Literature DB >> 12466546

HapScope: a software system for automated and visual analysis of functionally annotated haplotypes.

Jinghui Zhang1, William L Rowe, Jeffery P Struewing, Kenneth H Buetow.   

Abstract

We have developed a software analysis package, HapScope, which includes a comprehensive analysis pipeline and a sophisticated visualization tool for analyzing functionally annotated haplotypes. The HapScope analysis pipeline supports: (i) computational haplotype construction with an expectation-maximization or Bayesian statistical algorithm; (ii) SNP classification by protein coding change, homology to model organisms or putative regulatory regions; and (iii) minimum SNP subset selection by either a Brute Force Algorithm or a Greedy Partition Algorithm. The HapScope viewer displays genomic structure with haplotype information in an integrated environment, providing eight alternative views for assessing genetic and functional correlation. It has a user-friendly interface for: (i) haplotype block visualization; (ii) SNP subset selection; (iii) haplotype consolidation with subset SNP markers; (iv) incorporation of both experimentally determined haplotypes and computational results; and (v) data export for additional analysis. Comparison of haplotypes constructed by the statistical algorithms with those determined experimentally shows variation in haplotype prediction accuracies in genomic regions with different levels of nucleotide diversity. We have applied HapScope in analyzing haplotypes for candidate genes and genomic regions with extensive SNP and genotype data. We envision that the systematic approach of integrating functional genomic analysis with population haplotypes, supported by HapScope, will greatly facilitate current genetic disease research.

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Year:  2002        PMID: 12466546      PMCID: PMC137968          DOI: 10.1093/nar/gkf654

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  28 in total

1.  Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

Authors:  N Patil; A J Berno; D A Hinds; W A Barrett; J M Doshi; C R Hacker; C R Kautzer; D H Lee; C Marjoribanks; D P McDonough; B T Nguyen; M C Norris; J B Sheehan; N Shen; D Stern; R P Stokowski; D J Thomas; M O Trulson; K R Vyas; K A Frazer; S P Fodor; D R Cox
Journal:  Science       Date:  2001-11-23       Impact factor: 47.728

2.  Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Authors:  Gonçalo R Abecasis; Stacey S Cherny; William O Cookson; Lon R Cardon
Journal:  Nat Genet       Date:  2001-12-03       Impact factor: 38.330

3.  ViewGene: a graphical tool for polymorphism visualization and characterization.

Authors:  Carl Kashuk; Sanghamitra SenGupta; Evan Eichler; Aravinda Chakravarti
Journal:  Genome Res       Date:  2002-02       Impact factor: 9.043

4.  The structure of haplotype blocks in the human genome.

Authors:  Stacey B Gabriel; Stephen F Schaffner; Huy Nguyen; Jamie M Moore; Jessica Roy; Brendan Blumenstiel; John Higgins; Matthew DeFelice; Amy Lochner; Maura Faggart; Shau Neen Liu-Cordero; Charles Rotimi; Adebowale Adeyemo; Richard Cooper; Ryk Ward; Eric S Lander; Mark J Daly; David Altshuler
Journal:  Science       Date:  2002-05-23       Impact factor: 47.728

5.  The human genome browser at UCSC.

Authors:  W James Kent; Charles W Sugnet; Terrence S Furey; Krishna M Roskin; Tom H Pringle; Alan M Zahler; David Haussler
Journal:  Genome Res       Date:  2002-06       Impact factor: 9.043

Review 6.  Inference of haplotypes from PCR-amplified samples of diploid populations.

Authors:  A G Clark
Journal:  Mol Biol Evol       Date:  1990-03       Impact factor: 16.240

7.  Identification of the cystic fibrosis gene: genetic analysis.

Authors:  B Kerem; J M Rommens; J A Buchanan; D Markiewicz; T K Cox; A Chakravarti; M Buchwald; L C Tsui
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

8.  Bayesian analysis of haplotypes for linkage disequilibrium mapping.

Authors:  J S Liu; C Sabatti; J Teng; B J Keats; N Risch
Journal:  Genome Res       Date:  2001-10       Impact factor: 9.043

9.  Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's disease.

