( en | de | ru )

 

Disambiguation of "Carter, Hannah"

Author of the publication

copydeleteadd this publication to your clipboard
Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations.

, , , , , , , and . Cancer research, 69 (16): 6660--6667 (Aug 15, 2009)
DOI: 10.1158/0008-5472.can-09-1133

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. You can also use the button next to the name to display some publications already assigned to the person.

Ronald Carter

Carter Kniffler

Marina Carter

Henry Carter

Glyn Carter

 

Other publications of authors with the same name

Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations., , , , , , , and . Cancer research, 69 (16): 6660--6667 (Aug 15, 2009)Erratum: Identifying mutation specific cancer pathways using a structurally resolved protein interaction network., , and . PSB, page 634. (2018)CRAVAT: cancer-related analysis of variants toolkit., , , , , , , , and . Bioinform., 29 (5): 647-648 (2013)Evaluation and accurate diagnoses of pediatric diseases using artificial intelligence, , , , , , , , , and 61 other author(s). Nature Medicine, 25 (3): 433--438 (2019)Predictive analyses of regulatory sequences with EUGENe., , , , , , , and . Nat. Comput. Sci., 3 (11): 946-956 (2023)A Probabilistic Model to Predict Clinical Phenotypic Traits from Genome Sequencing., , , , , , , , , and 2 other author(s). PLoS Comput. Biol., (2014)Extracting allelic read counts from 250, 000 human sequencing runs in Sequence Read Archive., , , and . PSB, page 196-207. (2019)Interaction Landscape of Inherited Polymorphisms with Somatic Events in Cancer, , , , , , , , , and 6 other author(s). Cancer Discovery, 7 (4): 410--423 (February 2017)Network-based stratification of tumor mutations, , , , and . Nature Methods, 10 (11): 1108--1115 (Sep 15, 2013)CHASM and SNVBox: toolkit for detecting biologically important single nucleotide mutations in cancer., , , , , and . Bioinform., 27 (15): 2147-2148 (2011)