UNC School of Medicine Integrated Genomics Cores High Throughput Sequencing Core Facility (RRID:SCR_022620)Copy Citation Copied
URL: https://www.med.unc.edu/genomics/about/
Proper Citation: UNC School of Medicine Integrated Genomics Cores High Throughput Sequencing Core Facility (RRID:SCR_022620)
Description: Full service sequencing facility to assist with genetic and genomic research. Part of Integrated Genomics Cores. Offers comprehensive library services, NextGen sequencing and alternative technologies including long reads. Offers library preparations and multiple sequencing platforms including MiSeq, HiSeq, NovaSeq, NextSeq, BioNano, Oxford Nanopore. Services also include using techniques and data analyses via sister core BARC.
Abbreviations: HTSF
Synonyms: UNC School of Medicine Integrated Genomics Cores HighThroughput Sequencing Facility, University of North Carolina at Chapel Hill School of Medicine Integrated Genomics Cores High-Throughput Sequencing Facility, UNC School of Medicine HighThroughput Sequencing Facility
Resource Type: core facility, access service resource, service resource
Keywords: NextGen sequencing, library preparations, Illumina kits, non Illumina kits, novel R&D, Oxford Nanopore, BioNano, MiSeq, HiSeq, NovaSeq, NextSeq, BioNano, Oxford Nanopore, sequencing platforms, ABRF, USEDit
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University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA |
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