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0
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0
replies
9.7k
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Comment:
C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by
DVA
▴ 630
0
votes
0
replies
9.7k
views
Comment:
C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by
DVA
▴ 630
0
votes
0
replies
9.7k
views
Comment:
C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by
DVA
▴ 630
0
votes
0
replies
9.7k
views
Comment:
C: How do people know to use at least 30X coverage in WGS?
7.6 years ago by
DVA
▴ 630
1
vote
1
reply
1.2k
views
Comment:
C: Filter for Smith_Waterman local alignment algorithm
7.9 years ago by
DVA
▴ 630
1
vote
0
replies
10k
views
Comment:
C: How To Split Reads For Different Flowcell Lanes In Fastq Files?
7.9 years ago by
DVA
▴ 630
0
votes
0
replies
3.6k
views
Comment:
C: Does BWA (BWA-MEM) care about the identity and coverage of the mapped reads?
8.0 years ago by
DVA
▴ 630
0
votes
0
replies
4.2k
views
Comment:
C: about somatic mutation calling
8.0 years ago by
DVA
▴ 630
0
votes
0
replies
3.3k
views
Comment:
C: Non-cancer somatic mutation calling
8.0 years ago by
DVA
▴ 630
10
votes
8
replies
3.3k
views
Non-cancer somatic mutation calling
somatic mutations
mutect
varscan
samtools
gatk
8.0 years ago by
DVA
▴ 630
0
votes
1
reply
3.3k
views
Comment:
C: Non-cancer somatic mutation calling
8.0 years ago by
DVA
▴ 630
0
votes
0
replies
3.3k
views
Comment:
C: Non-cancer somatic mutation calling
8.0 years ago by
DVA
▴ 630
0
votes
0
replies
3.3k
views
Comment:
C: Non-cancer somatic mutation calling
8.0 years ago by
DVA
▴ 630
0
votes
1
reply
4.2k
views
Comment:
C: about somatic mutation calling
8.0 years ago by
DVA
▴ 630
0
votes
1
reply
4.2k
views
Comment:
C: about somatic mutation calling
8.0 years ago by
DVA
▴ 630
1
vote
0
replies
1.3k
views
Comment:
C: identifying aspecific snp in sequenced genes
8.0 years ago by
DVA
▴ 630
0
votes
1
reply
1.3k
views
Answer:
A: identifying aspecific snp in sequenced genes
8.0 years ago by
DVA
▴ 630
1
vote
0
replies
1.5k
views
Comment:
C: how to query dbsnp locally
8.0 years ago by
DVA
▴ 630
2
votes
0
replies
3.5k
views
Comment:
C: mate pair trimming ?
8.0 years ago by
DVA
▴ 630
3
votes
0
replies
4.1k
views
Answer:
A: Illumina's HiSeq strange Phred quality score
8.0 years ago by
DVA
▴ 630
1
vote
0
replies
2.1k
views
Answer:
A: The gene TGFb isn't measured in Affymetrix HT Human Genome U133 Array Plate Set?
8.0 years ago by
DVA
▴ 630
4
votes
1
reply
45k
views
Answer:
A: How To Sort Sam File
8.1 years ago by
DVA
▴ 630
1
vote
0
replies
2.3k
views
Answer:
A: VCFtools: how does --diff option consider genotypes
8.2 years ago by
DVA
▴ 630
1
vote
1
reply
2.3k
views
VCFtools: how does --diff option consider genotypes
vcf
updated 21 months ago by
Ram
43k • written 8.3 years ago by
DVA
▴ 630
0
votes
0
replies
3.6k
views
Output all allele counts at each position using bcftools
bcftools
samtools
8.2 years ago by
DVA
▴ 630
0
votes
0
replies
1.6k
views
Comment:
C: Extract genotype from hg19
8.2 years ago by
DVA
▴ 630
2
votes
2
replies
1.6k
views
Extract genotype from hg19
hg19
updated 8.2 years ago by
Chris Fields
★ 2.2k • written 8.2 years ago by
DVA
▴ 630
0
votes
0
replies
2.0k
views
Comment:
C: Can't locate dbSNP 131 anymore?
