The OMRF Genomics facility is a universally accessible resource able to provide investigators with massive amounts of sequencing, genotyping, or gene expression data in a relatively short period of time. Our Novaseq 6000, NextSeq 500, and Miseq instruments combine to provide researchers extreme flexibility in a very cost-efficient manner. The facility is capable of processing and analyzing all forms of sequencing projects, including whole genome sequencing, custom targeted resequencing including exome capture, RNA-seq, ChIP-seq, and MethylCap-Seq. Study sizes can range from singletons to over one thousand samples.
Our iScan system with Autoloader is capable of processing thousands of genotyping samples per week with arrays targeting hundreds to millions of variants per sample.
Generation of a 3'-end tag library using Lexogen Quanteq FWD kit followed by generation of 10M single end 75bp reads using either an Illumina NextSeq or NovaSeq
20M guaranteed mRNA reads with NEB Ultra II Directional mRNA (poly-A selected) kit. Sequenced on an Illumina NovaSeq S1 flowcell with PE50 reads. Initial RNA QC and final library QC by Kapa qPCR and Agilent Tapestation included. Deeper coverage prices on request.
10ng input required. Typical TAT of 35 days.
Chromatin Immunoprecipitation (ChIP) Assays Services
Next Generation Sequencing (NGS) Services
Oklahoma Medical Research - Next Generation Sequencing Core has not received any reviews.
Oklahoma Medical Research - Next Generation Sequencing Core has not received any endorsements.