acid features (microRNA)
+ Nucleic acid features (microRNA)
1.5
A report on microRNA sequence (miRNA) or precursor, microRNA targets, miRNA binding sites in an RNA sequence etc.
@@ -8300,7 +8298,7 @@
- DEP_Regular expression
+ Regular expression
beta12orEarlier
true
@@ -8511,7 +8509,7 @@
- DEP_Protein family signature
+ Protein family signature
A protein family signature (sequence classifier) from the InterPro database.
1.5
@@ -8527,7 +8525,7 @@
- DEP_Protein domain signature
+ Protein domain signature
Protein domain signatures identify structural or functional domains or other units with defined boundaries.
A protein domain signature (sequence classifier) from the InterPro database.
@@ -8543,7 +8541,7 @@
- DEP_Protein region signature
+ Protein region signature
A protein region signature defines a region which cannot be described as a protein family or domain signature.
1.5
@@ -8559,7 +8557,7 @@
- DEP_Protein repeat signature
+ Protein repeat signature
A protein repeat signature (sequence classifier) from the InterPro database.
beta12orEarlier
@@ -8575,7 +8573,7 @@
- DEP_Protein site signature
+ Protein site signature
1.5
true
@@ -9156,7 +9154,7 @@
- DEP_Sequence-profile alignment (HMM)
+ Sequence-profile alignment (HMM)
Alignment of molecular sequence(s) to a hidden Markov model(s).
true
@@ -9171,7 +9169,7 @@
- DEP_Sequence-profile alignment (fingerprint)
+ Sequence-profile alignment (fingerprint)
true
beta12orEarlier
@@ -9255,7 +9253,7 @@
- DEP_Phylogenetic report
+ Phylogenetic report
true
This is a broad data type and is used for example for reports on confidence, shape or stratigraphic (age) data derived from phylogenetic tree analysis.
@@ -9578,13 +9576,13 @@
-
+
-
+
3D coordinate and associated data for a carbohydrate (3D) structure.
@@ -9702,7 +9700,7 @@
- DEP_Protein structure (all atoms)
+ Protein structure (all atoms)
3D coordinate and associated data for a protein tertiary (3D) structure (all atoms).
true
@@ -9717,7 +9715,7 @@
- DEP_Protein structure (C-alpha atoms)
+ Protein structure (C-alpha atoms)
1.5
beta12orEarlier
@@ -9887,7 +9885,7 @@
- DEP_Structure alignment (protein all atoms)
+ Structure alignment (protein all atoms)
true
beta12orEarlier
@@ -9902,7 +9900,7 @@
- DEP_Structure alignment (protein C-alpha atoms)
+ Structure alignment (protein C-alpha atoms)
beta12orEarlier
true
@@ -10221,7 +10219,7 @@
- DEP_Enzyme report
+ Enzyme report
An informative report on a specific enzyme.
Enzyme report
@@ -10238,7 +10236,7 @@
- DEP_Restriction enzyme report
+ Restriction enzyme report
true
Restriction enzyme report
@@ -10722,7 +10720,7 @@
- DEP_DEP_CATH node
+ CATH node
CATH classification node report
true
@@ -10739,7 +10737,7 @@
- DEP_DEP_SCOP node
+ SCOP node
beta12orEarlier
1.5
@@ -10769,7 +10767,7 @@
- DEP_CATH class
+ CATH class
true
Information on a protein 'class' node from the CATH database.
@@ -10784,7 +10782,7 @@
- DEP_CATH architecture
+ CATH architecture
true
Information on a protein 'architecture' node from the CATH database.
@@ -10799,7 +10797,7 @@
- DEP_CATH topology
+ CATH topology
beta12orEarlier
Information on a protein 'topology' node from the CATH database.
@@ -10814,7 +10812,7 @@
- DEP_CATH homologous superfamily
+ CATH homologous superfamily
Information on a protein 'homologous superfamily' node from the CATH database.
beta12orEarlier
@@ -10829,7 +10827,7 @@
- DEP_CATH structurally similar group
+ CATH structurally similar group
Information on a protein 'structurally similar group' node from the CATH database.
beta12orEarlier
@@ -10844,7 +10842,7 @@
- DEP_CATH functional category
+ CATH functional category
beta12orEarlier
1.5
@@ -11465,7 +11463,7 @@
- DEP_MIRIAM datatype
+ MIRIAM datatype
1.5
true
@@ -11527,7 +11525,7 @@
- DEP_Database version information
+ Database version information
beta12orEarlier
Information on a database (or ontology) version, for example name, version number and release date.
@@ -11543,7 +11541,7 @@
- DEP_Tool version information
+ Tool version information
1.5
true
@@ -11603,7 +11601,7 @@
- DEP_Job status
+ Job status
Values for EBI services are 'DONE' (job has finished and the results can then be retrieved), 'ERROR' (the job failed or no results where found), 'NOT_FOUND' (the job id is no longer available; job results might be deleted, 'PENDING' (the job is in a queue waiting processing), 'RUNNING' (the job is currently being processed).
true
@@ -11633,7 +11631,7 @@
- DEP_Job type
+ Job type
A label (text token) describing the type of job, for example interactive or non-interactive.
beta12orEarlier
@@ -11648,7 +11646,7 @@
- DEP_Tool log
+ Tool log
beta12orEarlier
true
@@ -11877,7 +11875,7 @@
- DEP_Number of iterations
+ Number of iterations
beta12orEarlier
true
@@ -11892,7 +11890,7 @@
- DEP_Number of output entities
+ Number of output entities
true
beta12orEarlier
@@ -12303,7 +12301,7 @@
- DEP_Ontology relation type
+ Ontology relation type
A relation type defined in an ontology.
true
@@ -13276,7 +13274,7 @@
- DEP_Map type
+ Map type
beta12orEarlier
true
@@ -14109,7 +14107,7 @@
- DEP_Sequence mask parameter
+ Sequence mask parameter
Data used to replace (mask) characters in a molecular sequence.
true
@@ -14186,7 +14184,7 @@
- DEP_Genome version information
+ Genome version information
1.5
Information on a genome version.
@@ -14367,7 +14365,7 @@
- DEP_Search parameter
+ Search parameter
Some simple value controlling a search operation, typically a search of a database.
true
@@ -14396,7 +14394,7 @@
- DEP_Secondary structure
+ Secondary structure
The secondary structure assignment (predicted or real) of a nucleic acid or protein.
beta12orEarlier
@@ -14518,7 +14516,7 @@
- DEP_Database entry version information
+ Database entry version information
Information on a database (or ontology) entry version, such as name (or other identifier) or parent database, unique identifier of entry, data, author and so on.
1.5
@@ -14623,7 +14621,7 @@
- DEP_Type
+ Type
true
beta12orEarlier
@@ -14825,13 +14823,13 @@
-
+
-
+
beta12orEarlier
@@ -15034,7 +15032,7 @@
- DEP_Sequence profile type
+ Sequence profile type
beta12orEarlier
A label (text token) describing a type of sequence profile such as frequency matrix, Gribskov profile, hidden Markov model etc.
@@ -15094,7 +15092,7 @@
- DEP_Results sort order
+ Results sort order
A control of the order of data that is output, for example the order of sequences in an alignment.
1.5
@@ -15183,7 +15181,7 @@
- DEP_Window step size
+ Window step size
Size of the incremental 'step' a sequence window is moved over a sequence.
true
@@ -15228,7 +15226,7 @@
- DEP_Sequence offset
+ Sequence offset
An offset for a single-point sequence position.
1.5
@@ -15243,7 +15241,7 @@
- DEP_Threshold
+ Threshold
A value that serves as a threshold for a tool (usually to control scoring or output).
true
@@ -15320,7 +15318,7 @@
- DEP_Rendering parameter
+ Rendering parameter
Graphical parameter
Graphics parameter
@@ -15353,7 +15351,7 @@
- DEP_Date
+ Date
true
beta12orEarlier
@@ -15517,7 +15515,7 @@
- DEP_Nucleic acid features (siRNA)
+ Nucleic acid features (siRNA)
A report on siRNA duplexes in mRNA.
beta12orEarlier
@@ -15670,7 +15668,7 @@
- DEP_Error
+ Error
true
1.5
@@ -15850,7 +15848,7 @@
- DEP_Server metadata
+ Server metadata
true
1.5
@@ -15978,7 +15976,7 @@
- DEP_Sequence set (bootstrapped)
+ Sequence set (bootstrapped)
A collection of sequences output from a bootstrapping (resampling) procedure.
true
@@ -16009,7 +16007,7 @@
- DEP_Schema
+ Schema
1.5
A data schema for organising or transforming data of some type.
