Mark F. Rogers

13 papers A* 1Journal 10Unranked 2
YearRankTypeTitle / Venue / Authors
2021 J jnl
CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome.
Bioinform.
Mark F. Rogers, Tom R. Gaunt, Colin Campbell
2021 J jnl
Prediction of driver variants in the cancer genome via machine learning methodologies.
Briefings Bioinform.
Mark F. Rogers, Tom R. Gaunt, Colin Campbell
2020 J jnl
CScape-somatic: distinguishing driver and passenger point mutations in the cancer genome.
Bioinform.
Mark F. Rogers, Tom R. Gaunt, Colin Campbell
2018 J jnl
FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.
Bioinform.
Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell
2017 J jnl
An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.
BMC Bioinform.
Michael Ferlaino, Mark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell
2017 J jnl
GTB - an online genome tolerance browser.
BMC Bioinform.
Hashem A. Shihab, Mark F. Rogers, Michael Ferlaino, Colin Campbell, Tom R. Gaunt
2017 J jnl
HIPred: an integrative approach to predicting haploinsufficient genes.
Bioinform.
Hashem A. Shihab, Mark F. Rogers, Colin Campbell, Tom R. Gaunt
2015 J jnl
An integrative approach to predicting the functional effects of non-coding and coding sequence variation.
Bioinform.
Hashem A. Shihab, Mark F. Rogers, Julian Gough, Matthew E. Mort, David N. Cooper, Ian N. M. Day, Tom R. Gaunt, Colin Campbell
2015 — conf
Sequential data selection for predicting the pathogenic effects of sequence variation.
BIBM
Mark F. Rogers, Colin Campbell, Hashem A. Shihab, Tom R. Gaunt, Matthew E. Mort, David N. Cooper
2013 J jnl
ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data.
Nucleic Acids Res.
Milana Frenkel-Morgenstern, Alessandro Gorohovski, Vincent Lacroix, Mark F. Rogers, Kristina Ibáñez, Cesar Boullosa, Eduardo Andrés León, Asa Ben-Hur, Alfonso Valencia
2013 — conf
SpliceGrapherXT: From Splice Graphs to Transcripts Using RNA-Seq.
BCB
Mark F. Rogers, Christina Boucher, Asa Ben-Hur
2009 J jnl
The use of gene ontology evidence codes in preventing classifier assessment bias.
Bioinform.
Mark F. Rogers, Asa Ben-Hur
2006 A* conf
Looking for Shortcuts: Infeasible Search Analysis for Oversubscribed Scheduling Problems.
ICAPS
Mark F. Rogers, Adele E. Howe, L. Darrell Whitley