Literature DB >> 21666266

Parent-specific copy number in paired tumor-normal studies using circular binary segmentation.

Adam B Olshen1, Henrik Bengtsson, Pierre Neuvial, Paul T Spellman, Richard A Olshen, Venkatraman E Seshan.   

Abstract

MOTIVATION: High-throughput techniques facilitate the simultaneous measurement of DNA copy number at hundreds of thousands of sites on a genome. Older techniques allow measurement only of total copy number, the sum of the copy number contributions from the two parental chromosomes. Newer single nucleotide polymorphism (SNP) techniques can in addition enable quantifying parent-specific copy number (PSCN). The raw data from such experiments are two-dimensional, but are unphased. Consequently, inference based on them necessitates development of new analytic methods.
METHODS: We have adapted and enhanced the circular binary segmentation (CBS) algorithm for this purpose with focus on paired test and reference samples. The essence of paired parent-specific CBS (Paired PSCBS) is to utilize the original CBS algorithm to identify regions of equal total copy number and then to further segment these regions where there have been changes in PSCN. For the final set of regions, calls are made of equal parental copy number and loss of heterozygosity (LOH). PSCN estimates are computed both before and after calling.
RESULTS: The methodology is evaluated by simulation and on glioblastoma data. In the simulation, PSCBS compares favorably to established methods. On the glioblastoma data, PSCBS identifies interesting genomic regions, such as copy-neutral LOH. AVAILABILITY: The Paired PSCBS method is implemented in an open-source R package named PSCBS, available on CRAN (http://cran.r-project.org/).

Entities:  

Mesh:

Year:  2011        PMID: 21666266      PMCID: PMC3137217          DOI: 10.1093/bioinformatics/btr329

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  36 in total

1.  An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays.

Authors:  Xiaojun Zhao; Cheng Li; J Guillermo Paez; Koei Chin; Pasi A Jänne; Tzu-Hsiu Chen; Luc Girard; John Minna; David Christiani; Chris Leo; Joe W Gray; William R Sellers; Matthew Meyerson
Journal:  Cancer Res       Date:  2004-05-01       Impact factor: 12.701

2.  Spatial smoothing and hot spot detection for CGH data using the fused lasso.

Authors:  Robert Tibshirani; Pei Wang
Journal:  Biostatistics       Date:  2007-05-18       Impact factor: 5.899

3.  Stochastic segmentation models for array-based comparative genomic hybridization data analysis.

Authors:  Tze Leung Lai; Haipeng Xing; Nancy Zhang
Journal:  Biostatistics       Date:  2007-09-12       Impact factor: 5.899

4.  PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.

Authors:  Kai Wang; Mingyao Li; Dexter Hadley; Rui Liu; Joseph Glessner; Struan F A Grant; Hakon Hakonarson; Maja Bucan
Journal:  Genome Res       Date:  2007-10-05       Impact factor: 9.043

5.  High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.

Authors:  D Pinkel; R Segraves; D Sudar; S Clark; I Poole; D Kowbel; C Collins; W L Kuo; C Chen; Y Zhai; S H Dairkee; B M Ljung; J W Gray; D G Albertson
Journal:  Nat Genet       Date:  1998-10       Impact factor: 38.330

6.  A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6.

Authors:  Henrik Bengtsson; Pratyaksha Wirapati; Terence P Speed
Journal:  Bioinformatics       Date:  2009-06-17       Impact factor: 6.937

7.  A single-sample method for normalizing and combining full-resolution copy numbers from multiple platforms, labs and analysis methods.

