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Answer: A: Panel of Normals
5.7 years ago by markus.riester ▴ 550
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Comment: C: PureCN: Estimating tumor purity and ploidy
5.7 years ago by markus.riester ▴ 550
1
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1.3k
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Answer: A: Pool of Normals- PureCN
5.7 years ago by markus.riester ▴ 550
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1.5k
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Comment: C: PureCN: Estimating tumor purity and ploidy
5.7 years ago by markus.riester ▴ 550
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1.8k
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Comment: C: PureCN: Tool for estimation of tumor purity and ploidy
5.7 years ago by markus.riester ▴ 550
1
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1.8k
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Answer: A: PureCN: Tool for estimation of tumor purity and ploidy
5.7 years ago by markus.riester ▴ 550
1
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1.7k
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Answer: A: Are the somatic mutations in TCGA filtered for germline mutations?
5.8 years ago by markus.riester ▴ 550
1
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3.0k
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Answer: A: How to use result of CNVkit to estimate purity by PureCN
6.2 years ago by markus.riester ▴ 550
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1.6k
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Answer: A: Calling somatic muttaions in pediatric tumor samples without matched normal samp
6.5 years ago by markus.riester ▴ 550
2
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13k
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Comment: C: TMB Tumor Mutation Burden
6.8 years ago by markus.riester ▴ 550
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3.6k
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Comment: C: Infer somatic mutations without normal control
6.8 years ago by markus.riester ▴ 550
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3.6k
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Answer: A: Infer somatic mutations without normal control
6.9 years ago by markus.riester ▴ 550
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1.3k
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Answer: A: WES chromosome Y off-target reads coverage compare to autosome
6.9 years ago by markus.riester ▴ 550
1
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0
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3.9k
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Answer: A: Suggestions regarding bioinformatics journal
6.9 years ago by markus.riester ▴ 550
1
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0
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5.0k
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Answer: A: ABSOLUTE R package - CreateReviewObject Error, Error in seq_len(M) : argument mu
7.2 years ago by markus.riester ▴ 550
0
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0
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3.3k
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Comment: C: Tumor purity estimation by allele frequency of COSMIC identified somatic mutatio
7.2 years ago by markus.riester ▴ 550
2
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0
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3.0k
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Answer: A: CNV calls in VCF format, conversion to PCAWG-11 Calibration
7.2 years ago by markus.riester ▴ 550
0
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1
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7.4k
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Comment: C: tumor only variant calling tools
7.2 years ago by markus.riester ▴ 550
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0
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7.4k
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Comment: C: tumor only variant calling tools
7.2 years ago by markus.riester ▴ 550
0
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0
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4.4k
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Answer: A: WES samples failing ABSOLUTE
7.3 years ago by markus.riester ▴ 550
1
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0
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2.7k
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Answer: A: Merging CNVs from multiple tumor samples from the same patient
7.3 years ago by markus.riester ▴ 550
0
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1
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2.8k
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Comment: C: WES or WGS analysis of cancer samples with no matched germline
7.4 years ago by markus.riester ▴ 550
7
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1
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2.8k
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Answer: A: WES or WGS analysis of cancer samples with no matched germline
7.4 years ago by markus.riester ▴ 550
2
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0
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9.5k
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Answer: A: Tumor Mutation Burden calculation: all_mut vs non_synonym
7.4 years ago by markus.riester ▴ 550
1
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0
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1.3k
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Comment: C: Detecting CNV can't cover aneuploidy situation
7.4 years ago by markus.riester ▴ 550
0
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0
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3.5k
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Comment: C: "Shifted" copy number ratios coming from cnvkit?
7.5 years ago by markus.riester ▴ 550
2
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2
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3.5k
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Answer: A: "Shifted" copy number ratios coming from cnvkit?
7.5 years ago by markus.riester ▴ 550
2
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0
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3.8k
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Answer: C: Is there a consensus that Matlab is the wrong language for open-access bioinform
7.7 years ago by markus.riester ▴ 550
2
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0
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2.6k
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Answer: A: Comparison of exome variant allele frequencies
7.7 years ago by markus.riester ▴ 550
0
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0
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5.1k
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Answer: A: Copy Number Variation Tools
7.7 years ago by markus.riester ▴ 550
3
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1
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2.1k
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Answer: A: Somatic variant caller
7.7 years ago by markus.riester ▴ 550
0
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1
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1.6k
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Comment: C: SNP Array data with 0 copies for a segment
7.7 years ago by markus.riester ▴ 550
0
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0
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3.9k
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Comment: C: The ABSOLUTE input and HAPSEG output format
7.7 years ago by markus.riester ▴ 550
0
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1
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3.9k
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Answer: A: The ABSOLUTE input and HAPSEG output format
7.7 years ago by markus.riester ▴ 550
0
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0
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4.2k
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Answer: A: Ploidy in copy number analysis
7.7 years ago by markus.riester ▴ 550
0
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0
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3.3k
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Comment: C: General recommendations for cancer genomics studies
7.9 years ago by markus.riester ▴ 550
2
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1
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1.8k
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Answer: C: purify tumor samples and remove normal cells
8.0 years ago by markus.riester ▴ 550
87 results • Page 2 of 2
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