@@ -16024,7 +16022,7 @@
- DEP_DTD
+ DTD
1.5
beta12orEarlier
@@ -16039,7 +16037,7 @@
- DEP_XML Schema
+ XML Schema
1.5
true
@@ -16055,7 +16053,7 @@
- DEP_Relax-NG schema
+ Relax-NG schema
true
A relax-NG schema.
@@ -16070,7 +16068,7 @@
- DEP_XSLT stylesheet
+ XSLT stylesheet
true
An XSLT stylesheet.
@@ -16928,7 +16926,7 @@
- DEP_Protein signature type
+ Protein signature type
1.5
A label (text token) describing a type of protein family signature (sequence classifier) from the InterPro database.
@@ -16943,7 +16941,7 @@
- DEP_Domain-nucleic acid interaction report
+ Domain-nucleic acid interaction report
beta12orEarlier
An informative report on protein domain-DNA/RNA interaction(s).
@@ -17588,7 +17586,7 @@
- DEP_Protein-drug interaction report
+ Protein-drug interaction report
beta12orEarlier
1.5
@@ -17727,7 +17725,7 @@
- DEP_Molecule report
+ Molecule report
true
1.5
@@ -17981,7 +17979,7 @@
- DEP_Expressed gene list
+ Expressed gene list
A simple summary of expressed genes.
Gene annotation (expressed gene list)
@@ -19265,13 +19263,13 @@
-
+
-
+
Identifier of a carbohydrate.
@@ -20177,7 +20175,7 @@
- DEP_Embryo report
+ Embryo report
1.5
beta12orEarlier
@@ -20785,7 +20783,7 @@
- DEP_Term ID list
+ Term ID list
1.5
The concepts are typically provided as a persistent identifier or some other link the source ontologies. Evidence of the validity of the annotation might be included.
@@ -21633,7 +21631,7 @@
- DEP_Article metadata
+ Article metadata
1.5
Bibliographic data concerning scientific article(s).
@@ -21804,7 +21802,7 @@
- DEP_DRCAT resource
+ DRCAT resource
true
beta12orEarlier
@@ -21876,7 +21874,7 @@
- DEP_Secondary structure report
+ Secondary structure report
1.5
An informative report on general information, properties or features of one or more molecular secondary structures.
@@ -21907,7 +21905,7 @@
- DEP_RNA features report
+ RNA features report
Nucleic acid features (RNA features)
RNA features
@@ -22500,7 +22498,7 @@
- DEP_Article report
+ Article report
true
Data derived from the analysis of a scientific text such as a full text article from a scientific journal.
@@ -22657,7 +22655,7 @@
- DEP_Microarray image
+ Microarray image
true
An image from a microarray experiment which (typically) allows a visualisation of probe hybridisation and gene-expression data.
@@ -22735,7 +22733,7 @@
- DEP_Workflow
+ Workflow
A computational workflow.
1.5
@@ -22976,7 +22974,7 @@
- DEP_Classification report
+ Classification report
1.5
A report on a classification of molecular sequences, structures or other entities.
@@ -23207,7 +23205,7 @@
- DEP_Core data
+ Core data
beta13
true
@@ -23317,7 +23315,7 @@
- DEP_Protein domain classification node
+ Protein domain classification node
1.5
true
@@ -23379,7 +23377,7 @@
- DEP_Geotemporal metadata
+ Geotemporal metadata
Basic information concerning geographical location or time.
true
@@ -23584,7 +23582,7 @@
- DEP_Sequence features (compositionally-biased regions)
+ Sequence features (compositionally-biased regions)
A report of regions in a molecular sequence that are biased to certain characters.
true
@@ -23613,7 +23611,7 @@
- DEP_Nucleic acid features (difference and change)
+ Nucleic acid features (difference and change)
true
1.5
@@ -23751,7 +23749,7 @@
- DEP_Nucleic acid features (d-loop)
+ Nucleic acid features (d-loop)
A displacement loop is a region of mitochondrial DNA in which one of the strands is displaced by an RNA molecule.
A report on displacement loops in a mitochondrial DNA sequence.
@@ -23767,7 +23765,7 @@
- DEP_Nucleic acid features (stem loop)
+ Nucleic acid features (stem loop)
A stem loop is a hairpin structure; a double-helical structure formed when two complementary regions of a single strand of RNA or DNA molecule form base-pairs.
1.5
@@ -23844,7 +23842,7 @@
- DEP_Transcriptional features (report)
+ Transcriptional features (report)
beta13
Features concerning transcription of DNA into RNA including the regulation of transcription.
@@ -23876,7 +23874,7 @@
- DEP_Nucleic acid features (immunoglobulin gene structure)
+ Nucleic acid features (immunoglobulin gene structure)
A report on predicted or actual immunoglobulin gene structure including constant, switch and variable regions and diversity, joining and variable segments.
1.5
@@ -23891,7 +23889,7 @@
- DEP_SCOP class
+ SCOP class
Information on a 'class' node from the SCOP database.
true
@@ -23906,7 +23904,7 @@
- DEP_SCOP fold
+ SCOP fold
true
1.5
@@ -23921,7 +23919,7 @@
- DEP_SCOP superfamily
+ SCOP superfamily
true
1.5
@@ -23936,7 +23934,7 @@
- DEP_SCOP family
+ SCOP family
beta13
Information on a 'family' node from the SCOP database.
@@ -23951,7 +23949,7 @@
- DEP_SCOP protein
+ SCOP protein
1.5
beta13
@@ -23966,7 +23964,7 @@
- DEP_SCOP species
+ SCOP species
Information on a 'species' node from the SCOP database.
beta13
@@ -24217,7 +24215,7 @@
- DEP_Sequence feature type
+ Sequence feature type
1.5
1.3
@@ -24232,7 +24230,7 @@
- DEP_Gene homology (report)
+ Gene homology (report)
1.5
An informative report on gene homologues between species.
@@ -27212,46 +27210,46 @@
- BFO 'quality' is narrower in the sense that it is a 'dependent_continuant' (snap:DependentContinuant), and broader in the sense that it is any quality not just the data format.
+ GFO 'Perpetuant' is in general broader than format, but it may be seen narrower in the sense of being a concrete individual and in the way of exhibiting presentials.
-
-
-
- Data model
- A defined data format has its implicit or explicit data model, and EDAM does not distinguish the two. Some data models however do not have any standard way of serialisation into an exchange format, and those are thus not considered formats in EDAM. (Remark: even broader - or closely related - term to 'Data model' would be an 'Information model'.)
-
-
+
- GFO 'Perpetuant' is in general broader than format, but it may be seen narrower in the sense of being a concrete individual and in the way of exhibiting presentials.
+ Compression and encoding' defines additional 'formatting' and/or encoding on top of the primary format.
+
-
- Format can be a quality of a data record.
+ Closely related concept focusing on the specification of a data format.
+
-
- File format denotes only formats of a computer file, but the same formats apply also to data blobs or exchanged messages.
File format
+ File format denotes only formats of a computer file, but the same formats apply also to data blobs or exchanged messages.
- Closely related concept focusing on the specification of a data format.
+ Data model
+ A defined data format has its implicit or explicit data model, and EDAM does not distinguish the two. Some data models however do not have any standard way of serialisation into an exchange format, and those are thus not considered formats in EDAM. (Remark: even broader - or closely related - term to 'Data model' would be an 'Information model'.)
+
+
+
+
+ Format can be a quality of a data record.
-
+
- Compression and encoding' defines additional 'formatting' and/or encoding on top of the primary format.
+ BFO 'quality' is narrower in the sense that it is a 'dependent_continuant' (snap:DependentContinuant), and broader in the sense that it is any quality not just the data format.
