Purifying Selection Causes Widespread Distortions of Genealogical Structure on the Human X Chromosome

Por O’Fallon, Brendan
Publicado em 2013

TreesimJ: a flexible, forward time population genetic simulator

Por O'Fallon, Brendan
Publicado no Bioinformatics (2010)

ACG: rapid inference of population history from recombining nucleotide sequences

Por O'Fallon Brendan D
Publicado em 2013-02-01

ACG: rapid inference of population history from recombining nucleotide sequences

Por O'Fallon, Brendan D
Publicado em 2013

A Method for Accurate Inference of Population Size from Serially Sampled Genealogies Distorted by Selection

Por O'Fallon, Brendan D.
Publicado no Mol Biol Evol (2011)

Native Americans experienced a strong population bottleneck coincident with European contact

Por O'Fallon, Brendan D., Fehren-Schmitz, Lars
Publicado em 2011

A Continuous-State Coalescent and the Impact of Weak Selection on the Structure of Gene Genealogies

Por O'Fallon, Brendan D., Seger, Jon, Adler, Frederick R.
Publicado no Mol Biol Evol (2010)

Quasi-species evolution in subdivided populations favours maximally deleterious mutations

Por O'Fallon, Brendan D, Adler, Frederick R, Proulx, Stephen R
Publicado em 2007

VarRanker: rapid prioritization of sequence variations associated with human disease

Por O'Fallon, Brendan D, Wooderchak-Donahue, Whitney, Bayrak-Toydemir, Pinar, Crockett, David
Publicado em 2013

Variant Tool Chest: an improved tool to analyze and manipulate variant call format (VCF) files

Por Ebbert, Mark TW, Wadsworth, Mark E, Boehme, Kevin L, Hoyt, Kaitlyn L, Sharp, Aaron R, O'Fallon, Brendan D, Kauwe, John SK, Ridge, Perry G
Publicado em 2014

A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspective

Por Wooderchak-Donahue, Whitney L, O’Fallon, Brendan, Furtado, Larissa V, Durtschi, Jacob D, Plant, Parker, Ridge, Perry G, Rope, Alan F, Yetman, Angela T, Bayrak-Toydemir, Pinar
Publicado em 2012

BMP9 Mutations Cause a Vascular-Anomaly Syndrome with Phenotypic Overlap with Hereditary Hemorrhagic Telangiectasia

Por Wooderchak-Donahue, Whitney L., McDonald, Jamie, O’Fallon, Brendan, Upton, Paul D., Li, Wei, Roman, Beth L., Young, Sarah, Plant, Parker, Fülöp, Gyula T., Langa, Carmen, Morrell, Nicholas W., Botella, Luisa M., Bernabeu, Carmelo, Stevenson, David A., Runo, James R., Bayrak-Toydemir, Pinar
Publicado em 2013

The Genomic and Phenotypic Diversity of Schizosaccharomyces pombe

Por Jeffares, Daniel C., Rallis, Charalampos, Rieux, Adrien, Speed, Doug, Převorovský, Martin, Mourier, Tobias, Marsellach, Francesc X., Iqbal, Zamin, Lau, Winston, Cheng, Tammy M.K., Pracana, Rodrigo, Mülleder, Michael, Lawson, Jonathan L.D., Chessel, Anatole, Bala, Sendu, Hellenthal, Garrett, O’Fallon, Brendan, Keane, Thomas, Simpson, Jared T., Bischof, Leanne, Tomiczek, Bartlomiej, Bitton, Danny A., Sideri, Theodora, Codlin, Sandra, Hellberg, Josephine E.E.U., van Trigt, Laurent, Jeffery, Linda, Li, Juan-Juan, Atkinson, Sophie, Thodberg, Malte, Febrer, Melanie, McLay, Kirsten, Drou, Nizar, Brown, William, Hayles, Jacqueline, Carazo Salas, Rafael E., Ralser, Markus, Maniatis, Nikolas, Balding, David J., Balloux, Francois, Durbin, Richard, Bähler, Jürg
Publicado no Nat Genet (2015)