Hi everyone,
If I have a snp vcf file for allele-specific mode, however it was not generated from extract_snps.py, what should I do to reformat it for HiC-Pro analysis?
Those annotation line are necessory for HiC-Pro? For example,
##FILTER=<ID=PASS,Description="Allfilterspassed">
What about other columns like INFO?
Here is an example file generated from extract_snps.py
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#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT 129P2_OlaHsd-PWK_PhJ-F1
chr1 3000321 rs583231582 G T 999 PASS DP=1295;DP4=767,500,14,14;CSQ=T||||intergenic_variant|||||||| GT 0|1
chr1 3001313 rs582038162 C T 999 PASS DP=1661;DP4=794,750,63,54;CSQ=A||||intergenic_variant||||||||,T||||intergenic_variant|||||||| GT 0|1
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Here is part of my vcf file, we call snps and filter after we did whole-genome sequence.
chr1 3000287 . A G 635.03 PASS AC=2;AF=1.00;AN=2;DP=20;ExcessHet=3.0103;FS=0.000;MLEAC=2;MLEAF=1.00;MQ=31.37;QD=31.75;SOR=0.892 GT:AD:DP:GQ:PL 1/1:0,20:20:60:649,60,0
chr1 3000321 . G T 976.03 PASS AC=2;AF=1.00;AN=2;DP=22;ExcessHet=3.0103;FS=0.000;MLEAC=2;MLEAF=1.00;MQ=29.54;QD=25.36;SOR=1.609 GT:AD:DP:GQ:PL 1/1:0,22:22:66:990,66,0
Thanks!