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When looking at the documentation of a new nf-core pipeline, mostly care about two things:
What does it do (what kind of input data, which tools, output data)
How do I run it (minimal example)
I find it surprisingly hard to quickly find this information for a nf-core pipeline. I sometimes prefer reading the code over reading the documentation.
Here's the documentation website how I perceive it:
(Using RNA-seq as an example, but this applies more generally)
I know there's the usage the parameters sections, which are great, but I'm really missing a quick "getting started" overview for most pipelines.
Alternative suggestion:
(The docs of the rnaseq workflow rewritten, moving boilerplate text into external, linked documents)
Pipeline summary
nf-core/rnaseq is a bioinformatics pipeline that can be used to analyse RNA sequencing data obtained from organisms with a reference genome and annotation. It takes a samplesheet and FASTQ files as input, performs QC, trimming and (pseudo-)alignment, and produces a gene expression matrix and extensive QC report.
[subway map and tools as is]
Usage
If you are new to nextflow and nf-core, please refer to [central documentation page about setting up nextflow] on how to set-up nextflow.
First, you need to prepare a samplesheet with your input data that looks as follows:
Each row represents fastq file (single-end) or a pair of fastq files (paired end). Rows with the same sample identifier are considered technical replicates and merged automatically.
The output of the pipeline applied on an example dataset can be found here [link to AWS test].
For more details, please refer to the output documentation.
Online Videos
[current content as is]
Credits/Support/Citations
[current content as is]
The text was updated successfully, but these errors were encountered:
Description of feature
When looking at the documentation of a new nf-core pipeline, mostly care about two things:
I find it surprisingly hard to quickly find this information for a nf-core pipeline. I sometimes prefer reading the code over reading the documentation.
Here's the documentation website how I perceive it:
(Using RNA-seq as an example, but this applies more generally)
I know there's the usage the parameters sections, which are great, but I'm really missing a quick "getting started" overview for most pipelines.
Alternative suggestion:
(The docs of the rnaseq workflow rewritten, moving boilerplate text into external, linked documents)
Pipeline summary
nf-core/rnaseq is a bioinformatics pipeline that can be used to analyse RNA sequencing data obtained from organisms with a reference genome and annotation. It takes a samplesheet and FASTQ files as input, performs QC, trimming and (pseudo-)alignment, and produces a gene expression matrix and extensive QC report.
[subway map and tools as is]
Usage
If you are new to nextflow and nf-core, please refer to [central documentation page about setting up nextflow] on how to set-up nextflow.
First, you need to prepare a samplesheet with your input data that looks as follows:
samplesheet.csv:
Each row represents fastq file (single-end) or a pair of fastq files (paired end). Rows with the same sample identifier are considered technical replicates and merged automatically.
Now, you can run the pipeline using:
For more details, please refer to the usage documentation and the parameter documentation.
Pipeline output
The output of the pipeline applied on an example dataset can be found here [link to AWS test].
For more details, please refer to the output documentation.
Online Videos
[current content as is]
Credits/Support/Citations
[current content as is]
The text was updated successfully, but these errors were encountered: