Abstract
Motivation: The use of dense single nucleotide polymorphism (SNP) data in genetic linkage analysis of large pedigrees is impeded by significant technical, methodological and computational challenges. Here we describe Superlink-Online SNP, a new powerful online system that streamlines the linkage analysis of SNP data. It features a fully integrated flexible processing workflow comprising both well-known and novel data analysis tools, including SNP clustering, erroneous data filtering, exact and approximate LOD calculations and maximum-likelihood haplotyping. The system draws its power from thousands of CPUs, performing data analysis tasks orders of magnitude faster than a single computer. By providing an intuitive interface to sophisticated state-of-the-art analysis tools coupled with high computing capacity, Superlink-Online SNP helps geneticists unleash the potential of SNP data for detecting disease genes.Results: Computations performed by Superlink-Online SNP are automatically parallelized using novel paradigms, and executed on unlimited number of private or public CPUs. One novel service is large-scale approximate Markov Chain-Monte Carlo (MCMC) analysis. The accuracy of the results is reliably estimated by running the same computation on multiple CPUs and evaluating the Gelman-Rubin Score to set aside unreliable results. Another service within the workflow is a novel parallelized exact algorithm for inferring maximum-likelihood haplotyping. The reported system enables genetic analyses that were previously infeasible. We demonstrate the system capabilities through a study of a large complex pedigree affected with metabolic syndrome.
Original language | English |
---|---|
Pages (from-to) | 197-205 |
Number of pages | 9 |
Journal | Bioinformatics |
Volume | 29 |
Issue number | 2 |
DOIs | |
State | Published - 15 Jan 2013 |
Externally published | Yes |
Bibliographical note
Funding Information:Funding: This work was supported by the National Institutes of Health [5R01HG004175-03] (to D.G., R.D. and E.T.), the Israeli Science Foundation (to D.G.) and the Israeli Ministry of Science and Technology [3-8095] (to A.S. and Z.B.).
Funding
Funding: This work was supported by the National Institutes of Health [5R01HG004175-03] (to D.G., R.D. and E.T.), the Israeli Science Foundation (to D.G.) and the Israeli Ministry of Science and Technology [3-8095] (to A.S. and Z.B.).
Funders | Funder number |
---|---|
National Institutes of Health | 5R01HG004175-03 |
National Institute of General Medical Sciences | R37GM046255 |
Israel Science Foundation | |
Ministry of science and technology, Israel | 3-8095 |