Daicel Arbor Biosciences helps researchers working on human health and clinical research applications by providing solutions for targeted NGS and in situ hybridization (ISH) that:
- Enable high-resolution targeted NGS to identify relevant mutations of nearly any type–e.g. SNPs, short or long indels, rearrangements, and more– from nearly any sample type.
- Maximize use of bioinformatic and sequencing resources by screening only informative regions such as full or partial exomes, regulatory regions, or gene families.
- Integrate multiple NGS approaches such as DNA-seq, RNA-seq, methylation sequencing, ATAC-seq, Hi-C, and more.
- Deliver highly specific probes to identify desired DNA or RNA targets, and disqualify repeat-rich regions likely to produce unintended background signal.
Want a comprehensive solution for targeted or whole-genome sequencing? Check out our customized Sequencing and Bioinformatics services.
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