Your browser doesn't support javascript.
loading
Author Correction: Predicting the clinical impact of human mutation with deep neural networks.
Sundaram, Laksshman; Gao, Hong; Padigepati, Samskruthi Reddy; McRae, Jeremy F; Li, Yanjun; Kosmicki, Jack A; Fritzilas, Nondas; Hakenberg, Jörg; Dutta, Anindita; Shon, John; Xu, Jinbo; Batzoglou, Serafim; Li, Xiaolin; Farh, Kyle Kai-How.
Afiliação
  • Sundaram L; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Gao H; Department of Computer Science, Stanford University, Stanford, CA, USA.
  • Padigepati SR; National Science Foundation Center for Big Learning, University of Florida, Gainesville, FL, USA.
  • McRae JF; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Li Y; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Kosmicki JA; National Science Foundation Center for Big Learning, University of Florida, Gainesville, FL, USA.
  • Fritzilas N; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Hakenberg J; National Science Foundation Center for Big Learning, University of Florida, Gainesville, FL, USA.
  • Dutta A; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Shon J; Analytic and Translational Genetics Unit (ATGU), Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
  • Xu J; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Batzoglou S; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Li X; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
  • Farh KK; Illumina Artificial Intelligence Laboratory, Illumina Inc, San Diego, CA, USA.
Nat Genet ; 51(2): 364, 2019 02.
Article em En | MEDLINE | ID: mdl-30559491
ABSTRACT
In the version of this article originally published, the name of author Serafim Batzoglou was misspelled. The error has been corrected in the HTML and PDF versions of the article.
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Nat Genet Assunto da revista: GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos