An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.


Journal Article

BACKGROUND:There is tremendous potential for genome sequencing to improve clinical diagnosis and care once it becomes routinely accessible, but this will require formalizing research methods into clinical best practices in the areas of sequence data generation, analysis, interpretation and reporting. The CLARITY Challenge was designed to spur convergence in methods for diagnosing genetic disease starting from clinical case history and genome sequencing data. DNA samples were obtained from three families with heritable genetic disorders and genomic sequence data were donated by sequencing platform vendors. The challenge was to analyze and interpret these data with the goals of identifying disease-causing variants and reporting the findings in a clinically useful format. Participating contestant groups were solicited broadly, and an independent panel of judges evaluated their performance. RESULTS:A total of 30 international groups were engaged. The entries reveal a general convergence of practices on most elements of the analysis and interpretation process. However, even given this commonality of approach, only two groups identified the consensus candidate variants in all disease cases, demonstrating a need for consistent fine-tuning of the generally accepted methods. There was greater diversity of the final clinical report content and in the patient consenting process, demonstrating that these areas require additional exploration and standardization. CONCLUSIONS:The CLARITY Challenge provides a comprehensive assessment of current practices for using genome sequencing to diagnose and report genetic diseases. There is remarkable convergence in bioinformatic techniques, but medical interpretation and reporting are areas that require further development by many groups.

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Cited Authors

  • Brownstein, CA; Beggs, AH; Homer, N; Merriman, B; Yu, TW; Flannery, KC; DeChene, ET; Towne, MC; Savage, SK; Price, EN; Holm, IA; Luquette, LJ; Lyon, E; Majzoub, J; Neupert, P; McCallie, D; Szolovits, P; Willard, HF; Mendelsohn, NJ; Temme, R; Finkel, RS; Yum, SW; Medne, L; Sunyaev, SR; Adzhubey, I; Cassa, CA; de Bakker, PIW; Duzkale, H; Dworzyński, P; Fairbrother, W; Francioli, L; Funke, BH; Giovanni, MA; Handsaker, RE; Lage, K; Lebo, MS; Lek, M; Leshchiner, I; MacArthur, DG; McLaughlin, HM; Murray, MF; Pers, TH; Polak, PP; Raychaudhuri, S; Rehm, HL; Soemedi, R; Stitziel, NO; Vestecka, S; Supper, J; Gugenmus, C; Klocke, B; Hahn, A; Schubach, M; Menzel, M; Biskup, S; Freisinger, P; Deng, M; Braun, M; Perner, S; Smith, RJH; Andorf, JL; Huang, J; Ryckman, K; Sheffield, VC; Stone, EM; Bair, T; Black-Ziegelbein, EA; Braun, TA; Darbro, B; DeLuca, AP; Kolbe, DL; Scheetz, TE; Shearer, AE; Sompallae, R; Wang, K; Bassuk, AG; Edens, E; Mathews, K; Moore, SA; Shchelochkov, OA; Trapane, P; Bossler, A; Campbell, CA; Heusel, JW; Kwitek, A; Maga, T; Panzer, K; Wassink, T; Van Daele, D; Azaiez, H; Booth, K; Meyer, N; Segal, MM; Williams, MS; Tromp, G; White, P; Corsmeier, D; Fitzgerald-Butt, S; Herman, G; Lamb-Thrush, D; McBride, KL; Newsom, D; Pierson, CR; Rakowsky, AT; Maver, A; Lovrečić, L; Palandačić, A; Peterlin, B; Torkamani, A; Wedell, A; Huss, M; Alexeyenko, A; Lindvall, JM; Magnusson, M; Nilsson, D; Stranneheim, H; Taylan, F; Gilissen, C; Hoischen, A; van Bon, B; Yntema, H; Nelen, M; Zhang, W; Sager, J; Zhang, L; Blair, K; Kural, D; Cariaso, M; Lennon, GG; Javed, A; Agrawal, S; Ng, PC; Sandhu, KS; Krishna, S; Veeramachaneni, V; Isakov, O; Halperin, E; Friedman, E; Shomron, N; Glusman, G; Roach, JC; Caballero, J; Cox, HC; Mauldin, D; Ament, SA; Rowen, L; Richards, DR; San Lucas, FA; Gonzalez-Garay, ML; Caskey, CT; Bai, Y; Huang, Y; Fang, F; Zhang, Y; Wang, Z; Barrera, J; Garcia-Lobo, JM; González-Lamuño, D; Llorca, J; Rodriguez, MC; Varela, I; Reese, MG; De La Vega, FM; Kiruluta, E; Cargill, M; Hart, RK; Sorenson, JM; Lyon, GJ; Stevenson, DA; Bray, BE; Moore, BM; Eilbeck, K; Yandell, M; Zhao, H; Hou, L; Chen, X; Yan, X; Chen, M; Li, C; Yang, C; Gunel, M; Li, P; Kong, Y; Alexander, AC; Albertyn, ZI; Boycott, KM; Bulman, DE; Gordon, PMK; Innes, AM; Knoppers, BM; Majewski, J; Marshall, CR; Parboosingh, JS; Sawyer, SL; Samuels, ME; Schwartzentruber, J; Kohane, IS; Margulies, DM

Published Date

  • March 25, 2014

Published In

Volume / Issue

  • 15 / 3

Start / End Page

  • R53 -

PubMed ID

  • 24667040

Pubmed Central ID

  • 24667040

Electronic International Standard Serial Number (EISSN)

  • 1474-760X

International Standard Serial Number (ISSN)

  • 1474-7596

Digital Object Identifier (DOI)

  • 10.1186/gb-2014-15-3-r53


  • eng