mgkit.workflow.snp_parser module¶
Deprecated since version 0.5.7: This script is deprecated now, use pnps-gen vcf instead
Note
if you need to use the script, install HTSeq
This script parses results of SNPs analysis from any tool for SNP calling 1 and integrates them into a format that can be later used for other scripts in the pipeline.
It integrates coverage and expected number of syn/nonsyn change and taxonomy from a GFF file, SNP data from a VCF file.
Note
The script accept gzipped VCF files
- 1
GATK pipeline was tested, but it is possible to use samtools and bcftools
Changes¶
Changed in version 0.2.1: added -s option for VCF files generated using bcftools
Changed in version 0.1.16: reworkked internals and removed SNPDat, syn/nonsyn evaluation is internal
Changed in version 0.1.13: reworked the internals and the classes used, including options -m and -s
-
mgkit.workflow.snp_parser.
check_snp_in_set
(samples, snp_data, pos, change, annotations, seq)[source]¶ Used by
parse_vcf()
to check if a SNP- Parameters
samples (iterable) – list of samples that contain the SNP
snp_data (dict) – dictionary from
init_count_set()
with per sample SNPs information
-
mgkit.workflow.snp_parser.
parse_vcf
(vcf_file, snp_data, min_reads, min_af, min_qual, annotations, seqs, options, line_num=100000)[source]¶ Parse VCF file counts synonymous and non-synonymous SNPs
- Parameters
vcf_file (file) – file handle to a VCF file
snp_data (dict) – dictionary from
init_count_set()
with per sample SNPs informationmin_reads (int) – minimum number of reads to accept a SNP
min_af (float) – minimum allele frequency to accept a SNP
min_qual (int) – minimum quality (Phred score) to accept a SNP
annotations (dict) – annotations grouped by their reference sequence
seqs (dict) – reference sequences
line_num (int) – the interval in number of lines at which progress will be printed
-
mgkit.workflow.snp_parser.
save_data
(output_file, snp_data)[source]¶ Pickle data structures to the disk.
- Parameters
output_file (str) – base name for pickle files
snp_data (dict) – dictionary from
init_count_set()
with per sample SNPs information