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Resource

GenomeVIP: a cloud platform for genomic variant discovery and interpretation

R. Jay Mashl
Adam D. Scott
Kuan-lin Huang
Matthew A. Wyczalkowski
Christopher J. Yoon
Beifang Niu Erin DeNardo Venkata D. Yellapantula Robert E. Handsaker Ken Chen Daniel C. Koboldt Kai Ye
... [+7 authors] ...,
David Fenyö
Benjamin J. Raphael
Michael C. Wendl
Li Ding

First Published May 18, 2017

Research

Characteristics of de novo structural changes in the human genome

Wigard P. Kloosterman
Laurent C. Francioli
Fereydoun Hormozdiari
Tobias Marschall
Jayne Y. Hehir-Kwa
Abdel Abdellaoui Eric-Wubbo Lameijer Matthijs H. Moed Vyacheslav Koval Ivo Renkens Markus J. van Roosmalen Pascal Arp Lennart C. Karssen Bradley P. Coe Robert E. Handsaker Eka D. Suchiman Edwin Cuppen Djie Tjwan Thung Mitch McVey Michael C. Wendl André Uitterlinden Cornelia M. van Duijn Morris A. Swertz Cisca Wijmenga GertJan B. van Ommen P. Eline Slagboom Dorret I. Boomsma Alexander Schönhuth Evan E. Eichler Paul I.W. de Bakker Kai Ye Victor Guryev André Uitterlinden Cornelia M. van Duijn Morris A. Swertz Cisca Wijmenga GertJan B. van Ommen P. Eline Slagboom Dorret I. Boomsma Alexander Schönhuth
... [+35 authors] ...,
Evan E. Eichler
Paul I.W. de Bakker
Kai Ye
Victor Guryev

First Published April 16, 2015

Resource

MuSiC: Identifying mutational significance in cancer genomes

Nathan D. Dees
Qunyuan Zhang
Cyriac Kandoth
Michael C. Wendl
William Schierding
Daniel C. Koboldt Thomas B. Mooney Matthew B. Callaway
... [+3 authors] ...,
David Dooling
Elaine R. Mardis
Richard K. Wilson
Li Ding

First Published July 3, 2012

RESOURCE

PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data

Ken Chen
Michael D. McLellan
Li Ding
Michael C. Wendl
Yumi Kasai
Richard K. Wilson
Elaine R. Mardis

First Published April 6, 2007

LETTER

The portability of tagSNPs across populations: A worldwide survey

Anna González-Neira
Xiayi Ke
Oscar Lao
Francesc Calafell
Arcadi Navarro
David Comas Howard Cann Suzannah Bumpstead Jilur Ghori Sarah Hunt
... [+5 authors] ...,
Panos Deloukas
Ian Dunham
Lon R. Cardon
Jaume Bertranpetit

First Published February 8, 2006

LETTER

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants

Robert Lawrence
David M. Evans
Andrew P. Morris
Xiayi Ke
Sarah Hunt
Marta Paolucci
... [+1 authors] ...,
Jiannis Ragoussis
Panos Deloukas
David Bentley
Lon R. Cardon

First Published October 26, 2005

RESOURCE

Complete MHC Haplotype Sequencing for Common Disease Gene Mapping

C. Andrew Stewart
Roger Horton
Richard J.N. Allcock
Jennifer L. Ashurst
Alexey M. Atrazhev
Penny Coggill Ian Dunham Simon Forbes Karen Halls Joanna M.M. Howson Sean J. Humphray Sarah Hunt Andrew J. Mungall Kazutoyo Osoegawa Sophie Palmer Anne N. Roberts Jane Rogers Sarah Sims Yu Wang Laurens G. Wilming John F. Elliott Pieter J. de Jong
... [+17 authors] ...,
Stephen Sawcer
John A. Todd
John Trowsdale
Stephan Beck

First Published May 12, 2004

RESOURCE

A Whole-Genome Mouse BAC Microarray With 1-Mb Resolution for Analysis of DNA Copy Number Changes by Array Comparative Genomic Hybridization

Yeun-Jun Chung
Jos Jonkers
Hannah Kitson
Heike Fiegler
Sean Humphray
Carol Scott Sarah Hunt Yuejin Yu Ichiko Nishijima
... [+4 authors] ...,
Arno Velds
Henne Holstege
Nigel Carter
Allan Bradley

First Published January 5, 2004

METHODS

Generalized Gap Model for Bacterial Artificial Chromosome Clone Fingerprint Mapping and Shotgun Sequencing

Michael C. Wendl
Robert H. Waterston

First Published December 1, 2002

METHODS

Theories and Applications for Sequencing Randomly Selected Clones

Michael C. Wendl
Marco A. Marra
LaDeana W. Hillier
Asif T. Chinwalla
Richard K. Wilson
Robert H. Waterston

First Published January 18, 2001

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