Authors:  Henrik Bengtsson; Amrita Ray; Paul Spellman; Terence P Speed
Journal:  Bioinformatics       Date:  2009-02-04       Impact factor: 6.937

8.  QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.

Authors:  Stefano Colella; Christopher Yau; Jennifer M Taylor; Ghazala Mirza; Helen Butler; Penny Clouston; Anne S Bassett; Anneke Seller; Christopher C Holmes; Jiannis Ragoussis
Journal:  Nucleic Acids Res       Date:  2007-03-06       Impact factor: 16.971

9.  A Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arrays.

Authors:  Philippe Lamy; Claus L Andersen; Lars Dyrskjot; Niels Torring; Carsten Wiuf
Journal:  BMC Bioinformatics       Date:  2007-11-09       Impact factor: 3.169

10.  Major copy proportion analysis of tumor samples using SNP arrays.

Authors:  Cheng Li; Rameen Beroukhim; Barbara A Weir; Wendy Winckler; Levi A Garraway; William R Sellers; Matthew Meyerson
Journal:  BMC Bioinformatics       Date:  2008-04-21       Impact factor: 3.169

View more
  61 in total

1.  CalMaTe: a method and software to improve allele-specific copy number of SNP arrays for downstream segmentation.

Authors:  Maria Ortiz-Estevez; Ander Aramburu; Henrik Bengtsson; Pierre Neuvial; Angel Rubio
Journal:  Bioinformatics       Date:  2012-05-09       Impact factor: 6.937

2.  Genome-Informed Targeted Therapy for Osteosarcoma.

Authors:  Leanne C Sayles; Marcus R Breese; Amanda L Koehne; Stanley G Leung; Alex G Lee; Heng-Yi Liu; Aviv Spillinger; Avanthi T Shah; Bogdan Tanasa; Krystal Straessler; Florette K Hazard; Sheri L Spunt; Neyssa Marina; Grace E Kim; Soo-Jin Cho; Raffi S Avedian; David G Mohler; Mi-Ok Kim; Steven G DuBois; Douglas S Hawkins; E Alejandro Sweet-Cordero
Journal:  Cancer Discov       Date:  2018-09-28       Impact factor: 39.397

3.  Quantification of Multiple Tumor Clones Using Gene Array and Sequencing Data.

Authors:  Yichen Cheng; James Y Dai; Thomas G Paulson; Xiaoyu Wang; Xiaohong Li; Brian J Reid; Charles Kooperberg
Journal:  Ann Appl Stat       Date:  2017-07-20       Impact factor: 2.083

4.  Directional allelic imbalance profiling and visualization from multi-sample data with RECUR.

Authors:  Yasminka A Jakubek; F Anthony San Lucas; Paul Scheet
Journal:  Bioinformatics       Date:  2019-07-01       Impact factor: 6.937

5.  Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.

Authors:  Julia Richter; Matthias Schlesner; Steve Hoffmann; Markus Kreuz; Ellen Leich; Birgit Burkhardt; Maciej Rosolowski; Ole Ammerpohl; Rabea Wagener; Stephan H Bernhart; Dido Lenze; Monika Szczepanowski; Maren Paulsen; Simone Lipinski; Robert B Russell; Sabine Adam-Klages; Gordana Apic; Alexander Claviez; Dirk Hasenclever; Volker Hovestadt; Nadine Hornig; Jan O Korbel; Dieter Kube; David Langenberger; Chris Lawerenz; Jasmin Lisfeld; Katharina Meyer; Simone Picelli; Jordan Pischimarov; Bernhard Radlwimmer; Tobias Rausch; Marius Rohde; Markus Schilhabel; René Scholtysik; Rainer Spang; Heiko Trautmann; Thorsten Zenz; Arndt Borkhardt; Hans G Drexler; Peter Möller; Roderick A F MacLeod; Christiane Pott; Stefan Schreiber; Lorenz Trümper; Markus Loeffler; Peter F Stadler; Peter Lichter; Roland Eils; Ralf Küppers; Michael Hummel; Wolfram Klapper; Philip Rosenstiel; Andreas Rosenwald; Benedikt Brors; Reiner Siebert
Journal:  Nat Genet       Date:  2012-11-11       Impact factor: 38.330

6.  Many private mutations originate from the first few divisions of a human colorectal adenoma.

Authors:  Haeyoun Kang; Matthew P Salomon; Andrea Sottoriva; Junsong Zhao; Morgan Toy; Michael F Press; Christina Curtis; Paul Marjoram; Kimberly Siegmund; Darryl Shibata
Journal:  J Pathol       Date:  2015-08-03       Impact factor: 7.996

