Literature DB >> 35854733

Applying FHIR Genomics for Research - From Sequencing to Database.

Sean Hernandez1, Karen Fairchild2,3, Mark Pemberton4, Jonathan Dahmer2, Wei Zhang1, Matvey B Palchuk2, Umit Topaloglu1.   

Abstract

The availability of next-generation sequencing (NGS) technologies and their continually declining costs have resulted in the accumulation of large genomic data sets. NGS results have traditionally been delivered in PDF format, and in some cases, structured data, e.g., XML or JSON formats, are also made available, but there is a lack of uniformity around the profiling of external vendor testing platforms. Atrium Health Wake Forest Baptist and TriNetX have harmonized and mapped genomic data to FHIR Genomic standards and imported it into the TriNetX database through a data pipeline. This process is translatable to other sequencing platforms and to other institutions. The addition of genotypic data to the TriNetX database to the reservoir of phenotypic data will promote enhanced industry trial recruitment, (ii) comprehensive intra-institutional genomic benchmarking/quality improvement, and eventually (iii) sweeping inter-institutional genomic research and treatment paradigm shifts. ©2022 AMIA - All rights reserved.

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Year:  2022        PMID: 35854733      PMCID: PMC9285172     

Source DB:  PubMed          Journal:  AMIA Annu Symp Proc        ISSN: 1559-4076


  14 in total

1.  FHIR Lab Reports: using SMART on FHIR and CDS Hooks to increase the clinical utility of pharmacogenomic laboratory test results.

Authors:  Michael Watkins; Karen Eilbeck
Journal:  AMIA Jt Summits Transl Sci Proc       Date:  2020-05-30

2.  SMART on FHIR Genomics: facilitating standardized clinico-genomic apps.

Authors:  Gil Alterovitz; Jeremy Warner; Peijin Zhang; Yishen Chen; Mollie Ullman-Cullere; David Kreda; Isaac S Kohane
Journal:  J Am Med Inform Assoc       Date:  2015-07-21       Impact factor: 4.497

3.  CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.

Authors:  Brian H Shirts; Joseph S Salama; Samuel J Aronson; Wendy K Chung; Stacy W Gray; Lucia A Hindorff; Gail P Jarvik; Sharon E Plon; Elena M Stoffel; Peter Z Tarczy-Hornoch; Eliezer M Van Allen; Karen E Weck; Christopher G Chute; Robert R Freimuth; Robert W Grundmeier; Andrea L Hartzler; Rongling Li; Peggy L Peissig; Josh F Peterson; Luke V Rasmussen; Justin B Starren; Marc S Williams; Casey L Overby
Journal:  J Am Med Inform Assoc       Date:  2015-07-03       Impact factor: 4.497

4.  A turning point in cancer research: sequencing the human genome.

Authors:  R Dulbecco
Journal:  Science       Date:  1986-03-07       Impact factor: 47.728

5.  AACR Project GENIE: Powering Precision Medicine through an International Consortium.

Authors: 
Journal:  Cancer Discov       Date:  2017-06-01       Impact factor: 39.397

6.  Genomic considerations for FHIR®; eMERGE implementation lessons.

Authors:  Mullai Murugan; Lawrence J Babb; Casey Overby Taylor; Luke V Rasmussen; Robert R Freimuth; Eric Venner; Fei Yan; Victoria Yi; Stephen J Granite; Hana Zouk; Samuel J Aronson; Kevin Power; Alex Fedotov; David R Crosslin; David Fasel; Gail P Jarvik; Hakon Hakonarson; Hana Bangash; Iftikhar J Kullo; John J Connolly; Jordan G Nestor; Pedro J Caraballo; WeiQi Wei; Ken Wiley; Heidi L Rehm; Richard A Gibbs
Journal:  J Biomed Inform       Date:  2021-04-28       Impact factor: 8.000

7.  Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.

Authors:  Georgia L Wiesner; Alanna Kulchak Rahm; Paul Appelbaum; Sharon Aufox; Sarah T Bland; Carrie L Blout; Kurt D Christensen; Wendy K Chung; Ellen Wright Clayton; Robert C Green; Margaret H Harr; Nora Henrikson; Christin Hoell; Ingrid A Holm; Gail P Jarvik; Iftikhar J Kullo; Philip E Lammers; Eric B Larson; Noralane M Lindor; Maddalena Marasa; Melanie F Myers; Josh F Peterson; Cynthia A Prows; James D Ralston; Hila Milo Rasouly; Richard R Sharp; Maureen E Smith; Sara L Van Driest; Janet L Williams; Marc S Williams; Julia Wynn; Kathleen A Leppig
Journal:  J Pers Med       Date:  2020-04-27

8.  The growing role of precision and personalized medicine for cancer treatment.

Authors:  Paulina Krzyszczyk; Alison Acevedo; Erika J Davidoff; Lauren M Timmins; Ileana Marrero-Berrios; Misaal Patel; Corina White; Christopher Lowe; Joseph J Sherba; Clara Hartmanshenn; Kate M O'Neill; Max L Balter; Zachary R Fritz; Ioannis P Androulakis; Rene S Schloss; Martin L Yarmush
Journal:  Technology (Singap World Sci)       Date:  2019-01-11

9.  Genomic Information for Clinicians in the Electronic Health Record: Lessons Learned From the Clinical Genome Resource Project and the Electronic Medical Records and Genomics Network.

Authors:  Marc S Williams; Casey Overby Taylor; Nephi A Walton; Scott R Goehringer; Samuel Aronson; Robert R Freimuth; Luke V Rasmussen; Eric S Hall; Cynthia A Prows; Wendy K Chung; Alexander Fedotov; Jordan Nestor; Chunhua Weng; Robb K Rowley; Georgia L Wiesner; Gail P Jarvik; Guilherme Del Fiol
Journal:  Front Genet       Date:  2019-10-29       Impact factor: 4.599

10.  Integrating Genetic Data into Electronic Health Records: Medical Geneticists' Perspectives.

Authors:  Haleh Ayatollahi; Seyedeh Fatemeh Hosseini; Morteza Hemmat
Journal:  Healthc Inform Res       Date:  2019-10-31
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