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0
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1
reply
4.3k
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Comment:
C: High A in "Per base sequence content" of fastQC report
6.2 years ago by
DVA
▴ 630
0
votes
0
replies
4.3k
views
Comment:
C: High A in "Per base sequence content" of fastQC report
6.2 years ago by
DVA
▴ 630
5
votes
10
replies
4.3k
views
High A in "Per base sequence content" of fastQC report
fastqc
6.2 years ago by
DVA
▴ 630
0
votes
0
replies
4.3k
views
Comment:
C: High A in "Per base sequence content" of fastQC report
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
4.3k
views
Comment:
C: High A in "Per base sequence content" of fastQC report
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
4.3k
views
Comment:
C: High A in "Per base sequence content" of fastQC report
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
2.1k
views
Comment:
C: Analysis of sequencing duplicates
6.4 years ago by
DVA
▴ 630
2
votes
9
replies
2.1k
views
Analysis of sequencing duplicates
duplicate
updated 6.5 years ago by
GenoMax
142k • written 6.5 years ago by
DVA
▴ 630
0
votes
1
reply
2.1k
views
Comment:
C: Analysis of sequencing duplicates
6.5 years ago by
DVA
▴ 630
0
votes
1
reply
2.1k
views
Comment:
C: Analysis of sequencing duplicates
6.5 years ago by
DVA
▴ 630
0
votes
0
replies
1.1k
views
Locate LOH using SNV VCF files
snp
6.5 years ago by
DVA
▴ 630
0
votes
0
replies
2.2k
views
Comment:
C: Locate positions in a large bed file
6.6 years ago by
DVA
▴ 630
3
votes
4
replies
2.2k
views
Locate positions in a large bed file
bed
updated 6.6 years ago by
Alex Reynolds
35k • written 6.6 years ago by
DVA
▴ 630
0
votes
0
replies
2.2k
views
Comment:
C: Locate positions in a large bed file
6.6 years ago by
DVA
▴ 630
3
votes
5
replies
3.9k
views
Mutect 2 on WGS data takes too long to run
mutect
wgs
updated 6.8 years ago by
donfreed
★ 1.6k • written 6.8 years ago by
DVA
▴ 630
0
votes
1
reply
3.9k
views
Comment:
C: Mutect 2 on WGS data takes too long to run
6.8 years ago by
DVA
▴ 630
6
votes
3
replies
2.5k
views
somatic calls by somatic SNV caller differ a lot, when comparing with cancer minors normal germline calls
somatic
SNV
SNP
updated 6.8 years ago by
d-cameron
★ 2.9k • written 6.8 years ago by
DVA
▴ 630
0
votes
0
replies
2.5k
views
Comment:
C: GT field in VCF only has one number?
6.8 years ago by
DVA
▴ 630
0
votes
0
replies
2.5k
views
Comment:
C: somatic calls by somatic SNV caller differ a lot, when comparing with cancer min
6.8 years ago by
DVA
▴ 630
3
votes
3
replies
2.5k
views
GT field in VCF only has one number?
vcf
6.8 years ago by
DVA
▴ 630
0
votes
0
replies
2.5k
views
Comment:
C: GT field in VCF only has one number?
6.8 years ago by
DVA
▴ 630
0
votes
0
replies
2.3k
views
Comment:
C: Effectively search for positions in large bedgraph files using python (or other
6.8 years ago by
DVA
▴ 630
2
votes
2
replies
2.3k
views
Effectively search for positions in large bedgraph files using python (or other language if needed)
bedgraph
python
updated 6.8 years ago by
Alex Reynolds
35k • written 6.8 years ago by
DVA
▴ 630
0
votes
0
replies
1.7k
views
Comment:
C: how can I keep only those SNP in file "a" which match to SNPs in file "b"?
6.9 years ago by
DVA
▴ 630
0
votes
1
reply
1.7k
views
Answer:
A: how can I keep only those SNP in file "a" which match to SNPs in file "b"?
