... but most cancer genomics analyses to date have been relatively small scale (~1000s of genomes) and have largely ignored the non-coding regions. For example the recent Pan-Cancer analysis included only 2658 cancer genomes https://t.co/sPhymZomcj
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Open Access UCL Research: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes https://t.co/ye4P6fIyJ1
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RT @ctokheim: @jgschraiber @cj_battey In cancer for somatic variant interpretation, the conclusion of coding variants as high effect size i…
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@jgschraiber @cj_battey In cancer for somatic variant interpretation, the conclusion of coding variants as high effect size is completely justified. TCGA WES identifies many driver mutations (https://t.co/zVPyejjJzR), while ICGC WGS found only ~<10% …