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Linking common human diseases to their phenotypes; development of a resource for human phenomics
BACKGROUND: In recent years a large volume of clinical genomics data has become available due to rapid advances in sequencing technologies. Efficient exploitation of this genomics data requires linkage to patient phenotype profiles. Current resources providing disease-phenotype associations are not...
Autores principales: | Kafkas, Şenay, Althubaiti, Sara, Gkoutos, Georgios V., Hoehndorf, Robert, Schofield, Paul N. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383460/ https://www.ncbi.nlm.nih.gov/pubmed/34425897 http://dx.doi.org/10.1186/s13326-021-00249-x |
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