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multiSNV: a probabilistic approach for improving detection of somatic point mutations from multiple related tumour samples.
Josephidou, Malvina; Lynch, Andy G; Tavaré, Simon.
Affiliation
  • Josephidou M; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK malvina.josephidou@cruk.cam.ac.uk.
  • Lynch AG; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK.
  • Tavaré S; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Robinson Way, Cambridge CB2 0RE, UK simon.tavare@cruk.cam.ac.uk.
Nucleic Acids Res ; 43(9): e61, 2015 May 19.
Article in En | MEDLINE | ID: mdl-25722372
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Models, Statistical / Point Mutation / Neoplasms Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nucleic Acids Res Year: 2015 Type: Article Affiliation country: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Mutational Analysis / Models, Statistical / Point Mutation / Neoplasms Type of study: Diagnostic_studies / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Nucleic Acids Res Year: 2015 Type: Article Affiliation country: United kingdom