Identification of large rearrangements in cancer genomes with barcode linked reads-Reference-Cited by-同舟云学术

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Identification of large rearrangements in cancer genomes with barcode linked reads

Published:2017-11-25 Issue:4 Volume:46 Page:e19-e19
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Xia Li C¹^ORCID,Bell John M²,Wood-Bouwens Christina¹,Chen Jiamin J¹,Zhang Nancy R³,Ji Hanlee P¹²

Affiliation:

1. Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA

2. Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA

3. Department of Statistics, the Wharton School, University of Pennsylvania, Philadelphia, PA 18014, USA

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/46/4/e19/24214374/gkx1193.pdf

Reference49 articles.

1. Structural variation in the human genome;Feuk;Nat. Rev. Genet.,2006

2. Phenotypic impact of genomic structural variation: insights from and for human disease;Weischenfeldt;Nat. Rev. Genet.,2013

3. Mechanisms underlying structural variant formation in genomic disorders;Carvalho;Nat. Rev. Genet.,2016

4. The minute chromosome (Phl) in chronic granulocytic leukemia;Nowell;Blut,1962

5. The emerging complexity of gene fusions in cancer;Mertens;Nat. Rev. Cancer,2015

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