Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
Showing : comments
0
votes
1
reply
2.3k
views
Comment: C: WGS coverage (depth) for CNV detection
6.2 years ago by CY ▴ 750
0
votes
0
replies
1.7k
views
Comment: C: How representative the solid tumor sample is to that entire tumor lesion in term
6.2 years ago by CY ▴ 750
0
votes
1
reply
1.7k
views
Comment: C: How representative the solid tumor sample is to that entire tumor lesion in term
6.2 years ago by CY ▴ 750
0
votes
0
replies
2.7k
views
Comment: C: Reads aligning in unstranded RNA-Seq library
6.2 years ago by CY ▴ 750
0
votes
0
replies
17k
views
Comment: C: disadvantage of NextSeq 500 compared with MiSeq
6.3 years ago by CY ▴ 750
0
votes
0
replies
1.7k
views
Comment: C: ExAC includes WES of phenotyped population
6.3 years ago by CY ▴ 750
0
votes
0
replies
1.8k
views
Comment: C: Is DNA or RNA better to get somatic mutation profile for neoantigen estimation?
6.3 years ago by CY ▴ 750
0
votes
1
reply
3.1k
views
Comment: C: Infer somatic mutations without normal control
6.3 years ago by CY ▴ 750
0
votes
0
replies
3.1k
views
Comment: C: Infer somatic mutations without normal control
6.3 years ago by CY ▴ 750
1
vote
0
replies
3.1k
views
Comment: A: Infer somatic mutations without normal control
6.3 years ago by CY ▴ 750
0
votes
1
reply
2.2k
views
Comment: C: pipeline for neo-antigen identification
6.3 years ago by CY ▴ 750
0
votes
0
replies
1.5k
views
Comment: C: Why CNV calling using VarScan need two steps of fragments merging?
6.4 years ago by CY ▴ 750
0
votes
2
replies
5.1k
views
Comment: C: Fragment size and insert size
6.4 years ago by CY ▴ 750
0
votes
0
replies
5.1k
views
Comment: C: Fragment size and insert size
6.4 years ago by CY ▴ 750
0
votes
1
reply
1.5k
views
Comment: C: Why CNV calling using VarScan need two steps of fragments merging?
6.4 years ago by CY ▴ 750
0
votes
0
replies
5.1k
views
Comment: C: Fragment size and insert size
6.4 years ago by CY ▴ 750
1
vote
0
replies
2.8k
views
Comment: C: Can phasing or pre-phase during basecall cause indel?
6.4 years ago by CY ▴ 750
0
votes
1
reply
2.8k
views
Comment: C: Can phasing or pre-phase during basecall cause indel?
6.4 years ago by CY ▴ 750
0
votes
2
replies
2.8k
views
Comment: C: Can phasing or pre-phase during basecall cause indel?
6.4 years ago by CY ▴ 750
1
vote
2
replies
1.9k
views
Comment: C: Two confusion in bam format
6.6 years ago by CY ▴ 750
0
votes
0
replies
2.9k
views
Comment: C: Why perfectly match (150M) records are not primary alignment in SAM
6.6 years ago by CY ▴ 750
0
votes
0
replies
2.9k
views
Comment: C: Why perfectly match (150M) records are not primary alignment in SAM
6.6 years ago by CY ▴ 750
0
votes
2
replies
2.9k
views
Comment: C: Why perfectly match (150M) records are not primary alignment in SAM
6.6 years ago by CY ▴ 750
0
votes
1
reply
2.4k
views
Comment: C: What kind of advantage does PEAR bring?
6.6 years ago by CY ▴ 750
0
votes
1
reply
2.4k
views
Comment: C: What kind of advantage does PEAR bring?
6.6 years ago by CY ▴ 750
0
votes
0
replies
1.7k
views
Comment: C: A confusion regarding haplotype
6.6 years ago by CY ▴ 750
0
votes
1
reply
2.5k
views
Comment: C: Do multiple SNPs exist in same chromosome to be called allele?
6.6 years ago by CY ▴ 750
0
votes
2
replies
2.5k
views
Comment: C: Do multiple SNPs exist in same chromosome to be called allele?
6.6 years ago by CY ▴ 750
0
votes
0
replies
1.3k
views
Comment: C: Will random hexamer priming introduce SNP / SNV detection bias?
6.8 years ago by CY ▴ 750
0
votes
0
replies
7.0k
views
Comment: C: Bwa And Bwa Mem Produce Different Alignments
6.8 years ago by CY ▴ 750
0
votes
0
replies
1.3k
views
Comment: C: Will random hexamer priming introduce SNP / SNV detection bias?
6.8 years ago by CY ▴ 750
0
votes
0
replies
2.2k
views
Comment: C: Difference between Rad-Seq and amplicon seq
6.8 years ago by CY ▴ 750
0
votes
0
replies
2.2k
views
Comment: C: Difference between Rad-Seq and amplicon seq
6.8 years ago by CY ▴ 750
0
votes
1
reply
2.2k
views
Comment: C: Difference between Rad-Seq and amplicon seq
6.8 years ago by CY ▴ 750
0
votes
2
replies
2.2k
views
Comment: C: Difference between Rad-Seq and amplicon seq
6.8 years ago by CY ▴ 750
0
votes
0
replies
9.3k
views
Comment: C: STAR genomeLoad issue
6.8 years ago by CY ▴ 750
0
votes
1
reply
1.8k
views
Comment: C: What makes low frequency variants callers good at what they do?
6.8 years ago by CY ▴ 750
0
votes
1
reply
9.3k
views
Comment: C: STAR genomeLoad issue
6.8 years ago by CY ▴ 750
0
votes
1
reply
9.3k
views
Comment: C: STAR genomeLoad issue
6.8 years ago by CY ▴ 750
0
votes
0
replies
2.0k
views
Comment: C: Somatic variant caller
7.1 years ago by CY ▴ 750
0
votes
0
replies
5.1k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
7.5 years ago by CY ▴ 750
0
votes
1
reply
2.3k
views
Comment: C: Detecting variants at very low fractions from ctDNA
7.5 years ago by CY ▴ 750
0
votes
0
replies
1.7k
views
Comment: C: 11% mutation frequency of TP53 in non-cancer samples
7.5 years ago by CY ▴ 750
0
votes
1
reply
5.1k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
7.5 years ago by CY ▴ 750
0
votes
1
reply
5.1k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
7.5 years ago by CY ▴ 750
0
votes
0
replies
5.1k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
7.5 years ago by CY ▴ 750
0
votes
0
replies
5.1k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
7.5 years ago by CY ▴ 750
0
votes
1
reply
5.1k
views
Comment: C: Call variant from RNA-Seq data using Haplotypecaller
7.5 years ago by CY ▴ 750
148 results • Page 3 of 3
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