Harold R. Garner

According to our database, Harold R. Garner authored at least 27 papers between 2000 and 2021.

Collaborative distances:

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

2021

Scaling Out a Combinatorial Algorithm for Discovering Carcinogenic Gene Combinations to Thousands of GPUs.

Sajal Dash, Qais Al-Hajri, Wu-chun Feng, Harold R. Garner, Ramu Anandakrishnan

Proceedings of the 35th IEEE International Parallel and Distributed Processing Symposium, 2021

2019

Estimating the number of genetic mutations (hits) required for carcinogenesis based on the distribution of somatic mutations.

Ramu Anandakrishnan, Robin T. Varghese, Nicholas Kinney, Harold R. Garner

PLoS Comput. Biol., 2019

CAGm: a repository of germline microsatellite variations in the 1000 genomes project.

Nicholas Kinney, Kyle Titus-Glover, Jonathan D. Wren, Robin T. Varghese, Pawel Michalak, Han Liao, Ramu Anandakrishnan, Arichanah Pulenthiran, Lin Kang, Harold R. Garner

Nucleic Acids Res., 2019

2018

Quantifying medical student clinical experiences via an ICD Code Logging App.

Fred Rawlins, Cameron Sumpter, Dean Sutphin, Harold R. Garner

Int. J. Medical Informatics, 2018

2014

BioFlow: a web based workflow management software for design and execution of genomics pipelines.

Harold R. Garner, Ashwin Puthige

Source Code Biol. Medicine, 2014

EvoCor: a platform for predicting functionally related genes using phylogenetic and expression profiles.

W. James Dittmar, Lauren McIver, Pawel Michalak, Harold R. Garner, Gregorio Valdez

Nucleic Acids Res., 2014

Discretized Gaussian mixture for genotyping of microsatellite loci containing homopolymer runs.

Hongseok Tae, Dong-Yun Kim, John McCormick, Robert E. Settlage, Harold R. Garner

Bioinform., 2014

Updating microbial genomic sequences: improving accuracy & innovation.

Hongseok Tae, Enusha Karunasena, Jasmin H. Bavarva, Harold R. Garner

BioData Min., 2014

2013

ReviSTER: an automated pipeline to revise misaligned reads to simple tandem repeats.

Hongseok Tae, Kevin W. McMahon, Robert E. Settlage, Jasmin H. Bavarva, Harold R. Garner

Bioinform., 2013

2010

Identifying duplicate content using statistically improbable phrases.

Mounir Errami, Zhaohui Sun, Angela C. George, Tara C. Long, Michael A. Skinner, Jonathan D. Wren, Harold R. Garner

Bioinform., 2010

2009

Déjà vu: a database of highly similar citations in the scientific literature.

Mounir Errami, Zhaohui Sun, Tara C. Long, Angela C. George, Harold R. Garner

Nucleic Acids Res., 2009

Application of multiple statistical tests to enhance mass spectrometry-based biomarker discovery.

Niclas Chiang Tan, Wayne G. Fisher, Kevin P. Rosenblatt, Harold R. Garner

BMC Bioinform., 2009

2008

Exhaustive prediction of disease susceptibility to coding base changes in the human genome.

Vinayak Kulkarni, Mounir Errami, Robert Barber, Harold R. Garner

BMC Bioinform., 2008

Déjà vu - A study of duplicate citations in Medline.

Mounir Errami, Justin M. Hicks, Wayne G. Fisher, David Trusty, Jonathan D. Wren, Tara C. Long, Harold R. Garner

Bioinform., 2008

2007

eTBLAST: a web server to identify expert reviewers, appropriate journals and similar publications.

Mounir Errami, Jonathan D. Wren, Justin M. Hicks, Harold R. Garner

Nucleic Acids Res., 2007

A Robust Biomarker Discovery Pipeline for High-Performance Mass Spectrometry Data.

Wayne G. Fisher, Kevin P. Rosenblatt, David A. Fishman, Gordon R. Whiteley, Alvydas Mikulskis, Scott A. Kuzdzal, Mary F. Lopez, Niclas Chiang Tan, Dwight C. German, Harold R. Garner

J. Bioinform. Comput. Biol., 2007

sIR: siRNA Information Resource, a web-based tool for siRNA sequence design and analysis and an open access siRNA database.

Jyoti K. Shah, Harold R. Garner, Michael A. White, David S. Shames, John D. Minna

BMC Bioinform., 2007

Clustering microarray-derived gene lists through implicit literature relationships.

Mark F. Burkart, Jonathan D. Wren, Jason I. Herschkowitz, Charles M. Perou, Harold R. Garner

Bioinform., 2007

2006

Text similarity: an alternative way to search MEDLINE.

James Lewis, Stephan Ossowski, Justin M. Hicks, Mounir Errami, Harold R. Garner

Bioinform., 2006

2005

Biomedical term mapping databases.

Jonathan D. Wren, Jeffrey T. Chang, James Pustejovsky, Eytan Adar, Harold R. Garner, Russ B. Altman

Nucleic Acids Res., 2005

Evidence for the regulation of alternative splicing via complementary DNA sequence repeats.

Yun Lian, Harold R. Garner

Bioinform., 2005

2004

Shared relationship analysis: ranking set cohesion and commonalities within a literature-derived relationship network.

Jonathan D. Wren, Harold R. Garner

Bioinform., 2004

Knowledge discovery by automated identification and ranking of implicit relationships.

Jonathan D. Wren, Raffi Bekeredjian, Jelena A. Stewart, Ralph V. Shohet, Harold R. Garner

Bioinform., 2004

2002

SIGNAL-Sequence Information and GeNomic AnaLysis.

Jonathan D. Wren, David A. Mittelman, Harold R. Garner

Comput. Methods Programs Biomed., 2002

ARROGANT: an application to manipulate large gene collections.

Amit V. Kulkarni, Noelle Sevilir Williams, Yun Lian, Jonathan D. Wren, David Mittelman, Alexander Pertsemlidis, Harold R. Garner

Bioinform., 2002

Applied computational genomics: polymorphism prediction, data mining and genomic analysis.

Harold R. Garner

Proceedings of the Sixth Annual International Conference on Computational Biology, 2002

2000

MAD: a suite of tools for microarray data management and processing.

Birong Liao, Walker Hale, Charles B. Epstein, Ronald A. Butow, Harold R. Garner

Bioinform., 2000