Mark F. Rogers

Publication Activity (10 Years)

Years Active: 2006-2021
Publications (10 Years): 7

Top Topics

Learning Methodologies

Sequential Data

Top Venues

Briefings Bioinform.

Publications

Mark F. Rogers, Tom R. Gaunt, Colin Campbell
CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome. Bioinform. 37 (22) (2021)
Mark F. Rogers, Tom R. Gaunt, Colin Campbell
Prediction of driver variants in the cancer genome via machine learning methodologies. Briefings Bioinform. 22 (4) (2021)
Mark F. Rogers, Tom R. Gaunt, Colin Campbell
CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome. Bioinform. 36 (12) (2020)
Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features. Bioinform. 34 (3) (2018)
Hashem A. Shihab, Mark F. Rogers, Michael Ferlaino, Colin Campbell, Tom R. Gaunt
GTB - an online genome tolerance browser. BMC Bioinform. 18 (1) (2017)
Michael Ferlaino, Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome. BMC Bioinform. 18 (1) (2017)
Hashem A. Shihab, Mark F. Rogers, Colin Campbell, Tom R. Gaunt
HIPred: an integrative approach to predicting haploinsufficient genes. Bioinform. 33 (12) (2017)
Hashem A. Shihab, Mark F. Rogers, Julian Gough, Matthew E. Mort, David N. Cooper, Ian N. M. Day, Tom R. Gaunt, Colin Campbell
An integrative approach to predicting the functional effects of non-coding and coding sequence variation. Bioinform. 31 (10) (2015)
Mark F. Rogers, Colin Campbell, Hashem A. Shihab, Tom R. Gaunt, Matthew E. Mort, David N. Cooper
Sequential data selection for predicting the pathogenic effects of sequence variation. BIBM (2015)
Milana Frenkel-Morgenstern, Alessandro Gorohovski, Vincent Lacroix, Mark F. Rogers, Kristina Ibáñez, Cesar Boullosa, Eduardo Andrés León, Asa Ben-Hur, Alfonso Valencia
ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data. Nucleic Acids Res. 41 (Database-Issue) (2013)
Mark F. Rogers, Christina Boucher, Asa Ben-Hur
SpliceGrapherXT: From Splice Graphs to Transcripts Using RNA-Seq. BCB (2013)
Mark F. Rogers, Asa Ben-Hur
The use of gene ontology evidence codes in preventing classifier assessment bias. Bioinform. 25 (9) (2009)
Mark F. Rogers, Adele E. Howe, L. Darrell Whitley
Looking for Shortcuts: Infeasible Search Analysis for Oversubscribed Scheduling Problems. ICAPS (2006)