-
+
@@ -30137,15 +30135,15 @@
- Tabular format
- Many textual formats used in bioinformatics are tabular (tab-separated values, TSV). Typically with an additional header in their own format.
+ fileext.com synonyms are in general narrower in the sense of being defined only as file formats, as opposed to data formats.
+
- fileext.com synonyms are in general narrower in the sense of being defined only as file formats, as opposed to data formats.
+ Tabular format
+ Many textual formats used in bioinformatics are tabular (tab-separated values, TSV). Typically with an additional header in their own format.
-
@@ -30280,7 +30278,7 @@
-
+
@@ -30292,7 +30290,7 @@
-
+
BioXSD XML format of basic bioinformatics types of data (sequence records, alignments, feature records, references to resources, and more).
@@ -32256,70 +32254,70 @@
+ However, one may think that an operation is not a process.
+
+
+
+
+
However, operation is not a GFO 'Concept' present only in someone's mind.
- BFO 'function' is narrower in the sense that it is a 'realizable_entity' (snap:RealizableEntity) and a 'dependent_continuant' (snap:DependentContinuant), and broader in the sense that it does not need to have input(s) and output(s).
+ Process can have a function (as its quality/attribute), and can also perform an operation with inputs and outputs.
+ Process
-
- However, one may think that an operation is not a process.
+ BFO 'function' is narrower in the sense that it is a 'realizable_entity' (snap:RealizableEntity) and a 'dependent_continuant' (snap:DependentContinuant), and broader in the sense that it does not need to have input(s) and output(s).
-
+
- Function
- Operation is a function that is computational. It typically has input(s) and output(s), which are always data.
-
-
-
-
- GFO 'Perpetuant' is in general broader than operation, but it may be seen narrower in the sense of being a concrete individual and exhibiting presentials.
+ Function, including an operation, can have a role of a quality/property in semantic annotation of e.g. a computational tool.
-
+
- Process can have a function (as its quality/attribute), and can also perform an operation with inputs and outputs.
- Process
+ However, one may think that an operation is not a process and not a physical entity.
+
- Function, including an operation, can have a role of a quality/property in semantic annotation of e.g. a computational tool.
+ Operation is a function that is computational. It typically has input(s) and output(s), which are always data. In addition, one may think of 'biotop:Disposition' (parent of 'biotop:Function') being also a 'biotop:Quality'.
-
-
+
+
- Process can have a function (as its quality/property), and can also have (perform) an operation with inputs and outputs.
+ Method may in addition focus on how to achieve the result, not just on what to achieve as with operation.
+
-
- Function, including an operation, can be a quality/property of e.g. a computational tool.
+ Process can have a function (as its quality/property), and can also have (perform) an operation with inputs and outputs.
-
+
- Computational tool provides one or more operations.
Computational tool
+ Computational tool provides one or more operations.
- However, one may think that an operation is not a process and not a physical entity.
+ Function
+ Operation is a function that is computational. It typically has input(s) and output(s), which are always data.
-
-
+
Process can have a function (as its quality/property), and can also have (perform) an operation with inputs and outputs.
@@ -32328,22 +32326,22 @@
- Method may in addition focus on how to achieve the result, not just on what to achieve as with operation.
+ GFO 'Perpetuant' is in general broader than operation, but it may be seen narrower in the sense of being a concrete individual and exhibiting presentials.
-
+
Process can have a function (as its quality/property), and can also have (perform) an operation with inputs and outputs.
-
+
- Operation is a function that is computational. It typically has input(s) and output(s), which are always data. In addition, one may think of 'biotop:Disposition' (parent of 'biotop:Function') being also a 'biotop:Quality'.
+ Function, including an operation, can be a quality/property of e.g. a computational tool.
-
-
+
+
@@ -32351,22 +32349,25 @@
- Search and retrieval
+ Query and retrieval
-
-
+
+
-
-
+
+
+ Search
Database retrieval
Search or query a data resource and retrieve entries and / or annotation.
+ Retrieval
+ Query
beta12orEarlier
@@ -32394,7 +32395,7 @@
Annotation
-
+
@@ -32420,8 +32421,8 @@
- Data indexing
-
+ Indexing
+
@@ -32431,6 +32432,7 @@
Database indexing
Generate an index of (typically a file of) biological data.
beta12orEarlier
+ Data indexing
@@ -32442,25 +32444,14 @@
Data index analysis
-
-
-
-
-
-
-
-
-
-
-
-
-
+
beta12orEarlier
Analyse an index of biological data.
Database index analysis
-
-
-
+
+ 1.6
+ true
+
@@ -32484,7 +32475,8 @@
Sequence generation
-
+
+
Generate a molecular sequence by some means.
beta12orEarlier
@@ -32498,7 +32490,7 @@
Sequence editing
-
+
beta12orEarlier
Edit or change a molecular sequence, either randomly or specifically.
@@ -32529,6 +32521,7 @@
Sequence conversion
+
beta12orEarlier
Convert a molecular sequence from one type to another.
@@ -32571,14 +32564,14 @@
-
-
+
+
-
-
+
+
beta12orEarlier
@@ -32595,16 +32588,17 @@
Sequence composition calculation
+
-
-
+
+
-
-
+
+
Calculate character or word composition or frequency of a molecular sequence.
@@ -32642,7 +32636,12 @@
Sequence motif discovery
-
+
+
+
+
+
+
@@ -32665,17 +32664,16 @@
Sequence motif recognition
-
-
-
+
+
-
-
+
+
Sequence motif detection
@@ -32694,10 +32692,15 @@
Sequence motif comparison
-
+
+
+
+
+
+
@@ -32731,8 +32734,8 @@
Conserved transcription regulatory sequence identification
-
+
@@ -32798,7 +32801,8 @@
Protein structural motif recognition
-
+
+
@@ -32826,17 +32830,18 @@
Protein domain recognition
-
+
+
-
-
+
+
-
-
+
+
Identify structural domains in a protein structure from first principles (for example calculations on structural compactness).
@@ -32922,6 +32927,7 @@
Protein property calculation
+
@@ -32930,14 +32936,14 @@
-
-
+
+
-
-
+
+
Protein property rendering
@@ -32959,14 +32965,14 @@
-
-
+
+
-
-
+
+
Predict antigenicity, allergenicity / immunogenicity, allergic cross-reactivity etc of peptides and proteins.
@@ -32982,7 +32988,7 @@
- Feature prediction
+ Sequence feature detection
@@ -32999,8 +33005,9 @@
SO:0000110
beta12orEarlier
+ Sequence feature recognition
Predict, recognise and identify positional features in molecular sequences such as key functional sites or regions.
- Sequence feature detection
+ Sequence feature prediction
@@ -33027,30 +33034,13 @@
Feature table query
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+
Query the features (in a feature table) of molecular sequence(s).
beta12orEarlier
-
-
-
+
+ 1.6
+ true
+
@@ -33058,9 +33048,9 @@
- Feature comparison
+ Sequence feature comparison
+
-
@@ -33069,13 +33059,19 @@
+
+
+
+
+
+
Feature table comparison
+ Feature comparison
Compare the feature tables of two or more molecular sequences.
- Sequence feature comparison
beta12orEarlier
@@ -33103,8 +33099,13 @@
Sequence alignment analysis
-
-
+
+
+
+
+
+
+
@@ -33113,8 +33114,8 @@
-
-
+
+
beta12orEarlier
@@ -33147,6 +33148,7 @@
Sequence alignment conversion
+
Convert a molecular sequence alignment from one type to another (for example amino acid to coding nucleotide sequence).
beta12orEarlier
@@ -33176,6 +33178,7 @@
Nucleic acid property calculation
+
@@ -33252,25 +33255,25 @@
Protein secondary structure prediction
-
-
+
+
-
-
+
+
-
-
+
+
-
+
beta12orEarlier
@@ -33333,14 +33336,14 @@
-
-
+
+
-
-
+
+
Use this (or child) concept for analysis of transmembrane domains (buried and exposed faces), transmembrane helices, helix topology, orientation, inter-helical contacts, membrane dipping (re-entrant) loops and other secondary structure etc. Methods might use pattern discovery, hidden Markov models, sequence alignment, structural profiles, amino acid property analysis, comparison to known domains or some combination (hybrid methods).
