Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
1
reply
887
views
Comment: C: Different NGS runs for paired samples
4.0 years ago by gab ▴ 20
0
votes
1
reply
1.1k
views
Comment: C: VCF rare variants and exon
4.0 years ago by gab ▴ 20
0
votes
0
replies
955
views
Comment: C: different bam from same NGS data
5.3 years ago by gab ▴ 20
0
votes
0
replies
955
views
Comment: C: different bam from same NGS data
5.3 years ago by gab ▴ 20
0
votes
0
replies
3.1k
views
Comment: C: coverage of a SNP site?
5.5 years ago by gab ▴ 20
0
votes
1
reply
2.0k
views
Comment: C: Calling somatic variants with Varscan
5.5 years ago by gab ▴ 20
1
vote
0
replies
1.1k
views
Comment: C: Whole Exome Sequencing Depth
5.5 years ago by gab ▴ 20
0
votes
0
replies
1.3k
views
Comment: C: Losing somatic SNPs
5.7 years ago by gab ▴ 20
0
votes
1
reply
1.3k
views
Comment: C: Losing somatic SNPs
5.7 years ago by gab ▴ 20
9 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