The circadian dynamics of small nucleolar RNA in the mouse liver

por Aitken, Stuart, Semple, Colin A.
Publicado 2017

When TADs go bad: chromatin structure and nuclear organisation in human disease

por Kaiser, Vera B, Semple, Colin A
Publicado 2017

Chromatin loop anchors are associated with genome instability in cancer and recombination hotspots in the germline

por Kaiser, Vera B., Semple, Colin A.
Publicado 2018

Side Effects: Substantial Non-Neutral Evolution Flanking Regulatory Sites

por Prendergast, James G. D., Semple, Colin A.
Publicado 2013

Integrative modeling reveals the principles of multi-scale chromatin boundary formation in human nuclear organization

por Moore, Benjamin L, Aitken, Stuart, Semple, Colin A
Publicado 2015

Mutational Biases Drive Elevated Rates of Substitution at Regulatory Sites across Cancer Types

por Kaiser, Vera B., Taylor, Martin S., Semple, Colin A.
Publicado 2016

Divergence of Mammalian Higher Order Chromatin Structure Is Associated with Developmental Loci

por Chambers, Emily V., Bickmore, Wendy A., Semple, Colin A.
Publicado 2013

Posttranscriptional Regulation of miRNAs Harboring Conserved Terminal Loops

por Michlewski, Gracjan, Guil, Sonia, Semple, Colin A., Cáceres, Javier F.
Publicado 2008

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 2013

The genomic signature of trait-associated variants

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

Sequence-Level Mechanisms of Human Epigenome Evolution

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

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 2012

Heterotachy in Mammalian Promoter Evolution

por Taylor, Martin S, Kai, Chikatoshi, Kawai, Jun, Carninci, Piero, Hayashizaki, Yoshihide, Semple, Colin A. M
Publicado 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 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 2012

Modeling double strand break susceptibility to interrogate structural variation in cancer

por Ballinger, Tracy J., Bouwman, Britta A. M., Mirzazadeh, Reza, Garnerone, Silvano, Crosetto, Nicola, Semple, Colin A.
Publicado 2019

IMPROVE-DD: Integrating multiple phenotype resources optimizes variant evaluation in genetically determined developmental disorders

por Aitken, Stuart, Firth, Helen V., Wright, Caroline F., Hurles, Matthew E., FitzPatrick, David R., Semple, Colin A.
Publicado 2022

Abundant local interactions in the 4p16.1 region suggest functional mechanisms underlying SLC2A9 associations with human serum uric acid

por Wei, Wen-Hua, Guo, Yunfei, Kindt, Alida S.D., Merriman, Tony R., Semple, Colin A., Wang, Kai, Haley, Chris S.
Publicado 2014

Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome

por Kaiser, Vera B., Talmane, Lana, Kumar, Yatendra, Semple, Fiona, MacLennan, Marie, FitzPatrick, David R., Taylor, Martin S., Semple, Colin A.
Publicado 2021

Lsh regulates LTR retrotransposon repression independently of Dnmt3b function

por Dunican, Donncha S, Cruickshanks, Hazel A, Suzuki, Masako, Semple, Colin A, Davey, Tracey, Arceci, Robert J, Greally, John, Adams, Ian R, Meehan, Richard R
Publicado 2013