From post

копировать удалить добавить публикацию в буфер
Запись сообщества
посмотреть историю данной записи
URL
DOI
BibTeX
EndNote
APA
Chicago
DIN 1505
Harvard
MSOffice XML

Identifying Mutation Specific Cancer Pathways Using a Structurally Resolved Protein Interaction Network.

B. Engin, M. Hofree, и H. Carter. Pacific Symposium on Biocomputing, стр. 84-95. (2015)

Please choose a person to relate this publication to

To differ between persons with the same name, the academic degree and the title of an important publication will be displayed.

Ronald Carter

Carter Kniffler

Marina Carter

Henry Carter

Christopher Carter

Другие публикации лиц с тем же именем

Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations.H. Carter, S. Chen, L. Isik, S. Tyekucheva, V. Velculescu, K. Kinzler, B. Vogelstein, и R. Karchin. Cancer research, 69 (16): 6660--6667 (15.08.2009)CRAVAT: cancer-related analysis of variants toolkit.C. Douville, H. Carter, R. Kim, N. Niknafs, M. Diekhans, P. Stenson, D. Cooper, M. Ryan, и R. Karchin. Bioinform., 29 (5): 647-648 (2013)Erratum: Identifying mutation specific cancer pathways using a structurally resolved protein interaction network.B. Engin, M. Hofree, и H. Carter. PSB, стр. 634. (2018)Computational KIR copy number discovery reveals interaction between inhibitory receptor burden and survival.R. Pyke, R. Genolet, A. Harari, G. Coukos, D. Gfeller, и H. Carter. PSB, стр. 148-159. (2019)MODBASE, a database of annotated comparative protein structure models and associated resources.U. Pieper, N. Eswar, B. Webb, D. Eramian, L. Kelly, D. Barkan, H. Carter, P. Mankoo, R. Karchin, M. Martí-Renom и 2 other автор(ы). Nucleic Acids Res., 37 (Database-Issue): 347-354 (2009)The Cancer Epitope Database and Analysis Resource (CEDAR).Z. Kosaloglu-Yalçin, N. Blazeska, R. Vita, H. Carter, M. Nielsen, S. Schoenberger, A. Sette, и B. Peters. Nucleic Acids Res., 51 (D1): 845-852 (января 2023)Evaluation and accurate diagnoses of pediatric diseases using artificial intelligenceH. Liang, B. Tsui, H. Ni, C. Valentim, S. Baxter, G. Liu, W. Cai, D. Kermany, X. Sun, J. Chen и 61 other автор(ы). Nature Medicine, 25 (3): 433--438 (2019)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 и 2 other автор(ы). PLoS Comput. Biol., (2014)Predictive analyses of regulatory sequences with EUGENe.A. Klie, D. Laub, J. Talwar, H. Stites, T. Jores, J. Solvason, E. Farley, и H. Carter. Nat. Comput. Sci., 3 (11): 946-956 (2023)CHASM and SNVBox: toolkit for detecting biologically important single nucleotide mutations in cancer.W. Wong, D. Kim, H. Carter, M. Diekhans, M. Ryan, и R. Karchin. Bioinform., 27 (15): 2147-2148 (2011)

BibSonomy

Disambiguation