Provided by: seqan-apps_1.4.1+dfsg-2_amd64
NAME
snp_store - SnpStore SYNOPSIS snp_store [OPTIONS] "GENOME FILE" "MAPPED READ FILE(S)" DESCRIPTION SNP and Indel Calling in Mapped Read Data. -h, --help Displays this help message. --version Display version information Options: : -o, --output FILE Output file for SNPs (must be set, no default construction). -if, --input-format NUM Set input format: 0 for GFF format and 1 for SAM format (both must be sorted according to genome positions). Default: 0. -of, --output-format NUM Set output format: 0 to output all candidate snps amd 1 to output successful candidate snps only. Default: 0. -dc, --dont-clip Ignore clip tags in gff. Default: off. -mu, --multi Keep non-unique fragmentStore.alignedReadStore. Default: off. -hq, --hide-qualities Only show coverage (no qualities) in SNP output file. Default: off. -sqo, --solexa-qual-offset Base qualities are encoded as Ascii value - 64 (instead of Ascii - 33). -id, --indel-file FILE Output file for called indels in gff format. Default: off. -m, --method NUM Set method used for SNP calling: 0 for threshold method and 1 for maq method. Default: 1. -mp, --max-pile NUM Maximal number of matches allowed to pile up at the same genome position. -mmp, --merged-max-pile Do pile up correction on merged lanes. Default: off. -mc, --min-coverage NUM Minimal required number of reads covering a candidate position. -fc, --force-call NUM Always call base if count is >= fc, ignore other parameters. Default: off. In range [1..inf]. -oa, --orientation-aware Distinguish between forward and reverse reads. Default: off. -mpr, --max-polymer-run NUM Discard indels in homopolymer runs longer than mpr. -dp, --diff-pos NUM Minimal number of different read positions supporting the mutation. -eb, --exclude-border NUM Exclude read positions within eb base pairs of read borders for SNV calling. -su, --suboptimal Keep suboptimal reads. -re, --realign Realign reads around indel candidates. -pws, --parse-window-size NUM Genomic window size for parsing reads (concerns memory consumption, choose smaller windows for higher coverage). In range [1..100000]. SNP calling options: : Threshold method related: : -mm, --min-mutations NUM Minimal number of observed mutations for mutation to be called. -pt, --perc-threshold NUM Minimal percentage of mutational base for mutation to be called. -mq, --min-quality NUM Minimal average quality of mutational base for mutation to be called. Maq method related: : -th, --theta NUM Dependency coefficient. -hr, --hetero-rate NUM Heterozygote rate. -mmq, --min-map-quality NUM Minimum base call (mapping) quality for a match to be considered. -ch, --corrected-het Use amplification bias corrected distribution for heterozygotes. Default: off. -maf, --mean-alleleFreq NUM Mean ref allele frequency in heterozygotes. -ac, --amp-cycles NUM Number of amplification cycles. -ae, --amp-efficiency NUM Polymerase efficiency, probability of amplification. -in, --initial-N NUM Initial allele population size. -mec, --min-explained-column NUM Minimum fraction of alignment column reads explained by genotype call. Indel calling options: : -it, --indel-threshold NUM Minimal number of indel-supporting reads required for indel calling. -ipt, --indel-perc-threshold NUM Minimal ratio of indel-supporting/covering reads for indel to be called. -iqt, --indel-quality-thresh NUM Minimal average quality of inserted base/deletion-neighboring bases for indel to be called. -bsi, --both-strands-indel Both strands need to be observed for indel to be called. Default: off. -ebi, --exclude-border-indel NUM Same as option -eb but for indel candidates. Other options: : -lf, --log-file FILE Write log file to FILE. -v, --verbose Enable verbose output. -vv, --very-verbose Enable very verbose output. -q, --quiet Set verbosity to a minimum. VERSION snp_store version: 1.0.1 Last update March 14, 2013