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.
CITATION STYLE
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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