Health Care, Research, Academia
We provide high-quality sequence analysis specifically focused on your research using the latest sequencing technology and our own proprietary sample preparation techniques. We develop a close relationship with you and your research team to ensure you get the focused support you need to turn your extracted samples to scientific discovery.
Design Your Run
Your sequencing design must include sufficient replicates and depth of coverage. We are available to consult with you on your experimental design.
Sequencing Prep
Sequencing prep is as important as the sequencing run. We tailor our prep using modern prep kits to ensure a high quality sequencing library with adequate coverage and unique dual indexes.
Sequencing That Matches Your Science
We prepare for and run on multiple NextGen platforms, and we have experience across a broad variety of organisms (e.g., prokaryotes, eukaryotes, octoploidal organisms) and sample conditions (e.g., modern, ancient, fragmented).
DNA and RNA quantification, chemical or mechanical fragmentation, bead-based size selection, amplification, sequencing library preparation and normalization, sequencing, and analysis.
Next Gen Sequencing Services
Sequencing design and solutions for investigating metagenomes, whole genomes, exomes, transcriptomes, and targeted sequences.
Genomics Support Services
Upon request, we can work with you on your experimental design to ensure sufficient coverage in areas of interest. We also consult with you to analyze your sequencing data.
Library Preparation Solutions
NextGen sequencing library preparation involves generating a library of dual-index-labeled DNA fragments that will flow across the sequencer's flow cell for sequencing by synthesis.
Next Gen Sequencing Services
We are equipped to handle most sample types and workflows offering a variety of library preparation solutions, sequencing, and data analyses.
Genomics Support Services
To ensure a successful sequencing run, the sample must meet sufficient purity, quantity, and quality standards. Your submitted samples will be validated through quality control analyses before executing your sequencing order.
Library Preparation Solutions
Next-generation sequencing (NGS) library preparation involves generating a collection of DNA fragments for sequencing. NGS libraries are pooled samples of DNA fragments that have unique indexes applied. The sequencers then run the pooled samples together and use the indexes to ``demultiplex`` the sequencing data so that each sample can be independently analyzed.