8.2 years ago by
DVA
▴ 630
2
votes
0
replies
2.0k
views
Answer:
Answer: Can't locate dbSNP 131 anymore?
updated 22 months ago by
Ram
43k • written 8.2 years ago by
DVA
▴ 630
3
votes
5
replies
2.0k
views
Can't locate dbSNP 131 anymore?
dbsnp
updated 22 months ago by
Ram
43k • written 8.2 years ago by
DVA
▴ 630
0
votes
0
replies
2.0k
views
Comment:
Comment: Can't locate dbSNP 131 anymore?
updated 22 months ago by
Ram
43k • written 8.2 years ago by
DVA
▴ 630
0
votes
1
reply
1.3k
views
Microarray vs WGS using a real dataset?
microarray
wgs
updated 21 months ago by
Ram
43k • written 8.3 years ago by
DVA
▴ 630
0
votes
0
replies
4.4k
views
Comment:
C: Why do people not call normal and tumor variant separately for somatic mutation
8.3 years ago by
DVA
▴ 630
0
votes
0
replies
4.4k
views
Comment:
C: Why do people not call normal and tumor variant separately for somatic mutation
8.3 years ago by
DVA
▴ 630
13
votes
6
replies
4.4k
views
Why do people not call normal and tumor variant separately for somatic mutation identification?
snp
updated 8.3 years ago by
Chris Miller
22k • written 8.3 years ago by
DVA
▴ 630
0
votes
1
reply
2.1k
views
Read Orientations in IGV view of Bisulfite Sequencing
igv
bisulfite-sequencing
updated 20 months ago by
Ram
43k • written 8.6 years ago by
DVA
▴ 630
0
votes
1
reply
3.6k
views
Comment:
C: Manually edit the flags in a sam file
8.6 years ago by
DVA
▴ 630
0
votes
1
reply
3.6k
views
Comment:
C: Manually edit the flags in a sam file
8.6 years ago by
DVA
▴ 630
0
votes
0
replies
3.6k
views
Comment:
Comment: Manually edit the flags in a sam file
updated 20 months ago by
Ram
43k • written 8.6 years ago by
DVA
▴ 630
0
votes
0
replies
3.6k
views
Comment:
Comment: Manually edit the flags in a sam file
updated 20 months ago by
Ram
43k • written 8.6 years ago by
DVA
▴ 630
4
votes
8
replies
3.6k
views
Manually edit the flags in a sam file
sam
updated 20 months ago by
Ram
43k • written 8.6 years ago by
DVA
▴ 630
0
votes
0
replies
6.4k
views
Comment:
C: Identify point mutations from each read in sam files
8.7 years ago by
DVA
▴ 630
0
votes
1
reply
6.4k
views
Comment:
C: Identify point mutations from each read in sam files
8.7 years ago by
DVA
▴ 630
0
votes
1
reply
6.4k
views
Comment:
Comment: Identify point mutations from each read in sam files
updated 19 months ago by
Ram
43k • written 8.7 years ago by
DVA
▴ 630
0
votes
0
replies
6.4k
views
Comment:
C: Identify point mutations from each read in sam files
8.7 years ago by
DVA
▴ 630
6
votes
12
replies
6.4k
views
Identify point mutations from each read in sam files
sam
mutations
updated 19 months ago by
Ram
43k • written 8.7 years ago by
DVA
▴ 630
0
votes
0
replies
4.0k
views
Comment:
C: Question about Details in Picard MarkDuplicates
8.9 years ago by
DVA
▴ 630
4
votes
2
replies
4.0k
views
Question about Details in Picard MarkDuplicates
sequence
updated 16 months ago by
Ram
43k • written 8.9 years ago by
DVA
▴ 630
0
votes
0
replies
3.7k
views
Comment:
C: Remove both pair end reads with low mapping quality using Samtools
9.4 years ago by
DVA
▴ 630
0
votes
0
replies
3.7k
views
Comment:
C: Remove both pair end reads with low mapping quality using Samtools
9.4 years ago by
DVA
▴ 630
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