@@ -33358,17 +33361,17 @@
Structure prediction
-
+
-
-
+
+
-
-
+
+
beta12orEarlier
@@ -33432,8 +33435,8 @@
Protein-protein interaction prediction (from protein sequence)
+
-
Identify or predict protein-protein interactions, interfaces, binding sites etc in protein sequences.
beta12orEarlier
@@ -33447,8 +33450,9 @@
Protein-protein interaction prediction (from protein structure)
+
-
+
Identify or predict protein-protein interactions, interfaces, binding sites etc in protein structures.
beta12orEarlier
@@ -33462,7 +33466,6 @@
Protein interaction network analysis
-
@@ -33473,6 +33476,12 @@
+
+
+
+
+
+
@@ -33511,23 +33520,24 @@
RNA secondary structure prediction
+
-
-
+
+
-
-
+
+
- Methods might use RNA motifs, predicted intermolecular contacts, or RNA sequence-structure compatibility (inverse RNA folding).
beta12orEarlier
Predict RNA secondary structure (for example knots, pseudoknots, alternative structures etc).
+ Methods might use RNA motifs, predicted intermolecular contacts, or RNA sequence-structure compatibility (inverse RNA folding).
@@ -33538,19 +33548,20 @@
- Nucleic acid folding analysis
+ Nucleic acid folding prediction
-
+
+
-
-
+
+
-
-
+
+
Nucleic acid folding
@@ -33601,6 +33612,7 @@
Genetic mapping
+
@@ -33608,6 +33620,7 @@
Functional mapping
+ Genetic map construction
Generate a genetic (linkage) map of a DNA sequence (typically a chromosome) showing the relative positions of genetic markers based on estimation of non-physical distances.
Mapping involves ordering genetic loci along a chromosome and estimating the physical distance between loci. A genetic map shows the relative (not physical) position of known genes and genetic markers.
Genetic map generation
@@ -33653,12 +33666,14 @@
Codon usage table generation
+
+ Codon usage table construction
beta12orEarlier
Calculate codon usage statistics and create a codon usage table.
@@ -33687,7 +33702,7 @@
Codon usage analysis
-
+
@@ -33696,14 +33711,14 @@
-
-
+
+
-
+
@@ -33714,8 +33729,8 @@
-
-
+
+
synon: Codon usage table analysis
@@ -33734,16 +33749,17 @@
Base position variability plotting
+
-
-
+
+
-
-
+
+
beta12orEarlier
@@ -33774,6 +33790,7 @@
Sequence distance matrix generation
+
@@ -33787,6 +33804,7 @@
Calculate a sequence distance matrix or otherwise estimate genetic distances between molecular sequences.
+ Sequence distance matrix construction
beta12orEarlier
Phylogenetic distance matrix generation
@@ -33800,19 +33818,13 @@
Sequence redundancy removal
-
+
-
-
-
-
-
-
Compare two or more molecular sequences, identify and remove redundant sequences based on some criteria.
beta12orEarlier
@@ -33827,8 +33839,14 @@
Sequence clustering
-
-
+
+
+
+
+
+
+
+
@@ -33838,6 +33856,7 @@
Sequence cluster generation
Build clusters of similar sequences, typically using scores from pair-wise alignment or other comparison of the sequences.
beta12orEarlier
+ Sequence cluster construction
The clusters may be output or used internally for some other purpose.
@@ -33849,27 +33868,33 @@
- Sequence alignment construction
+ Sequence alignment generation
+
-
+
+
+
+
+
+
-
-
+
+
Sequence alignment computation
Sequence alignment
- Sequence alignment generation
Align (identify equivalent sites within) molecular sequences.
beta12orEarlier
+ Sequence alignment construction
@@ -33882,6 +33907,7 @@
Hybrid sequence alignment construction
+ Hybrid sequence alignment generation
Align two or more molecular sequences of different types (for example genomic DNA to EST, cDNA or mRNA).
beta12orEarlier
beta13
@@ -33896,7 +33922,7 @@
- Structure-based sequence alignment construction
+ Structure-based sequence alignment
@@ -33905,8 +33931,12 @@
Align molecular sequences using sequence and structural information.
- beta12orEarlier
+ Structure-based sequence alignment generation
Structure-based sequence alignment
+ Sequence alignment (structure-based)
+ beta12orEarlier
+ Structure-based sequence alignment construction
+ Sequence alignment generation (structure-based)
@@ -33917,10 +33947,10 @@
- Structure alignment construction
+ Structure alignment generation
+
-
@@ -33928,8 +33958,11 @@
Structure alignment
- Align (superimpose) molecular tertiary structures.
+ Multiple structure alignment generation
+ Multiple structure alignment construction
beta12orEarlier
+ Structure alignment construction
+ Align (superimpose) molecular tertiary structures.
@@ -33941,8 +33974,14 @@
Sequence profile generation
-
-
+
+
+
+
+
+
+
+
@@ -33955,8 +33994,9 @@
- Generate some type of sequence profile (for example a hidden Markov model) from a sequence alignment.
beta12orEarlier
+ Sequence profile construction
+ Generate some type of sequence profile (for example a hidden Markov model) from a sequence alignment.
@@ -33967,14 +34007,13 @@
- Structural (3D) profile generation
-
-
-
+ 3D profile generation
+
+
-
-
+
+
@@ -33985,11 +34024,12 @@
-
-
+
+
beta12orEarlier
+ Structural profile construction
Generate some type of structural (3D) profile or template from a structure or structure alignment.
Structural profile generation
@@ -34002,9 +34042,8 @@
- Sequence profile alignment construction
-
-
+ Profile-to-profile alignment
+
@@ -34017,7 +34056,15 @@
+
+
+
+
+
+
Align sequence profiles (representing sequence alignments).
+ Sequence profile alignment generation
+ Sequence profile alignment construction
See also 'Sequence alignment comparison'.
beta12orEarlier
Sequence profile alignment
@@ -34031,13 +34078,13 @@
- Structural (3D) profile alignment construction
-
+ 3D profile-to-3D profile alignment
+
-
-
+
+
@@ -34048,13 +34095,18 @@
-
-
+
+
- Structural (3D) profile alignment
Align structural (3D) profiles or templates (representing structures or structure alignments).
+ Structural profile alignment construction
+ Structural profile alignment generation
Structural profile alignment
+ Structural profile alignment construction (multiple)
+ Multiple 3D profile alignment construction
+ 3D profile alignment
+ 3D profile alignment (multiple)
beta12orEarlier
@@ -34066,10 +34118,14 @@
- Sequence-profile alignment construction
-
-
-
+ Sequence-to-profile alignment
+
+
+
+
+
+
+
@@ -34078,14 +34134,16 @@
-
-
+
+
A sequence profile typically represents a sequence alignment. Methods might perform one-to-one, one-to-many or many-to-many comparisons.
Sequence-profile alignment
Align molecular sequence(s) to sequence profile(s).
beta12orEarlier
+ Sequence-profile alignment generation
+ Sequence-profile alignment construction
@@ -34096,25 +34154,26 @@
- Sequence-3D profile alignment construction
+ Sequence-to-3D-profile alignment
-
-
-
+
+
-
-
+
+
Sequence-3D profile alignment
Methods might perform one-to-one, one-to-many or many-to-many comparisons.
+ Sequence-3D profile alignment generation
Align molecular sequence(s) to structural (3D) profile(s) or template(s) (representing a structure or structure alignment).
+ Sequence-3D profile alignment construction
beta12orEarlier
@@ -34137,14 +34196,14 @@
-
-
+
+
-
-
+
+
Sequence-structure alignment
@@ -34162,9 +34221,10 @@
Protein fold recognition
-
-
+
+
+
@@ -34192,7 +34252,7 @@
- Data retrieval (metadata and documentation)
+ Metadata retrieval
@@ -34242,17 +34302,17 @@
Text mining
-
+
-
-
+
+
-
-
+
+
@@ -34304,14 +34364,14 @@
-
-
+
+
-
-
+
+
Design or predict oligonucleotide primers for PCR and DNA amplification etc.
