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Links from PubMed

Items: 3

1.

Markov Models for inferring copy number variations from genotype data on Illumina platforms.

Wang H, Veldink JH, Blauw H, van den Berg LH, Ophoff RA, Sabatti C.

Hum Hered. 2009;68(1):1-22. doi: 10.1159/000210445. Epub 2009 Apr 1.

2.

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

Seiser EL, Innocenti F.

Cancer Inform. 2015 Jan 27;13(Suppl 7):77-83. doi: 10.4137/CIN.S16345. eCollection 2014. Review.

3.

Copy-number variation and association studies of human disease.

McCarroll SA, Altshuler DM.

Nat Genet. 2007 Jul;39(7 Suppl):S37-42. Review.

PMID:
17597780

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