I am working on a pooled samples re-sequencing project. There are 10 pools for cases and controls respectively. I am calling SNV using SNVer, just wondering do I need to call SNV in cases and controls separately? do I can call them simutaneously?
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##fileformat=VCFv4.0
##INFO=<ID=DP,Number=1,Type=Integer,Description="Total Depth">
##INFO=<ID=AF,Number=.,Type=Float,Description="Alternative Allele Frequency">
##INFO=<ID=NP,Number=1,Type=Integer,Description="Number of Pools">
##INFO=<ID=PV,Number=.,Type=Float,Description="Pvalue generated by SNVer">
##FORMAT=<ID=AC,Number=1,Type=Integer,Description="Alternative Allele Count">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT S1P1 S1P10 S1P11 S1P12 S1P13 S1P14 S1P15 S1P16 S1P17 S1P18 S1P19 S1P2 S1P20 S1P21 S1P22 S1P23 S1P24 S1P3 S1P4 S1P5 S1P6 S1P7 S1P8 S1P9
chr1 1234567 . C T . PASS DP=13135;AF=0.005;NP=22;PV=2.4424906541753444E-15 ACP 0:598 0:518 0:259 62:594 NA:NA 0:462 0:627 0:579 0:427 0:652 0:543 0:645 0:594 0:410 0:402 0:407 0:313 0:590 0:547 0:820 NA:NA 0:570 0:587 0:721
BTW, our design is : 10 individuals a pool; targeted sequencing of a few regions; so around 20 pools were sequenced in a single lane. these 20 pools consist of both cases and controls.
So your suggestion is:
call cases and controls separately; do I need to call SNV base on lane as well?Last edited by lung1212; 01-16-2014, 05:59 PM.
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