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Computational methods and resources for the interpretation of genomic variants in cancer

The recent improvement of the high-throughput sequencing technologies is having a strong impact on the detection of genetic variations associated with cancer. Several institutions worldwide have been sequencing the whole exomes and or genomes of cancer patients in the thousands, thereby providing an...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:BMC Genomics
मुख्य लेखकों: Tian, Rui, Basu, Malay K, Capriotti, Emidio
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: BioMed Central 2015
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC4480958/
https://ncbi.nlm.nih.gov/pubmed/26111056
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-16-S8-S7
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