Literature DB >> 19503625

Comparison of comparative genomic hybridization technologies across microarray platforms.

Susan D Hester1, Laura Reid, Norma Nowak, Wendell D Jones, Joel S Parker, Kevin Knudtson, William Ward, Jay Tiesman, Nancy D Denslow.   

Abstract

In the 2007 Association of Biomolecular Resource Facilities Microarray Research Group project, we analyzed HL-60 DNA with five platforms: Agilent, Affymetrix 500K, Affymetrix U133 Plus 2.0, Illumina, and RPCI 19K BAC arrays. Copy number variation was analyzed using circular binary segmentation (CBS) analysis of log ratio scores from four independently assessed hybridizations of each platform. Data obtained from these platforms were assessed for reproducibility and the ability to detect formerly reported copy number variations in HL-60. In HL-60, all of the tested platforms detected genomic DNA amplification of the 8q24 locus, trisomy 18, and monosomy X; and deletions at loci 5q11.2~q31, 9p21.3~p22, 10p12~p15, 14q22~q31, and 17p12~p13.3. In the HL-60 genome, at least two of the five platforms detected five novel losses and five novel gains. This report provides guidance in the selection of platforms based on this wide-ranging evaluation of available CGH platforms.

Entities:  

Keywords:  BAC array; HL-60; arrayCGH

Mesh:

Year:  2009        PMID: 19503625      PMCID: PMC2685605     

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  29 in total

1.  Assembly of microarrays for genome-wide measurement of DNA copy number.

Authors:  A M Snijders; N Nowak; R Segraves; S Blackwood; N Brown; J Conroy; G Hamilton; A K Hindle; B Huey; K Kimura; S Law; K Myambo; J Palmer; B Ylstra; J P Yue; J W Gray; A N Jain; D Pinkel; D G Albertson
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

2.  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

3.  Detection of large-scale variation in the human genome.

Authors:  A John Iafrate; Lars Feuk; Miguel N Rivera; Marc L Listewnik; Patricia K Donahoe; Ying Qi; Stephen W Scherer; Charles Lee
Journal:  Nat Genet       Date:  2004-08-01       Impact factor: 38.330

4.  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

5.  Characterization of the continuous, differentiating myeloid cell line (HL-60) from a patient with acute promyelocytic leukemia.

Authors:  R Gallagher; S Collins; J Trujillo; K McCredie; M Ahearn; S Tsai; R Metzgar; G Aulakh; R Ting; F Ruscetti; R Gallo
Journal:  Blood       Date:  1979-09       Impact factor: 22.113

Review 6.  Genomic microarrays in human genetic disease and cancer.

Authors:  Donna G Albertson; Daniel Pinkel
Journal:  Hum Mol Genet       Date:  2003-08-05       Impact factor: 6.150

7.  Large-scale copy number polymorphism in the human genome.

Authors:  Jonathan Sebat; B Lakshmi; Jennifer Troge; Joan Alexander; Janet Young; Pär Lundin; Susanne Månér; Hillary Massa; Megan Walker; Maoyen Chi; Nicholas Navin; Robert Lucito; John Healy; James Hicks; Kenny Ye; Andrew Reiner; T Conrad Gilliam; Barbara Trask; Nick Patterson; Anders Zetterberg; Michael Wigler
Journal:  Science       Date:  2004-07-23       Impact factor: 47.728

8.  Karyotypic complexity of the NCI-60 drug-screening panel.

Authors:  Anna V Roschke; Giovanni Tonon; Kristen S Gehlhaus; Nicolas McTyre; Kimberly J Bussey; Samir Lababidi; Dominic A Scudiero; John N Weinstein; Ilan R Kirsch
Journal:  Cancer Res       Date:  2003-12-15       Impact factor: 12.701

9.  Comprehensive genome-wide comparison of DNA and RNA level scan using microarray technology for identification of candidate cancer-related genes in the HL-60 cell line.

Authors:  Celal Ulger; Gokce A Toruner; Mualla Alkan; Mansoor Mohammed; Shamsha Damani; Jason Kang; Anthony Galante; Hana Aviv; Patricia Soteropoulos; Peter P Tolias; Marvin N Schwalb; James J Dermody
Journal:  Cancer Genet Cytogenet       Date:  2003-11

10.  Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays.

Authors:  Herbert Auer; David L Newsom; Norma J Nowak; Kirk M McHugh; Sunita Singh; Chack-Yung Yu; Yan Yang; Gail D Wenger; Julie M Gastier-Foster; Karl Kornacker
Journal:  BMC Genomics       Date:  2007-04-30       Impact factor: 3.969

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  12 in total

1.  Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.

Authors:  Dalila Pinto; Katayoon Darvishi; Xinghua Shi; Diana Rajan; Diane Rigler; Tom Fitzgerald; Anath C Lionel; Bhooma Thiruvahindrapuram; Jeffrey R Macdonald; Ryan Mills; Aparna Prasad; Kristin Noonan; Susan Gribble; Elena Prigmore; Patricia K Donahoe; Richard S Smith; Ji Hyeon Park; Matthew E Hurles; Nigel P Carter; Charles Lee; Stephen W Scherer; Lars Feuk
Journal:  Nat Biotechnol       Date:  2011-05-08       Impact factor: 54.908

2.  Copy number profiling of Oncotype DX genes reveals association with survival of breast cancer patients.

Authors:  Washaakh Ahmed; Muhammad Faraz Arshad Malik; Muhammad Saeed; Farhan Haq
Journal:  Mol Biol Rep       Date:  2018-09-17       Impact factor: 2.316

3.  DeepCNV: a deep learning approach for authenticating copy number variations.

Authors:  Joseph T Glessner; Xiurui Hou; Cheng Zhong; Jie Zhang; Munir Khan; Fabian Brand; Peter Krawitz; Patrick M A Sleiman; Hakon Hakonarson; Zhi Wei
Journal:  Brief Bioinform       Date:  2021-09-02       Impact factor: 11.622

4.  Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data.

Authors:  Soon-Young Kim; Ji-Hong Kim; Yeun-Jun Chung
Journal:  Genomics Inform       Date:  2012-09-28

5.  A discovery resource of rare copy number variations in individuals with autism spectrum disorder.

Authors:  Aparna Prasad; Daniele Merico; Bhooma Thiruvahindrapuram; John Wei; Anath C Lionel; Daisuke Sato; Jessica Rickaby; Chao Lu; Peter Szatmari; Wendy Roberts; Bridget A Fernandez; Christian R Marshall; Eli Hatchwell; Peggy S Eis; Stephen W Scherer
Journal:  G3 (Bethesda)       Date:  2012-12-01       Impact factor: 3.154

6.  CNV-WebStore: online CNV analysis, storage and interpretation.

Authors:  Geert Vandeweyer; Edwin Reyniers; Wim Wuyts; Liesbeth Rooms; R Frank Kooy
Journal:  BMC Bioinformatics       Date:  2011-01-05       Impact factor: 3.307

7.  Evaluation of high-resolution microarray platforms for genomic profiling of bone tumours.

Authors:  Stine H Kresse; Karoly Szuhai; Ana H Barragan-Polania; Halfdan Rydbeck; Anne-Marie Cleton-Jansen; Ola Myklebost; Leonardo A Meza-Zepeda
Journal:  BMC Res Notes       Date:  2010-08-08

Review 8.  Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays.

Authors:  Eric L Seiser; Federico Innocenti
Journal:  Cancer Inform       Date:  2015-01-27

9.  Robust BRCA1-like classification of copy number profiles of samples repeated across different datasets and platforms.

Authors:  Philip C Schouten; Anita Grigoriadis; Thomas Kuilman; Hasan Mirza; Johnathan A Watkins; Saskia A Cooke; Ewald van Dyk; Tesa M Severson; Oscar M Rueda; Marlous Hoogstraat; Caroline V M Verhagen; Rachael Natrajan; Suet-Feung Chin; Esther H Lips; Janneke Kruizinga; Arno Velds; Marja Nieuwland; Ron M Kerkhoven; Oscar Krijgsman; Conchita Vens; Daniel Peeper; Petra M Nederlof; Carlos Caldas; Andrew N Tutt; Lodewyk F Wessels; Sabine C Linn
Journal:  Mol Oncol       Date:  2015-03-20       Impact factor: 6.603

10.  Expanding probe repertoire and improving reproducibility in human genomic hybridization.

Authors:  Stephanie N Dorman; Ben C Shirley; Joan H M Knoll; Peter K Rogan
Journal:  Nucleic Acids Res       Date:  2013-02-01       Impact factor: 16.971

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