Leveraging network analytics to infer patient syndrome and identify causal genes in rare disease cases-Reference-Cited by-同舟云学术

Leveraging network analytics to infer patient syndrome and identify causal genes in rare disease cases

Published:2017-08 Issue:S5 Volume:18 Page:
ISSN:1471-2164
Container-title:BMC Genomics
language:en
Short-container-title:BMC Genomics

Author:

Krämer Andreas,Shah Sohela,Rebres Robert Anthony,Tang Susan,Richards Daniel Rene

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Biotechnology

Link

http://link.springer.com/content/pdf/10.1186/s12864-017-3910-4.pdf

Reference43 articles.

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3. Valencia CA, et al. Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center’s Experience. Front Pediatr. 2015; doi: 10.3389/fped.2015.00067 .

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