Linking common human diseases to their phenotypes; development of a resource for human phenomics
Abstract 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...
Furkejuvvon:
| Váldodahkkit: | , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
BMC
2021-08-01
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| Ráidu: | Journal of Biomedical Semantics |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1186/s13326-021-00249-x |
| Fáddágilkorat: |
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