Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

PURPOSE: Genomic sequencing has become an increasingly powerful and relevant tool to be leveraged for the discovery of genetic aberrations underlying rare, Mendelian conditions. Although the computational tools incorporated into diagnostic workflows for this task are continually evolving and improvi...

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Detalles Bibliográficos
Autores principales: Kobren, Shilpa Nadimpalli, Baldridge, Dustin, Velinder, Matt, Krier, Joel B., LeBlanc, Kimberly, Esteves, Cecilia, Pusey, Barbara N., Züchner, Stephan, Blue, Elizabeth, Lee, Hane, Huang, Alden, Bastarache, Lisa, Bican, Anna, Cogan, Joy, Marwaha, Shruti, Alkelai, Anna, Murdock, David R., Liu, Pengfei, Wegner, Daniel J., Paul, Alexander J., Sunyaev, Shamil R., Kohane, Isaac S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187147/
https://www.ncbi.nlm.nih.gov/pubmed/33580225
http://dx.doi.org/10.1038/s41436-020-01084-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187147/
https://www.ncbi.nlm.nih.gov/pubmed/33580225
http://dx.doi.org/10.1038/s41436-020-01084-8

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