Authors:  J C Lambert; C Berr; F Pasquier; A Delacourte; B Frigard; D Cottel; J Pérez-Tur; V Mouroux; M Mohr; D Cécyre; D Galasko; C Lendon; J Poirier; J Hardy; D Mann; P Amouyel; M C Chartier-Harlin
Journal:  Hum Mol Genet       Date:  1998-09       Impact factor: 6.150

10.  Sequence variation in the human angiotensin converting enzyme.

Authors:  M J Rieder; S L Taylor; A G Clark; D A Nickerson
Journal:  Nat Genet       Date:  1999-05       Impact factor: 38.330

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  14 in total

1.  Haploscope: a tool for the graphical display of haplotype structure in populations.

Authors:  F Anthony San Lucas; Noah A Rosenberg; Paul Scheet
Journal:  Genet Epidemiol       Date:  2011-12-06       Impact factor: 2.135

2.  PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level.

Authors:  Lucía Conde; Juan M Vaquerizas; Javier Santoyo; Fátima Al-Shahrour; Sergio Ruiz-Llorente; Mercedes Robledo; Joaquín Dopazo
Journal:  Nucleic Acids Res       Date:  2004-07-01       Impact factor: 16.971

3.  Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses.

Authors:  Montserrat García-Closas; Kathleen M Egan; Polly A Newcomb; Louise A Brinton; Linda Titus-Ernstoff; Stephen Chanock; Robert Welch; Jolanta Lissowska; Beata Peplonska; Neonila Szeszenia-Dabrowska; Witold Zatonski; Alicja Bardin-Mikolajczak; Jeffery P Struewing
Journal:  Hum Genet       Date:  2006-02-17       Impact factor: 4.132

4.  Reconstructing patterns of reticulate evolution in plants.

Authors:  C Randal Linder; Loren H Rieseberg
Journal:  Am J Bot       Date:  2004-10       Impact factor: 3.844

5.  CREBBP mutations in relapsed acute lymphoblastic leukaemia.

Authors:  Charles G Mullighan; Jinghui Zhang; Lawryn H Kasper; Stephanie Lerach; Debbie Payne-Turner; Letha A Phillips; Sue L Heatley; Linda Holmfeldt; J Racquel Collins-Underwood; Jing Ma; Kenneth H Buetow; Ching-Hon Pui; Sharyn D Baker; Paul K Brindle; James R Downing
Journal:  Nature       Date:  2011-03-10       Impact factor: 49.962

6.  Genomewide distribution of high-frequency, completely mismatching SNP haplotype pairs observed to be common across human populations.

Authors:  Jinghui Zhang; William L Rowe; Andrew G Clark; Kenneth H Buetow
Journal:  Am J Hum Genet       Date:  2003-10-14       Impact factor: 11.025

7.  Thyroid nodules, polymorphic variants in DNA repair and RET-related genes, and interaction with ionizing radiation exposure from nuclear tests in Kazakhstan.

Authors:  Alice J Sigurdson; Charles E Land; Parveen Bhatti; Marbin Pineda; Alina Brenner; Zhanat Carr; Boris I Gusev; Zhaxibay Zhumadilov; Steven L Simon; Andre Bouville; Joni L Rutter; Elaine Ron; Jeffery P Struewing
Journal:  Radiat Res       Date:  2009-01       Impact factor: 2.841

8.  Systematic analysis of genetic alterations in tumors using Cancer Genome WorkBench (CGWB).

Authors:  Jinghui Zhang; Richard P Finney; William Rowe; Michael Edmonson; Sei Hoon Yang; Tatiana Dracheva; Jin Jen; Jeffery P Struewing; Kenneth H Buetow
Journal:  Genome Res       Date:  2007-05-24       Impact factor: 9.043

Review 9.  A comprehensive literature review of haplotyping software and methods for use with unrelated individuals.

Authors:  Rany M Salem; Jennifer Wessel; Nicholas J Schork
Journal:  Hum Genomics       Date:  2005-03       Impact factor: 4.639

10.  A survey of current software for haplotype phase inference.

Authors:  Michael E Weale
Journal:  Hum Genomics       Date:  2004-01       Impact factor: 4.639

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