Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • gibberwocky
    Junior Member
    • Mar 2013
    • 8

    #1

    GATK VariantsToBinaryPed and PLINK

    Hopefully someone can point out what I'm doing wrong.

    I have called variants for 4 chickens separately in GATK using the Haplotype caller, and the VCF files have later been combined using the CombineVariants tool. The resulting VCF file has then been converted to PED format using the VariantsToBinaryPed tool. No errors were generated at any point.

    However, when using the binary file set in plink there appears to be an issue. For instance, when calculating allele frequency for 77k SNPs the MAF is NA for all SNPs, as the NCHROBS is 0 for all SNPs, e.g.

    Code:
     CHR              SNP   A1   A2          MAF  NCHROBS
      24      Var-24-1055    A    T           NA        0
      24      Var-24-1137    T    A           NA        0
      24      Var-24-1263    G    A           NA        0
    Looking at the VCF file that was fed into the VariantsToBinaryPed tool indicates that these SNPs are present and genotyped, e.g.

    Code:
    #CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	HA1A22AHB1A16A	JA1A17A	JB1A25B
    24	1055	.	T	A	484.77	PASS	AC=8;AF=1.00;AN=8;DP=129;FS=0.000;MLEAC=2;MLEAF=1.00;MQ0=0;set=Intersection	GT:AD:DP:GQ:PL	1/1:0,26:26:54:513,54,0	1/1:0,38:38:99:1138,117,0	1/1:0,35:35:99:977,108,0	1/1:0,30:30:93:890,93,0
    24	1137	.	A	T	181.77	PASS	AC=2;AF=0.500;AN=4;DP=65;MLEAC=1;MLEAF=0.500;MQ0=0;set=HA1A22A-JB1A25B	GT:AD:DP:GQ:PL	0/1:16,10:26:99:210,0,208	./.	./.	0/1:19,20:39:99:372,0,261
    24	1263	.	A	G	170.77	PASS	AC=2;AF=0.500;AN=4;DP=38;MLEAC=1;MLEAF=0.500;MQ0=0;set=HA1A22A-JB1A25B	GT:AD:DP:GQ:PL	0/1:14,10:24:99:199,0,172	./.	./.	0/1:6,8:14:89:122,0,89
    Can anyone advise?

    Cheers

    D
  • chrchang
    Member
    • Jun 2013
    • 15

    #2
    PLINK assumes chromosome 24 is the Y chromosome, and forces all nonmale Y chromosome genotypes to missing.

    With PLINK 1.07, you can hack your way around this by using --dog to force the correct chromosome count. PLINK 1.9 has the more general --chr-set flag for this (and it can also directly import VCF files with --vcf).

    Comment

    • gibberwocky
      Junior Member
      • Mar 2013
      • 8

      #3
      Much obliged, that solved the problem, figured it would be something trivial.

      D

      Comment

      Latest Articles

      Collapse

      • kinpict.com
        Reply to 16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
        by kinpict.com
        The part about this topic feels surprisingly grounded, and the details on the page is the bit that made me slow down. I’d keep <a href="https://kinpict.com/">ai family photo generator</a> bookmarked for later.
        Today, 06:37 PM
      • SEQadmin2
        16S/ITS Profiling vs. Shotgun Metagenomics: What Changes in Your Workflow?
        by SEQadmin2





        NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification,...
        10-30-2026, 06:46 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by SEQadmin2, 11-12-2026, 07:59 AM
      0 responses
      28 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 11-05-2026, 09:25 AM
      0 responses
      35 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 11-03-2026, 11:54 AM
      2 responses
      56 views
      0 reactions
      Last Post kinpict.com  
      Started by SEQadmin2, 10-28-2026, 09:57 AM
      0 responses
      175 views
      0 reactions
      Last Post SEQadmin2  
      Working...