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Navigating the phenotype frontier: The monarch initiative

  • Author(s): McMurry, JA
  • Köhler, S
  • Washington, NL
  • Balhoff, JP
  • Borromeo, C
  • Brush, M
  • Carbon, S
  • Conlin, T
  • Dunn, N
  • Engelstad, M
  • Foster, E
  • Gourdine, JP
  • Jacobsen, JOB
  • Keith, D
  • Laraway, B
  • Xuan, JN
  • Shefchek, K
  • Vasilevsky, NA
  • Yuan, Z
  • Lewis, SE
  • Hochheiser, H
  • Groza, T
  • Smedley, D
  • Robinson, PN
  • Mungall, CJ
  • Haendel, MA
  • et al.

Published Web Location

http://www.genetics.org/content/genetics/203/4/1491.full.pdf
No data is associated with this publication.
Abstract

© 2016 by the Genetics Society of America. The principles of genetics apply across the entire tree of life. At the cellular level we share biological mechanisms with species from which we diverged millions, even billions of years ago. We can exploit this common ancestry to learn about health and disease, by analyzing DNA and protein sequences, but also through the observable outcomes of genetic differences, i.e. phenotypes. To solve challenging disease problems we need to unify the heterogeneous data that relates genomics to disease traits. Without a big-picture view of phenotypic data, many questions in genetics are difficult or impossible to answer. The Monarch Initiative (https://monarchinitiative.org) provides tools for genotype-phenotype analysis, genomic diagnostics, and precision medicine across broad areas of disease.

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