Literature DB >> 19276148

Smoothing waves in array CGH tumor profiles.

Mark A van de Wiel1, Rebecca Brosens, Paul H C Eilers, Candy Kumps, Gerrit A Meijer, Björn Menten, Erik Sistermans, Frank Speleman, Marieke E Timmerman, Bauke Ylstra.   

Abstract

MOTIVATION: Many high-resolution array comparative genomic hybridization tumor profiles contain a wave bias, which makes accurate detection of breakpoints in such profiles more difficult.
RESULTS: An efficient and highly effective algorithm that largely removes the wave bias from tumor profiles by regressing the tumor profile data on data of profiles from the clinical genetics practice. Results are illustrated on two independent datasets. The algorithm is shown to be robust against the presence of true copy number aberrations. Moreover, the smoothed profiles are able to recapitulate the aberration location and signal for simulated tumor profiles. AVAILABILITY: Easy-to-use R scripts, user instructions and data are available from http://www.few.vu.nl/~mavdwiel/nowaves.html. SUPPLEMENTARY INFORMATION: Supplementary information are available at Bioinformatics online.

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Year:  2009        PMID: 19276148     DOI: 10.1093/bioinformatics/btp132

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


  37 in total

1.  A novel signal processing approach for the detection of copy number variations in the human genome.

Authors:  Catherine Stamoulis; Rebecca A Betensky
Journal:  Bioinformatics       Date:  2011-07-12       Impact factor: 6.937

2.  Novel multisample scheme for inferring phylogenetic markers from whole genome tumor profiles.

Authors:  Ayshwarya Subramanian; Stanley Shackney; Russell Schwartz
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2013 Nov-Dec       Impact factor: 3.710

3.  WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.

Authors:  Lennart Raman; Annelies Dheedene; Matthias De Smet; Jo Van Dorpe; Björn Menten
Journal:  Nucleic Acids Res       Date:  2019-02-28       Impact factor: 16.971

4.  Performance assessment of copy number microarray platforms using a spike-in experiment.

Authors:  Eitan Halper-Stromberg; Laurence Frelin; Ingo Ruczinski; Robert Scharpf; Chunfa Jie; Benilton Carvalho; Haiping Hao; Kurt Hetrick; Anne Jedlicka; Amanda Dziedzic; Kim Doheny; Alan F Scott; Steve Baylin; Jonathan Pevsner; Forrest Spencer; Rafael A Irizarry
Journal:  Bioinformatics       Date:  2011-04-15       Impact factor: 6.937

5.  Two types of primary mucinous ovarian tumors can be distinguished based on their origin.

Authors:  Michiel Simons; Femke Simmer; Johan Bulten; Marjolijn J Ligtenberg; Harry Hollema; Shannon van Vliet; Richarda M de Voer; Eveline J Kamping; Dirk F van Essen; Bauke Ylstra; Lauren E Schwartz; Yihong Wang; Leon F Massuger; Iris D Nagtegaal; Robert J Kurman
Journal:  Mod Pathol       Date:  2019-11-06       Impact factor: 7.842

6.  CGHpower: exploring sample size calculations for chromosomal copy number experiments.

Authors:  Ilari Scheinin; José A Ferreira; Sakari Knuutila; Gerrit A Meijer; Mark A van de Wiel; Bauke Ylstra
Journal:  BMC Bioinformatics       Date:  2010-06-17       Impact factor: 3.169

7.  Multiple pathways in the FGF signaling network are frequently deregulated by gene amplification in oral dysplasias.

Authors:  Ivy F L Tsui; Catherine F Poh; Cathie Garnis; Miriam P Rosin; Lewei Zhang; Wan L Lam
Journal:  Int J Cancer       Date:  2009-11-01       Impact factor: 7.396

8.  Multisample aCGH data analysis via total variation and spectral regularization.

Authors:  Xiaowei Zhou; Can Yang; Xiang Wan; Hongyu Zhao; Weichuan Yu
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2013 Jan-Feb       Impact factor: 3.710

9.  Waved aCGH: to smooth or not to smooth.

Authors:  F Leprêtre; C Villenet; S Quief; O Nibourel; C Jacquemin; X Troussard; F Jardin; F Gibson; J P Kerckaert; C Roumier; M Figeac
Journal:  Nucleic Acids Res       Date:  2010-01-13       Impact factor: 16.971

10.  Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays.

Authors:  Tatiana Popova; Elodie Manié; Dominique Stoppa-Lyonnet; Guillem Rigaill; Emmanuel Barillot; Marc Henri Stern
Journal:  Genome Biol       Date:  2009-11-11       Impact factor: 13.583

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