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10.1186/s13073-018-0531-8

http://scihub22266oqcxt.onion/10.1186/s13073-018-0531-8
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suck abstract from ncbi


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pmid29592813      Genome+Med 2018 ; 10 (ä): ä
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  • Cancer Genome Interpreter annotates the biological and clinical relevance of tumor alterations #MMPMID29592813
  • Tamborero D; Rubio-Perez C; Deu-Pons J; Schroeder MP; Vivancos A; Rovira A; Tusquets I; Albanell J; Rodon J; Tabernero J; de Torres C; Dienstmann R; Gonzalez-Perez A; Lopez-Bigas N
  • Genome Med 2018[]; 10 (ä): ä PMID29592813show ga
  • While tumor genome sequencing has become widely available in clinical and research settings, the interpretation of tumor somatic variants remains an important bottleneck. Here we present the Cancer Genome Interpreter, a versatile platform that automates the interpretation of newly sequenced cancer genomes, annotating the potential of alterations detected in tumors to act as drivers and their possible effect on treatment response. The results are organized in different levels of evidence according to current knowledge, which we envision can support a broad range of oncology use cases. The resource is publicly available at http://www.cancergenomeinterpreter.org.Electronic supplementary material: The online version of this article (10.1186/s13073-018-0531-8) contains supplementary material, which is available to authorized users.
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