@@ -34330,29 +34390,29 @@
Microarray probe design
-
+
-
+
-
-
+
+
-
-
+
+
-
+
Microarray probe prediction
@@ -34369,9 +34429,8 @@
Sequence assembly
-
-
+
@@ -34398,17 +34457,17 @@
Microarray data standardization and normalization
-
+
-
+
-
+
@@ -34442,6 +34501,7 @@
Gene expression profile clustering
+
@@ -34460,18 +34520,21 @@
- Gene expression profile generation
-
+ Gene expression profiling
+
+
- Gene expression profiling
+ Gene expression profile generation
beta12orEarlier
- Expression profiling
Generate a gene expression profile or pattern, for example from microarray data.
+ Functional profiling
+ Gene expression profile construction
+ Expression profiling
@@ -34483,7 +34546,7 @@
Gene expression profile comparison
-
+
@@ -34551,11 +34614,16 @@
Protein secondary structure assignment
-
+
+
+
+
+
+
@@ -34578,11 +34646,12 @@
Protein structure assignment
-
+
+
-
-
+
+
@@ -34591,6 +34660,12 @@
+
+
+
+
+
+
Assign a protein tertiary structure (3D coordinates) from raw experimental data.
beta12orEarlier
@@ -34603,31 +34678,31 @@
- Protein model evaluation
+ Protein model validation
-
+
-
+
-
+
-
+
@@ -34651,12 +34726,11 @@
Protein model refinement
-
The PDB file format has had difficulties, inconsistencies and errors. Corrections can include identifying a meaningful sequence, removal of alternate atoms, correction of nomenclature problems, removal of incomplete residues and spurious waters, addition or removal of water, modelling of missing side chains, optimisation of cysteine bonds, regularisation of bond lengths, bond angles and planarities etc.
+ Refine (after evaluation) a model of protein structure to reduce steric clashes, volume irregularities etc.
beta12orEarlier
WHATIF: CorrectedPDBasXML
- Refine (after evlauation) a model of protein structure to reduce steric clashes, volume irregularities etc.
@@ -34667,22 +34741,21 @@
- Phylogenetic tree construction
+ Phylogenetic tree generation
-
+
-
-
+
+
-
-
+
+
- Phylogenetic tree generation
beta12orEarlier
Construct a phylogenetic tree.
Phylogenetic trees are usually constructed from a set of sequences from which an alignment (or data matrix) is calculated.
@@ -34701,14 +34774,14 @@
-
-
+
+
-
-
+
+
Analyse an existing phylogenetic tree or trees, typically to detect features or make predictions.
@@ -34724,8 +34797,8 @@
Phylogenetic tree comparison
-
+
For example, to produce a consensus tree, subtrees, supertrees, calculate distances between trees or test topological similarity between trees (e.g. a congruence index) etc.
Compare two or more phylogenetic trees.
beta12orEarlier
@@ -34744,13 +34817,13 @@
-
+
-
+
@@ -34818,6 +34891,7 @@
Protein SNP mapping
+
@@ -34872,6 +34946,7 @@
Immunogen design
+
beta12orEarlier
beta12orEarlier
@@ -34886,19 +34961,18 @@
- Zinc finger protein domain prediction and optimisation
+ Zinc finger prediction
-
-
-
+
+
-
-
+
+
beta12orEarlier
@@ -34939,11 +35013,15 @@
- File format conversion
+ Formatting
+ File format conversion
File reformatting
+ File formatting
+ Format conversion
Reformat a file of data (or equivalent entity in memory).
beta12orEarlier
+ Reformatting
@@ -34954,10 +35032,11 @@
- File validation
+ Format validation
beta12orEarlier
+ File format validation
Test and validate the format and content of a data file.
@@ -34969,28 +35048,28 @@
- Plotting and rendering
+ Visualisation
-
-
+
+
-
-
+
+
-
-
+
+
+ Rendering
Visualise, plot or render (graphically) biomolecular data such as molecular sequences or structures.
- Visualisation
beta12orEarlier
@@ -35032,17 +35111,16 @@
Structure database search
-
-
-
+
+
-
-
+
+
Search a tertiary structure database by sequence and/or structure comparison and retrieve structures and associated data.
@@ -35059,17 +35137,17 @@
Protein secondary database search
-
+
-
-
+
+
-
-
+
+
Sequence profile database search
@@ -35090,7 +35168,6 @@
Motif database search
-
@@ -35140,12 +35217,13 @@
Sequence retrieval (by code)
-
+
beta12orEarlier
Query a database and retrieve sequences with a given entry code or accession number.
-
-
-
+
+ 1.6
+ true
+
@@ -35154,12 +35232,13 @@
Sequence retrieval (by keyword)
-
+
beta12orEarlier
Query a database and retrieve sequences containing a given keyword.
-
-
-
+
+ 1.6
+ true
+
@@ -35169,8 +35248,6 @@
Sequence database search (by sequence)
-
-
Search a sequence database and retrieve sequences that are similar to a query sequence.
beta12orEarlier
Sequence similarity search
@@ -35206,24 +35283,13 @@
Sequence database search (by amino acid composition)
-
-
-
-
-
-
-
-
-
-
-
-
-
+
beta12orEarlier
Search a sequence database and retrieve sequences of a given amino acid composition.
-
-
-
+
+ 1.6
+ true
+
@@ -35231,10 +35297,10 @@
- Sequence database search (by physicochemical property)
+ Sequence database search (by property)
beta12orEarlier
- Search a sequence database and retrieve sequences with a specified physicochemical property.
+ Search a sequence database and retrieve sequences with a specified property, typically a physicochemical or compositional property.
@@ -35246,15 +35312,15 @@
Sequence database search (by sequence using word-based methods)
-
-
+
Search a sequence database and retrieve sequences that are similar to a query sequence using a word-based method.
Sequence similarity search (word-based methods)
Word-based methods (for example BLAST, gapped BLAST, MEGABLAST, WU-BLAST etc.) are usually quicker than alignment-based methods. They may or may not handle gaps.
beta12orEarlier
-
-
-
+
+ 1.6
+ true
+
@@ -35263,15 +35329,15 @@
Sequence database search (by sequence using profile-based methods)
-
-
+
This includes tools based on PSI-BLAST.
beta12orEarlier
Search a sequence database and retrieve sequences that are similar to a query sequence using a sequence profile-based method, or with a supplied profile as query.
Sequence similarity search (profile-based methods)
-
-
-
+
+ 1.6
+ true
+
@@ -35280,21 +35346,15 @@
Sequence database search (by sequence using local alignment-based methods)
-
-
-
-
-
-
-
-
+
This includes tools based on the Smith-Waterman algorithm or FASTA.
Sequence similarity search (local alignment-based methods)
beta12orEarlier
Search a sequence database for sequences that are similar to a query sequence using a local alignment-based method.
-
-
-
+
+ 1.6
+ true
+
@@ -35303,21 +35363,15 @@
Sequence database search (by sequence using global alignment-based methods)
-
-
-
-
-
-
-
-
+
beta12orEarlier
Sequence similarity search (global alignment-based methods)
Search sequence(s) or a sequence database for sequences that are similar to a query sequence using a global alignment-based method.
This includes tools based on the Needleman and Wunsch algorithm.
-
-
-
+
+ 1.6
+ true
+
@@ -35326,20 +35380,15 @@
Sequence database search (by sequence for primer sequences)
-
-
-
-
-
-
-
+
Sequence similarity search (primer sequences)
STSs are genetic markers that are easily detected by the polymerase chain reaction (PCR) using specific primers.
Search a DNA database (for example a database of conserved sequence tags) for matches to Sequence-Tagged Site (STS) primer sequences.
beta12orEarlier
-
-
-
+
+ 1.6
+ true
+
@@ -35348,32 +35397,15 @@
Sequence database search (by molecular weight)
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
- beta12orEarlier
+
Peptide mass fingerprinting
- Search sequence(s) or a sequence database for sequences which match a set of peptide masses, for example a peptide mass fingerprint from mass spectrometry.
+ beta12orEarlier
Protein fingerprinting
-
-
-
+ Search sequence(s) or a sequence database for sequences which match a set of peptide masses, for example a peptide mass fingerprint from mass spectrometry.
