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In Silico Discrimination of Single Nucleotide Polymorphisms and Pathological Mutations in Human Gene Promoter Regions by Means of Local DNA Sequence Context and Regularity.

I. Khan, M. Mort, P. Buckland, M. O'Donovan, D. Cooper, and N. Chuzhanova. In Silico Biology, 6 (1-2): 23-34 (2006)

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David N Ehrat

n n n

Cooper Baker

Jason Cooper

Simon Cooper

Other publications of authors with the same name

DDIG-in: detecting disease-causing genetic variations due to frameshifting indels and nonsense mutations employing sequence and structural properties at nucleotide and protein levels.L. Folkman, Y. Yang, Z. Li, B. Stantic, A. Sattar, M. Mort, D. Cooper, Y. Liu, and Y. Zhou. Bioinform., 31 (10): 1599-1606 (2015)Structure-based kernels for the prediction of catalytic residues and their involvement in human inherited disease.F. Xin, S. Myers, Y. Li, D. Cooper, S. Mooney, and P. Radivojac. Bioinform., 26 (16): 1975-1982 (2010)Inferring the genetic relationship between brain imaging-derived phenotypes and risk of complex diseases by Mendelian randomization and genome-wide colocalization.S. Lin, H. Zhang, M. Qi, D. Cooper, Y. Yang, Y. Yang, and H. Zhao. NeuroImage, (October 2023)RegulationSpotter: annotation and interpretation of extratranscriptic DNA variants.J. Schwarz, D. Hombach, S. Köhler, D. Cooper, M. Schuelke, and D. Seelow. Nucleic Acids Res., 47 (Webserver-Issue): W106-W113 (2019)When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.K. Pagel, V. Pejaver, G. Lin, H. Nam, M. Mort, D. Cooper, J. Sebat, L. Iakoucheva, S. Mooney, and P. Radivojac. Bioinform., 33 (14): i389-i398 (2017)A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing.Y. Chen, C. Douville, C. Wang, N. Niknafs, G. Yeo, V. Guthrie, H. Carter, P. Stenson, D. Cooper, B. Li and 2 other author(s). PLoS Comput. Biol., (2014)Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.K. Pagel, D. Antaki, A. Lian, M. Mort, D. Cooper, J. Sebat, L. Iakoucheva, S. Mooney, and P. Radivojac. PLoS Comput. Biol., (2019)Mining clinical attributes of genomic variants through assisted literature curation in Egas.S. Matos, D. Campos, R. Pinho, R. Silva, M. Mort, D. Cooper, and J. Oliveira. Database J. Biol. Databases Curation, (2016)MutationTaster2021.R. Steinhaus, S. Proft, M. Schuelke, D. Cooper, J. Schwarz, and D. Seelow. Nucleic Acids Res., 49 (Webserver-Issue): 446-451 (2021)CRAVAT: cancer-related analysis of variants toolkit.C. Douville, H. Carter, R. Kim, N. Niknafs, M. Diekhans, P. Stenson, D. Cooper, M. Ryan, and R. Karchin. Bioinform., 29 (5): 647-648 (2013)

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Disambiguation of "Cooper, David N."