Name: POGENOM
Owner: Environmental Genomics Group SciLifeLab/KTH Stockholm
Description: Population genomics from metagenomes
Created: 2017-06-09 07:48:24.0
Updated: 2017-06-09 13:03:06.0
Pushed: 2017-08-17 14:52:24.0
Homepage: null
Size: 32
Language: Perl
GitHub Committers
User | Most Recent Commit | # Commits |
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Anders Andersson | 2018-01-15 12:53:21.0 | 21 |
Other Committers
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Population genomics from metagenomes
POGENOM takes as input a file of the variant call format (VCF). This is generated by mapping one or several metagenome samples against a reference genome with a read aligner and calling variants using a variant caller. POGENOM calculates the nucleotide diversity (?) within each sample. If a multiple sample vcf file is provided as input, the fixation index (FST) will also be calculated between each pair of samples. If, in addition to the VCF file, an annotation file of the General Feature Format (GFF) is provided as input, gene-wise ? and FST will also be calculated. If further a genetic code file is provided, gene-wise ? and FST will be calculated also at the amino acid level. Now also non-synonymous to synonymous polymorphism rates (pN/pS) will be calculated for each gene in each sample. POGENOM also calculates some of the above parameters for all samples collectively, treating them as a metasample.
Download the latest POGENOM distribution from https://github.com/EnvGen/POGENOM/releases and extract the files. You need to have Perl installed on your computer to run POGENOM. When running POGENOM, either move to the directory where you have put the files or give the path to the files when running, i.e. perl path/to/pogenom.pl ...
Either:
perl pogenom.pl --vcf_file VCF_FILE --out OUTPUT_FILES_PREFIX --genome_size GENOME_SIZE [--help]
Or:
perl pogenom.pl -vcf_file VCF_FILE --out OUTPUT_FILES_PREFIX --gff_file GFF_FILE [--help]
--vcf_file VCF_FILE
Specify vcf file with data from a single or multiple samples.
--out OUTPUT_FILES_PREFIX
Specify the prefix of the output file name(s) (overwrites existing files with same names).
--genome_size GENOME_SIZE
Specify genome size (in bp; integer). Not required if --gff_file
is given.
--gff_file GFF_FILE
Specify gff file. Either this or --genome_size
must be given.
--genetic_code_file GENETIC_CODE_FILE
Specify genetic code file. E.g. standard_genetic_code.txt
in the POGENOM distribution.
--loci_file LOCI_FILE
Specify file with ids for loci to include.
--min_count MIN_COUNT
Specify minimum coverage for a locus to be included for the sample.
--min_found MIN_FOUND_IN
Specify minimum number samples that a locus need to be present in to be included.
--subsample SUBSAMPLE
Specify coverage level at which to subsample.
--keep_haplotypes
If this is used, POGENOM will not split haplotypes into single-nucleotide variants, which is otherwise the default behaviour.
--vcf_version
Specify VCF file format version. Can be set to 4.2 or 4.1 (default).
--help
To print help message on screen.
POGENOM doesn't have a paper yet, meanwhile please cite it like this:
Andersson AF, Sjöqvist C (2017). POGENOM: population genomics from metagenomes. https://github.com/EnvGen/POGENOM.