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Comment: C: Different NGS runs for paired samples
4.7 years ago by gab ▴ 20
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Comment: C: VCF rare variants and exon
4.7 years ago by gab ▴ 20
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Comment: C: different bam from same NGS data
5.9 years ago by gab ▴ 20
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Comment: C: different bam from same NGS data
5.9 years ago by gab ▴ 20
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Comment: C: coverage of a SNP site?
6.1 years ago by gab ▴ 20
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Comment: C: Calling somatic variants with Varscan
6.2 years ago by gab ▴ 20
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Comment: C: Whole Exome Sequencing Depth
6.2 years ago by gab ▴ 20
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Comment: C: Losing somatic SNPs
6.4 years ago by gab ▴ 20
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Comment: C: Losing somatic SNPs
6.4 years ago by gab ▴ 20
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