Literature DB >> 20926418

CopyMap: localization and calling of copy number variation by joint analysis of hybridization data from multiple individuals.

Sebastian Zöllner1.   

Abstract

SUMMARY: The program package CopyMap identifies copy number variation from oligo-hybridization and CGH data. Using a time-dependent hidden Markov model to combine evidence of copy number variants (CNVs) across multiple carriers, CopyMap is substantially more accurate than standard hidden Markov methods in identifying CNVs and calling CNV-carriers. Moreover, CopyMap provides more precise estimates of CNV-boundaries. AVAILABILITY: The C-source code and detailed documentation for the program CopyMap is available on the Internet at http://www.sph.umich.edu/csg/szoellner/

Mesh:

Year:  2010        PMID: 20926418      PMCID: PMC2981497          DOI: 10.1093/bioinformatics/btq515

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  10 in total

1.  Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.

Authors:  Sebastian Zöllner; Gang Su; William C L Stewart; Yi Chen; Melvin G McInnis; Margit Burmeister
Journal:  Genet Epidemiol       Date:  2009-05       Impact factor: 2.135

2.  Segmental copy number variation shapes tissue transcriptomes.

Authors:  Charlotte N Henrichsen; Nicolas Vinckenbosch; Sebastian Zöllner; Evelyne Chaignat; Sylvain Pradervand; Frédéric Schütz; Manuel Ruedi; Henrik Kaessmann; Alexandre Reymond
Journal:  Nat Genet       Date:  2009-03-08       Impact factor: 38.330

3.  Integrated detection and population-genetic analysis of SNPs and copy number variation.

Authors:  Steven A McCarroll; Finny G Kuruvilla; Joshua M Korn; Simon Cawley; James Nemesh; Alec Wysoker; Michael H Shapero; Paul I W de Bakker; Julian B Maller; Andrew Kirby; Amanda L Elliott; Melissa Parkin; Earl Hubbell; Teresa Webster; Rui Mei; James Veitch; Patrick J Collins; Robert Handsaker; Steve Lincoln; Marcia Nizzari; John Blume; Keith W Jones; Rich Rava; Mark J Daly; Stacey B Gabriel; David Altshuler
Journal:  Nat Genet       Date:  2008-09-07       Impact factor: 38.330

4.  Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA.

Authors:  Michael T Barrett; Alicia Scheffer; Amir Ben-Dor; Nick Sampas; Doron Lipson; Robert Kincaid; Peter Tsang; Bo Curry; Kristin Baird; Paul S Meltzer; Zohar Yakhini; Laurakay Bruhn; Stephen Laderman
Journal:  Proc Natl Acad Sci U S A       Date:  2004-12-10       Impact factor: 11.205

5.  Detecting copy number variations from array CGH data based on a conditional random field model.

Authors:  Xiao-Lin Yin; Jing Li
Journal:  J Bioinform Comput Biol       Date:  2010-04       Impact factor: 1.122

6.  Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation.

Authors:  Robert Lucito; John Healy; Joan Alexander; Andrew Reiner; Diane Esposito; Maoyen Chi; Linda Rodgers; Amy Brady; Jonathan Sebat; Jennifer Troge; Joseph A West; Seth Rostan; Ken C Q Nguyen; Scott Powers; Kenneth Q Ye; Adam Olshen; Ennapadam Venkatraman; Larry Norton; Michael Wigler
Journal:  Genome Res       Date:  2003-09-15       Impact factor: 9.043

7.  Origins and functional impact of copy number variation in the human genome.

Authors:  Donald F Conrad; Dalila Pinto; Richard Redon; Lars Feuk; Omer Gokcumen; Yujun Zhang; Jan Aerts; T Daniel Andrews; Chris Barnes; Peter Campbell; Tomas Fitzgerald; Min Hu; Chun Hwa Ihm; Kati Kristiansson; Daniel G Macarthur; Jeffrey R Macdonald; Ifejinelo Onyiah; Andy Wing Chun Pang; Sam Robson; Kathy Stirrups; Armand Valsesia; Klaudia Walter; John Wei; Chris Tyler-Smith; Nigel P Carter; Charles Lee; Stephen W Scherer; Matthew E Hurles
Journal:  Nature       Date:  2009-10-07       Impact factor: 49.962

8.  Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.

Authors:  Joshua M Korn; Finny G Kuruvilla; Steven A McCarroll; Alec Wysoker; James Nemesh; Simon Cawley; Earl Hubbell; Jim Veitch; Patrick J Collins; Katayoon Darvishi; Charles Lee; Marcia M Nizzari; Stacey B Gabriel; Shaun Purcell; Mark J Daly; David Altshuler
Journal:  Nat Genet       Date:  2008-09-07       Impact factor: 38.330

9.  Identification of small gains and losses in single cells after whole genome amplification on tiling oligo arrays.

Authors:  Jochen B Geigl; Anna C Obenauf; Julie Waldispuehl-Geigl; Eva M Hoffmann; Martina Auer; Martina Hörmann; Maria Fischer; Zlatko Trajanoski; Michael A Schenk; Lars O Baumbusch; Michael R Speicher
Journal:  Nucleic Acids Res       Date:  2009-06-18       Impact factor: 16.971

10.  Mouse segmental duplication and copy number variation.

Authors:  Xinwei She; Ze Cheng; Sebastian Zöllner; Deanna M Church; Evan E Eichler
Journal:  Nat Genet       Date:  2008-05-22       Impact factor: 38.330

  10 in total
  5 in total

Review 1.  Systems genetics in "-omics" era: current and future development.

Authors:  Hong Li
Journal:  Theory Biosci       Date:  2012-11-09       Impact factor: 1.919

2.  Fast detection of de novo copy number variants from SNP arrays for case-parent trios.

Authors:  Robert B Scharpf; Terri H Beaty; Holger Schwender; Samuel G Younkin; Alan F Scott; Ingo Ruczinski
Journal:  BMC Bioinformatics       Date:  2012-12-12       Impact factor: 3.169

3.  Parsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.

Authors:  Michael Seifert; André Gohr; Marc Strickert; Ivo Grosse
Journal:  PLoS Comput Biol       Date:  2012-01-12       Impact factor: 4.475

4.  Diversity and regulatory impact of copy number variation in the primate Macaca fascicularis.

Authors:  Andreas R Gschwind; Anjali Singh; Ulrich Certa; Alexandre Reymond; Tobias Heckel
Journal:  BMC Genomics       Date:  2017-02-10       Impact factor: 3.969

5.  A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk.

Authors:  Samuel G Younkin; Robert B Scharpf; Holger Schwender; Margaret M Parker; Alan F Scott; Mary L Marazita; Terri H Beaty; Ingo Ruczinski
Journal:  BMC Genet       Date:  2014-02-14       Impact factor: 2.797

  5 in total

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