Anthony P. Fejes

According to our database, Anthony P. Fejes authored at least 5 papers between 2008 and 2018.

Collaborative distances:

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

2018

The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool.

Steven Flygare, Edgar Javier Hernandez, Lon Phan, Barry Moore, Man Li, Anthony P. Fejes, Hao Hu, Karen Eilbeck, Chad D. Huff, Lynn Jorde, Martin G. Reese, Mark Yandell

BMC Bioinform., 2018

2013

Identifying cancer mutation targets across thousands of samples: MuteProc, a high throughput mutation analysis pipeline.

Alireza Hadj Khodabakhshi, Anthony P. Fejes, Inanç Birol, Steven J. M. Jones

BMC Bioinform., 2013

2011

Human variation database: an open-source database template for genomic discovery.

Anthony P. Fejes, Alireza Hadj Khodabakhshi, Inanç Birol, Steven J. M. Jones

Bioinform., 2011

2010

Genomic analysis of a rare human tumor.

Steven J. M. Jones, Janessa Laskin, Yvonne Y. Li, Obi L. Griffith, Jianghong An, Mikhail Bilenky, Yaron S. N. Butterfield, Timothee Cezard, Eric Chuah, Richard Corbett, Anthony P. Fejes, Malachi Griffith, John Yee, Montgomery Martin, Michael Mayo, Nataliya Melnyk, Ryan D. Morin, Trevor J. Pugh, Tesa Severson, Sohrab P. Shah, Margaret Sutcliffe, Angela Tam, Jefferson Terry, Nina Thiessen, Thomas Thomson, Richard Varhol, Thomas Zeng, Yongjun Zhao, Richard A. Moore, David G. Huntsman, Inanç Birol, Martin Hirst, Robert A. Holt, Marco A. Marra

BMC Bioinform., 2010

2008

FindPeaks 3.1: a tool for identifying areas of enrichment from massively parallel short-read sequencing technology.

Anthony P. Fejes, Gordon Robertson, Mikhail Bilenky, Richard Varhol, Matthew N. Bainbridge, Steven J. M. Jones

Bioinform., 2008