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Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy

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 ac...

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Autores principales: Bell, John M., Lau, Billy T., Greer, Stephanie U., Wood-Bouwens, Christina, Xia, Li C., Connolly, Ian D., Gephart, Melanie H., Ji, Hanlee P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737808/
https://www.ncbi.nlm.nih.gov/pubmed/28977555
http://dx.doi.org/10.1093/nar/gkx712
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author Bell, John M.
Lau, Billy T.
Greer, Stephanie U.
Wood-Bouwens, Christina
Xia, Li C.
Connolly, Ian D.
Gephart, Melanie H.
Ji, Hanlee P.
author_facet Bell, John M.
Lau, Billy T.
Greer, Stephanie U.
Wood-Bouwens, Christina
Xia, Li C.
Connolly, Ian D.
Gephart, Melanie H.
Ji, Hanlee P.
author_sort Bell, John M.
collection PubMed
description 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.
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spelling pubmed-57378082018-01-04 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. Nucleic Acids Res Methods Online 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. Oxford University Press 2017-11-02 2017-08-16 /pmc/articles/PMC5737808/ /pubmed/28977555 http://dx.doi.org/10.1093/nar/gkx712 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Bell, John M.
Lau, Billy T.
Greer, Stephanie U.
Wood-Bouwens, Christina
Xia, Li C.
Connolly, Ian D.
Gephart, Melanie H.
Ji, Hanlee P.
Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
title Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
title_full Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
title_fullStr Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
title_full_unstemmed Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
title_short Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
title_sort chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737808/
https://www.ncbi.nlm.nih.gov/pubmed/28977555
http://dx.doi.org/10.1093/nar/gkx712
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