Literature DB >> 16685644

Online system for faster multipoint linkage analysis via parallel execution on thousands of personal computers.

M Silberstein1, A Tzemach, N Dovgolevsky, M Fishelson, A Schuster, D Geiger.   

Abstract

Computation of LOD scores is a valuable tool for mapping disease-susceptibility genes in the study of Mendelian and complex diseases. However, computation of exact multipoint likelihoods of large inbred pedigrees with extensive missing data is often beyond the capabilities of a single computer. We present a distributed system called "SUPERLINK-ONLINE," for the computation of multipoint LOD scores of large inbred pedigrees. It achieves high performance via the efficient parallelization of the algorithms in SUPERLINK, a state-of-the-art serial program for these tasks, and through the use of the idle cycles of thousands of personal computers. The main algorithmic challenge has been to efficiently split a large task for distributed execution in a highly dynamic, nondedicated running environment. Notably, the system is available online, which allows computationally intensive analyses to be performed with no need for either the installation of software or the maintenance of a complicated distributed environment. As the system was being developed, it was extensively tested by collaborating medical centers worldwide on a variety of real data sets, some of which are presented in this article.

Mesh:

Year:  2006        PMID: 16685644      PMCID: PMC1474109          DOI: 10.1086/504158

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  32 in total

1.  Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.

Authors:  K Strauch; R Fimmers; T Kurz; K A Deichmann; T F Wienker; M P Baur
Journal:  Am J Hum Genet       Date:  2000-05-04       Impact factor: 11.025

2.  Allegro, a new computer program for multipoint linkage analysis.

Authors:  D F Gudbjartsson; K Jonasson; M L Frigge; A Kong
Journal:  Nat Genet       Date:  2000-05       Impact factor: 38.330

3.  On the parallelization of linkmap from the LINKAGE/FASTLINK package.

Authors:  A Rai; N Lopez-Benitez; J D Hargis; S E Poduslo
Journal:  Comput Biomed Res       Date:  2000-10

4.  Amish brittle hair syndrome gene maps to 7p14.1.

Authors:  Eric Seboun; Arnaud Lemainque; Charles E Jackson
Journal:  Am J Med Genet A       Date:  2005-04-30       Impact factor: 2.802

5.  Maximum likelihood haplotyping for general pedigrees.

Authors:  Ma'ayan Fishelson; Nickolay Dovgolevsky; Dan Geiger
Journal:  Hum Hered       Date:  2005       Impact factor: 0.444

6.  Software for constructing and verifying pedigrees within large genealogies and an application to the Old Order Amish of Lancaster County.

Authors:  R Agarwala; L G Biesecker; K A Hopkins; C A Francomano; A A Schaffer
Journal:  Genome Res       Date:  1998-03       Impact factor: 9.043

7.  Parametric and nonparametric linkage analysis: a unified multipoint approach.

Authors:  L Kruglyak; M J Daly; M P Reeve-Daly; E S Lander
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

8.  Faster linkage analysis computations for pedigrees with loops or unused alleles.

Authors:  A A Schäffer
Journal:  Hum Hered       Date:  1996 Jul-Aug       Impact factor: 0.444

9.  Faster multipoint linkage analysis using Fourier transforms.

Authors:  L Kruglyak; E S Lander
Journal:  J Comput Biol       Date:  1998       Impact factor: 1.479

10.  Can we rely on the family history?

Authors:  J Zlotogora; B Bisharat; S Barges
Journal:  Am J Med Genet       Date:  1998-04-28
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  43 in total

1.  Hyperchlorhidrosis caused by homozygous mutation in CA12, encoding carbonic anhydrase XII.

Authors:  Maya Feldshtein; Suliman Elkrinawi; Baruch Yerushalmi; Barak Marcus; Daniela Vullo; Hila Romi; Rivka Ofir; Daniel Landau; Sara Sivan; Claudiu T Supuran; Ohad S Birk
Journal:  Am J Hum Genet       Date:  2010-10-28       Impact factor: 11.025

2.  Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.

Authors:  Miora Feinstein; Barak Markus; Iris Noyman; Hannah Shalev; Hagit Flusser; Ilan Shelef; Keren Liani-Leibson; Zamir Shorer; Idan Cohen; Shareef Khateeb; Sara Sivan; Ohad S Birk
Journal:  Am J Hum Genet       Date:  2010-11-18       Impact factor: 11.025

3.  Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity.

Authors:  Kouji Maeda; Ryuji Kaji; Katsuhito Yasuno; Jamiyansuren Jambaldorj; Hiroyuki Nodera; Hiroshi Takashima; Masanori Nakagawa; Satoshi Makino; Gen Tamiya
Journal:  J Hum Genet       Date:  2007-10-02       Impact factor: 3.172

4.  Multilocus lod scores in large pedigrees: combination of exact and approximate calculations.

Authors:  Liping Tong; Elizabeth Thompson
Journal:  Hum Hered       Date:  2007-10-12       Impact factor: 0.444

5.  Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5.

Authors:  Daniella Magen; Ayala Ofir; Liron Berger; Dorit Goldsher; Ayelet Eran; Nasser Katib; Nassser Katib; Yousif Nijem; Euvgeni Vlodavsky; Shay Tzur; Shay Zur; Doron M Behar; Yakov Fellig; Hanna Mandel
Journal:  Hum Genet       Date:  2015-01-06       Impact factor: 4.132

6.  Isolated foveal hypoplasia with secondary nystagmus and low vision is associated with a homozygous SLC38A8 mutation.

Authors:  Yonatan Perez; Libe Gradstein; Hagit Flusser; Barak Markus; Idan Cohen; Yshaia Langer; Mira Marcus; Tova Lifshitz; Rotem Kadir; Ohad S Birk
Journal:  Eur J Hum Genet       Date:  2013-09-18       Impact factor: 4.246

7.  Targeted next-generation sequencing appoints c16orf57 as clericuzio-type poikiloderma with neutropenia gene.

Authors:  Ludovica Volpi; Gaia Roversi; Elisa Adele Colombo; Nico Leijsten; Daniela Concolino; Andrea Calabria; Maria Antonietta Mencarelli; Michele Fimiani; Fabio Macciardi; Rolph Pfundt; Eric F P M Schoenmakers; Lidia Larizza
Journal:  Am J Hum Genet       Date:  2009-12-10       Impact factor: 11.025

8.  Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis.

Authors:  Rahim Ullah; Muhammad Ansar; Zaka Ullah Durrani; Kwanghyuk Lee; Regie Lyn P Santos-Cortez; Dost Muhammad; Mahboob Ali; Muhammad Zia; Muhammad Ayub; Suliman Khan; Josh D Smith; Deborah A Nickerson; Jay Shendure; Michael Bamshad; Suzanne M Leal; Wasim Ahmad
Journal:  Int J Dermatol       Date:  2015-11-17       Impact factor: 2.736

9.  Estimating genome-wide IBD sharing from SNP data via an efficient hidden Markov model of LD with application to gene mapping.

Authors:  Sivan Bercovici; Christopher Meek; Ydo Wexler; Dan Geiger
Journal:  Bioinformatics       Date:  2010-06-15       Impact factor: 6.937

10.  Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.

Authors:  Muhammad Salman Chishti; Kwanghyuk Lee; Merry-Lynn McDonald; Muhammad Jawad Hassan; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal
Journal:  J Hum Genet       Date:  2009-02-20       Impact factor: 3.172

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