Literature DB >> 27896972

DATA SHARING AND REPRODUCIBLE CLINICAL GENETIC TESTING: SUCCESSES AND CHALLENGES.

Shan Yang1, Melissa Cline, Can Zhang, Benedict Paten, Stephen E Lincoln.   

Abstract

Open sharing of clinical genetic data promises to both monitor and eventually improve the reproducibility of variant interpretation among clinical testing laboratories. A significant public data resource has been developed by the NIH ClinVar initiative, which includes submissions from hundreds of laboratories and clinics worldwide. We analyzed a subset of ClinVar data focused on specific clinical areas and we find high reproducibility (>90% concordance) among labs, although challenges for the community are clearly identified in this dataset. We further review results for the commonly tested BRCA1 and BRCA2 genes, which show even higher concordance, although the significant fragmentation of data into different silos presents an ongoing challenge now being addressed by the BRCA Exchange. We encourage all laboratories and clinics to contribute to these important resources.

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Year:  2017        PMID: 27896972      PMCID: PMC5340191          DOI: 10.1142/9789813207813_0017

Source DB:  PubMed          Journal:  Pac Symp Biocomput        ISSN: 2335-6928


  15 in total

1.  Diagnostic concordance among pathologists interpreting breast biopsy specimens.

Authors:  Joann G Elmore; Gary M Longton; Patricia A Carney; Berta M Geller; Tracy Onega; Anna N A Tosteson; Heidi D Nelson; Margaret S Pepe; Kimberly H Allison; Stuart J Schnitt; Frances P O'Malley; Donald L Weaver
Journal:  JAMA       Date:  2015-03-17       Impact factor: 56.272

2.  Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.

Authors:  Nadine Tung; Chiara Battelli; Brian Allen; Rajesh Kaldate; Satish Bhatnagar; Karla Bowles; Kirsten Timms; Judy E Garber; Christina Herold; Leif Ellisen; Jill Krejdovsky; Kim DeLeonardis; Kristin Sedgwick; Kathleen Soltis; Benjamin Roa; Richard J Wenstrup; Anne-Renee Hartman
Journal:  Cancer       Date:  2014-09-03       Impact factor: 6.860

3.  A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients.

Authors:  Stephen E Lincoln; Yuya Kobayashi; Michael J Anderson; Shan Yang; Andrea J Desmond; Meredith A Mills; Geoffrey B Nilsen; Kevin B Jacobs; Federico A Monzon; Allison W Kurian; James M Ford; Leif W Ellisen
Journal:  J Mol Diagn       Date:  2015-07-22       Impact factor: 5.568

4.  Variability in Pathologists' Interpretations of Individual Breast Biopsy Slides: A Population Perspective.

Authors:  Joann G Elmore; Heidi D Nelson; Margaret S Pepe; Gary M Longton; Anna N A Tosteson; Berta Geller; Tracy Onega; Patricia A Carney; Sara L Jackson; Kimberly H Allison; Donald L Weaver
Journal:  Ann Intern Med       Date:  2016-03-22       Impact factor: 25.391

5.  Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.

Authors:  Mitzi L Murray; Felecia Cerrato; Robin L Bennett; Gail P Jarvik
Journal:  Genet Med       Date:  2011-12       Impact factor: 8.822

6.  Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Authors:  Sue Richards; Nazneen Aziz; Sherri Bale; David Bick; Soma Das; Julie Gastier-Foster; Wayne W Grody; Madhuri Hegde; Elaine Lyon; Elaine Spector; Karl Voelkerding; Heidi L Rehm
Journal:  Genet Med       Date:  2015-03-05       Impact factor: 8.822

