Abstract
New computational and database-driven tools are emerging to aid in the interpretation of cancer genomic data as its use becomes more common in clinical evidence-based cancer medicine. Two such open source tools, published recently in Genome Medicine, provide important advances to address the clinical cancer genomics data interpretation bottleneck.
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CITATION STYLE
APA
Mardis, E. R. (2018, April 13). New additions to the cancer precision medicine toolkit. Genome Medicine. BioMed Central Ltd. https://doi.org/10.1186/s13073-018-0540-7
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