Literature DB >> 31489360

Detection of Local DNA Copy Number Changes in Lung Cancer Population Analyses Using A Multi-Scale Approach.

Nezamoddin N Kachouie1, Xihong Lin2, David C Christiani3,4, Armin Schwartzman5.   

Abstract

Emerging advances in genomic sequencing have prompted the development of new computational methods for studying the genomic sources of human diseases. This paper presents a recent statistical approach for detection of local regions with significant copy number alterations (CNAs) in lung cancer population. Mapping such regions is of interest as they are potentially associated with lung cancer. Conventional application of multiple testing methods corresponds to testing for CNAs at each probe separately and thresholding the t-statistics as test statistics. Due to the large number of probes, this approach often fails to detect CNA regions. In contrast, the proposed method uses the heights of located peaks and improves the detection power. This is achieved by taking advantage of the spatial structure in the data as well as reducing the number of tests in the multiple comparisons problem. In copy number analysis, it is common to apply segmentation or change detection tools to each individual genomic sample. However, since segmentation results vary among subjects, it becomes difficult to find the common genomic regions in population analyses. Our approach solves this problem by performing the analysis using summary statistics to study at population level directly. Hence, the region detection is performed on the summary t-statistic map. The proposed method is applied to lung cancer data and shows promise for detection of local regions with significant CNAs.

Entities:  

Keywords:  Copy number alterations (CNAs); Gene-Cancer association; Local region detection; Lung cancer

Year:  2016        PMID: 31489360      PMCID: PMC6727850          DOI: 10.1080/23737484.2016.1197079

Source DB:  PubMed          Journal:  Commun Stat Case Stud Data Anal Appl        ISSN: 2373-7484


  19 in total

1.  Genome-wide analysis of DNA copy-number changes using cDNA microarrays.

Authors:  J R Pollack; C M Perou; A A Alizadeh; M B Eisen; A Pergamenschikov; C F Williams; S S Jeffrey; D Botstein; P O Brown
Journal:  Nat Genet       Date:  1999-09       Impact factor: 38.330

2.  Circular binary segmentation for the analysis of array-based DNA copy number data.

Authors:  Adam B Olshen; E S Venkatraman; Robert Lucito; Michael Wigler
Journal:  Biostatistics       Date:  2004-10       Impact factor: 5.899

3.  Denoising array-based comparative genomic hybridization data using wavelets.

Authors:  Li Hsu; Steven G Self; Douglas Grove; Tim Randolph; Kai Wang; Jeffrey J Delrow; Lenora Loo; Peggy Porter
Journal:  Biostatistics       Date:  2005-04       Impact factor: 5.899

4.  High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.

Authors:  Helen Davies; Ed Dicks; Philip Stephens; Charles Cox; Jon Teague; Chris Greenman; Graham Bignell; Sarah O'meara; Sarah Edkins; Adrian Parker; Claire Stevens; Andrew Menzies; Matt Blow; Bill Bottomley; Mark Dronsfield; P Andrew Futreal; Michael R Stratton; Richard Wooster
Journal:  Genomics       Date:  2006-01-09       Impact factor: 5.736

Review 5.  Methods and strategies for analyzing copy number variation using DNA microarrays.

Authors:  Nigel P Carter
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

6.  A statistical method to detect chromosomal regions with DNA copy number alterations using SNP-array-based CGH data.

Authors:  Yinglei Lai; Hongyu Zhao
Journal:  Comput Biol Chem       Date:  2005-02       Impact factor: 2.877

7.  Characterizing the cancer genome in lung adenocarcinoma.

Authors:  Barbara A Weir; Michele S Woo; Gad Getz; Sven Perner; Li Ding; Rameen Beroukhim; William M Lin; Michael A Province; Aldi Kraja; Laura A Johnson; Kinjal Shah; Mitsuo Sato; Roman K Thomas; Justine A Barletta; Ingrid B Borecki; Stephen Broderick; Andrew C Chang; Derek Y Chiang; Lucian R Chirieac; Jeonghee Cho; Yoshitaka Fujii; Adi F Gazdar; Thomas Giordano; Heidi Greulich; Megan Hanna; Bruce E Johnson; Mark G Kris; Alex Lash; Ling Lin; Neal Lindeman; Elaine R Mardis; John D McPherson; John D Minna; Margaret B Morgan; Mark Nadel; Mark B Orringer; John R Osborne; Brad Ozenberger; Alex H Ramos; James Robinson; Jack A Roth; Valerie Rusch; Hidefumi Sasaki; Frances Shepherd; Carrie Sougnez; Margaret R Spitz; Ming-Sound Tsao; David Twomey; Roel G W Verhaak; George M Weinstock; David A Wheeler; Wendy Winckler; Akihiko Yoshizawa; Soyoung Yu; Maureen F Zakowski; Qunyuan Zhang; David G Beer; Ignacio I Wistuba; Mark A Watson; Levi A Garraway; Marc Ladanyi; William D Travis; William Pao; Mark A Rubin; Stacey B Gabriel; Richard A Gibbs; Harold E Varmus; Richard K Wilson; Eric S Lander; Matthew Meyerson
Journal:  Nature       Date:  2007-11-04       Impact factor: 49.962

8.  Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors.

Authors:  A Kallioniemi; O P Kallioniemi; D Sudar; D Rutovitz; J W Gray; F Waldman; D Pinkel
Journal:  Science       Date:  1992-10-30       Impact factor: 47.728

9.  ERBB2 amplification in breast cancer analyzed by fluorescence in situ hybridization.

Authors:  O P Kallioniemi; A Kallioniemi; W Kurisu; A Thor; L C Chen; H S Smith; F M Waldman; D Pinkel; J W Gray
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-15       Impact factor: 11.205

10.  The potential of copy number gains and losses, detected by array-based comparative genomic hybridization, for computational differential diagnosis of B-cell lymphomas and genetic regions involved in lymphomagenesis.

Authors:  Ichiro Takeuchi; Hiroyuki Tagawa; Akira Tsujikawa; Masao Nakagawa; Miyuki Katayama-Suguro; Ying Guo; Masao Seto
Journal:  Haematologica       Date:  2008-11-23       Impact factor: 9.941

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