Skip to main navigation
Skip to search
Skip to main content
University of Kentucky Home
LOGIN & Help
English
Español
Home
Research units
Researchers
Projects & Grants
Research Output
Facilities & Equipment
Honors & Awards
Activities
Search by expertise, name or affiliation
Resolving the full MAPT H2 inverted haplotype using optical genome mapping and ultra-long-read nanopore sequencing
Ebbert, Mark T. W.
(PI)
Fardo, David
(CoI)
Nelson, Peter
(CoI)
Sanders-Brown Center on Aging (SBCoA)
Internal Medicine
Neuroscience
Neuroscience Research Priority Area
Institute for Biomedical Informatics
Center for Computational Sciences
Biostatistics
Pathology and Lab Medicine
Neurosurgery
Overview
Fingerprint
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.
Sort by
Weight
Alphabetically
Neuroscience
Nanopore Sequencing
100%
Haplotype
100%
Genetic Mapping
100%
Alzheimer's Disease
60%
Telomere
60%
Centromere
20%
Frontotemporal Dementia
20%
Reference Genome
20%
Parkinson's Disease
20%
Neurodegenerative Disorder
20%
Medicine and Dentistry
Optical Genome Mapping
100%
Haplotype
100%
Alzheimer's Disease
60%
Telomere
60%
Long-read Sequencing
40%
Centromere
20%
Parkinson's Disease
20%
Diseases
20%
Frontotemporal Lobar Degeneration
20%
Degenerative Disease
20%
Biochemistry, Genetics and Molecular Biology
Optical Genome Mapping
100%
Haplotype
100%
Telomere
60%
Genomics
20%
Centromere
20%