Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
0
replies
651
views
Comment: Comment: Don't see uploaded files for linking in EGA (European Genome Archive)
11 months ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.9k
views
Comment: Comment: Singularity image is not working in nextflow
12 months ago by optimistsso4co3 ▴ 110
0
votes
2
replies
1.9k
views
Comment: Comment: Singularity image is not working in nextflow
12 months ago by optimistsso4co3 ▴ 110
0
votes
1
reply
764
views
Comment: Comment: How to interpret deletion the length of chromosome?
15 months ago by optimistsso4co3 ▴ 110
0
votes
0
replies
1.2k
views
Comment: Comment: How to filter VCF for only variants present in particular sample?
21 months ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.2k
views
Comment: Comment: How to filter VCF for only variants present in particular sample?
21 months ago by optimistsso4co3 ▴ 110
0
votes
0
replies
1.0k
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
21 months ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.0k
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
21 months ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.0k
views
Comment: Comment: Is it possible to query column of particular sample on VCF?
21 months ago by optimistsso4co3 ▴ 110
0
votes
0
replies
956
views
Comment: Comment: Research Scientist (Fungal & Algal Program)
22 months ago by optimistsso4co3 ▴ 110
0
votes
0
replies
620
views
Comment: Comment: Mobile element discovery with MELT brings different results when chromosomes are
23 months ago by optimistsso4co3 ▴ 110
0
votes
0
replies
746
views
Comment: Comment: How to correct for allele frequency mismatches?
2.2 years ago by optimistsso4co3 ▴ 110
1
vote
0
replies
1.6k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
2.4 years ago by optimistsso4co3 ▴ 110
0
votes
0
replies
1.6k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
2.4 years ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.6k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
2.4 years ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.6k
views
Comment: Comment: Why isn't it a common practice to call variant for every position in human genom
2.4 years ago by optimistsso4co3 ▴ 110
0
votes
0
replies
744
views
Comment: Comment: Wha does combineGVCFs does to loci with variant only in gVCF from another analys
2.5 years ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.2k
views
Comment: Comment: What are "must have" data types one should extract from WGS .fq data?
2.5 years ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.2k
views
Comment: Comment: What are "must have" data types one should extract from WGS .fq data?
2.5 years ago by optimistsso4co3 ▴ 110
0
votes
1
reply
810
views
Comment: Comment: Is it ok to replace missing WGS calls with reference notation "0/0"?
2.5 years ago by optimistsso4co3 ▴ 110
0
votes
1
reply
1.9k
views
Comment: Comment: How to pass custom software specific variables to nf-core/sarek nextflow pipelin
2.8 years ago by optimistsso4co3 ▴ 110
0
votes
2
replies
1.9k
views
Comment: Comment: How to pass custom software specific variables to nf-core/sarek nextflow pipelin
2.8 years ago by optimistsso4co3 ▴ 110
0
votes
0
replies
1.2k
views
Comment: Comment: How to paralle trim_galore for single sample?
2.8 years ago by optimistsso4co3 ▴ 110
0
votes
0
replies
2.9k
views
Comment: C: GTEX - how to upload more than one rsIDs to get gene expression or eQTL informat
3.6 years ago by optimistsso4co3 ▴ 110
0
votes
0
replies
1.6k
views
Comment: C: Whats the point of genotype pruning before imputation?
4.8 years ago by optimistsso4co3 ▴ 110
25 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