Children’s rare disease cohorts: an integrative research and clinical genomics initiative

While genomic data is frequently collected under distinct research protocols and disparate clinical and research regimes, there is a benefit in streamlining sequencing strategies to create harmonized databases, particularly in the area of pediatric rare disease. Research hospitals seeking to impleme...

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Detalles Bibliográficos
Autores principales: Rockowitz, Shira, LeCompte, Nicholas, Carmack, Mary, Quitadamo, Andrew, Wang, Lily, Park, Meredith, Knight, Devon, Sexton, Emma, Smith, Lacey, Sheidley, Beth, Field, Michael, Holm, Ingrid A., Brownstein, Catherine A., Agrawal, Pankaj B., Kornetsky, Susan, Poduri, Annapurna, Snapper, Scott B., Beggs, Alan H., Yu, Timothy W., Williams, David A., Sliz, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338382/
https://www.ncbi.nlm.nih.gov/pubmed/32655885
http://dx.doi.org/10.1038/s41525-020-0137-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338382/
https://www.ncbi.nlm.nih.gov/pubmed/32655885
http://dx.doi.org/10.1038/s41525-020-0137-0

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