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SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays.
Bioinformatics ; 23(1): 57-63, 2007 Jan 01.
Article en En | MEDLINE | ID: mdl-17062589
ABSTRACT
MOTIVATION The technology to genotype single nucleotide polymorphisms (SNPs) at extremely high densities provides for hypothesis-free genome-wide scans for common polymorphisms associated with complex disease. However, we find that some errors introduced by commonly employed genotyping algorithms may lead to inflation of false associations between markers and phenotype.

RESULTS:

We have developed a novel SNP genotype calling program, SNiPer-High Density (SNiPer-HD), for highly accurate genotype calling across hundreds of thousands of SNPs. The program employs an expectation-maximization (EM) algorithm with parameters based on a training sample set. The algorithm choice allows for highly accurate genotyping for most SNPs. Also, we introduce a quality control metric for each assayed SNP, such that poor-behaving SNPs can be filtered using a metric correlating to genotype class separation in the calling algorithm. SNiPer-HD is superior to the standard dynamic modeling algorithm and is complementary and non-redundant to other algorithms, such as BRLMM. Implementing multiple algorithms together may provide highly accurate genotyping calls, without inflation of false positives due to systematically miss-called SNPs. A reliable and accurate set of SNP genotypes for increasingly dense panels will eliminate some false association signals and false negative signals, allowing for rapid identification of disease susceptibility loci for complex traits.

AVAILABILITY:

SNiPer-HD is available at TGen's website http//www.tgen.org/neurogenomics/data.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Algoritmos / Biología Computacional / Análisis de Secuencia por Matrices de Oligonucleótidos / Polimorfismo de Nucleótido Simple Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2007 Tipo del documento: Article
Search on Google
Banco de datos: MEDLINE Asunto principal: Algoritmos / Biología Computacional / Análisis de Secuencia por Matrices de Oligonucleótidos / Polimorfismo de Nucleótido Simple Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2007 Tipo del documento: Article