Literature DB >> 19381971

Comparative genomic hybridization: microarray design and data interpretation.

Richard Redon1, Nigel P Carter.   

Abstract

Microarray-based Comparative Genomic Hybridization (array-CGH) has been applied for a decade to screen for submicroscopic DNA gains and losses in tumor and constitutional DNA samples. This method has become increasingly flexible with the integration of new biological resources generated by genome sequencing projects. In this chapter, we describe alternative strategies for whole genome screening and high resolution breakpoint mapping of copy number changes by array-CGH, as well as tools available for accurate analysis of array-CGH experiments. Although most methods listed here have been designed for microarrays comprising large-insert clones, they can be adapted easily to other types of microarray platforms, such as those constructed from printed or synthesized oligonucleotides.

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Year:  2009        PMID: 19381971      PMCID: PMC2871310          DOI: 10.1007/978-1-59745-538-1_3

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  19 in total

1.  Breakpoint identification and smoothing of array comparative genomic hybridization data.

Authors:  Kees Jong; Elena Marchiori; Gerrit Meijer; A V D Vaart; Bauke Ylstra
Journal:  Bioinformatics       Date:  2004-06-16       Impact factor: 6.937

2.  Accurate and reliable high-throughput detection of copy number variation in the human genome.

Authors:  Heike Fiegler; Richard Redon; Dan Andrews; Carol Scott; Robert Andrews; Carol Carder; Richard Clark; Oliver Dovey; Peter Ellis; Lars Feuk; Lisa French; Paul Hunt; Dimitrios Kalaitzopoulos; James Larkin; Lyndal Montgomery; George H Perry; Bob W Plumb; Keith Porter; Rachel E Rigby; Diane Rigler; Armand Valsesia; Cordelia Langford; Sean J Humphray; Stephen W Scherer; Charles Lee; Matthew E Hurles; Nigel P Carter
Journal:  Genome Res       Date:  2006-11-22       Impact factor: 9.043

Review 3.  Copy-number variation and association studies of human disease.

Authors:  Steven A McCarroll; David M Altshuler
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

4.  Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances.

Authors:  S Solinas-Toldo; S Lampel; S Stilgenbauer; J Nickolenko; A Benner; H Döhner; T Cremer; P Lichter
Journal:  Genes Chromosomes Cancer       Date:  1997-12       Impact factor: 5.006

5.  Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome.

Authors:  Richard Redon; Geneviève Baujat; Damien Sanlaville; Martine Le Merrer; Michel Vekemans; Arnold Munnich; Nigel P Carter; Valérie Cormier-Daire; Laurence Colleaux
Journal:  Eur J Hum Genet       Date:  2006-06       Impact factor: 4.246

6.  Global variation in copy number in the human genome.

Authors:  Richard Redon; Shumpei Ishikawa; Karen R Fitch; Lars Feuk; George H Perry; T Daniel Andrews; Heike Fiegler; Michael H Shapero; Andrew R Carson; Wenwei Chen; Eun Kyung Cho; Stephanie Dallaire; Jennifer L Freeman; Juan R González; Mònica Gratacòs; Jing Huang; Dimitrios Kalaitzopoulos; Daisuke Komura; Jeffrey R MacDonald; Christian R Marshall; Rui Mei; Lyndal Montgomery; Kunihiro Nishimura; Kohji Okamura; Fan Shen; Martin J Somerville; Joelle Tchinda; Armand Valsesia; Cara Woodwark; Fengtang Yang; Junjun Zhang; Tatiana Zerjal; Jane Zhang; Lluis Armengol; Donald F Conrad; Xavier Estivill; Chris Tyler-Smith; Nigel P Carter; Hiroyuki Aburatani; Charles Lee; Keith W Jones; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2006-11-23       Impact factor: 49.962

7.  Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.

Authors:  Pawandeep Dhami; Alison J Coffey; Stephen Abbs; Joris R Vermeesch; Jan P Dumanski; Karen J Woodward; Robert M Andrews; Cordelia Langford; David Vetrie
Journal:  Am J Hum Genet       Date:  2005-03-08       Impact factor: 11.025

8.  Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

Authors:  Rebecca R Selzer; Todd A Richmond; Nathan J Pofahl; Roland D Green; Peggy S Eis; Prakash Nair; Arthur R Brothman; Raymond L Stallings
Journal:  Genes Chromosomes Cancer       Date:  2005-11       Impact factor: 5.006

9.  Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization.

Authors:  S du Manoir; M R Speicher; S Joos; E Schröck; S Popp; H Döhner; G Kovacs; M Robert-Nicoud; P Lichter; T Cremer
Journal:  Hum Genet       Date:  1993-02       Impact factor: 4.132

10.  SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.

Authors:  Thomas S Price; Regina Regan; Richard Mott; Asa Hedman; Ben Honey; Rachael J Daniels; Lee Smith; Andy Greenfield; Ana Tiganescu; Veronica Buckle; Nicki Ventress; Helena Ayyub; Anita Salhan; Susana Pedraza-Diaz; John Broxholme; Jiannis Ragoussis; Douglas R Higgs; Jonathan Flint; Samantha J L Knight
Journal:  Nucleic Acids Res       Date:  2005-06-16       Impact factor: 16.971

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  6 in total

Review 1.  Efficient genome-wide genotyping strategies and data integration in crop plants.

Authors:  Davoud Torkamaneh; Brian Boyle; François Belzile
Journal:  Theor Appl Genet       Date:  2018-01-19       Impact factor: 5.699

2.  CNARA: reliability assessment for genomic copy number profiles.

Authors:  Ni Ai; Haoyang Cai; Caius Solovan; Michael Baudis
Journal:  BMC Genomics       Date:  2016-10-12       Impact factor: 3.969

3.  High-throughput Molecular Analysis of Pseudohypoparathyroidism 1b Patients Reveals Novel Genetic and Epigenetic Defects.

Authors:  Jennifer Danzig; Dong Li; Suzanne Jan de Beur; Michael A Levine
Journal:  J Clin Endocrinol Metab       Date:  2021-10-21       Impact factor: 6.134

4.  Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes.

Authors:  Debora Mancini-DiNardo; Thaddeus Judkins; Nick Woolstenhulme; Collin Burton; Jeremy Schoenberger; Matthew Ryder; Adam Murray; Natalia Gutin; Aaron Theisen; Jayson Holladay; Jonathan Craft; Christopher Arnell; Kelsey Moyes; Benjamin Roa
Journal:  J Exp Clin Cancer Res       Date:  2014-09-11

5.  Laboratory Medicine in the Scope of Proteomics and Genomics.

Authors:  Urszula Demkow
Journal:  EJIFCC       Date:  2010-10-29

Review 6.  Potential Clinical Application of Genomics in Multiple Myeloma.

Authors:  Cinnie Yentia Soekojo; Sanjay de Mel; Melissa Ooi; Benedict Yan; Wee Joo Chng
Journal:  Int J Mol Sci       Date:  2018-06-10       Impact factor: 5.923

  6 in total

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