Literature DB >> 17276656

Resolving the resolution of array CGH.

Bradley P Coe1, Bauke Ylstra, Beatriz Carvalho, Gerrit A Meijer, Calum Macaulay, Wan L Lam.   

Abstract

Many recent technologies have been designed to supplant conventional metaphase CGH technology with the goal of refining the description of segmental copy number status throughout the genome. However, the emergence of new technologies has led to confusion as to how to describe adequately the capabilities of each array platform. The design of a CGH array can incorporate a uniform or a highly variable element distribution. This can lead to bias in the reporting of average or median resolutions, making it difficult to provide a fair comparison of platforms. In this report, we propose a new definition of resolution for array CGH technology, termed "functional resolution," that incorporates the uniformity of element spacing on the array, as well as the sensitivity of each platform to single-copy alterations. Calculation of these metrics is automated through the development of a Java-based application, "ResCalc," which is applicable to any array CGH platform.

Mesh:

Year:  2007        PMID: 17276656     DOI: 10.1016/j.ygeno.2006.12.012

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  58 in total

1.  High-resolution genomic profiling of thyroid lesions uncovers preferential copy number gains affecting mitochondrial biogenesis loci in the oncocytic variants.

Authors:  Ivana Kurelac; Dario de Biase; Claudia Calabrese; Claudio Ceccarelli; Charlotte Ky Ng; Raymond Lim; Alan MacKay; Britta Weigelt; Anna Maria Porcelli; Jorge S Reis-Filho; Giovanni Tallini; Giuseppe Gasparre
Journal:  Am J Cancer Res       Date:  2015-05-15       Impact factor: 6.166

2.  Comparison of comparative genomic hybridization technologies across microarray platforms.

Authors:  Susan D Hester; Laura Reid; Norma Nowak; Wendell D Jones; Joel S Parker; Kevin Knudtson; William Ward; Jay Tiesman; Nancy D Denslow
Journal:  J Biomol Tech       Date:  2009-04

3.  MSB: a mean-shift-based approach for the analysis of structural variation in the genome.

Authors:  Lu-Yong Wang; Alexej Abyzov; Jan O Korbel; Michael Snyder; Mark Gerstein
Journal:  Genome Res       Date:  2008-11-26       Impact factor: 9.043

4.  Detection of novel copy number variants in uterine leiomyomas using high-resolution SNP arrays.

Authors:  Wayne Bowden; Josh Skorupski; Ertug Kovanci; Aleksandar Rajkovic
Journal:  Mol Hum Reprod       Date:  2009-06-30       Impact factor: 4.025

5.  Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history.

Authors:  Philip M Kim; Hugo Y K Lam; Alexander E Urban; Jan O Korbel; Jason Affourtit; Fabian Grubert; Xueying Chen; Sherman Weissman; Michael Snyder; Mark B Gerstein
Journal:  Genome Res       Date:  2008-10-08       Impact factor: 9.043

6.  Copy number variant analysis of human embryonic stem cells.

Authors:  Hao Wu; Kevin J Kim; Kshama Mehta; Salvatore Paxia; Andrew Sundstrom; Thomas Anantharaman; Ali I Kuraishy; Tri Doan; Jayati Ghosh; April D Pyle; Amander Clark; William Lowry; Guoping Fan; Tim Baxter; Bud Mishra; Yi Sun; Michael A Teitell
Journal:  Stem Cells       Date:  2008-03-27       Impact factor: 6.277

7.  Absence/presence calling in microarray-based CGH experiments with non-model organisms.

Authors:  Martijs J Jonker; Wim C de Leeuw; Marino Marinković; Floyd R A Wittink; Han Rauwerda; Oskar Bruning; Wim A Ensink; Ad C Fluit; C H Boel; Mark de Jong; Timo M Breit
Journal:  Nucleic Acids Res       Date:  2014-04-25       Impact factor: 16.971

8.  Genomic deletions correlate with underexpression of novel candidate genes at six loci in pediatric pilocytic astrocytoma.

Authors:  Nicola Potter; Aikaterini Karakoula; Kim P Phipps; William Harkness; Richard Hayward; Dominic N P Thompson; Thomas S Jacques; Brian Harding; David G T Thomas; Rodger W Palmer; Jeremy Rees; John Darling; Tracy J Warr
Journal:  Neoplasia       Date:  2008-08       Impact factor: 5.715

9.  Statistical aspects of discerning indel-type structural variation via DNA sequence alignment.

Authors:  Michael C Wendl; Richard K Wilson
Journal:  BMC Genomics       Date:  2009-08-05       Impact factor: 3.969

10.  Integrative molecular profiling of triple negative breast cancers identifies amplicon drivers and potential therapeutic targets.

Authors:  N Turner; M B Lambros; H M Horlings; A Pearson; R Sharpe; R Natrajan; F C Geyer; M van Kouwenhove; B Kreike; A Mackay; A Ashworth; M J van de Vijver; J S Reis-Filho
Journal:  Oncogene       Date:  2010-01-18       Impact factor: 9.867

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