The Comparative Proteomics of Ubiquitination in Mouse

Por Semple, Colin A.M.
Publicado em 2003

Widespread signatures of recent selection linked to nucleosome positioning in the human lineage

Por Prendergast, James G.D., Semple, Colin A.M.
Publicado em 2011

Properties of Local Interactions and Their Potential Value in Complementing Genome-Wide Association Studies

Por Wei, Wenhua, Gyenesei, Attila, Semple, Colin A. M., Haley, Chris S.
Publicado em 2013

The genomic signature of trait-associated variants

Por Kindt, Alida S D, Navarro, Pau, Semple, Colin A M, Haley, Chris S
Publicado em 2013

Corrigendum of ‘High throughput analysis of epistasis in genome-wide association studies with BiForce’

Por Gyenesei, Attila, Semple, Colin A.M., Haley, Chris S., Wei, Wen-Hua
Publicado em 2013

Sequence-Level Mechanisms of Human Epigenome Evolution

Por Prendergast, James G.D., Chambers, Emily V., Semple, Colin A.M.
Publicado em 2014

Computational Comparison of Human Genomic Sequence Assemblies for a Region of Chromosome 4

Por Semple, Colin A.M., Morris, Stewart W., Porteous, David J., Evans, Kathryn L.
Publicado em 2002

High-throughput analysis of epistasis in genome-wide association studies with BiForce

Por Gyenesei, Attila, Moody, Jonathan, Semple, Colin A.M., Haley, Chris S., Wei, Wen-Hua
Publicado em 2012

Heterotachy in Mammalian Promoter Evolution

Por Taylor, Martin S, Kai, Chikatoshi, Kawai, Jun, Carninci, Piero, Hayashizaki, Yoshihide, Semple, Colin A. M
Publicado em 2006

BiForce Toolbox: powerful high-throughput computational analysis of gene–gene interactions in genome-wide association studies

Por Gyenesei, Attila, Moody, Jonathan, Laiho, Asta, Semple, Colin A.M., Haley, Chris S., Wei, Wen-Hua
Publicado em 2012

A genome-wide screen in human embryonic stem cells reveals novel sites of allele-specific histone modification associated with known disease loci

Por Prendergast, James G D, Tong, Pin, Hay, David C, Farrington, Susan M, Semple, Colin A M
Publicado em 2012

SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis

Por Le Hellard, Stéphanie, Ballereau, Stéphane J., Visscher, Peter M., Torrance, Helen S., Pinson, Jeni, Morris, Stewart W., Thomson, Marian L., Semple, Colin A. M., Muir, Walter J., Blackwood, Douglas H. R., Porteous, David J., Evans, Kathryn L.
Publicado em 2002

Computational disease gene identification: a concert of methods prioritizes type 2 diabetes and obesity candidate genes

Por Tiffin, Nicki, Adie, Euan, Turner, Frances, Brunner, Han G., van Driel, Marc A., Oti, Martin, Lopez-Bigas, Nuria, Ouzounis, Christos, Perez-Iratxeta, Carolina, Andrade-Navarro, Miguel A., Adeyemo, Adebowale, Patti, Mary Elizabeth, Semple, Colin A. M., Hide, Winston
Publicado em 2006