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Beagle: Skip intervals with no common markers
beagle plink vcf conformgt
updated 4.0 years ago by ▴ 20 • written 5.3 years ago by ▴ 10
0
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0
replies
968
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Comment: C: None of the variants updated from hg18 to 19
5.3 years ago by NS ▴ 10
0
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2
replies
968
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None of the variants updated from hg18 to 19
LiftOver Plink Imputation GenomeBuild
5.3 years ago by NS ▴ 10
1
vote
1
reply
2.4k
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How to create manifest file for Illumnina GTCtoVCF
illumnia gtc idat genotype sequencing
updated 5.5 years ago by ▴ 630 • written 6.0 years ago by ▴ 10
0
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0
replies
9.7k
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Comment: A: Read binary Illumina GTC files (1000 genomes)
6.0 years ago by NS ▴ 10
0
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0
replies
3.9k
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Answer: A: genotyping according to the red/green intensity for illumina microarray?
6.0 years ago by NS ▴ 10
0
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0
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3.2k
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Comment: C: Extracting Ancestral allele from INFO column of vcf file
6.2 years ago by NS ▴ 10
1
vote
3
replies
3.2k
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Extracting Ancestral allele from INFO column of vcf file
vcf SNP ancestral allele shell linux
6.2 years ago by NS ▴ 10
0
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0
replies
2.1k
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Comment: A: Reference and ALT allele list for all SNPs
6.2 years ago by NS ▴ 10
0
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4
replies
2.1k
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Reference and ALT allele list for all SNPs
snp
6.2 years ago by NS ▴ 10
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