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Related Concept Videos

Genomics02:02

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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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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Related Experiment Video

Updated: Mar 14, 2026

Heuristic Mining of Hierarchical Genotypes and Accessory Genome Loci in Bacterial Populations
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Practical considerations for implementing genomic information resources. Experiences from eMERGE and CSER.

Luke V Rasmussen1, Casey L Overby, John Connolly

  • 1Luke Rasmussen, Division of Health and Biomedical Informatics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, 750 North Lake Shore Drive, 11th Floor, Rubloff Building, Chicago, IL 60611, Phone: 312-503-2823.

Applied Clinical Informatics
|September 22, 2016
PubMed
Summary

Genomic medicine requires better information resources for patients and providers. A survey revealed a need for improved access and delivery of genomic content, with opportunities for collaboration between institutions and vendors.

Keywords:
Electronic health recordsclinical decision supporteducationgeneticsmedicine

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Area of Science:

  • Genomic Medicine
  • Clinical Informatics
  • Health Information Resources

Background:

  • Genomic medicine is rapidly evolving, necessitating effective information resources for clinical practice.
  • Current delivery methods for genomic information in healthcare settings show significant variability.

Purpose of the Study:

  • To assess current perceptions and usage of genomic information resources.
  • To understand the delivery approaches for genomic content in clinical settings.

Main Methods:

  • A survey was administered to representatives from the electronic Medical Records and Genomics (eMERGE) network and the Clinical Sequencing Exploratory Research (CSER) consortium.
  • Data were collected in 2014 from ten institutions across eight eMERGE and two CSER sites.

Main Results:

  • Provider-facing genomic content is predominantly delivered via electronic health records (EHRs).
  • Patient-facing genomic content is primarily disseminated through paper pamphlets.
  • A strong consensus (91%) exists on the need for new genomic content for both patients and providers.
  • A majority (73%) agreed on the need for shared content across institutions, alongside site-specific requirements.

Conclusions:

  • There is a clear demand for enhanced access to and a broader range of information resources to support genomic medicine.
  • Opportunities exist for content developers and EHR vendors to collaborate with healthcare institutions.
  • Developing a central, multi-modal content repository with customization options is recommended to streamline resource utilization.