Searching journal content for articles similar to Helman et al. 24 (7): 1053.

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  1. ...Consortium (ICGC) (Zhang et al. 2019), and the Pan-Cancer Analysis of Whole Genomes (PCAWG) project (The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020) to characterize thousands of cancers across dozens of cancer types. Building on these population-scale efforts, the Catalogue Of Somatic...
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  2. ...Genomes Consortium 2020) with our method and compared them against somatic and germline variants detected by the Pan-Cancer Analysis of Whole Genomes (PCAWG) project (The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020). To compare our results with somatic consensus indels from the four...
  3. ...behavior. Whole-genome and -exome sequencing has contributed to the characterization of the mutational spectrum of the disease, but the underlying transcriptional profile is still poorly understood. We have performed deep RNA sequencing in different subpopulations of normal B-lymphocytes and CLL cells from...
  4. ...-associated mutationsIn cancer s, APOBEC-induced localized hypermutation events are frequently observed (Nik-Zainal et al. 2012a; The ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium 2020). Across the mutations detected in our hGOiA3A and TP53KO-hGOiA3A lines, ∼5% of the 29,650 acquired base substitutions were...
  5. ...genomic structural variation in human cancer cell lines and primary tumors. Whole-genome sequencing revealed HPV integrants flanking and bridging extensive host genomic amplifications and rearrangements, including deletions, inversions, and chromosomal translocations. We present a model of “looping...
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