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HIVE-heptagon: A sensible variant-calling algorithm with post-alignment quality controls.
Simonyan, Vahan; Chumakov, Konstantin; Donaldson, Eric; Karagiannis, Konstantinos; Lam, Phuc VinhNguyen; Dingerdissen, Hayley; Voskanian, Alin.
Afiliación
  • Simonyan V; Center for Biologics Evaluation and Research, US Food and Drug Administration, 10993 New Hampshire Ave., Silver Spring, MD, United States. Electronic address: Vahan.simonyan@fda.hhs.gov.
  • Chumakov K; Center for Biologics Evaluation and Research, US Food and Drug Administration, 10993 New Hampshire Ave., Silver Spring, MD, United States. Electronic address: Konstantin.Chumakov@fda.hhs.gov.
  • Donaldson E; Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, MD, 10993 New Hampshire Ave., United States. Electronic address: Eric.Donaldson@fda.hhs.gov.
  • Karagiannis K; Center for Biologics Evaluation and Research, US Food and Drug Administration, 10993 New Hampshire Ave., Silver Spring, MD, United States; Department of Biochemistry and Molecular Medicine, George Washington University Medical Center, 2300 Eye St. NW, Washington DC, United States. Electronic address
  • Lam PV; Center for Biologics Evaluation and Research, US Food and Drug Administration, 10993 New Hampshire Ave., Silver Spring, MD, United States. Electronic address: LamPhuc.VinhNguyen@fda.hhs.gov.
  • Dingerdissen H; Center for Biologics Evaluation and Research, US Food and Drug Administration, 10993 New Hampshire Ave., Silver Spring, MD, United States; Department of Biochemistry and Molecular Medicine, George Washington University Medical Center, 2300 Eye St. NW, Washington DC, United States. Electronic address
  • Voskanian A; Center for Biologics Evaluation and Research, US Food and Drug Administration, 10993 New Hampshire Ave., Silver Spring, MD, United States. Electronic address: Alin.Voskanian-Kordi@fda.hhs.gov.
Genomics ; 109(3-4): 131-140, 2017 07.
Article en En | MEDLINE | ID: mdl-28188908
ABSTRACT
Advances in high-throughput sequencing (HTS) technologies have greatly increased the availability of genomic data and potential discovery of clinically significant genomic variants. However, numerous issues still exist with the analysis of these data, including data complexity, the absence of formally agreed upon best practices, and inconsistent reproducibility. Toward a more robust and reproducible variant-calling paradigm, we propose a series of selective noise filtrations and post-alignment quality control (QC) techniques that may reduce the rate of false variant calls. We have implemented both novel and refined post-alignment QC mechanisms to augment existing pre-alignment QC measures. These techniques can be used independently or in combination to identify and correct issues caused during data generation or early analysis stages. The adoption of these procedures by the broader scientific community is expected to improve the identification of clinically significant variants both in terms of computational efficiency and in the confidence of the results.

AVAILABILITY:

https//hive.biochemistry.gwu.edu/.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimorfismo Genético / Control de Calidad / Algoritmos / Genoma Humano / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: Genomics Asunto de la revista: GENETICA Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polimorfismo Genético / Control de Calidad / Algoritmos / Genoma Humano / Secuenciación de Nucleótidos de Alto Rendimiento Tipo de estudio: Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: Genomics Asunto de la revista: GENETICA Año: 2017 Tipo del documento: Article