+
+ 1.6
+ true
+
@@ -35382,18 +35414,13 @@
Sequence database search (by isoelectric point)
-
-
-
-
-
-
-
+
Search sequence(s) or a sequence database for sequences of a given isoelectric point.
beta12orEarlier
-
-
-
+
+ 1.6
+ true
+
@@ -35402,12 +35429,13 @@
Structure retrieval (by code)
-
+
beta12orEarlier
Query a tertiary structure database and retrieve entries with a given entry code or accession number.
-
-
-
+
+ 1.6
+ true
+
@@ -35416,12 +35444,13 @@
Structure retrieval (by keyword)
-
+
beta12orEarlier
Query a tertiary structure database and retrieve entries containing a given keyword.
-
-
-
+
+ 1.6
+ true
+
@@ -35432,7 +35461,6 @@
Structure database search (by sequence)
-
Search a tertiary structure database and retrieve structures with a sequence similar to a query sequence.
Structure retrieval by sequence
beta12orEarlier
@@ -35541,14 +35569,14 @@
-
-
+
+
-
-
+
+
Generate digest fragments for a nucleotide sequence containing restriction sites.
@@ -36031,21 +36059,21 @@
- Ramachandran plot evaluation
+ Ramachandran plot validation
-
-
+
+
-
-
+
+
- Analyse (typically to validate) a Ramachandran plot of a protein structure.
+ Validate a Ramachandran plot of a protein structure.
beta12orEarlier
@@ -36145,6 +36173,7 @@
Protein titration curve plotting
+
@@ -36239,6 +36268,7 @@
Protein hydrophobic moment plotting
+
@@ -36361,15 +36391,15 @@
Protein feature prediction (from sequence)
-
-
+
Predict, recognise and identify positional features in protein sequences such as functional sites or regions and secondary structure.
Sequence feature detection (protein)
beta12orEarlier
Methods typically involve scanning for known motifs, patterns and regular expressions.
-
-
-
+
+ 1.6
+ true
+
@@ -36377,23 +36407,23 @@
- Nucleic acid feature prediction
-
-
+ Nucleic acid feature detection
-
-
+
+
-
-
+
+
+ Nucleic acid feature prediction
+ Nucleic acid feature recognition
beta12orEarlier
Methods typically involve scanning for known motifs, patterns and regular expressions.
Predict, recognise and identify features in nucleotide sequences such as functional sites or regions, typically by scanning for known motifs, patterns and regular expressions.
@@ -36413,14 +36443,14 @@
-
-
+
+
-
-
+
+
Epitope mapping is commonly done during vaccine design.
@@ -36468,14 +36498,14 @@
-
-
+
+
-
-
+
+
Detect or predict signal peptides and signal peptide cleavage sites in protein sequences.
@@ -36491,12 +36521,13 @@
- Binding site prediction (from sequence)
+ Protein binding site detection
beta12orEarlier
Ligand-binding and active site prediction (from sequence)
Predict catalytic residues, active sites or other ligand-binding sites in protein sequences.
+ Binding site prediction (from sequence)
@@ -36552,14 +36583,14 @@
-
-
+
+
-
-
+
+
Detect or predict cleavage sites (enzymatic or chemical) in protein sequences.
@@ -36632,7 +36663,7 @@
Transposon prediction
-
+
@@ -36652,7 +36683,7 @@
PolyA signal detection
-
+
@@ -36672,7 +36703,7 @@
Quadruplex formation site detection
-
+
@@ -36700,7 +36731,7 @@
CpG island and isochore detection
-
+
@@ -36729,7 +36760,7 @@
Restriction site recognition
-
+
@@ -36761,7 +36792,7 @@
Nucleosome formation or exclusion sequence prediction
-
+
@@ -36781,17 +36812,17 @@
Splice site prediction
-
+
-
-
+
+
-
-
+
+
Methods might require a pre-mRNA or genomic DNA sequence.
@@ -37058,11 +37089,12 @@
- Sequence alignment quality evaluation
+ Sequence alignment validation
beta12orEarlier
Evaluate molecular sequence alignment accuracy.
+ Sequence alignment quality evaluation
Evaluation might be purely sequence-based or use structural information.
@@ -37105,8 +37137,9 @@
- Sequence alignment analysis (chimeric sequence detection)
+ Chimeric sequence detection
+ Sequence alignment analysis (chimeric sequence detection)
Detects chimeric sequences (chimeras) from a sequence alignment.
A chimera includes regions from two or more phylogenetically distinct sequences. They are usually artifacts of PCR and are thought to occur when a prematurely terminated amplicon reanneals to another DNA strand and is subsequently copied to completion in later PCR cycles.
beta12orEarlier
@@ -37120,11 +37153,12 @@
- Sequence alignment analysis (recombination detection)
+ Recombination detection
Tools might use a genetic algorithm, quartet-mapping, bootscanning, graphical methods, random forest model and so on.
Detect recombination (hotspots and coldspots) and identify recombination breakpoints in a sequence alignment.
beta12orEarlier
+ Sequence alignment analysis (recombination detection)
@@ -37135,10 +37169,11 @@
- Sequence alignment analysis (indel detection)
+ Indel detection
Identify insertion, deletion and duplication events from a sequence alignment.
Tools might use a genetic algorithm, quartet-mapping, bootscanning, graphical methods, random forest model and so on.
+ Sequence alignment analysis (indel detection)
beta12orEarlier
@@ -37187,6 +37222,7 @@
Nucleic acid melting profile plotting
+
@@ -37464,14 +37500,14 @@
-
-
+
+
-
-
+
+
G protein-coupled receptor (GPCR) analysis
@@ -37489,13 +37525,13 @@
Protein structure prediction
-
+
-
-
+
+
@@ -37506,8 +37542,8 @@
-
-
+
+
Predict tertiary structure (backbone and side-chain conformation) of protein sequences.
@@ -37525,18 +37561,17 @@
Nucleic acid structure prediction
-
-
-
+
+
-
-
+
+
Methods might identify thermodynamically stable or evolutionarily conserved structures.
@@ -37604,20 +37639,20 @@
-
-
+
+
-
-
+
+
-
+
This includes protein-protein interactions, protein-nucleic acid, protein-ligand binding etc. Methods might predict whether the molecules are likely to bind in vivo, their conformation when bound, the strength of the interaction, possible mutations to achieve bonding and so on.
@@ -37706,7 +37741,6 @@
Structured RNA prediction and optimisation
-
@@ -37735,9 +37769,9 @@
SNP detection
-
-
+
+
@@ -37808,6 +37842,7 @@
beta12orEarlier
Infer haplotypes, either alleles at multiple loci that are transmitted together on the same chromosome, or a set of single nucleotide polymorphisms (SNPs) on a single chromatid that are statistically associated.
Haplotype inference
+ Haplotype map generation
@@ -37863,6 +37898,7 @@
Dotplot plotting
+
@@ -37881,8 +37917,8 @@
- Pairwise sequence alignment construction
-
+ Pairwise sequence alignment
+
@@ -37890,9 +37926,11 @@
beta12orEarlier
- Align exactly two molecular sequences.
+ Pairwise sequence alignment construction
Methods might perform one-to-one, one-to-many or many-to-many comparisons.
Pairwise sequence alignment
+ Align exactly two molecular sequences.
+ Pairwise sequence alignment generation
@@ -37903,12 +37941,14 @@
- Multiple sequence alignment construction
+ Multiple sequence alignment
+ Multiple sequence alignment generation
beta12orEarlier
Multiple sequence alignment
This includes methods that use an existing alignment, for example to incorporate sequences into an alignment, or combine several multiple alignments into a single, improved alignment.
Align two or more molecular sequences.
+ Multiple sequence alignment construction
@@ -37919,16 +37959,19 @@
- Pairwise sequence alignment construction (local)
-
+ Pairwise sequence alignment generation (local)
+
+ Pairwise sequence alignment construction (local)
Local alignment methods identify regions of local similarity.
Local pairwise sequence alignment construction
beta12orEarlier
Pairwise sequence alignment (local)
Locally align exactly two molecular sequences.
-
-
-
+
+
+ 1.6
+ true
+
@@ -37936,16 +37979,19 @@
- Pairwise sequence alignment construction (global)
-
+ Pairwise sequence alignment generation (global)
+
beta12orEarlier
Global alignment methods identify similarity across the entire length of the sequences.
Globally align exactly two molecular sequences.
