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Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy.
Bell, John M; Lau, Billy T; Greer, Stephanie U; Wood-Bouwens, Christina; Xia, Li C; Connolly, Ian D; Gephart, Melanie H; Ji, Hanlee P.
Afiliación
  • Bell JM; Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
  • Lau BT; Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
  • Greer SU; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Wood-Bouwens C; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Xia LC; Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Connolly ID; Department of Neurosurgery, Stanford University Hospital and Clinics, Stanford, CA 94305, USA.
  • Gephart MH; Department of Neurosurgery, Stanford University Hospital and Clinics, Stanford, CA 94305, USA.
  • Ji HP; Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
Nucleic Acids Res ; 45(19): e162, 2017 Nov 02.
Article en En | MEDLINE | ID: mdl-28977555
ABSTRACT
Genomic instability is a frequently occurring feature of cancer that involves large-scale structural alterations. These somatic changes in chromosome structure include duplication of entire chromosome arms and aneuploidy where chromosomes are duplicated beyond normal diploid content. However, the accurate determination of aneuploidy events in cancer genomes is a challenge. Recent advances in sequencing technology allow the characterization of haplotypes that extend megabases along the human genome using high molecular weight (HMW) DNA. For this study, we employed a library preparation method in which sequence reads have barcodes linked to single HMW DNA molecules. Barcode-linked reads are used to generate extended haplotypes on the order of megabases. We developed a method that leverages haplotypes to identify chromosomal segmental alterations in cancer and uses this information to join haplotypes together, thus extending the range of phased variants. With this approach, we identified mega-haplotypes that encompass entire chromosome arms. We characterized the chromosomal arm changes and aneuploidy events in a manner that offers similar information as a traditional karyotype but with the benefit of DNA sequence resolution. We applied this approach to characterize aneuploidy and chromosomal alterations from a series of primary colorectal cancers.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Haplotipos / Aneuploidia / Neoplasias Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Haplotipos / Aneuploidia / Neoplasias Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Nucleic Acids Res Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos