Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
1
reply
406
views
Comment: Comment: How to interpret deletion the length of chromosome?
9 weeks ago by optimistsso4co3 ▴ 100
0
votes
0
replies
615
views
Comment: Comment: How to filter VCF for only variants present in particular sample?
7 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
615
views
Comment: Comment: How to filter VCF for only variants present in particular sample?
7 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
638
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
7 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
638
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
7 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
638
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
7 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
659
views
Comment: Comment: Research Scientist (Fungal & Algal Program)
9 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
404
views
Comment: Comment: Mobile element discovery with MELT brings different results when chromosomes are
9 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
433
views
Comment: Comment: How to correct for allele frequency mismatches?
14 months ago by optimistsso4co3 ▴ 100
1
vote
0
replies
992
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
15 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
992
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
15 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
992
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
15 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
992
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
15 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
525
views
Comment: Comment: Wha does combineGVCFs does to loci with variant only in gVCF from another analys
16 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
831
views
Comment: Comment: What are "must have" data types one should extract from WGS .fq data?
16 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
831
views
Comment: Comment: What are "must have" data types one should extract from WGS .fq data?
16 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
571
views
Comment: Comment: Is it ok to replace missing WGS calls with reference notation "0/0"?
16 months ago by optimistsso4co3 ▴ 100
0
votes
1
reply
1.3k
views
Comment: Comment: How to pass custom software specific variables to nf-core/sarek nextflow pipelin
20 months ago by optimistsso4co3 ▴ 100
0
votes
2
replies
1.3k
views
Comment: Comment: How to pass custom software specific variables to nf-core/sarek nextflow pipelin
20 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
818
views
Comment: Comment: How to paralle trim_galore for single sample?
20 months ago by optimistsso4co3 ▴ 100
0
votes
0
replies
2.2k
views
Comment: C: GTEX - how to upload more than one rsIDs to get gene expression or eQTL informat
2.5 years ago by optimistsso4co3 ▴ 100
0
votes
0
replies
1.3k
views
Comment: C: Whats the point of genotype pruning before imputation?
3.7 years ago by optimistsso4co3 ▴ 100
22 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