pFst1

Usage

Overview

pFst is a probabilistic approach for detecting differences in allele frequencies between two populations.

Options

**pFst** is a likelihood ratio test (LRT) quantifying allele frequency
differences between populations.  The LRT by default uses the binomial
distribution.  If Genotype likelihoods are provided it uses a modified
binomial that weights each allele count by its certainty.  If type is
set to 'PO' the LRT uses a beta distribution to fit the allele
frequency spectrum of the target and background.  PO requires the AD
and DP genotype fields and requires at least two pools for the target
and background.  The p-value calculated in **pFst** is based on the
chi-squared distribution with one degree of freedom.
Output : 3 columns :     
     1. seqid            
     2. position         
     3. **pFst** probability 
required: t,target     -- argument: a zero based comma separated list of target individuals corresponding to VCF columns       
required: b,background -- argument: a zero based comma separated list of background individuals corresponding to VCF columns   
required: f,file       -- argument: a properly formatted VCF.                                                                  
required: y,type       -- argument: genotype likelihood format ; genotypes: GP, GL or PL; pooled: PO                           
optional: d,deltaaf    -- argument: skip sites where the difference in allele frequencies is less than deltaaf, default is zero
optional: r,region     -- argument: a tabix compliant genomic range : seqid or seqid:start-end                                 
optional: c,counts     -- switch  : use genotype counts rather than genotype likelihoods to estimate parameters, default false 
Type: statistics

Exit status

0

Success

not 0

Failure

Other