- Wide range of supported reads: Illumina, Oxford Nanopore, PacBio, BGI.
- Short read multi-threaded processing: QC, filtering, trimming, overlapped pairs merging.
- Assemblies from short reads, long reads or hybrid assembly using modern and powerful assemblers: SPAdes, Unicycler, Flye or MEGAHIT.
- Quality control of assembly: completeness and contamination assessment with CheckM as well as PhiX detection.
- Fast annotation of bacterial and archeal genome assemblies with bakta.
- No High Performance Computing needed. The pipeline works on laptop or desktop.
ZGA is written in Python and tested with Python 3.8 - 3.10.
The simplest way to install ZGA and all dependencies is conda:
-
You need to install conda, e.g. miniconda. Python 3.8 or newer is preferred.
-
After installation You should add channels - the conda's software sources:
conda config --add channels bioconda
conda config --add channels conda-forge -
At the end You should install ZGA to an existing active environment (Python 3.8+):
conda install zga
or create a fresh environment and activate it:
conda create -n zga zga
conda activate zga
If You have troubles with bioconda channel try to use my personal channel https://anaconda.org/laxeye/zga conda install -c laxeye zga
Run pip install zga. Biopython is the only one dependency installed from PyPI. All other dependencies You should install manually or using conda as mentioned above. CheckM is available on PyPi, but it's easier to install it using conda.
You can get ZGA by cloning from the repository with git clone https://github.com/laxeye/zga.git or by downloading an archive. After downloading enter the directory cd zga and run python3 setup.py install.
Don't forget to install dependecies (see bellow).
ZGA uses several software and libraries including:
- fastp
- BBmap
- NxTrim
- mash
- SPAdes (>= 3.12 to support merged paired-end reads, >= 3.5.0 to support Nanopore reads)
- Unicycler
- Flye >= 2.6
- MEGAHIT
- minimap2
- racon
- CheckM >= 1.2.1
- BioPython
- NCBI BLAST+
- bakta
You may install all dependencies separately using conda. It's highly recommended to create a new conda environment:
conda create -n zga "python>=3.8" fastp "spades>=3.12" unicycler checkm-genome bakta bbmap blast biopython nxtrim "mash>=2" flye minimap2 racon "samtools>=1.9" megahit
and activate it
conda activate zga
Otherwise you may install dependencies to existing conda environment:
conda install "python>=3.8" fastp "spades>=3.12" unicycler checkm-genome bakta bbmap blast biopython nxtrim "mash>=2" flye minimap2 racon "samtools>=1.9" megahit
Of course, it's possible to use another ways even compile all tools from source code. In this case you should check if binaries are in your '$PATH' variable.
After installation you need to download bakta database, please read detailed instructions. Shortly you need to run:
bakta_db download --output <output-path> --type [light|full]
ZGA was tested on Ubuntu 18.04, 19.10, 20.04, 22.04 and EndeavourOS. Most probably any modern 64-bit Linux distribuition is suitable.
Your feedback on other OS is welcome!
Run zga -h to get a help message.
ZGA includes several steps:
- Read quality check ('readqc')
- Read processing ('preprocessing')
- Genome assembling ('assembling')
- Genome polishing ('polishing')
- Genome quality assessment ('check_genome')
- Genome annotation ('annotation')
You may start from any step and finish at any step providing arguments -s or --first-step and -l or --last-step followed by step designation (in brackets in the list above).
E.g. if You like to perform read processing, genome assembling and genome polishing You should run
zga --first-step preprocessing --last-step polishing ...
ZGA may use unprocessed or processed sequencing reads from different platforms as well as genome assemblies to perform assembly polishing, assembly quality assessment and assembly annotation. FASTQ format gzipped or not is required for sequencing reads. Paired-end reads shoul be provided in separate files, not interleaved. Sequencing reads should be provided as space separated list after corresponding argument:
-1 or --pe-1 for forward paired-end reads (Illumina, BGI)
-2 or --pe-2 for reverse paired-end reads
-S or --single-end for unpaired short reads
--pe-merged for merged overlapping paired-end reads (if You performed merging earlier)
--mp-1 for first mate-pair reads, RF orientation is supposed
--mp-2 for second mate-pair reads
--pacbio for PacBio single-end sequencing reads
--nanopore for Oxford Nanopore sequencing reads
When bbduk.sh (short read trimming tool) throws an exception ZGA tries to repair reads with repair.sh (from BBMap).
zga -1 Raw.R1.fq.gz -2 Raw.R2.fq.gz unprocessed paired-end reads
zga -1 Unmerged_1.fq -2 Unmerged_2.fq --pe-merged Merged.fq reads after processing (overlapping reads merging)
zga -1 Lib1.R1.fq.gz Lib2.R1.fq -2 Lib1.R2.fq Lib2.R2.fq combination of reads from two sequencing libraries
ZGA produces up to 4 sub-folders in output folder:
- readQC - results of reaq quality control with fastp,
- reads - processed reads,
- assembly - folder produced by genomic assembler,
- annotation - annotated genome.
Log-file zga.log is available in the output folder.
