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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Updated: Jan 3, 2026

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Correction: The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning

Kenneth D Mandl1,2,3, Tracy Glauser4,5, Ian D Krantz6,7

  • 1Computational Health Informatics Program, Boston Children's Hospital, Boston, MA, USA. kenneth_mandl@harvard.edu.

Genetics in Medicine : Official Journal of the American College of Medical Genetics
|November 28, 2019
PubMed
Summary

An amendment to this paper has been published. Please refer to the link at the top of the document for the updated version.

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Area of Science:

  • Not specified in the provided abstract.

Context:

  • The original paper has been amended.

Purpose:

  • To inform readers about a published amendment.

Summary:

  • An amendment to the paper is now available.
  • Access the amendment via the link provided at the top of the paper.

Impact:

  • Ensures readers access the most current and accurate information.
  • Facilitates informed understanding based on revised content.