Autor der Publikation

Kopieren Löschen Diese Publikation zur Ablage hinzufügen
Community-Eintrag
Versionsverlauf dieses Eintrags
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Overview of the interactive task in BioCreative V.

Q. Wang, S. Abdul, L. Almeida, S. Ananiadou, Y. Balderas-Martínez, R. Batista-Navarro, D. Campos, L. Chilton, H. Chou, G. Contreras, L. Cooper, H. Dai, B. Ferrell, J. Fluck, S. Gama-Castro, N. George, G. Gkoutos, A. Irin, L. Jensen, S. Jimenez, T. Jue, I. Keseler, S. Madan, S. Matos, P. McQuilton, M. Milacic, M. Mort, J. Natarajan, E. Pafilis, E. Pereira, S. Rao, F. Rinaldi, K. Rothfels, D. Salgado, R. Silva, O. Singh, R. Stefancsik, C. Su, S. Subramani, H. Tadepally, L. Tsaprouni, N. Vasilevsky, X. Wang, A. Chatr aryamontri, S. Laulederkind, S. Matis-Mitchell, J. McEntyre, S. Orchard, S. Pundir, R. Rodriguez-Esteban, K. Auken, Z. Lu, M. Schaeffer, C. Wu, L. Hirschman, und C. Arighi. Database, (2016)

Bitte wählen Sie eine Person um die Publikation zuzuordnen

Um zwischen Personen mit demselben Namen zu unterscheiden, wird der akademische Grad und der Titel einer wichtigen Publikation angezeigt. Zudem lassen sich über den Button neben dem Namen einige der Person bereits zugeordnete Publikationen anzeigen.

E. Garrelts

E. Zafeiriou

Dr. -Ing. Claudiu Mortan University of Stuttgart

Matthew Joliffe University of Stuttgart

Ph. D. Matthew Millard University of Stuttgart

Weitere Publikationen von Autoren mit dem selben Namen

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, und Y. Zhou. Bioinformatics, 31 (10): 1599-1606 (2015)An integrative approach to predicting the functional effects of non-coding and coding sequence variation.H. Shihab, M. Rogers, J. Gough, M. Mort, D. Cooper, I. Day, T. Gaunt, und C. Campbell. Bioinformatics, 31 (10): 1536-1543 (2015)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, und N. Chuzhanova. In Silico Biology, 6 (1-2): 23-34 (2006)regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions.M. Teng, S. Ichikawa, L. Padgett, Y. Wang, M. Mort, D. Cooper, D. Koller, T. Foroud, H. Edenberg, M. Econs und 1 andere Autor(en). Bioinformatics, 28 (14): 1879-1886 (2012)The Loss and Gain of Functional Amino Acid Residues Is a Common Mechanism Causing Human Inherited Disease.J. Lugo-Martinez, V. Pejaver, K. Pagel, S. Jain, M. Mort, D. Cooper, S. Mooney, und P. Radivojac. PLoS Computational Biology, (2016)Sequential data selection for predicting the pathogenic effects of sequence variation.M. Rogers, C. Campbell, H. Shihab, T. Gaunt, M. Mort, und D. Cooper. BIBM, Seite 639-644. IEEE Computer Society, (2015)An integrative approach to predicting the functional effects of small indels in non-coding regions of the human genome.M. Ferlaino, M. Rogers, H. Shihab, M. Mort, D. Cooper, T. Gaunt, und C. Campbell. BMC Bioinformatics, 18 (1): 442:1-442:8 (2017)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, und P. Radivojac. Bioinformatics, 33 (14): i389-i398 (2017)FATHMM-XF: accurate prediction of pathogenic point mutations via extended features.M. Rogers, H. Shihab, M. Mort, D. Cooper, T. Gaunt, und C. Campbell. Bioinformatics, 34 (3): 511-513 (2018)Automated inference of molecular mechanisms of disease from amino acid substitutions.B. Li, V. Krishnan, M. Mort, F. Xin, K. Kamati, D. Cooper, S. Mooney, und P. Radivojac. Bioinformatics, 25 (21): 2744-2750 (2009)