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comments
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2
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4.4k
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Comment:
C: Why do people not call normal and tumor variant separately for somatic mutation
updated 4.4 years ago by
Ram
43k • written 8.3 years ago by
DVA
▴ 630
0
votes
0
replies
6.4k
views
Comment:
C: Identify point mutations from each read in sam files
updated 4.5 years ago by
Ram
43k • written 8.7 years ago by
DVA
▴ 630
0
votes
0
replies
1.3k
views
Comment:
C: What happens when SNV caller looks at a SV (e.g. deletion) region?
5.2 years ago by
DVA
▴ 630
0
votes
0
replies
1.0k
views
Comment:
C: How to handle RNASeq reads that can map to both human and mouse ref (e.g. conser
5.5 years ago by
DVA
▴ 630
0
votes
0
replies
1.9k
views
Comment:
C: CIGAR and sequence length are inconsistent after HISAT alignment
5.5 years ago by
DVA
▴ 630
1
vote
0
replies
1.2k
views
Comment:
C: Count 0, 5, 20 covered sites in bam
5.7 years ago by
DVA
▴ 630
0
votes
0
replies
1.2k
views
Comment:
C: Count 0, 5, 20 covered sites in bam
5.7 years ago by
DVA
▴ 630
0
votes
0
replies
1.2k
views
Comment:
C: Count 0, 5, 20 covered sites in bam
5.7 years ago by
DVA
▴ 630
0
votes
0
replies
1.7k
views
Comment:
C: Pathway enrichment with differential expression p-values
5.9 years ago by
DVA
▴ 630
0
votes
1
reply
3.5k
views
Comment:
C: Horizontal lines in MA plot (DESeq2)
6.0 years ago by
DVA
▴ 630
0
votes
0
replies
4.5k
views
Comment:
C: Which annotation file to use
6.0 years ago by
DVA
▴ 630
0
votes
0
replies
4.5k
views
Comment:
C: Which annotation file to use
6.0 years ago by
DVA
▴ 630
0
votes
0
replies
6.4k
views
Comment:
C: High Unassigned Ambiguity in Feature Counts
6.0 years ago by
DVA
▴ 630
0
votes
2
replies
4.5k
views
Comment:
C: Which annotation file to use
6.1 years ago by
DVA
▴ 630
0
votes
1
reply
4.5k
views
Comment:
C: Which annotation file to use
6.1 years ago by
DVA
▴ 630
0
votes
0
replies
4.5k
views
Comment:
C: Which annotation file to use
6.1 years ago by
DVA
▴ 630
0
votes
1
reply
6.4k
views
Comment:
C: High Unassigned Ambiguity in Feature Counts
6.1 years ago by
DVA
▴ 630
0
votes
1
reply
2.0k
views
Comment:
C: Mask gtf file for cufflinks
6.1 years ago by
DVA
▴ 630
1
vote
0
replies
2.0k
views
Comment:
C: Mask gtf file for cufflinks
6.1 years ago by
DVA
▴ 630
0
votes
1
reply
2.0k
views
Comment:
C: Mask gtf file for cufflinks
6.1 years ago by
DVA
▴ 630
2
votes
0
replies
2.4k
views
Comment:
C: HISAT2 tmo and rna-strandness options not working as expected
6.1 years ago by
DVA
▴ 630
0
votes
1
reply
2.3k
views
Comment:
C: Reasons for polyA in RNA Seq Reads
6.2 years ago by
DVA
▴ 630
0
votes
0
replies
2.2k
views
Comment:
C: Base pair order in sequencer vs in fastq
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
5.4k
views
Comment:
C: Best way to trim PolyA in RNA Seq reads?
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
5.4k
views
Comment:
C: Best way to trim PolyA in RNA Seq reads?
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
5.4k
views
Comment:
C: Best way to trim PolyA in RNA Seq reads?
6.2 years ago by
DVA
▴ 630
0
votes
0
replies
5.4k
views
Comment:
C: Best way to trim PolyA in RNA Seq reads?
6.2 years ago by
DVA
▴ 630
0
votes
1
reply
5.4k
views
Comment:
C: Best way to trim PolyA in RNA Seq reads?
6.2 years ago by
DVA
▴ 630
0
votes
0
replies
5.4k
views
Comment:
C: Best way to trim PolyA in RNA Seq reads?
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
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
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
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
2.2k
views
Comment:
C: Locate positions in a large bed file
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
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
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
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
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
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
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
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