Whole genome sequencing analysis for cancer genomics and precision medicine. Issue 3 (26th February 2018)

• Record Type: Journal Article
• Authors: Nakagawa, Hidewaki; Fujita, Masashi
• Is Part Of: Cancer science. Volume 109:Issue 3(2018)
• Page Start: 513
• Page End: 522
• Publication Date: 2018-02-26
• Subjects: cancer genome -- mutational signature -- non‐coding mutation -- structural variant -- whole genome sequencing; Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.13505
• Languages: English
• ISSNs: 1347-9032

Abstract

Abstract : Explosive advances in next‐generation sequencer (NGS) and computational analyses have enabled exploration of somatic protein‐altered mutations in most cancer types, with coding mutation data intensively accumulated. However, there is limited information on somatic mutations in non‐coding regions, including introns, regulatory elements and non‐coding RNA. Structural variants and pathogen in cancer genomes remain widely unexplored. Whole genome sequencing (WGS) approaches can be used to comprehensively explore all types of genomic alterations in cancer and help us to better understand the whole landscape of driver mutations and mutational signatures in cancer genomes and elucidate the functional or clinical implications of these unexplored genomic regions and mutational signatures. This review describes recently developed technical approaches for cancer WGS and the future direction of cancer WGS, and discusses its utility and limitations as an analysis platform and for mutation interpretation for cancer genomics and cancer precision medicine. Taking into account the diversity of cancer genomes and phenotypes, interpretation of abundant mutation information from WGS, especially non‐coding and structure variants, requires the analysis of large‐scale WGS data integrated with RNA‐Seq, epigenomics, immuno‐genomic and clinic‐pathological information. Abstract : A representative Circos plot of cancer genome structure from whole genome sequencing analysis, which indicates SVs and CNAs in all of human chromosomes (1‐22+XY). Chromothripsis in chromosome 1 and 14 was observed.