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1.
BMC Bioinformatics ; 10: 81, 2009 Mar 09.
Article de Anglais | MEDLINE | ID: mdl-19267942

RÉSUMÉ

BACKGROUND: Genotyping of single-nucleotide polymorphisms (SNPs) is a fundamental technology in modern genetics. The SNPlex mid-throughput genotyping system (Applied Biosystems, Foster City, CA, USA) enables the multiplexed genotyping of up to 48 SNPs simultaneously in a single DNA sample. The high level of automation and the large amount of data produced in a high-throughput laboratory require advanced software tools for quality control and workflow management. RESULTS: We have developed two programs, which address two main aspects of quality control in a SNPlex genotyping environment: GMFilter improves the analysis of SNPlex plates by removing wells with a low overall signal intensity. It enables scientists to automatically process the raw data in a standardized way before analyzing a plate with the proprietary GeneMapper software from Applied Biosystems. SXTestPlate examines the genotype concordance of a SNPlex test plate, which was typed with a control SNP set. This program allows for regular quality control checks of a SNPlex genotyping platform. It is compatible to other genotyping methods as well. CONCLUSION: GMFilter and SXTestPlate provide a valuable tool set for laboratories engaged in genotyping based on the SNPlex system. The programs enhance the analysis of SNPlex plates with the GeneMapper software and enable scientists to evaluate the performance of their genotyping platform.


Sujet(s)
Génotype , Polymorphisme de nucléotide simple/génétique , Logiciel , Bases de données génétiques , Génome humain , Humains , Mémorisation et recherche des informations , Séquençage par oligonucléotides en batterie/méthodes , Interface utilisateur
2.
Mutat Res ; 573(1-2): 111-35, 2005 Jun 03.
Article de Anglais | MEDLINE | ID: mdl-15829242

RÉSUMÉ

In this review we describe the principles, protocols, and applications of two commercially available SNP genotyping platforms, the TaqMan SNP Genotyping Assays and the SNPlex Genotyping System. Combined, these two technologies meet the requirements of multiple SNP applications in genetics research and pharmacogenetics. We also describe a set of SNP selection tools and validated assay resources which we developed to accelerate the cycle of experimentation on these platforms. Criteria for selecting the more appropriate of these two genotyping technologies are presented: the genetic architecture of the trait of interest, the throughput required, and the number of SNPs and samples needed for a successful study. Overall, the TaqMan assay format is suitable for low- to mid-throughput applications in which a high assay conversion rate, simple assay workflow, and low cost of automation are desirable. The SNPlex Genotyping System, on the other hand, is well suited for SNP applications in which throughput and cost-efficiency are essential, e.g., applications requiring either the testing of large numbers of SNPs and samples, or the flexibility to select various SNP subsets.


Sujet(s)
Génotype , Polymorphisme de nucléotide simple , Fréquence d'allèle , Humains , Déséquilibre de liaison , Pharmacogénétique/méthodes , Logiciel
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