Data resources for the identification and interpretation of actionable mutations by clinicians.

Prawira, A; Pugh, T J; Stockley, T L; Siu, L L

Prawira, A; Pugh, T J; Stockley, T L; Siu, L L.

Affiliation

Prawira A; Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto.
Pugh TJ; Cancer Genomics Program, Princess Margaret Cancer Centre, University Health Network, Toronto.
Stockley TL; Cancer Genomics Program, Princess Margaret Cancer Centre, University Health Network, Toronto.
Siu LL; Department of Medical Biophysics, University of Toronto, Toronto.

Ann Oncol ; 28(5): 946-957, 2017 05 01.

Article in En | MEDLINE | ID: mdl-28327901

Subject(s)

Genome, Human/genetics; Genomics; Neoplasms/genetics; Precision Medicine; Databases, Genetic; High-Throughput Nucleotide Sequencing; Humans; Mutation/genetics

Key words

actionable mutations; data resources; next-generation sequencing; somatic variants

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Human / Genomics / Precision Medicine / Neoplasms Type of study: Diagnostic_studies / Guideline Limits: Humans Language: En Journal: Ann Oncol Journal subject: NEOPLASIAS Year: 2017 Document type: Article

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