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The Matchmaker Exchange API: automating patient matching through the exchange of structured phenotypic and genotypic profiles
Despite the increasing prevalence of clinical sequencing, the difficulty of identifying additional affected families is a key obstacle to solving many rare diseases. There may only be a handful of similar patients worldwide, and their data may be stored in diverse clinical and research databases. Co...
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| Publicado en: | Hum Mutat |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4775166/ https://ncbi.nlm.nih.gov/pubmed/26255989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22850 |
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