Man page - bfst(1)
Packages contains this manual
- vcflib-api(1)
- vcfannotategenotypes(1)
- vcfcat(1)
- vcfgeno2alleles(1)
- vcfroc(1)
- vcfhethomratio(1)
- vcfcountalleles(1)
- vcfaddinfo(1)
- vcfrandomsample(1)
- vcfbreakmulti(1)
- vcfcheck(1)
- vcfsitesummarize(1)
- vcfdistance(1)
- vcfglbound(1)
- pyvcflib(1)
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- vcflib(1)
- vcfnumalt(1)
- vcfsample2info(1)
- vcfkeepgeno(1)
- vcfgeno2haplo(1)
- vcfallelicprimitives(1)
- vcfindex(1)
- vcfecho(1)
- vcfwave(1)
- vcf2tsv(1)
- vcffixup(1)
- vcfremap(1)
- vcfnullgenofields(1)
- vcfoverlay(1)
- vcfremoveaberrantgenotypes(1)
- vcfflatten(1)
- vcfintersect(1)
- vcfprimers(1)
- vcfgenosamplenames(1)
- vcfafpath(1)
- vcfinfo2qual(1)
- vcfparsealts(1)
- vcffilter(1)
- vcfuniqalleles(1)
- vcfgenotypes(1)
- vcfsamplenames(1)
- vcfaltcount(1)
- vcfcombine(1)
- vcfuniq(1)
- vcf2dag(1)
- vcfgenotypecompare(1)
- vcfhetcount(1)
- vcfclassify(1)
- vcfkeepsamples(1)
- vcf2fasta(1)
- vcflength(1)
- vcfleftalign(1)
- vcfcommonsamples(1)
- vcfglxgt(1)
- vcfentropy(1)
- vcfrandom(1)
- vcfcreatemulti(1)
- vcfnulldotslashdot(1)
- vcfgenosummarize(1)
- vcfstats(1)
- vcfannotate(1)
- smoother(1)
- vcfstreamsort(1)
- vcfevenregions(1)
- vcfld(1)
- vcfkeepinfo(1)
- vcfqual2info(1)
- vcfremovesamples(1)
- abba-baba(1)
- vcfcleancomplex(1)
- vcfsamplediff(1)
apt-get install libvcflib-tools
Manual
BFST
NAMESYNOPSIS
DESCRIPTION
OPTIONS
EXIT VALUES
SEE ALSO
OTHER
LICENSE
AUTHORS
NAME
bFst
SYNOPSIS
bFst ātarget 0,1,2,3,4,5,6,7 ābackground 11,12,13,16,17,19,22 āfile my.vcf ādeltaaf 0.1
DESCRIPTION
bFst is a Bayesian approach to Fst. Importantly bFst accounts for genotype uncertainty in the model using genotype likelihoods. For a more detailed description see: `A Bayesian approach to inferring population structure from dominant markersā by Holsinger et al.Ā Molecular Ecology Vol 11, issue 7 2002. The likelihood function has been modified to use genotype likelihoods provided by variant callers. There are five free parameters estimated in the model: each subpopulationās allele frequency and Fis (fixation index, within each subpopulation), a free parameter for the total populationās allele frequency, and Fst.
OPTIONS
Output : 11 columns :
1. Seqid
2. Position
3. Observed allele frequency in target.
4. Estimated allele frequency in target.
5. Observed allele frequency in background.
6. Estimated allele frequency in background.
7. Observed allele frequency combined.
8. Estimated allele frequency in combined.
9. ML estimate of Fst (mean)
10. Lower bound of the 95% credible interval
11. Upper bound of the 95% credible interval
required: t,target -- a zero bases comma separated list of target individuals corrisponding to VCF columns
required: b,background -- a zero bases comma separated list of background individuals corrisponding to VCF columns
required: f,file a -- a proper formatted VCF file. the FORMAT field MUST contain "PL"
required: d,deltaaf -- skip sites were the difference in allele frequency is less than deltaaf
Type: statistics
EXIT VALUES
|
0 |
Success |
|||
|
not 0 |
Failure |
SEE ALSO
vcflib (1)
OTHER
LICENSE
Copyright 2011-2024 (C) Erik Garrison and vcflib contributors. MIT licensed. Copyright 2020-2024 (C) Pjotr Prins.
AUTHORS
Erik Garrison and vcflib contributors.