Probabilistic inference and ranking of gene regulatory pathways as a shortest-path problem

por Jensen, James D, Jensen, Daniel M, Clement, Mark J, Snell, Quinn O
Publicado 2013

Effects of error-correction of heterozygous next-generation sequencing data

por Fujimoto, M Stanley, Bodily, Paul M, Okuda, Nozomu, Clement, Mark J, Snell, Quinn
Publicado 2014

Detecting false positive sequence homology: a machine learning approach

por Fujimoto, M. Stanley, Suvorov, Anton, Jensen, Nicholas O., Clement, Mark J., Bybee, Seth M.
Publicado 2016

A novel approach for multi-SNP GWAS and its application in Alzheimer’s disease

por Bodily, Paul M., Fujimoto, M. Stanley, Page, Justin T., Clement, Mark J., Ebbert, Mark T. W., Ridge, Perry G.
Publicado 2016

Heterozygous genome assembly via binary classification of homologous sequence

por Bodily, Paul M, Fujimoto, M Stanley, Ortega, Cameron, Okuda, Nozomu, Price, Jared C, Clement, Mark J, Snell, Quinn
Publicado 2015

Probabilistic alignment leads to improved accuracy and read coverage for bisulfite sequencing data

por Hong, Changjin, Clement, Nathan L, Clement, Spencer, Hammoud, Saher Sue, Carrell, Douglas T, Cairns, Bradley R, Snell, Quinn, Clement, Mark J, Johnson, William Evan
Publicado 2013

Targeted Amplicon Sequencing (TAS): A Scalable Next-Gen Approach to Multilocus, Multitaxa Phylogenetics

por Bybee, Seth M., Bracken-Grissom, Heather, Haynes, Benjamin D., Hermansen, Russell A., Byers, Robert L., Clement, Mark J., Udall, Joshua A., Wilcox, Edward R., Crandall, Keith A.
Publicado 2011

Pathoscope: Species identification and strain attribution with unassembled sequencing data

por Francis, Owen E., Bendall, Matthew, Manimaran, Solaiappan, Hong, Changjin, Clement, Nathan L., Castro-Nallar, Eduardo, Snell, Quinn, Schaalje, G. Bruce, Clement, Mark J., Crandall, Keith A., Johnson, W. Evan
Publicado 2013