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Stephen J. Chanock
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2020 – today
- 2022
- [j10]Eric Ruan, Erika Nemeth, Richard A. Moffitt
, Lorena Sandoval, Mitchell J. Machiela, Neal D. Freedman, Wen-Yi Huang
PLCOjs, a FAIR GWAS web SDK for the NCI Prostate, Lung, Colorectal and Ovarian Cancer Genetic Atlas project. Bioinform. 38(18): 4434-4436 (2022) - [c1]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
ImmunoTyper-SR: A Novel Computational Approach for Genotyping Immunoglobulin Heavy Chain Variable Genes Using Short Read Data. RECOMB 2022: 382-384 - [i1]Praphulla M. S. Bhawsar, Erich Bremer, Máire A. Duggan, Stephen J. Chanock, Montserrat Garcia-Closas, Joel H. Saltz, Jonas S. Almeida:
ImageBox3: No-Server Tile Serving to Traverse Whole Slide Images on the Web. CoRR abs/2207.01734 (2022)
2010 – 2019
- 2019
- [j9]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
Viral coinfection analysis using a MinHash toolkit. BMC Bioinform. 20(1): 389:1-389:10 (2019) - 2018
- [j8]Mitchell J. Machiela
LDassoc: an online tool for interactively exploring genome-wide association study results and prioritizing variants for functional investigation. Bioinform. 34(5): 887-889 (2018) - 2016
- [j7]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
GWASdb v2: an update database for human genetic variants identified by genome-wide association studies. Nucleic Acids Res. 44(Database-Issue): 869-876 (2016) - 2015
- [j6]Mitchell J. Machiela
LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants. Bioinform. 31(21): 3555-3557 (2015) - 2012
- [j5]Mulin Jun Li, Panwen Wang, Xiaorong Liu
GWASdb: a database for human genetic variants identified by genome-wide association studies. Nucleic Acids Res. 40(Database-Issue): 1047-1054 (2012) - 2011
- [j4]Juan R. González
A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data. BMC Bioinform. 12: 166 (2011)
2000 – 2009
- 2008
- [j3]Leah E. Mechanic, Brian T. Luke, Julie E. Goodman
Polymorphism Interaction Analysis (PIA): a method for investigating complex gene-gene interactions. BMC Bioinform. 9 (2008) - 2006
- [j2]Bernice R. Packer, Meredith Yeager, Laura Burdett, Robert Welch, Michael Beerman, Liqun Qi, Hugues Sicotte, Brian Staats
SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes. Nucleic Acids Res. 34(Database-Issue): 617-621 (2006) - 2004
- [j1]Bernice R. Packer, Meredith Yeager, Brian Staats
SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes. Nucleic Acids Res. 32(Database-Issue): 528-532 (2004)
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