6.9 years ago by
DVA
▴ 630
3
votes
2
replies
2.4k
views
snpEff database to annotate b37 GATK output
snpeff
gatk
updated 6.9 years ago by
hns
▴ 150 • written 7.1 years ago by
DVA
▴ 630
2
votes
0
replies
3.5k
views
Comment:
C: Seeking private tutor to learn RNA/ChIP-Seq data analysis
6.9 years ago by
DVA
▴ 630
4
votes
5
replies
4.2k
views
No output from samtools index?
samtools
7.0 years ago by
DVA
▴ 630
0
votes
0
replies
4.2k
views
Comment:
C: No output from samtools index?
7.0 years ago by
DVA
▴ 630
0
votes
0
replies
4.2k
views
Comment:
C: No output from samtools index?
7.0 years ago by
DVA
▴ 630
0
votes
0
replies
10k
views
Comment:
C: COSMIC vcf file compatibility for Mutect2
7.1 years ago by
DVA
▴ 630
0
votes
1
reply
1.6k
views
Comment:
C: snp frequency with annovar
7.2 years ago by
DVA
▴ 630
0
votes
0
replies
2.7k
views
Comment:
C: Running iqtree in a python script?
7.3 years ago by
DVA
▴ 630
1
vote
0
replies
4.4k
views
Answer:
A: Help: Read Sam File and find chromosome
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
5.5k
views
Comment:
C: Develop an R package for CRAN vs BioConductor
7.3 years ago by
DVA
▴ 630
50
votes
17
replies
5.5k
views
7 follow
Develop an R package for CRAN vs BioConductor
bioconductor
cran
r
packages
updated 7.3 years ago by
ddiez
★ 2.0k • written 7.3 years ago by
DVA
▴ 630
0
votes
1
reply
5.5k
views
Comment:
C: Develop an R package for CRAN vs BioConductor
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
5.5k
views
Comment:
C: Develop an R package for CRAN vs BioConductor
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
5.5k
views
Comment:
C: Develop an R package for CRAN vs BioConductor
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
5.5k
views
Comment:
C: Develop an R package for CRAN vs BioConductor
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
7.6k
views
Comment:
C: Extract surrounding genome sequences given certain locations using R
7.3 years ago by
DVA
▴ 630
10
votes
11
replies
7.6k
views
Extract surrounding genome sequences given certain locations using R
R
package
genome
sequence
updated 7.3 years ago by
ddiez
★ 2.0k • written 7.3 years ago by
DVA
▴ 630
0
votes
0
replies
7.6k
views
Comment:
C: Extract surrounding genome sequences given certain locations using R
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
7.6k
views
Comment:
C: Extract surrounding genome sequences given certain locations using R
7.3 years ago by
DVA
▴ 630
0
votes
0
replies
1.5k
views
Comment:
C: Convert BLAST NC_ labels to chromosome label
7.4 years ago by
DVA
▴ 630
3
votes
2
replies
1.5k
views
Convert BLAST NC_ labels to chromosome label
blast
updated 7.4 years ago by
mastal511
★ 2.1k • written 7.4 years ago by
DVA
▴ 630
0
votes
1
reply
1.3k
views
Other genetic variants representation format besides VCF
vcf
variants
updated 7.4 years ago by
Brian Bushnell
20k • written 7.4 years ago by
DVA
▴ 630
10
votes
10
replies
9.7k
views
How do people know to use at least 30X coverage in WGS?
sequencing
wgs
coverage
updated 7.5 years ago by
Brian Bushnell
20k • written 7.6 years ago by
DVA
▴ 630
0
votes
0
replies
2.8k
views
Comment:
C: Large input when using jellyfish
7.5 years ago by
DVA
▴ 630
2
votes
2
replies
2.8k
views
Large input when using jellyfish
jellyfish
next-gen
whole genome seq
7.5 years ago by
DVA
▴ 630
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