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Comment: C: Different NGS runs for paired samples
3.0 years ago by gab ▴ 20
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879
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Comment: C: VCF rare variants and exon
3.0 years ago by gab ▴ 20
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757
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Comment: C: different bam from same NGS data
4.2 years ago by gab ▴ 20
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757
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Comment: C: different bam from same NGS data
4.2 years ago by gab ▴ 20
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2.8k
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Comment: C: coverage of a SNP site?
4.4 years ago by gab ▴ 20
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1.5k
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Comment: C: Calling somatic variants with Varscan
4.5 years ago by gab ▴ 20
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Comment: C: Whole Exome Sequencing Depth
4.5 years ago by gab ▴ 20
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1.1k
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Comment: C: Losing somatic SNPs
4.7 years ago by gab ▴ 20
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1.1k
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Comment: C: Losing somatic SNPs
4.7 years ago by gab ▴ 20
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