Using large-scale genome variation cohorts to decipher the molecular mechanism of cancer-Reference-Cited by-同舟云学术

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Using large-scale genome variation cohorts to decipher the molecular mechanism of cancer

Published:2016-07 Issue:7-8 Volume:339 Page:308-313
ISSN:1631-0691
Container-title:Comptes Rendus Biologies
language:en
Short-container-title:Comptes Rendus Biologies

Author:

Habermann Nina,Mardin Balca R.,Yakneen Sergei,Korbel Jan O.

Publisher

Elsevier BV

Subject

General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference21 articles.

1. Data analysis: create a cloud commons;Stein;Nature,2015

2. Evolution of the cancer genome;Yates;Nat. Rev. Genet.,2012

3. Massive genomic rearrangement acquired in a single catastrophic event during cancer development;Stephens;Cell,2011

4. Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations;Rausch;Cell,2012

5. Whole-genome sequencing identifies genomic heterogeneity at a nucleotide and chromosomal level in bladder cancer;Morrison;Proc. Natl. Acad. Sci. U. S. A.,2014

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chromothripsis—Explosion in Genetic Science;Cells;2021-05-04

2. Butler enables rapid cloud-based analysis of thousands of human genomes;Nature Biotechnology;2020-02-05

3. Mutational game changer: Chromothripsis and its emerging relevance to cancer;Mutation Research/Reviews in Mutation Research;2018-07

4. Enabling rapid cloud-based analysis of thousands of human genomes via Butler;2017-09-07

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