Dear All,

I have performed samtools for variant calling I have found variants in 
pileup file but not in vcf file. please find below one example for your 
concern.

chromosome    1082014    G    230 
a$,aaAAaaAAAAA,,a,aaaaaAaaaaaaAAaaa.ATaaAaaAaa,aaaAAAaaAtAa.A,,taaaa.AAa,aaAa,,aAaAaataaAaaaaAA,taaaAaaA,,,aaaa,AAAAAatA.a.,aA.taaAa.a,,,,aaa,aaaAAaAaAaaAA...aa,aAA,a,AaaAa,AAAAaA.aaa,aaaaaaAA..,a.t,aaaaa
 
'A>=<<@AF<<..FFFAFFFAAFAFFFFFC..FFF..AFFC.<A.FCFF8AF?.A.AFFFFF.FF.F7FF)FA)7.FFF.FF.F)FAFFAFFFFF)<FFF..F.FFFFFFFFFA)FF7<FFAF.FF.FF<F7)FFFF))F<..FAFAF7F.<FFAFF7)F.FFFFFABFAFFFFFFFFA..<FF.FFF7.C7FFFF.F8....

parameters:
/data/ngs/Programs/samtools-0.1.18/samtools mpileup -d 10000 -f ref.fa 
sorted.bam >mpileup.txt

/data/ngs/Programs/samtools-0.1.18/samtools mpileup -d 10000 -L 10000 -u 
-f sorted.bam > bcf.txt

/data/ngs/Programs/samtools-0.1.18/bcftools/bcftools view -ANvcgbcf 
bcf.txt  >vcf

Looking forward for your reply,

Thanks,
Manoharan

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