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4
votes
6
replies
5.1k
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Taking the difference of two VCFs (or removing singletons)
genome sequencing singleton SNP filter
updated 18 months ago by ▴ 20 • written 11.1 years ago by ▴ 40
4
votes
11
replies
18k
views
11 follow
Getting data into Plink! and TreeMix
genome next-gen SNP
updated 3.6 years ago by • 0 • written 11.1 years ago by ▴ 40
1
vote
1
reply
18k
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Answer: A: Getting data into Plink! and TreeMix
updated 6.7 years ago by 45k • written 8.6 years ago by ▴ 40
1
vote
0
replies
1.9k
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Comment: C: Variant caller comparison for non-human data (highly varied populations)
7.9 years ago by hermathena ▴ 40
3
votes
2
replies
1.9k
views
Variant caller comparison for non-human data (highly varied populations)
variant calling genotyping GATK FreeBayes Platypus
8.0 years ago by hermathena ▴ 40
0
votes
0
replies
3.3k
views
Comment: C: Recalculate QUAL and INFO fields for a subset of samples in a VCF
9.7 years ago by hermathena ▴ 40
0
votes
7
replies
3.3k
views
Recalculate QUAL and INFO fields for a subset of samples in a VCF
SNP next-gen
updated 9.8 years ago by 12k • written 9.8 years ago by ▴ 40
0
votes
0
replies
5.1k
views
Comment: A: Taking the difference of two VCFs (or removing singletons)
11.1 years ago by hermathena ▴ 40
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