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From: Mao J. <jia...@gm...> - 2011-04-07 15:37:33
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Dear Petr, Thanks a lot for your kind reply. I will try them out. But, please see the followings. 2011/4/7 Petr Danecek <pd...@sa...>: > Hi Mao, > > if you want to use existing tools, the script fill-an-ac can calculate > the value of AN and AC tags. Then you could get the stats using > vcf-stats -f INFO/AN,INFO/AC. I have no idea about AN and AC tags. I have not find enough INFO about them. I want to understand them more. Could you please give me more explanation on them, or point out where I can find them in detail? I am new to genomics, and I have no colleagues who use VCF and VCFTools tool. So my improvement depends on the mailing list. Thanks in advance. > > For the second task I'd create one VCF file per population using > vcf-subset and then vcf-compare to get the numbers you want. > > Hope this helps, > Petr > > > On Thu, 2011-04-07 at 11:42 +0200, Mao Jianfeng wrote: >> Dear vcftools-listers, >> >> VCF format and VCFTOOLS eased my work of NGS genomics. Thanks a lot >> for its generation. >> >> I am facing problem, when I attempt to calculate the frequency >> distribution of different types of variations in accessions and >> populations. I am new to genomics and not good at computer. I would >> like to hear advice/directions from you. >> >> I have NGS genomic data from 100 individuals of 10 geographic regions. >> The data (snp, indels) have been in VCF format. Now, I asked two >> problems. >> >> (1) what is the frequency distribution of genomic variants (snp, >> indel) in the different numbers of individuals? For example, in my >> case, I want to count how many snp/indel occurred in 10 individuals, >> 20 individuals, 30, 40 ,50 ,60, 70, 80, 90, 100 (the whole data). >> >> (2) what is the frequency distribution of genomic variants (snp, >> indel) in the different numbers of populations? For example, in my >> case, I want to count how many snp/indel occurred in 2 populations, 4 >> populations, 6, 8, 10 (the whole data). >> >> I check the manu for VCFTOOLS, but I have not find functionality for >> these two jobs. Have you, any listers, faced the same problems? What >> is your strategy for that? Could you please share any hints with me? >> And, I think you advice should be valuable for all the VCF users. >> >> Thanks a lot in advance. >> >> ------------------------------------------------------------------------------ >> Xperia(TM) PLAY >> It's a major breakthrough. An authentic gaming >> smartphone on the nation's most reliable network. >> And it wants your games. >> http://p.sf.net/sfu/verizon-sfdev >> _______________________________________________ >> Vcftools-help mailing list >> Vcf...@li... >> https://lists.sourceforge.net/lists/listinfo/vcftools-help > > > > > -- > The Wellcome Trust Sanger Institute is operated by Genome Research > Limited, a charity registered in England with number 1021457 and a > company registered in England with number 2742969, whose registered > office is 215 Euston Road, London, NW1 2BE. > |