Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
1
reply
1.1k
views
Comment: Comment: ancestral allele SNP mouse biomart
2.6 years ago by serpalma.v ▴ 80
0
votes
0
replies
972
views
Comment: C: Insert size 350bp vs 400bp, any major downstream difference?
4.0 years ago by serpalma.v ▴ 80
0
votes
1
reply
1.2k
views
Comment: C: How to extract intervals for regions that are masked?
4.1 years ago by serpalma.v ▴ 80
0
votes
0
replies
1.5k
views
Comment: C: Are there any issues with using sample reads coming from different technologies
4.2 years ago by serpalma.v ▴ 80
0
votes
1
reply
1.5k
views
Comment: C: Are there any issues with using sample reads coming from different technologies
4.2 years ago by serpalma.v ▴ 80
0
votes
0
replies
1.9k
views
Comment: C: What test to apply to detect genomic signatures of selection?
updated 4.4 years ago by 43k • written 8.3 years ago by ▴ 80
0
votes
0
replies
1.9k
views
Comment: C: How does plink calculates linkage disequilibrium (r2) in unphased data?
4.7 years ago by serpalma.v ▴ 80
0
votes
1
reply
1.4k
views
Comment: C: Interpretation of full LD between extremely distant SNPs
4.9 years ago by serpalma.v ▴ 80
0
votes
1
reply
16k
views
Comment: C: Best tool for variant calling
5.1 years ago by serpalma.v ▴ 80
0
votes
1
reply
16k
views
Comment: C: Best tool for variant calling
5.2 years ago by serpalma.v ▴ 80
0
votes
1
reply
16k
views
Comment: C: Best tool for variant calling
5.2 years ago by serpalma.v ▴ 80
0
votes
0
replies
1.1k
views
Comment: C: How to select SNPs the most conservative way after WGS Variant Calling?
5.2 years ago by serpalma.v ▴ 80
0
votes
1
reply
16k
views
Comment: C: Best tool for variant calling
5.2 years ago by serpalma.v ▴ 80
0
votes
0
replies
4.8k
views
Comment: C: Overrepresented stretches of Gs in NovaSeq library
5.3 years ago by serpalma.v ▴ 80
0
votes
1
reply
14k
views
Comment: C: what cause poly-G from NextSeq
5.3 years ago by serpalma.v ▴ 80
0
votes
2
replies
4.8k
views
Comment: C: Overrepresented stretches of Gs in NovaSeq library
5.3 years ago by serpalma.v ▴ 80
0
votes
1
reply
3.5k
views
Comment: C: bcftool (mpileup, call) extremely slow on 60 BAMs (WGS 20x)
5.4 years ago by serpalma.v ▴ 80
0
votes
1
reply
3.5k
views
Comment: C: bcftool (mpileup, call) extremely slow on 60 BAMs (WGS 20x)
5.4 years ago by serpalma.v ▴ 80
0
votes
0
replies
2.5k
views
Comment: C: GATK variantFiltration unexpected behaviour?
5.4 years ago by serpalma.v ▴ 80
0
votes
1
reply
3.2k
views
Comment: C: Only females but still few reads map to Y chromosome
5.4 years ago by serpalma.v ▴ 80
0
votes
1
reply
3.2k
views
Comment: C: Only females but still few reads map to Y chromosome
5.4 years ago by serpalma.v ▴ 80
0
votes
0
replies
3.2k
views
Comment: C: Only females but still few reads map to Y chromosome
5.4 years ago by serpalma.v ▴ 80
0
votes
0
replies
2.2k
views
Comment: C: Per base GC content with a shoulder after adapter removal and trimming
5.6 years ago by serpalma.v ▴ 80
0
votes
1
reply
2.2k
views
Comment: C: Per base GC content with a shoulder after adapter removal and trimming
5.6 years ago by serpalma.v ▴ 80
0
votes
0
replies
1.3k
views
Comment: C: what is the conventional apporach to calculate depth of coverage?
5.6 years ago by serpalma.v ▴ 80
0
votes
1
reply
2.2k
views
Comment: C: Which indication of a failure can be found in bwa-mem or samtools' output?
5.7 years ago by serpalma.v ▴ 80
0
votes
1
reply
2.2k
views
Comment: C: Which indication of a failure can be found in bwa-mem or samtools' output?
5.7 years ago by serpalma.v ▴ 80
0
votes
1
reply
2.2k
views
Comment: C: Which indication of a failure can be found in bwa-mem or samtools' output?
5.7 years ago by serpalma.v ▴ 80
0
votes
0
replies
2.7k
views
Comment: C: Adding read group to bam files from multiplexed samples
5.8 years ago by serpalma.v ▴ 80
0
votes
1
reply
2.7k
views
Comment: C: Adding read group to bam files from multiplexed samples
5.8 years ago by serpalma.v ▴ 80
0
votes
0
replies
3.6k
views
Comment: C: Fix per tile sequence quality?
5.8 years ago by serpalma.v ▴ 80
0
votes
0
replies
2.8k
views
Comment: C: How to find the self aligned repeat region in human genome
6.7 years ago by serpalma.v ▴ 80
0
votes
1
reply
2.0k
views
Comment: C: Feasible Annotation of 4 million unique SNPs
6.8 years ago by serpalma.v ▴ 80
0
votes
0
replies
2.0k
views
Comment: C: Feasible Annotation of 4 million unique SNPs
6.8 years ago by serpalma.v ▴ 80
0
votes
1
reply
4.0k
views
Comment: C: basic concepts behind --sjdbOverhang (STAR)
7.1 years ago by serpalma.v ▴ 80
0
votes
1
reply
1.3k
views
Comment: C: How to project the read count?(HiSeq2500, mouse genome, resequencing)
7.8 years ago by serpalma.v ▴ 80
0
votes
0
replies
1.2k
views
Comment: C: Assigning time to data analysis (detection of signatures of selection)
7.8 years ago by serpalma.v ▴ 80
0
votes
0
replies
5.8k
views
Comment: Comment: topGO approach for a list a genes without expression
updated 3.1 years ago by 43k • written 9.5 years ago by ▴ 80
0
votes
0
replies
3.5k
views
Comment: C: Max Length With Fastx Tookit
10.4 years ago by serpalma.v ▴ 80
0
votes
1
reply
3.5k
views
Comment: C: Max Length With Fastx Tookit
10.4 years ago by serpalma.v ▴ 80
40 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