BioMed Central | Articles which cite: Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan.

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PubMed Central articles that cite the above article:

1.	QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data. Colella S, Yau C, Taylor JM, Mirza G, Butler H, Clouston P, Bassett AS, Seller A, Holmes CC, Ragoussis J Nucleic Acids Res 2007, 35:2013-25 [PubMed Central] [PubMed] [Related articles]
2.	The application of single nucleotide polymorphism microarrays in cancer research. Mao X, Young BD, Lu YJ Curr Genomics 2007 Jun, 8:219-28 [PubMed Central] [PubMed] [Related articles]
3.	Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays. Scharpf RB, Parmigiani G, Pevsner J, Ruczinski I Ann Appl Stat 2008 Jun 1, 2:687-713 [PubMed Central] [PubMed] [Related articles]
4.	A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6. Bengtsson H, Wirapati P, Speed TP Bioinformatics 2009 Sep 1, 25:2149-56 [PubMed Central] [PubMed] [Related articles]

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