Using the Sankey diagram to visualize article features on the topics of whole-exome sequencing (WES) and whole-genome sequencing (WGS) since 2012: Bibliometric analysis
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference55 articles.
1. Rapid phenotype-driven gene sequencing with the NeoSeq panel: a diagnostic tool for critically ill newborns with suspected genetic disease.;de Castro;J Clin Med,2020
2. Clinical exome sequencing for genetic identification of rare Mendelian disorders.;Lee;JAMA,2014
3. Infant mortality: the contribution of genetic disorders.;Wojcik;J Perinatol,2019
4. Genetic disorders and mortality in infancy and early childhood: delayed diagnoses and missed opportunities.;Wojcik;Genet Med,2018
5. High-throughput sequencing technologies.;Reuter;Mol Cell,2015
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