A phenome-wide association study identifies effects of copy number variation of VNTRs and multicopy genes on multiple human traits is a research paper published in medRxiv (2022). On theSindex it has a DataRank of 0. It has been cited 2 times.
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National Institutes of Health
Grant: 3R01NS105781-03S1
Pilot investigation of tandem repeat variation as a cause of Alzheimer's disease using whole genome sequencing data
National Institutes of Health
Grant: 5F31NS108797-02
Identification of novel pathogenic tandem repeat expansions using long read sequencing
National Institutes of Health
Grant: 1S10OD018522-01
Transforming Genomics with 5 PB Big Omics Data Engine Cray CS300-AC Supercomputer
National Institutes of Health
Grant: 1U01NS120241-01
Development and application of a pipeline to identify tandem repeat expansions as a cause of Parkinson's disease in the AMP PD cohort
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