A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.

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作者： Kathrin,Klein ^[1] ; Roman,Tremmel ^[2] ; Stefan,Winter ^[1] ; Sarah,Fehr ^[2] ; Florian,Battke ^[1] ; Tim,Scheurenbrand ^[2] ; Elke,Schaeffeler ^[3] ; Saskia,Biskup ^[4] ; Matthias,Schwab ^[3] ; Ulrich M,Zanger ^[4]

作者单位： Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, Germany. ^[1] Medical School, University of Tübingen, Tübingen, Germany. ^[2] CeGaT GmbH, Tübingen, Germany. ^[3] Praxis für Humangenetik Tübingen, Tübingen, Germany. ^[4] Department of Clinical Pharmacology, University Hospital Tübingen, Tübingen, Germany. ^[5] Department of Pharmacy and Biochemistry, University of Tübingen, Tübingen, Germany. ^[6]

关键词 ADME eQTL analysis next generation sequencing pharmacogenomics rare variants

DOI 10.3389/fgene.2019.00007

PMID 30766545

发布时间 2024-07-14

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Frontiers in genetics

2019年10卷

7页

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A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.

Frontiers in genetics

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Frontiers in genetics

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A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort.

Frontiers in genetics

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Frontiers in genetics

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