7.  Analysis of protein-coding genetic variation in 60,706 humans.

Authors:  Monkol Lek; Konrad J Karczewski; Eric V Minikel; Kaitlin E Samocha; Eric Banks; Timothy Fennell; Anne H O'Donnell-Luria; James S Ware; Andrew J Hill; Beryl B Cummings; Taru Tukiainen; Daniel P Birnbaum; Jack A Kosmicki; Laramie E Duncan; Karol Estrada; Fengmei Zhao; James Zou; Emma Pierce-Hoffman; Joanne Berghout; David N Cooper; Nicole Deflaux; Mark DePristo; Ron Do; Jason Flannick; Menachem Fromer; Laura Gauthier; Jackie Goldstein; Namrata Gupta; Daniel Howrigan; Adam Kiezun; Mitja I Kurki; Ami Levy Moonshine; Pradeep Natarajan; Lorena Orozco; Gina M Peloso; Ryan Poplin; Manuel A Rivas; Valentin Ruano-Rubio; Samuel A Rose; Douglas M Ruderfer; Khalid Shakir; Peter D Stenson; Christine Stevens; Brett P Thomas; Grace Tiao; Maria T Tusie-Luna; Ben Weisburd; Hong-Hee Won; Dongmei Yu; David M Altshuler; Diego Ardissino; Michael Boehnke; John Danesh; Stacey Donnelly; Roberto Elosua; Jose C Florez; Stacey B Gabriel; Gad Getz; Stephen J Glatt; Christina M Hultman; Sekar Kathiresan; Markku Laakso; Steven McCarroll; Mark I McCarthy; Dermot McGovern; Ruth McPherson; Benjamin M Neale; Aarno Palotie; Shaun M Purcell; Danish Saleheen; Jeremiah M Scharf; Pamela Sklar; Patrick F Sullivan; Jaakko Tuomilehto; Ming T Tsuang; Hugh C Watkins; James G Wilson; Mark J Daly; Daniel G MacArthur
Journal:  Nature       Date:  2016-08-18       Impact factor: 49.962

8.  The next controversy in genetic testing: clinical data as trade secrets?

Authors:  Robert Cook-Deegan; John M Conley; James P Evans; Daniel Vorhaus
Journal:  Eur J Hum Genet       Date:  2012-11-14       Impact factor: 4.246

9.  Distributing the future: The weak justifications for keeping human genomic databases secret and the challenges and opportunities in reverse engineering them.

Authors:  Misha Angrist; Robert Cook-Deegan
Journal:  Appl Transl Genom       Date:  2014-12-01

10.  ClinVar: public archive of interpretations of clinically relevant variants.

Authors:  Melissa J Landrum; Jennifer M Lee; Mark Benson; Garth Brown; Chen Chao; Shanmuga Chitipiralla; Baoshan Gu; Jennifer Hart; Douglas Hoffman; Jeffrey Hoover; Wonhee Jang; Kenneth Katz; Michael Ovetsky; George Riley; Amanjeev Sethi; Ray Tully; Ricardo Villamarin-Salomon; Wendy Rubinstein; Donna R Maglott
Journal:  Nucleic Acids Res       Date:  2015-11-17       Impact factor: 16.971

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  4 in total

1.  METHODS TO ENSURE THE REPRODUCIBILITY OF BIOMEDICAL RESEARCH.

Authors:  Konrad J Karczewski; Nicholas P Tatonetti; Arjun K Manrai; Chirag J Patel; C Titus Brown; John P A Ioannidis
Journal:  Pac Symp Biocomput       Date:  2017

2.  A new era in the interpretation of human genomic variation.

Authors:  Heidi L Rehm
Journal:  Genet Med       Date:  2017-07-13       Impact factor: 8.822

3.  Consistency of BRCA1 and BRCA2 Variant Classifications Among Clinical Diagnostic Laboratories.

Authors:  Stephen E Lincoln; Shan Yang; Melissa S Cline; Yuya Kobayashi; Can Zhang; Scott Topper; David Haussler; Benedict Paten; Robert L Nussbaum
Journal:  JCO Precis Oncol       Date:  2017-04-11

4.  Sources of discordance among germ-line variant classifications in ClinVar.

Authors:  Shan Yang; Stephen E Lincoln; Yuya Kobayashi; Keith Nykamp; Robert L Nussbaum; Scott Topper
Journal:  Genet Med       Date:  2017-06-01       Impact factor: 8.822

  4 in total

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