Pairwise sequence alignment (global)
+ Pairwise sequence alignment construction (global)
Global pairwise sequence alignment construction
-
-
-
+
+
+ 1.6
+ true
+
@@ -37953,9 +37999,12 @@
- Multiple sequence alignment construction (local)
-
+ Local sequence alignment
+
Locally align two or more molecular sequences.
+ Sequence alignment (local)
+ Sequence alignment generation (local)
+ Multiple sequence alignment construction (local)
Local alignment methods identify regions of local similarity.
beta12orEarlier
Local multiple sequence alignment construction
@@ -37970,13 +38019,16 @@
- Multiple sequence alignment construction (global)
-
- beta12orEarlier
+ Global sequence alignment
+
Global alignment methods identify similarity across the entire length of the sequences.
+ Sequence alignment generation (global)
+ Globally align two or more molecular sequences.
+ Multiple sequence alignment construction (global)
+ Sequence alignment (global)
+ beta12orEarlier
Multiple sequence alignment (global)
Global multiple sequence alignment construction
- Globally align two or more molecular sequences.
@@ -37987,12 +38039,15 @@
- Multiple sequence alignment construction (constrained)
-
+ Constrained sequence alignment
+
Constrained multiple sequence alignment construction
Multiple sequence alignment (constrained)
+ Multiple sequence alignment construction (constrained)
+ Sequence alignment generation (constrained)
Align two or more molecular sequences with user-defined constraints.
beta12orEarlier
+ Sequence alignment (constrained)
@@ -38003,12 +38058,15 @@
- Multiple sequence alignment construction (consensus)
-
- Multiple sequence alignment (consensus)
+ Consensus-based sequence alignment
+
Align two or more molecular sequences using multiple methods to achieve higher quality.
- beta12orEarlier
+ Sequence alignment generation (consensus)
Consensus multiple sequence alignment construction
+ Multiple sequence alignment (consensus)
+ Multiple sequence alignment construction (consensus)
+ beta12orEarlier
+ Sequence alignment (consensus)
@@ -38019,19 +38077,22 @@
- Multiple sequence alignment construction (phylogenetic tree-based)
-
+ Tree-based sequence alignment
+
+ Multiple sequence alignment (phylogenetic tree-based)
+ Multiple sequence alignment construction (phylogenetic tree-based)
+ Sequence alignment (phylogenetic tree-based)
+ Align multiple sequences using relative gap costs calculated from neighbors in a supplied phylogenetic tree.
Phylogenetic tree-based multiple sequence alignment construction
beta12orEarlier
This is supposed to give a more biologically meaningful alignment than standard alignments.
- Multiple sequence alignment (phylogenetic tree-based)
- Align multiple sequences using relative gap costs calculated from neighbors in a supplied phylogenetic tree.
+ Sequence alignment generation (phylogenetic tree-based)
@@ -38042,28 +38103,16 @@
- Secondary structure alignment construction
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+ Secondary structure alignment generation
+
Align molecular secondary structure (represented as a 1D string).
- beta12orEarlier
Secondary structure alignment
-
-
-
+ Secondary structure alignment construction
+ beta12orEarlier
+
+ 1.6
+ true
+
@@ -38071,19 +38120,26 @@
- Protein secondary structure alignment construction
-
+ Protein secondary structure alignment generation
+
+
+
+
+
+
+
- Protein secondary structure alignment
Secondary structure alignment (protein)
- beta12orEarlier
Align protein secondary structures.
+ Protein secondary structure alignment
+ beta12orEarlier
+ Protein secondary structure alignment construction
@@ -38094,13 +38150,13 @@
- RNA secondary structure alignment construction
-
+ RNA secondary structure alignment
+
-
-
+
+
@@ -38109,10 +38165,18 @@
+
+
+
+
+
+
beta12orEarlier
Secondary structure alignment (RNA)
+ RNA secondary structure alignment construction
Align RNA secondary structures.
RNA secondary structure alignment
+ RNA secondary structure alignment generation
@@ -38123,9 +38187,10 @@
- Pairwise structure alignment construction
+ Pairwise structure alignment generation
Align (superimpose) exactly two molecular tertiary structures.
+ Pairwise structure alignment construction
Pairwise structure alignment
beta12orEarlier
@@ -38139,14 +38204,15 @@
Multiple structure alignment construction
-
+
beta12orEarlier
Multiple structure alignment
This includes methods that use an existing alignment.
Align (superimpose) two or more molecular tertiary structures.
-
-
-
+
+ 1.6
+ true
+
@@ -38184,16 +38250,19 @@
- Pairwise structure alignment construction (local)
-
+ Pairwise structure alignment generation (local)
+
+ Pairwise structure alignment construction (local)
Local alignment methods identify regions of local similarity, common substructures etc.
Pairwise structure alignment (local)
beta12orEarlier
Local pairwise structure alignment construction
Locally align (superimpose) exactly two molecular tertiary structures.
-
-
-
+
+
+ 1.6
+ true
+
@@ -38201,16 +38270,19 @@
- Pairwise structure alignment construction (global)
-
+ Pairwise structure alignment generation (global)
+
beta12orEarlier
Pairwise structure alignment (global)
Global alignment methods identify similarity across the entire structures.
Globally align (superimpose) exactly two molecular tertiary structures.
Global pairwise structure alignment construction
-
-
-
+ Pairwise structure alignment construction (global)
+
+
+ 1.6
+ true
+
@@ -38218,12 +38290,15 @@
- Multiple structure alignment construction (local)
-
- beta12orEarlier
+ Local structure alignment
+
+ Structure alignment generation (local)
+ Multiple structure alignment construction (local)
Multiple structure alignment (local)
- Local alignment methods identify regions of local similarity, common substructures etc.
Locally align (superimpose) two or more molecular tertiary structures.
+ beta12orEarlier
+ Structure alignment construction (local)
+ Local alignment methods identify regions of local similarity, common substructures etc.
Local multiple structure alignment construction
@@ -38235,13 +38310,16 @@
- Multiple structure alignment construction (global)
-
- beta12orEarlier
- Global multiple structure alignment construction
+ Global structure alignment
+
Globally align (superimpose) two or more molecular tertiary structures.
- Multiple structure alignment (global)
+ Global multiple structure alignment construction
Global alignment methods identify similarity across the entire structures.
+ beta12orEarlier
+ Multiple structure alignment construction (global)
+ Structure alignment generation (global)
+ Multiple structure alignment (global)
+ Structure alignment construction (global)
@@ -38252,13 +38330,16 @@
- Sequence profile alignment construction (pairwise)
+ Profile-to-profile alignment (pairwise)
+ Sequence profile alignment generation (pairwise)
Align exactly two molecular profiles.
- Pairwise sequence profile alignment construction
beta12orEarlier
Sequence profile alignment (pairwise)
+ Sequence profile alignment construction (pairwise)
+ Pairwise sequence profile alignment construction
Methods might perform one-to-one, one-to-many or many-to-many comparisons.
+ Sequence alignment generation (pairwise profile)
@@ -38269,15 +38350,18 @@
- Sequence profile alignment construction (multiple)
-
+ Sequence alignment generation (multiple profile)
+
Sequence profile alignment (multiple)
+ Sequence profile alignment construction (multiple)
Multiple sequence profile alignment construction
+ Sequence profile alignment generation (multiple)
beta12orEarlier
Align two or more molecular profiles.
-
-
-
+
+ 1.6
+ true
+
@@ -38285,13 +38369,15 @@
- Structural (3D) profile alignment construction (pairwise)
+ 3D profile-to-3D profile alignment (pairwise)
beta12orEarlier
- Align exactly two molecular Structural (3D) profiles.
+ Structural profile alignment construction (pairwise)
Structural (3D) profile alignment (pairwise)
- Pairwise structural (3D) profile alignment construction
Methods might perform one-to-one, one-to-many or many-to-many comparisons.
+ Structural profile alignment generation (pairwise)
+ Align exactly two molecular Structural (3D) profiles.
+ Pairwise structural (3D) profile alignment construction
@@ -38302,15 +38388,17 @@
- Structural (3D) profile alignment construction (multiple)
-
+ Structural profile alignment generation (multiple)
+
Structural (3D) profile alignment (multiple)
beta12orEarlier
Multiple structural (3D) profile alignment construction
Align two or more molecular 3D profiles.
