Literature DB >> 18252739

ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays.

Guillem Rigaill1, Philippe Hupé, Anna Almeida, Philippe La Rosa, Jean-Philippe Meyniel, Charles Decraene, Emmanuel Barillot.   

Abstract

MOTIVATION: Affymetrix SNP arrays can be used to determine the DNA copy number measurement of 11 000-500 000 SNPs along the genome. Their high density facilitates the precise localization of genomic alterations and makes them a powerful tool for studies of cancers and copy number polymorphism. Like other microarray technologies it is influenced by non-relevant sources of variation, requiring correction. Moreover, the amplitude of variation induced by non-relevant effects is similar or greater than the biologically relevant effect (i.e. true copy number), making it difficult to estimate non-relevant effects accurately without including the biologically relevant effect.
RESULTS: We addressed this problem by developing ITALICS, a normalization method that estimates both biological and non-relevant effects in an alternate, iterative manner, accurately eliminating irrelevant effects. We compared our normalization method with other existing and available methods, and found that ITALICS outperformed these methods for several in-house datasets and one public dataset. These results were validated biologically by quantitative PCR. AVAILABILITY: The R package ITALICS (ITerative and Alternative normaLIzation and Copy number calling for affymetrix Snp arrays) has been submitted to Bioconductor.

Entities:  

Mesh:

Year:  2008        PMID: 18252739     DOI: 10.1093/bioinformatics/btn048

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


  13 in total

1.  ACNE: a summarization method to estimate allele-specific copy numbers for Affymetrix SNP arrays.

Authors:  Maria Ortiz-Estevez; Henrik Bengtsson; Angel Rubio
Journal:  Bioinformatics       Date:  2010-06-06       Impact factor: 6.937

2.  Joint estimation of copy number variation and reference intensities on multiple DNA arrays using GADA.

Authors:  Roger Pique-Regi; Antonio Ortega; Shahab Asgharzadeh
Journal:  Bioinformatics       Date:  2009-03-10       Impact factor: 6.937

Review 3.  Statistical issues in the analysis of DNA Copy Number Variations.

Authors:  Nathan E Wineinger; Richard E Kennedy; Stephen W Erickson; Mary K Wojczynski; Carl E Bruder; Hemant K Tiwari
Journal:  Int J Comput Biol Drug Des       Date:  2008

4.  PAIR: paired allelic log-intensity-ratio-based normalization method for SNP-CGH arrays.

Authors:  Shengping Yang; Stanley Pounds; Kun Zhang; Zhide Fang
Journal:  Bioinformatics       Date:  2012-11-29       Impact factor: 6.937

Review 5.  Current analysis platforms and methods for detecting copy number variation.

Authors:  Wenli Li; Michael Olivier
Journal:  Physiol Genomics       Date:  2012-11-06       Impact factor: 3.107

6.  A genomic and transcriptomic approach for a differential diagnosis between primary and secondary ovarian carcinomas in patients with a previous history of breast cancer.

Authors:  Jean-Philippe Meyniel; Paul H Cottu; Charles Decraene; Marc-Henri Stern; Jérôme Couturier; Ingrid Lebigot; André Nicolas; Nina Weber; Virginie Fourchotte; Séverine Alran; Audrey Rapinat; David Gentien; Sergio Roman-Roman; Laurent Mignot; Xavier Sastre-Garau
Journal:  BMC Cancer       Date:  2010-05-21       Impact factor: 4.430

7.  Spatial normalization improves the quality of genotype calling for Affymetrix SNP 6.0 arrays.

Authors:  High Seng Chai; Terry M Therneau; Kent R Bailey; Jean-Pierre A Kocher
Journal:  BMC Bioinformatics       Date:  2010-06-29       Impact factor: 3.169

Review 8.  Cancer gene discovery in mouse and man.

Authors:  Jenny Mattison; Louise van der Weyden; Tim Hubbard; David J Adams
Journal:  Biochim Biophys Acta       Date:  2009-03-12

9.  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

10.  Integrated study of copy number states and genotype calls using high-density SNP arrays.

Authors:  Wei Sun; Fred A Wright; Zhengzheng Tang; Silje H Nordgard; Peter Van Loo; Tianwei Yu; Vessela N Kristensen; Charles M Perou
Journal:  Nucleic Acids Res       Date:  2009-07-06       Impact factor: 16.971

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