Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias

BACKGROUND: High-density genotyping arrays that measure hybridization of genomic DNA fragments to allele-specific oligonucleotide probes are widely used to genotype single nucleotide polymorphisms (SNPs) in genetic studies, including human genome-wide association studies. Hybridization intensities a...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Didion, John P, Yang, Hyuna, Sheppard, Keith, Fu, Chen-Ping, McMillan, Leonard, de Villena, Fernando Pardo-Manuel, Churchill, Gary A
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2012
Témata:
Methodology Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3305361/
https://ncbi.nlm.nih.gov/pubmed/22260749
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-34
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky