Literature DB >> 24969160

Visualization of haplotype sharing patterns in pedigree samples.

Sulgi Kim1, Mohamad Saad, Debby W Tsuang, Ellen M Wijsman.   

Abstract

OBJECTIVES: A particular approach to the visualization of descent of founder DNA copies in a pedigree has been suggested, which helps to understand haplotype sharing patterns among subjects of interest. However, the approach does not provide the information in an ideal format to show haplotype sharing patterns. Therefore, we aimed to find an efficient way to visualize such sharing patterns and to demonstrate that our tool provides useful information for finding an informative subset of subjects for a sequence study.
METHODS: The visualization package, SharedHap, computes and visualizes a novel metric, the SharedHap proportion, which quantifies haplotype sharing among a set of subjects of interest. We applied SharedHap to simulated and real pedigree datasets to illustrate the approach.
RESULTS: SharedHap successfully represents haplotype sharing patterns that contribute to linkage signals in both simulated and real datasets. Using the visualizations we were also able to find ideal sets of subjects for sequencing studies.
CONCLUSIONS: Our novel metric that can be computed using the SharedHap package provides useful information about haplotype sharing patterns among subjects of interest. The visualization of the SharedHap proportion provides useful information in pedigree studies, allowing for a better selection of candidate subjects for use in further sequencing studies.
© 2014 S. Karger AG, Basel.

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Year:  2014        PMID: 24969160      PMCID: PMC4112026          DOI: 10.1159/000358171

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  28 in total

1.  Increasing the power and efficiency of disease-marker case-control association studies through use of allele-sharing information.

Authors:  Tasha E Fingerlin; Michael Boehnke; Gonçalo R Abecasis
Journal:  Am J Hum Genet       Date:  2004-02-02       Impact factor: 11.025

Review 2.  Linkage analysis in the next-generation sequencing era.

Authors:  Joan E Bailey-Wilson; Alexander F Wilson
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

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Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

4.  Report of the Committee on Methods of Linkage Analysis and Reporting.

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5.  Department of Veterans Affairs Cooperative Studies Program genetic linkage study of schizophrenia: ascertainment methods and sample description.

Authors:  M T Tsuang; S V Faraone; S Bingham; K Young; S Prabhudesai; S L Haverstock; F Mena; A S Menon; J Pepple; J Johnson; C Baldwin; D Weiss; J Collins
Journal:  Am J Med Genet       Date:  2000-06-12

Review 6.  Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease.

Authors:  David Botstein; Neil Risch
Journal:  Nat Genet       Date:  2003-03       Impact factor: 38.330

7.  Exome sequencing of a pedigree with Tourette syndrome or chronic tic disorder.

Authors:  Senthil K Sundaram; Ahm M Huq; Zhen Sun; Wu Yu; Lindsey Bennett; Benjamin J Wilson; Michael E Behen; Harry T Chugani
Journal:  Ann Neurol       Date:  2011-05       Impact factor: 10.422

8.  Construction of multilocus genetic linkage maps in humans.

Authors:  E S Lander; P Green
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

9.  Genome-wide search for schizophrenia susceptibility loci: the NIMH Genetics Initiative and Millennium Consortium.

Authors:  C R Cloninger; C A Kaufmann; S V Faraone; D Malaspina; D M Svrakic; J Harkavy-Friedman; B K Suarez; T C Matise; D Shore; H Lee; C L Hampe; D Wynne; C Drain; P D Markel; C T Zambuto; K Schmitt; M T Tsuang
Journal:  Am J Med Genet       Date:  1998-07-10

10.  Strategies for selection of subjects for sequencing after detection of a linkage peak.

Authors:  Kristina Allen-Brady; James Farnham; Lisa Cannon-Albright
Journal:  BMC Proc       Date:  2011-11-29
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