Perform all steps: read qc, read trimming and merging, assembly, CheckM assesment with default (bacterial) marker set, bakta annotation and use 4 CPU threads where possible:
zga -1 R1.fastq.gz -2 R2.fastq.gz --bbmerge --threads 4 -o my_assembly
Assemble with SPAdes using paired-end and nanopore reads of archaeal genome (CheckM will use archaeal markers) altering memory limit to 16 GB:
zga -1 R1.fastq.gz -2 R2.fastq.gz --nanopore MiniION.fastq.gz -a spades --threads 4 --memory-limit 16 --domain archaea -o my_assembly
Short read correction with SPAdes is a computationally expensive step, You may run read-correction with tadpole including --tadpole-correct option which is much faster and needs less memory.
zga --tadpole-correct -1 R1.fastq.gz -2 R2.fastq.gz --threads 4 -o my_assembly
Assemble long reads with Flye skipping long read polishing and perfom short-read polishing with racon:
zga -1 R1.fastq.gz -2 R2.fastq.gz --nanopore MiniION.fastq.gz -a flye --threads 4 --domain archaea -o my_assembly --flye-short-polish --flye-skip-long-polish
Assemble from Nanopore reads using unicycler:
zga -a unicycler --nanopore MiniION.fastq -o nanopore_assembly
Perform assesment and annotation of genome assembly with e.g. Pectobacterium CheckM marker set:
zga --first-step check_genome -g pectobacterium_sp.fasta --checkm_rank genus --checkm_taxon Pectobacterium -o my_output_dir
Let CheckM to infer the right marker set:
zga --first-step check_genome -g my_genome.fa --checkm_mode lineage -o my_output_dir
ZGA is in the stage of active development.
Known issues and limitations:
- Unicycler can't use mate-pair reads or multiple libraries of same type.
Don't hesitate to report bugs or features!
It's a great pleasure to know, that your software is useful. Please cite ZGA:
Korzhenkov A. 2021. ZGA: a flexible pipeline for read processing, de novo assembly and annotation of prokaryotic genomes. bioRxiv https://doi.org/10.1101/2021.04.27.441618
And of course tools it's using:
Chen, S., Zhou, Y., Chen, Y., & Gu, J. (2018). fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinformatics, 34(17), i884-i890. https://doi.org/10.1093/bioinformatics/bty560
Bushnell, B., Rood, J., & Singer, E. (2017). BBMerge–accurate paired shotgun read merging via overlap. PloS one, 12(10). https://doi.org/10.1371/journal.pone.0185056
Bankevich, A., Nurk, S., Antipov, D., Gurevich, A. A., Dvorkin, M., Kulikov, A. S., ... & Pyshkin, A. V. (2012). SPAdes: a new genome assembly algorithm and its applications to single-cell sequencing. Journal of computational biology, 19(5), 455-477. https://dx.doi.org/10.1089/cmb.2012.0021
Wick, R. R., Judd, L. M., Gorrie, C. L., & Holt, K. E. (2017). Unicycler: resolving bacterial genome assemblies from short and long sequencing reads. PLoS computational biology, 13(6), e1005595. https://doi.org/10.1371/journal.pcbi.1005595
Vaser, R., Sović, I., Nagarajan, N., & Šikić, M. (2017). Fast and accurate de novo genome assembly from long uncorrected reads. Genome research, 27(5), 737-746. https://genome.cshlp.org/content/27/5/737.full
Li, D., Liu, C-M., Luo, R., Sadakane, K., and Lam, T-W., (2015) MEGAHIT: An ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph. Bioinformatics, doi: 10.1093/bioinformatics/btv033 https://doi.org/10.1093/bioinformatics/btv033
Li, H. (2018). Minimap2: pairwise alignment for nucleotide sequences. Bioinformatics, 34:3094-3100. https://dx.doi.org/10.1093/bioinformatics/bty191
Kolmogorov, M., Yuan, J., Lin, Y., & Pevzner, P. A. (2019). Assembly of long, error-prone reads using repeat graphs. Nature biotechnology, 37(5), 540-546. https://doi.org/10.1038/s41587-019-0072-8
Parks, D. H., Imelfort, M., Skennerton, C. T., Hugenholtz, P., & Tyson, G. W. (2015). CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome research, 25(7), 1043-1055. https://dx.doi.org/10.1101/gr.186072.114
Schwengers O., Jelonek L., Dieckmann M. A., Beyvers S., Blom J., Goesmann A. (2021). Bakta: rapid and standardized annotation of bacterial genomes via alignment-free sequence identification. Microbial Genomics, 7(11). https://doi.org/10.1099/mgen.0.000685
Camacho, C., Coulouris, G., Avagyan, V. et al. (2009). BLAST+: architecture and applications. BMC Bioinformatics 10, 421. https://doi.org/10.1186/1471-2105-10-421
Cock, P. J., Antao, T., Chang, J. T., Chapman, B. A., Cox, C. J., Dalke, A., ... & De Hoon, M. J. (2009). Biopython: freely available Python tools for computational molecular biology and bioinformatics. Bioinformatics, 25(11), 1422-1423. https://doi.org/10.1093/bioinformatics/btp163
O’Connell, J., et al. (2015) NxTrim: optimized trimming of Illumina mate pair reads. Bioinformatics 31(12), 2035-2037. https://doi.org/10.1093/bioinformatics/btv057
Ondov, B.D., Treangen, T.J., Melsted, P. et al. Mash: fast genome and metagenome distance estimation using MinHash. Genome Biol 17, 132 (2016). https://doi.org/10.1186/s13059-016-0997-x