7.  SPARSE INTEGRATIVE CLUSTERING OF MULTIPLE OMICS DATA SETS.

Authors:  Ronglai Shen; Sijian Wang; Qianxing Mo
Journal:  Ann Appl Stat       Date:  2013-04-09       Impact factor: 2.083

8.  Allelic loss of 9p21.3 is a prognostic factor in 1p/19q codeleted anaplastic gliomas.

Authors:  Agustí Alentorn; Caroline Dehais; François Ducray; Catherine Carpentier; Karima Mokhtari; Dominique Figarella-Branger; Olivier Chinot; Elisabeth Cohen-Moyal; Carole Ramirez; Hugues Loiseau; Selma Elouahdani-Hamdi; Patrick Beauchesne; Olivier Langlois; Christine Desenclos; Jean-Sébastien Guillamo; Phong Dam-Hieu; François Ghiringhelli; Philippe Colin; Joel Godard; Fabrice Parker; Frédéric Dhermain; Antoine F Carpentier; Jean-Sebastien Frenel; Philippe Menei; Luc Bauchet; Thierry Faillot; Mélanie Fesneau; Denys Fontaine; Marie-Jeannette Motuo-Fotso; Elodie Vauleon; Claude Gaultier; Caroline Le Guerinel; Edouard-Marcel Gueye; Georges Noel; Nicolas Desse; Xavier Durando; Eduardo Barrascout; Michel Wager; Damien Ricard; Ioana Carpiuc; Jean-Yves Delattre; Ahmed Idbaih
Journal:  Neurology       Date:  2015-09-18       Impact factor: 9.910

9.  Spatial mutation patterns as markers of early colorectal tumor cell mobility.

Authors:  Marc D Ryser; Byung-Hoon Min; Kimberly D Siegmund; Darryl Shibata
Journal:  Proc Natl Acad Sci U S A       Date:  2018-05-14       Impact factor: 11.205

10.  The landscape of genomic alterations across childhood cancers.

Authors:  Susanne N Gröbner; Barbara C Worst; Joachim Weischenfeldt; Ivo Buchhalter; Kortine Kleinheinz; Vasilisa A Rudneva; Pascal D Johann; Gnana Prakash Balasubramanian; Maia Segura-Wang; Sebastian Brabetz; Sebastian Bender; Barbara Hutter; Dominik Sturm; Elke Pfaff; Daniel Hübschmann; Gideon Zipprich; Michael Heinold; Jürgen Eils; Christian Lawerenz; Serap Erkek; Sander Lambo; Sebastian Waszak; Claudia Blattmann; Arndt Borkhardt; Michaela Kuhlen; Angelika Eggert; Simone Fulda; Manfred Gessler; Jenny Wegert; Roland Kappler; Daniel Baumhoer; Stefan Burdach; Renate Kirschner-Schwabe; Udo Kontny; Andreas E Kulozik; Dietmar Lohmann; Simone Hettmer; Cornelia Eckert; Stefan Bielack; Michaela Nathrath; Charlotte Niemeyer; Günther H Richter; Johannes Schulte; Reiner Siebert; Frank Westermann; Jan J Molenaar; Gilles Vassal; Hendrik Witt; Birgit Burkhardt; Christian P Kratz; Olaf Witt; Cornelis M van Tilburg; Christof M Kramm; Gudrun Fleischhack; Uta Dirksen; Stefan Rutkowski; Michael Frühwald; Katja von Hoff; Stephan Wolf; Thomas Klingebiel; Ewa Koscielniak; Pablo Landgraf; Jan Koster; Adam C Resnick; Jinghui Zhang; Yanling Liu; Xin Zhou; Angela J Waanders; Danny A Zwijnenburg; Pichai Raman; Benedikt Brors; Ursula D Weber; Paul A Northcott; Kristian W Pajtler; Marcel Kool; Rosario M Piro; Jan O Korbel; Matthias Schlesner; Roland Eils; David T W Jones; Peter Lichter; Lukas Chavez; Marc Zapatka; Stefan M Pfister
Journal:  Nature       Date:  2018-02-28       Impact factor: 49.962

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.