-
-
-
+ Structural profile alignment construction (multiple)
+
+ 1.6
+ true
+
@@ -38319,20 +38407,15 @@
Data retrieval (tool metadata)
-
-
-
-
-
-
-
+
Tool information retrieval
beta12orEarlier
Search and retrieve names of or documentation on bioinformatics tools, for example by keyword or which perform a particular function.
Data retrieval (tool annotation)
-
-
-
+
+ 1.6
+ true
+
@@ -38341,20 +38424,15 @@
Data retrieval (database metadata)
-
-
-
-
-
-
-
+
Database information retrieval
Search and retrieve names of or documentation on bioinformatics databases or query terms, for example by keyword.
Data retrieval (database annotation)
beta12orEarlier
-
-
-
+
+ 1.6
+ true
+
@@ -38467,8 +38545,8 @@
Sequence assembly (mapping assembly)
The final sequence will resemble the backbone sequence. Mapping assemblers are usually much faster and less memory intensive than de-novo assemblers.
- Sequence assembly by combining fragments using an existing backbone sequence.
beta12orEarlier
+ Sequence assembly by combining fragments using an existing backbone sequence, typically a reference genome.
@@ -38483,7 +38561,7 @@
beta12orEarlier
De-novo assemblers are much slower and more memory intensive than mapping assemblers.
- Sequence assembly by combining fragments into a new, previously unknown sequence.
+ Sequence assembly by combining fragments without the aid of a reference sequence or genome.
@@ -38596,6 +38674,7 @@
Heat map generation
+
@@ -38603,6 +38682,7 @@
Generate a heat map of gene expression from microarray data.
+ Heat map construction
The heat map usually uses a coloring scheme to represent clusters. They can show how expression of mRNA by a set of genes was influenced by experimental conditions.
beta12orEarlier
@@ -38616,19 +38696,14 @@
Gene expression profile analysis
-
-
-
-
-
-
-
+
Analyse one or more gene expression profiles, typically to interpret them in functional terms.
beta12orEarlier
Functional profiling
-
-
-
+
+ 1.6
+ true
+
@@ -38637,7 +38712,8 @@
Gene expression profile pathway mapping
-
+
+
@@ -38659,7 +38735,7 @@
Protein secondary structure assignment (from coordinate data)
-
+
Assign secondary structure from protein coordinate data.
beta12orEarlier
@@ -38732,10 +38808,11 @@
- Phylogenetic tree construction (data centric)
+ Phylogenetic tree generation (data centric)
Construct a phylogenetic tree from a specific type of data.
beta12orEarlier
+ Phylogenetic tree construction (data centric)
@@ -38746,10 +38823,11 @@
- Phylogenetic tree construction (method centric)
+ Phylogenetic tree generation (method centric)
beta12orEarlier
Construct a phylogenetic tree using a specific method.
+ Phylogenetic tree construction (method centric)
@@ -38764,6 +38842,7 @@
Methods typically compare multiple molecular sequence and estimate evolutionary distances and relationships to infer gene families or make functional predictions.
+ Phylogenetic tree generation (from molecular sequences)
beta12orEarlier
Phylogenetic tree construction from molecular sequences.
@@ -38786,6 +38865,7 @@
Phylogenetic tree construction from continuous quantitative character data.
beta12orEarlier
+ Phylogenetic tree generation (from continuous quantitative characters)
@@ -38810,6 +38890,7 @@
+ Phylogenetic tree generation (from gene frequencies)
beta12orEarlier
Phylogenetic tree construction from gene frequency data.
@@ -38831,6 +38912,7 @@
beta12orEarlier
+ Phylogenetic tree generation (from polymorphism data)
Phylogenetic tree construction from polymorphism data including microsatellites, RFLP (restriction fragment length polymorphisms), RAPD (random-amplified polymorphic DNA) and AFLP (amplified fragment length polymorphisms) data.
@@ -38845,6 +38927,7 @@
Phylogenetic species tree construction
beta12orEarlier
+ Phylogenetic species tree generation
Construct a phylogenetic species tree, for example, from a genome-wide sequence comparison.
@@ -38856,11 +38939,12 @@
- Phylogenetic tree construction (parsimony methods)
+ Phylogenetic tree generation (parsimony methods)
beta12orEarlier
This includes evolutionary parsimony (invariants) methods.
Construct a phylogenetic tree by computing a sequence alignment and searching for the tree with the fewest number of character-state changes from the alignment.
+ Phylogenetic tree construction (parsimony methods)
@@ -38871,9 +38955,10 @@
- Phylogenetic tree construction (minimum distance methods)
+ Phylogenetic tree generation (minimum distance methods)
Construct a phylogenetic tree by computing (or using precomputed) distances between sequences and searching for the tree with minimal discrepancies between pairwise distances.
+ Phylogenetic tree construction (minimum distance methods)
beta12orEarlier
This includes neighbor joining (NJ) clustering method.
@@ -38886,11 +38971,12 @@
- Phylogenetic tree construction (maximum likelihood and Bayesian methods)
+ Phylogenetic tree generation (maximum likelihood and Bayesian methods)
beta12orEarlier
Maximum likelihood methods search for a tree that maximizes a likelihood function, i.e. that is most likely given the data and model. Bayesian analysis estimate the probability of tree for branch lengths and topology, typically using a Monte Carlo algorithm.
Construct a phylogenetic tree by relating sequence data to a hypothetical tree topology using a model of sequence evolution.
+ Phylogenetic tree construction (maximum likelihood and Bayesian methods)
@@ -38901,9 +38987,10 @@
- Phylogenetic tree construction (quartet methods)
+ Phylogenetic tree generation (quartet methods)
Construct a phylogenetic tree by computing four-taxon trees (4-trees) and searching for the phylogeny that matches most closely.
+ Phylogenetic tree construction (quartet methods)
beta12orEarlier
@@ -38915,9 +39002,10 @@
- Phylogenetic tree construction (AI methods)
+ Phylogenetic tree generation (AI methods)
beta12orEarlier
+ Phylogenetic tree construction (AI methods)
Construct a phylogenetic tree by using artificial-intelligence methods, for example genetic algorithms.
@@ -38929,7 +39017,7 @@
- Sequence alignment analysis (phylogenetic modelling)
+ DNA substitution modelling
@@ -38946,6 +39034,7 @@
Identify a plausible model of DNA substitution that explains a DNA sequence alignment.
beta12orEarlier
+ Sequence alignment analysis (phylogenetic modelling)
@@ -39027,9 +39116,10 @@
- Phylogenetic tree construction (consensus)
+ Phylogenetic tree generation (consensus)
+ Phylogenetic tree construction (consensus)
beta12orEarlier
Methods typically test for topological similarity between trees using for example a congruence index.
Compare two or more phylogenetic trees to produce a consensus tree.
@@ -39079,7 +39169,6 @@
Phylogenetic tree annotation
-
Annotate a phylogenetic tree with terms from a controlled vocabulary.
beta12orEarlier
@@ -39093,9 +39182,8 @@
- Peptide immunogen prediction and optimisation
+ Immunogenicity prediction
-
@@ -39104,17 +39192,18 @@
-
-
+
+
-
-
+
+
Predict and optimise peptide ligands that elicit an immunological response.
+ Peptide immunogen prediction
beta12orEarlier
@@ -39126,8 +39215,8 @@
- DNA vaccine prediction and optimisation
-
+ DNA vaccine design
+
@@ -39153,18 +39242,17 @@
- Sequence reformatting
+ Sequence formatting
-
-
+
-
+
@@ -39181,9 +39269,8 @@
- Sequence alignment reformatting
+ Sequence alignment formatting
-
@@ -39208,7 +39295,7 @@
- Codon usage table reformatting
+ Codon usage table formatting
@@ -39237,17 +39324,17 @@
Sequence rendering
-
+
-
-
+
+
-
-
+
+
Visualise, format or render a molecular sequence, possibly with sequence features or properties shown.
@@ -39264,7 +39351,13 @@
Sequence alignment rendering
-
+
+
+
+
+
+
+
@@ -39291,7 +39384,12 @@