Mark F. Rogers

According to our database, Mark F. Rogers authored at least 12 papers between 2006 and 2021.

Collaborative distances:

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

2021

Prediction of driver variants in the cancer genome via machine learning methodologies.

Mark F. Rogers, Tom R. Gaunt, Colin Campbell

Briefings Bioinform., 2021

2020

CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome.

Mark F. Rogers, Tom R. Gaunt, Colin Campbell

Bioinform., 2020

2018

FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.

Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell

Bioinform., 2018

2017

GTB - an online genome tolerance browser.

Hashem A. Shihab, Mark F. Rogers, Michael Ferlaino, Colin Campbell, Tom R. Gaunt

BMC Bioinform., 2017

An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.

Michael Ferlaino, Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell

BMC Bioinform., 2017

HIPred: an integrative approach to predicting haploinsufficient genes.

Hashem A. Shihab, Mark F. Rogers, Colin Campbell, Tom R. Gaunt

Bioinform., 2017

2015

An integrative approach to predicting the functional effects of non-coding and coding sequence variation.

Hashem A. Shihab, Mark F. Rogers, Julian Gough, Matthew E. Mort, David N. Cooper, Ian N. M. Day, Tom R. Gaunt, Colin Campbell

Bioinform., 2015

Sequential data selection for predicting the pathogenic effects of sequence variation.

Mark F. Rogers, Colin Campbell, Hashem A. Shihab, Tom R. Gaunt, Matthew E. Mort, David N. Cooper

Proceedings of the 2015 IEEE International Conference on Bioinformatics and Biomedicine, 2015

2013

ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data.

Milana Frenkel-Morgenstern, Alessandro Gorohovski, Vincent Lacroix, Mark F. Rogers, Kristina Ibáñez, Cesar Boullosa, Eduardo Andrés León, Asa Ben-Hur, Alfonso Valencia

Nucleic Acids Res., 2013

SpliceGrapherXT: From Splice Graphs to Transcripts Using RNA-Seq.

Mark F. Rogers, Christina Boucher, Asa Ben-Hur

Proceedings of the ACM Conference on Bioinformatics, 2013

2009

The use of gene ontology evidence codes in preventing classifier assessment bias.

Mark F. Rogers, Asa Ben-Hur

Bioinform., 2009

2006

Looking for Shortcuts: Infeasible Search Analysis for Oversubscribed Scheduling Problems.

Mark F. Rogers, Adele E. Howe, L. Darrell Whitley

Proceedings of the Sixteenth International Conference on Automated Planning and Scheduling, 2006