Stephen J. Chanock

According to our database, Stephen J. Chanock authored at least 12 papers between 2004 and 2022.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of three.

2022

ImageBox3: No-Server Tile Serving to Traverse Whole Slide Images on the Web.

Praphulla M. S. Bhawsar, Erich Bremer, Máire A. Duggan, Stephen J. Chanock, Montserrat Garcia-Closas, Joel H. Saltz, Jonas S. Almeida

CoRR, 2022

PLCOjs, a FAIR GWAS web SDK for the NCI Prostate, Lung, Colorectal and Ovarian Cancer Genetic Atlas project.

Eric Ruan, Erika Nemeth, Richard A. Moffitt, Lorena Sandoval, Mitchell J. Machiela, Neal D. Freedman, Wen-Yi Huang, Wendy Wong, Kai-Ling Chen, Brian Park, Kevin Jiang, Belynda Hicks, Jia Liu, Daniel E. Russ, Lori M. Minasian, Paul F. Pinsky, Stephen J. Chanock, Montserrat Garcia-Closas, Jonas S. Almeida

Bioinform., 2022

ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes Using Short Read Data.

Michael Ford, Ananth Hari, Oscar Rodriguez, Junyan Xu, Justin Lack, Cihan Oguz, Yu Zhang, Sarah Weber, Mary Magliocco, Jason Barnett, Sandhya Xirasagar, Smilee Samuel, Luisa Imberti, Paolo Bonfanti, Andrea Biondi, Clifton L. Dalgard, Stephen J. Chanock, Lindsey Rosen, Steven Holland, Helen Su, Luigi Notarangelo, Uzi Vishkin, Corey Watson, Süleyman Cenk Sahinalp

Proceedings of the Research in Computational Molecular Biology, 2022

2019

Viral coinfection analysis using a MinHash toolkit.

Eric T. Dawson, Sarah Wagner, David Roberson, Meredith Yeager, Joseph Boland, Erik Garrison, Stephen J. Chanock, Mark Schiffman, Tina Raine-Bennett, Thomas Lorey, Phillip E. Castle, Lisa Mirabello, Richard Durbin

BMC Bioinform., 2019

2018

LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation.

Mitchell J. Machiela, Stephen J. Chanock

Bioinform., 2018

2016

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.

Mulin Jun Li, Zipeng Liu, Panwen Wang, Maria P. Wong, Matthew R. Nelson, Jean-Pierre A. Kocher, Meredith Yeager, Pak Chung Sham, Stephen J. Chanock, Zhengyuan Xia, Junwen Wang

Nucleic Acids Res., 2016

2015

LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants.

Mitchell J. Machiela, Stephen J. Chanock

Bioinform., 2015

2012

GWASdb: a database for human genetic variants identified by genome-wide association studies.

Mulin Jun Li, Panwen Wang, Xiaorong Liu, Ee Lyn Lim, Zhangyong Wang, Meredith Yeager, Maria P. Wong, Pak Chung Sham, Stephen J. Chanock, Junwen Wang

Nucleic Acids Res., 2012

2011

A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data.

Juan R. González, Benjamin Rodriguez-Santiago, Alejandro Cáceres, Roger Pique-Regi, Nathaniel Rothman, Stephen J. Chanock, Lluís Armengol, Luis A. Pérez-Jurado

BMC Bioinform., 2011

2008

Polymorphism Interaction Analysis (PIA): a method for investigating complex gene-gene interactions.

Leah E. Mechanic, Brian T. Luke, Julie E. Goodman, Stephen J. Chanock, Curtis C. Harris

BMC Bioinform., 2008

2006

SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes.

Bernice R. Packer, Meredith Yeager, Laura Burdett, Robert Welch, Michael Beerman, Liqun Qi, Hugues Sicotte, Brian Staats, Mekhala Acharya, Andrew Crenshaw, Andrew Eckert, Vinita Puri, Daniela S. Gerhard, Stephen J. Chanock

Nucleic Acids Res., 2006

2004

SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes.

Bernice R. Packer, Meredith Yeager, Brian Staats, Robert Welch, Andrew Crenshaw, Maureen Kiley, Andrew Eckert, Michael Beerman, Edward Miller, Andrew Bergen, Nathaniel Rothman, Robert Strausberg, Stephen J. Chanock

Nucleic Acids Res., 2004