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4
votes
6
replies
4.2k
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Taking the difference of two VCFs (or removing singletons)
genome sequencing singleton SNP filter
updated 7 months ago by ▴ 20 • written 10.3 years ago by ▴ 40
4
votes
11
replies
16k
views
11 follow
Getting data into Plink! and TreeMix
genome next-gen SNP
updated 2.8 years ago by • 0 • written 10.2 years ago by ▴ 40
1
vote
1
reply
16k
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Answer: A: Getting data into Plink! and TreeMix
updated 5.9 years ago by 44k • written 7.8 years ago by ▴ 40
1
vote
0
replies
1.6k
views
Comment: C: Variant caller comparison for non-human data (highly varied populations)
7.1 years ago by hermathena ▴ 40
3
votes
2
replies
1.6k
views
Variant caller comparison for non-human data (highly varied populations)
variant calling genotyping GATK FreeBayes Platypus
7.1 years ago by hermathena ▴ 40
0
votes
0
replies
2.7k
views
Comment: C: Recalculate QUAL and INFO fields for a subset of samples in a VCF
8.9 years ago by hermathena ▴ 40
0
votes
7
replies
2.7k
views
Recalculate QUAL and INFO fields for a subset of samples in a VCF
SNP next-gen
updated 8.9 years ago by 12k • written 8.9 years ago by ▴ 40
0
votes
0
replies
4.2k
views
Comment: A: Taking the difference of two VCFs (or removing singletons)
10.2 years ago by hermathena ▴ 40
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