Gene-based burden scores identify rare variant associations for 28 blood biomarkers.

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作者： Rana,Aldisi ^[1] ; Emadeldin,Hassanin ^[2] ; Sugirthan,Sivalingam ^[3] ; Andreas,Buness ^[2] ; Hannah,Klinkhammer ^[4] ; Andreas,Mayr ^[5] ; Holger,Fröhlich ^[2] ; Peter,Krawitz ^[4] ; Carlo,Maj ^[5]

作者单位： Institute of Genomic Statistic and Bioinformatics, University Hospital Bonn, Bonn, Germany. s0raaldi@uni-bonn.de. ^[1] Institute of Genomic Statistic and Bioinformatics, University Hospital Bonn, Bonn, Germany. ^[2] Luxembourg Center for Systems Biomedicine, University of Luxembourg, Esch-Sur-Alzette, Luxembourg. ^[3] Core Unit for Bioinformatics Analysis, University Hospital Bonn, Bonn, Germany. ^[4] Institute of Medical Biometry, Informatics and Epidemiology, University Hospital Bonn, Bonn, Germany. ^[5] Fraunhofer Institute for Algorithms and Scientific Computing, Sankt Augustin, Germany. ^[6] Bonn-Aachen International Center for IT (b-it), University of Bonn, Bonn, Germany. ^[7] Centre for Human Genetics, University of Marburg, Marburg, Germany. ^[8]

关键词 Blood biomarkers Complex phenotypes Gene associations Genetic prediction PRS Rare variants

主题词人类(Humans);疾病遗传易感性(Genetic Predisposition to Disease);表型(Phenotype);多因子遗传(Multifactorial Inheritance)

DOI 10.1186/s12863-023-01155-0

PMID 37667186

发布时间 2023-11-21

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BMC genomic data

2023年24卷1期

50页

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Gene-based burden scores identify rare variant associations for 28 blood biomarkers.

BMC genomic data

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BMC genomic data

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Gene-based burden scores identify rare variant associations for 28 blood biomarkers.

BMC genomic data

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BMC genomic data

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