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Comment: C: call somatic CNV from cfDNA with normal control
6.6 years ago by CY ▴ 750
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2.5k
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Comment: C: WGS coverage (depth) for CNV detection
6.6 years ago by CY ▴ 750
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1.9k
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Comment: C: How representative the solid tumor sample is to that entire tumor lesion in term
6.6 years ago by CY ▴ 750
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1.9k
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Comment: C: How representative the solid tumor sample is to that entire tumor lesion in term
6.6 years ago by CY ▴ 750
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2.9k
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Comment: C: Reads aligning in unstranded RNA-Seq library
6.7 years ago by CY ▴ 750
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18k
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Comment: C: disadvantage of NextSeq 500 compared with MiSeq
6.7 years ago by CY ▴ 750
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1.9k
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Comment: C: ExAC includes WES of phenotyped population
6.7 years ago by CY ▴ 750
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2.0k
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Comment: C: Is DNA or RNA better to get somatic mutation profile for neoantigen estimation?
6.7 years ago by CY ▴ 750
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3.5k
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Comment: C: Infer somatic mutations without normal control
6.7 years ago by CY ▴ 750
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3.5k
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Comment: C: Infer somatic mutations without normal control
6.7 years ago by CY ▴ 750
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3.5k
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Comment: A: Infer somatic mutations without normal control
6.8 years ago by CY ▴ 750
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2.3k
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Comment: C: pipeline for neo-antigen identification
6.8 years ago by CY ▴ 750
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1.7k
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Comment: C: Why CNV calling using VarScan need two steps of fragments merging?
6.8 years ago by CY ▴ 750
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2
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5.6k
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Comment: C: Fragment size and insert size
6.8 years ago by CY ▴ 750
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5.6k
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Comment: C: Fragment size and insert size
6.8 years ago by CY ▴ 750
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1
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1.7k
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Comment: C: Why CNV calling using VarScan need two steps of fragments merging?
6.8 years ago by CY ▴ 750
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5.6k
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Comment: C: Fragment size and insert size
6.9 years ago by CY ▴ 750
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3.2k
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Comment: C: Can phasing or pre-phase during basecall cause indel?
6.9 years ago by CY ▴ 750
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3.2k
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Comment: C: Can phasing or pre-phase during basecall cause indel?
6.9 years ago by CY ▴ 750
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3.2k
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Comment: C: Can phasing or pre-phase during basecall cause indel?
6.9 years ago by CY ▴ 750
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2.0k
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Comment: C: Two confusion in bam format
7.0 years ago by CY ▴ 750
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3.0k
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Comment: C: Why perfectly match (150M) records are not primary alignment in SAM
7.0 years ago by CY ▴ 750
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3.0k
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Comment: C: Why perfectly match (150M) records are not primary alignment in SAM
7.0 years ago by CY ▴ 750
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2
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3.0k
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Comment: C: Why perfectly match (150M) records are not primary alignment in SAM
7.1 years ago by CY ▴ 750
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1
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2.6k
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Comment: C: What kind of advantage does PEAR bring?
7.1 years ago by CY ▴ 750
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1
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2.6k
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Comment: C: What kind of advantage does PEAR bring?
7.1 years ago by CY ▴ 750
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1.9k
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Comment: C: A confusion regarding haplotype
7.1 years ago by CY ▴ 750
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2.7k
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Comment: C: Do multiple SNPs exist in same chromosome to be called allele?
7.1 years ago by CY ▴ 750
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2
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2.7k
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Comment: C: Do multiple SNPs exist in same chromosome to be called allele?
7.1 years ago by CY ▴ 750
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1.5k
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Comment: C: Will random hexamer priming introduce SNP / SNV detection bias?
7.2 years ago by CY ▴ 750
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7.2k
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Comment: C: Bwa And Bwa Mem Produce Different Alignments
7.2 years ago by CY ▴ 750
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1.5k
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Comment: C: Will random hexamer priming introduce SNP / SNV detection bias?
7.2 years ago by CY ▴ 750
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2.4k
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Comment: C: Difference between Rad-Seq and amplicon seq
7.2 years ago by CY ▴ 750
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2.4k
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Comment: C: Difference between Rad-Seq and amplicon seq
7.2 years ago by CY ▴ 750
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1
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2.4k
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Comment: C: Difference between Rad-Seq and amplicon seq
7.2 years ago by CY ▴ 750
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2.4k
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Comment: C: Difference between Rad-Seq and amplicon seq
7.2 years ago by CY ▴ 750
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10.0k
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Comment: C: STAR genomeLoad issue
7.3 years ago by CY ▴ 750
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1
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1.9k
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Comment: C: What makes low frequency variants callers good at what they do?
7.3 years ago by CY ▴ 750
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1
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10.0k
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Comment: C: STAR genomeLoad issue
7.3 years ago by CY ▴ 750
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1
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10.0k
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Comment: C: STAR genomeLoad issue
7.3 years ago by CY ▴ 750
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2.1k
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Comment: C: Somatic variant caller
7.6 years ago by CY ▴ 750
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5.4k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.0 years ago by CY ▴ 750
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1
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2.5k
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Comment: C: Detecting variants at very low fractions from ctDNA
8.0 years ago by CY ▴ 750
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1.8k
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Comment: C: 11% mutation frequency of TP53 in non-cancer samples
8.0 years ago by CY ▴ 750
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1
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5.4k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.0 years ago by CY ▴ 750
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1
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5.4k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.0 years ago by CY ▴ 750
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5.4k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.0 years ago by CY ▴ 750
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0
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5.4k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.0 years ago by CY ▴ 750
0
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1
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5.4k
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Comment: C: Call variant from RNA-Seq data using Haplotypecaller
8.0 years ago by CY ▴ 750
149 results • Page 3 of 3
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