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SNP dataset and Z Score
gwas z-score snp written 2.4 years ago by nkhan.mscs15seecs70 • updated 18 hours ago by zx87549.6k
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Negative Fst values from VCFtools result
genome vcftool fst snp written 1 day ago by nitinra0 • updated 1 day ago by genomax90k
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Handing scafflold names for plink bed file
bedfile genome plink snp written 3 days ago by nitinra0 • updated 2 days ago by genomax90k
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Error while merging multiple vcf files using Picard MergeVcfs
genome gatk picard tool snp written 3 days ago by nitinra0 • updated 3 days ago by Medhat8.8k
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How do I subset VCF based on genotype?
snp written 3 days ago by Tine10 • updated 3 days ago by Kevin Blighe66k
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Microarry (GSA) manifest file and CytoSNP-850K manifest file comparison
snp written 4 days ago by MOJ0 • updated 4 days ago by curious440
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Allele frequency calculation for genotype dosage value
snp written 3.2 years ago by drsachinbioinfo20 • updated 4 days ago by Biostar ♦♦ 20
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Annotating VCF files
snp written 4 days ago by vinayjrao180
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bcftools error duplicate samples
gene R snp written 5 days ago by abyousaf0
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Unrecognized flag in Plink2
genome snp written 5 days ago by A.Mubashir 0
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GCTA-COJO slct conceptual question
snp written 5 days ago by brighteyes10170 • updated 5 days ago by genomax90k
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Finding unique variants by sample ID in a multisample vcf
vcf bcftools vep snp written 6 days ago by tacrolimus50 • updated 6 days ago by brunobsouzaa290
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In Need of Help with NCBI Database
ncbi mutation entrez snp written 7 days ago by deemassh0 • updated 7 days ago by h.mon31k
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merging multiple vcfs by column in Picard
vcf genome picard snp written 7 days ago by nitinra0 • updated 7 days ago by Pierre Lindenbaum130k
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Converting MNP to SNP
vcf freebayes snp written 2.9 years ago by finswimmer13k • updated 8 days ago by cicindel20
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Visualizing gene variants (gviz)
gviz snp written 9 days ago by bsmith030465150
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How to incorporate interaction between two alleles in ApoE for Alzheimer's polygenic risk score?
snp written 22 months ago by kl10 • updated 11 days ago by Biostar ♦♦ 20
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