Daicel Arbor Biosciences helps scientists in both research and industry settings overcome these challenges with solutions for sensitive, effective targeted NGS that:
- Enable sequencing of even extremely rare, damaged, and short molecules (<50bp) that are impossible to assay with traditional PCR-based amplicon sequencing.
- Tolerate significant nucleotide-level dissimilarity between bait reference sequence and target molecules, which is frequently present in older samples.
- Are suited for any scale of genetic study, from single loci such as mitochondrial DNA, to hundreds to thousands of custom loci or markers, to entire eukaryotic nuclear genomes.
- Offer dedicated, tested protocols for sensitive DNA enrichment from ancient, museum, forensic, or other compromised DNA samples.
Want a comprehensive solution for targeted or whole-genome sequencing? Check out our customized Sequencing and Bioinformatics services.
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