Richard A. Gibbs

According to our database, Richard A. Gibbs authored at least 17 papers between 1991 and 2024.

Collaborative distances:

• Dijkstra number of five.
• Erdős number of three.

2024

Empowering personalized pharmacogenomics with generative AI solutions.

Mullai Murugan, Bo Yuan, Eric Venner, Christie M. Ballantyne, Katherine M. Robinson, James C. Coons, Liwen Wang, Philip E. Empey, Richard A. Gibbs

J. Am. Medical Informatics Assoc., 2024

2021

Genomic considerations for FHIR®; eMERGE implementation lessons.

Mullai Murugan, Lawrence J. Babb, Casey Overby Taylor, Luke V. Rasmussen, Robert R. Freimuth, Eric Venner, Fei Yan, Victoria Yi, Stephen J. Granite, Hana Zouk, Samuel J. Aronson, Kevin Power, Alexander Fedotov, David R. Crosslin, David Fasel, Gail P. Jarvik, Hakon Hakonarson, Hana Bangash, Iftikhar J. Kullo, John J. Connolly, Jordan G. Nestor, Pedro J. Caraballo, Wei-Qi Wei, Ken Wiley, Heidi L. Rehm, Richard A. Gibbs

J. Biomed. Informatics, 2021

2019

ARBoR: an identity and security solution for clinical reporting.

Eric Venner, Mullai Murugan, Walker Hale, Jordan M. Jones, Shan Lu, Victoria Yi, Richard A. Gibbs

J. Am. Medical Informatics Assoc., 2019

2018

Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.

Samuel J. Aronson, Lawrence J. Babb, Darren C. Ames, Richard A. Gibbs, Eric Venner, John J. Connelly, Keith Marsolo, Chunhua Weng, Marc S. Williams, Andrea L. Hartzler, Wayne H. Liang, James D. Ralston, Emily Beth Devine, Shawn N. Murphy, Christopher G. Chute, Pedro J. Caraballo, Iftikhar J. Kullo, Robert R. Freimuth, Luke V. Rasmussen, Firas H. Wehbe, Josh F. Peterson, Jamie R. Robinson, Ken Wiley, Casey Overby Taylor, eMERGE Network EHRI Working Group

J. Am. Medical Informatics Assoc., 2018

2017

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.

Yong Chen, Li Zhao, Yi Wang, Ming Cao, Violet Gelowani, Mingchu Xu, Smriti A. Agrawal, Yumei Li, Stephen P. Daiger, Richard A. Gibbs, Fei Wang, Rui Chen

BMC Bioinform., 2017

2016

SV-STAT accurately detects structural variation via alignment to reference-based assemblies.

Caleb F. Davis, Deborah I. Ritter, David A. Wheeler, Hongmei Wang, Yan Ding, Shannon P. Dugan, Matthew N. Bainbridge, Donna M. Muzny, Pulivarthi H. Rao, Tsz-Kwong Man, Sharon E. Plon, Richard A. Gibbs, Ching C. Lau

Source Code Biol. Medicine, 2016

ITD assembler: an algorithm for internal tandem duplication discovery from short-read sequencing data.

Navin Rustagi, Oliver A. Hampton, Jie Li, Liu Xi, Richard A. Gibbs, Sharon E. Plon, Marek Kimmel, David A. Wheeler

BMC Bioinform., 2016

A hybrid computational strategy to address WGS variant analysis in >5000 samples.

Zhuoyi Huang, Navin Rustagi, Narayanan Veeraraghavan, Andrew Carroll, Richard A. Gibbs, Eric Boerwinkle, Manjunath Gorentla Venkata, Fuli Yu

BMC Bioinform., 2016

DNAism: exploring genomic datasets on the web with Horizon Charts.

David Rio Deiros, Richard A. Gibbs, Jeffrey Rogers

BMC Bioinform., 2016

2015

Tissue-specific transcriptome sequencing analysis expands the non-human primate reference transcriptome resource (NHPRTR).

Xinxia Peng, Jean Thierry-Mieg, Danielle Thierry-Mieg, Andrew Nishida, Lenore Pipes, Marjan Bozinoski, Matthew J. Thomas, Sara Kelly, Jeffrey M. Weiss, Muthuswamy Raveendran, Donna M. Muzny, Richard A. Gibbs, Jeffrey Rogers, Gary P. Schroth, Michael G. Katze, Christopher E. Mason

Nucleic Acids Res., 2015

2014

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.

Jeffrey G. Reid, Andrew Carroll, Narayanan Veeraraghavan, Mahmoud Dahdouli, Andreas Sundquist, Adam C. English, Matthew N. Bainbridge, Simon White, William J. Salerno, Christian Buhay, Fuli Yu, Donna M. Muzny, Richard Daly, Geoff Duyk, Richard A. Gibbs, Eric Boerwinkle

BMC Bioinform., 2014

2012

An integrative variant analysis suite for whole exome next-generation sequencing data.

Danny Challis, Jin Yu, Uday S. Evani, Andrew R. Jackson, Sameer Paithankar, Cristian Coarfa, Aleksandar Milosavljevic, Richard A. Gibbs, Fuli Yu

BMC Bioinform., 2012

2005

SNPdetector: A Software Tool for Sensitive and Accurate SNP Detection.

Jinghui Zhang, David A. Wheeler, Imtiaz Yakub, Sharon Wei, Raman Sood, William Rowe, Paul P. Liu, Richard A. Gibbs, Kenneth H. Buetow

PLoS Comput. Biol., 2005

Computational and Conformational Evaluation of FTase Alternative Substrates: Insight into a Novel Enzyme Binding Pocket.

Brian S. Henriksen, Todd J. Zahn, Jeffrey D. Evanseck, Steven M. Firestine, Richard A. Gibbs

J. Chem. Inf. Model., 2005

2000

The Human Transcript Database: a catalogue of full length cDNA inserts.

John Bouck, Michael P. McLeod, Kim Worley, Richard A. Gibbs

Bioinform., 2000

1995

Accurate determination of DNA in agarose gels using the novel algorithm GelScann(1.0).

Michael L. Metzker, Kyle M. Allain, Richard A. Gibbs

Comput. Appl. Biosci., 1995

1991

Distinct distance sets in a graph.

Richard A. Gibbs, Peter J. Slater

Discret. Math., 1991