Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
2
votes
5
replies
3.9k
views
Beagle: Skip intervals with no common markers
beagle plink vcf conformgt
updated 3.4 years ago by ▴ 20 • written 4.8 years ago by ▴ 10
0
votes
0
replies
847
views
Comment: C: None of the variants updated from hg18 to 19
4.8 years ago by NS ▴ 10
0
votes
2
replies
847
views
None of the variants updated from hg18 to 19
LiftOver Plink Imputation GenomeBuild
4.8 years ago by NS ▴ 10
1
vote
1
reply
2.2k
views
How to create manifest file for Illumnina GTCtoVCF
illumnia gtc idat genotype sequencing
updated 4.9 years ago by ▴ 570 • written 5.4 years ago by ▴ 10
0
votes
0
replies
8.9k
views
Comment: A: Read binary Illumina GTC files (1000 genomes)
5.4 years ago by NS ▴ 10
0
votes
0
replies
3.6k
views
Answer: A: genotyping according to the red/green intensity for illumina microarray?
5.4 years ago by NS ▴ 10
0
votes
0
replies
2.9k
views
Comment: C: Extracting Ancestral allele from INFO column of vcf file
5.6 years ago by NS ▴ 10
1
vote
3
replies
2.9k
views
Extracting Ancestral allele from INFO column of vcf file
vcf SNP ancestral allele shell linux
5.6 years ago by NS ▴ 10
0
votes
0
replies
2.0k
views
Comment: A: Reference and ALT allele list for all SNPs
5.6 years ago by NS ▴ 10
0
votes
4
replies
2.0k
views
Reference and ALT allele list for all SNPs
snp
5.6 years ago by NS ▴ 10
10 results • Page 1 of 1
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6