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Mutation extraction tools can be combined for robust recognition of genetic variants in the literature

As the cost of genomic sequencing continues to fall, the amount of data being collected and studied for the purpose of understanding the genetic basis of disease is increasing dramatically. Much of the source information relevant to such efforts is available only from unstructured sources such as th...

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Detalhes bibliográficos
Main Authors: Jimeno Yepes, Antonio, Verspoor, Karin
Formato: Artigo
Idioma:Inglês
Publicado em: F1000Research 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4176422/
https://ncbi.nlm.nih.gov/pubmed/25285203
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.3-18.v2
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