Mark F. Rogers - researchr alias

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Viewing Publication 1 - 13 from 13

2021

CScape-somatic: distinguishing driver and passenger point mutations in the cancer genomeMark F. Rogers, Tom R. Gaunt, Colin Campbell. bioinformatics, 37(22):4298, November 2021. [doi]

Prediction of driver variants in the cancer genome via machine learning methodologiesMark F. Rogers, Tom R. Gaunt, Colin Campbell. bib, 22(4), 2021. [doi]

2020

CScape-somatic: distinguishing driver and passenger point mutations in the cancer genomeMark F. Rogers, Tom R. Gaunt, Colin Campbell. bioinformatics, 36(12):3637-3644, 2020. [doi]

2018

FATHMM-XF: accurate prediction of pathogenic point mutations via extended featuresMark F. Rogers, Hashem A. Shihab, Matthew E. Mort, David N. Cooper, Tom R. Gaunt, Colin Campbell. bioinformatics, 34(3):511-513, 2018. [doi]

2017

2015

2013

ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing dataMilana Frenkel-Morgenstern, Alessandro Gorohovski, Vincent Lacroix, Mark F. Rogers, Kristina Ibanez, Cesar Boullosa, Eduardo Andrés León, Asa Ben-Hur, Alfonso Valencia. nar, 41(Database-Issue):142-151, 2013. [doi]

SpliceGrapherXT: From Splice Graphs to Transcripts Using RNA-SeqMark F. Rogers, Christina Boucher, Asa Ben-Hur. bcb 2013: 247 [doi]

2009

The use of gene ontology evidence codes in preventing classifier assessment biasMark F. Rogers, Asa Ben-Hur. bioinformatics, 25(9):1173-1177, 2009. [doi]

2006

Looking for Shortcuts: Infeasible Search Analysis for Oversubscribed Scheduling ProblemsMark F. Rogers, Adele E. Howe, Darrell Whitley. aips 2006: 314-323

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