Literature DB >> 25903743

Somatic structural variation and cancer.

Jose M C Tubio.   

Abstract

With the advent of next-generation sequencing technologies, we have witnessed a rapid pace of discovery of new patterns of somatic structural variation in cancer genomes, and an attempt to figure out their underlying mechanisms. Some of these mechanisms are associated with particular cancer types, and in some cases are the main cause of the structural mutations that drive the oncogenic process. This review provides an overview of the patterns of somatic structural variation and chromosomal structures that characterize cancer genomes, their causal mechanisms and their impact in oncogenesis.
© The Author 2015. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Entities:  

Keywords:  cancer genome; driver mutation; mutational process; somatic structural variation

Mesh:

Year:  2015        PMID: 25903743     DOI: 10.1093/bfgp/elv016

Source DB:  PubMed          Journal:  Brief Funct Genomics        ISSN: 2041-2649            Impact factor:   4.241


  10 in total

Review 1.  Long-read sequencing in deciphering human genetics to a greater depth.

Authors:  Mohit K Midha; Mengchu Wu; Kuo-Ping Chiu
Journal:  Hum Genet       Date:  2019-09-19       Impact factor: 4.132

2.  Integrated analysis of optical mapping and whole-genome sequencing reveals intratumoral genetic heterogeneity in metastatic lung squamous cell carcinoma.

Authors:  Yizhou Peng; Chongze Yuan; Xiaoting Tao; Yue Zhao; Xingxin Yao; Lingdun Zhuge; Jianwei Huang; Qiang Zheng; Yue Zhang; Hui Hong; Haiquan Chen; Yihua Sun
Journal:  Transl Lung Cancer Res       Date:  2020-06

3.  Copy number variant analysis using genome-wide mate-pair sequencing.

Authors:  James B Smadbeck; Sarah H Johnson; Stephanie A Smoley; Athanasios Gaitatzes; Travis M Drucker; Roman M Zenka; Farhad Kosari; Stephen J Murphy; Nicole Hoppman; Umut Aypar; William R Sukov; Robert B Jenkins; Hutton M Kearney; Andrew L Feldman; George Vasmatzis
Journal:  Genes Chromosomes Cancer       Date:  2018-07-30       Impact factor: 5.006

4.  Micro-Inversions In Human Cancer Genomes.

Authors:  Li Qu; Huaiqiu Zhu; May Wang
Journal:  Annu Int Conf IEEE Eng Med Biol Soc       Date:  2018-07

Review 5.  Breaking point: the genesis and impact of structural variation in tumours.

Authors:  Ailith Ewing; Colin Semple
Journal:  F1000Res       Date:  2018-11-19

6.  TSD: A Computational Tool To Study the Complex Structural Variants Using PacBio Targeted Sequencing Data.

Authors:  Guofeng Meng; Ying Tan; Yue Fan; Yan Wang; Guang Yang; Gregory Fanning; Yang Qiu
Journal:  G3 (Bethesda)       Date:  2019-05-07       Impact factor: 3.154

7.  Large Fragment InDels Reshape Genome Structure of Porcine Alveolar Macrophage 3D4/21 Cells.

Authors:  Xiaolong Li; Xiaoqian Zhang; Yandong Luo; Ru Liu; Yan Sun; Shuhong Zhao; Mei Yu; Jianhua Cao
Journal:  Genes (Basel)       Date:  2022-08-24       Impact factor: 4.141

8.  Association of structural variation with cardiometabolic traits in Finns.

Authors:  Lei Chen; Haley J Abel; Indraniel Das; David E Larson; Liron Ganel; Krishna L Kanchi; Allison A Regier; Erica P Young; Chul Joo Kang; Alexandra J Scott; Colby Chiang; Xinxin Wang; Shuangjia Lu; Ryan Christ; Susan K Service; Charleston W K Chiang; Aki S Havulinna; Johanna Kuusisto; Michael Boehnke; Markku Laakso; Aarno Palotie; Samuli Ripatti; Nelson B Freimer; Adam E Locke; Nathan O Stitziel; Ira M Hall
Journal:  Am J Hum Genet       Date:  2021-04-01       Impact factor: 11.025

9.  Landscape of somatic mutations in 560 breast cancer whole-genome sequences.

Authors:  Serena Nik-Zainal; Helen Davies; Johan Staaf; Manasa Ramakrishna; Dominik Glodzik; Xueqing Zou; Inigo Martincorena; Ludmil B Alexandrov; Sancha Martin; David C Wedge; Peter Van Loo; Young Seok Ju; Marcel Smid; Arie B Brinkman; Sandro Morganella; Miriam R Aure; Ole Christian Lingjærde; Anita Langerød; Markus Ringnér; Sung-Min Ahn; Sandrine Boyault; Jane E Brock; Annegien Broeks; Adam Butler; Christine Desmedt; Luc Dirix; Serge Dronov; Aquila Fatima; John A Foekens; Moritz Gerstung; Gerrit K J Hooijer; Se Jin Jang; David R Jones; Hyung-Yong Kim; Tari A King; Savitri Krishnamurthy; Hee Jin Lee; Jeong-Yeon Lee; Yilong Li; Stuart McLaren; Andrew Menzies; Ville Mustonen; Sarah O'Meara; Iris Pauporté; Xavier Pivot; Colin A Purdie; Keiran Raine; Kamna Ramakrishnan; F Germán Rodríguez-González; Gilles Romieu; Anieta M Sieuwerts; Peter T Simpson; Rebecca Shepherd; Lucy Stebbings; Olafur A Stefansson; Jon Teague; Stefania Tommasi; Isabelle Treilleux; Gert G Van den Eynden; Peter Vermeulen; Anne Vincent-Salomon; Lucy Yates; Carlos Caldas; Laura van't Veer; Andrew Tutt; Stian Knappskog; Benita Kiat Tee Tan; Jos Jonkers; Åke Borg; Naoto T Ueno; Christos Sotiriou; Alain Viari; P Andrew Futreal; Peter J Campbell; Paul N Span; Steven Van Laere; Sunil R Lakhani; Jorunn E Eyfjord; Alastair M Thompson; Ewan Birney; Hendrik G Stunnenberg; Marc J van de Vijver; John W M Martens; Anne-Lise Børresen-Dale; Andrea L Richardson; Gu Kong; Gilles Thomas; Michael R Stratton
Journal:  Nature       Date:  2016-05-02       Impact factor: 49.962

10.  Somatic structural variation targets neurodevelopmental genes and identifies SHANK2 as a tumor suppressor in neuroblastoma.

Authors:  Gonzalo Lopez; Karina L Conkrite; Miriam Doepner; Komal S Rathi; Apexa Modi; Zalman Vaksman; Lance M Farra; Eric Hyson; Moataz Noureddine; Jun S Wei; Malcolm A Smith; Shahab Asgharzadeh; Robert C Seeger; Javed Khan; Jaime Guidry Auvil; Daniela S Gerhard; John M Maris; Sharon J Diskin
Journal:  Genome Res       Date:  2020-08-13       Impact factor: 9.043

  10 in total

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