Development and application of a computable genotype model in the GA4GH Variation Representation Specification
暂无分享,去创建一个
Andrew D. Yates | Reece K. Hart | H. Rehm | A. Prlić | Kevin P. Riehle | R. Freimuth | S. Chamala | L. Babb | T. Nelson | A. Wagner | Wesley Goar | Melissa Cline | Kori Kuzma | Jennifer Lee | Anastasia Smith | Kathryn Stahl | Melissa S. Cline | K. Kuzma
[1] Matthew H. Brush,et al. The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identification , 2021, Cell genomics.
[2] Grant M. Wood,et al. GA4GH: International policies and standards for data sharing across genomic research and healthcare , 2021, Cell genomics.
[3] John J. Connolly,et al. Genomic considerations for FHIR®; eMERGE implementation lessons , 2021, J. Biomed. Informatics.
[4] Alex H. Wagner,et al. A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer , 2020, Nature Genetics.
[5] Neil A. Miller,et al. PharmVar and the Landscape of Pharmacogenetic Resources , 2019, Clinical pharmacology and therapeutics.
[6] Lon Phan,et al. SPDI: Data Model for Variants and Applications at NCBI , 2019, bioRxiv.
[7] Aleksandar Milosavljevic,et al. ClinGen Allele Registry links information about genetic variants , 2018, Human mutation.
[8] Michelle Whirl-Carrillo,et al. Standardization can accelerate the adoption of pharmacogenomics: current status and the path forward. , 2018, Pharmacogenomics.
[9] S. Jackson,et al. Haplotype-Based Genotyping in Polyploids , 2018, Front. Plant Sci..
[10] T. Klein,et al. New Pharmacogenomics Research Network: An Open Community Catalyzing Research and Translation in Precision Medicine , 2017, Clinical pharmacology and therapeutics.
[11] R. Durbin,et al. Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly , 2016, bioRxiv.
[12] Raymond Dalgleish,et al. HGVS Recommendations for the Description of Sequence Variants: 2016 Update , 2016, Human mutation.
[13] M Schwab,et al. Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting , 2016, Clinical pharmacology and therapeutics.
[14] Ulrich Broeckel,et al. Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project. , 2016, The Journal of molecular diagnostics : JMD.
[15] G. Escaramís,et al. A decade of structural variants: description, history and methods to detect structural variation. , 2015, Briefings in functional genomics.
[16] J. Fagerness,et al. Pharmacogenomic and pharmacogenetic-guided therapy as a tool in precision medicine: current state and factors impacting acceptance by stakeholders , 2015, Genetics research.
[17] Mario Pazzagli,et al. Is laboratory medicine ready for the era of personalized medicine? A survey addressed to laboratory directors of hospitals/academic schools of medicine in Europe , 2015, Clinical chemistry and laboratory medicine.
[18] K. Yamamoto,et al. GLOBAL ALLIANCE FOR GENOMICS AND HEALTH , 2015 .
[19] O. Gottesman,et al. Implementation and utilization of genetic testing in personalized medicine , 2014, Pharmacogenomics and personalized medicine.
[20] David S. Jones. How Personalized Medicine Became Genetic, and Racial: Werner Kalow and the Formations of Pharmacogenetics , 2012, Journal of the history of medicine and allied sciences.
[21] R. Altman,et al. Pharmacogenomics Knowledge for Personalized Medicine , 2012, Clinical pharmacology and therapeutics.
[22] G. Kuo,et al. Clinical Application of Pharmacogenomics , 2012, Journal of pharmacy and practice.
[23] R. Verbrugge,et al. Adoption of Pharmacogenomic Testing by US Physicians: Results of a Nationwide Survey , 2012, Clinical pharmacology and therapeutics.
[24] Gonçalo R. Abecasis,et al. The variant call format and VCFtools , 2011, Bioinform..
[25] Jeroen F. J. Laros,et al. LOVD v.2.0: the next generation in gene variant databases , 2011, Human mutation.
[26] R. Altman,et al. Databases in the area of pharmacogenetics , 2011, Human mutation.
[27] T. Klein,et al. CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network , 2011, Clinical pharmacology and therapeutics.
[28] Aaron R. Quinlan,et al. Bioinformatics Applications Note Genome Analysis Bedtools: a Flexible Suite of Utilities for Comparing Genomic Features , 2022 .
[29] E. Lyon,et al. Characterization of 107 Genomic DNA Reference Materials for CYP 2 D 6 , CYP 2 C 19 , CYP 2 C 9 , VKORC 1 , and UGT 1 A 1 A GeT-RM and Association for Molecular Pathology Collaborative Project , 2010 .
[30] G. Kuo,et al. Pharmacogenomics: bridging the gap between science and practice. , 2010, Journal of the American Pharmacists Association : JAPhA.
[31] D. Flockhart,et al. The Star‐Allele Nomenclature: Retooling for Translational Genomics , 2007, Clinical pharmacology and therapeutics.
[32] Henk-Jan Guchelaar,et al. Translating Pharmacogenomics: Challenges on the Road to the Clinic , 2007, PLoS medicine.
[33] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[34] D W Nebert,et al. Suggestions for the nomenclature of human alleles: relevance to ecogenetics, pharmacogenetics and molecular epidemiology. , 2000, Pharmacogenetics.
[35] R. Angell,et al. First-meiotic-division nondisjunction in human oocytes. , 1997, American journal of human genetics.
[36] P. Frazier. Bridging the Gap Between Science and Practice. , 1992 .