Products

myBaits® Compass 1.2M SNP Kit

Retrieve millions of human genome-wide SNPs for FGG and other research

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myBaits® FORCE kit

The FORensic Capture Enrichment (FORCE) panel is an all-in-one SNP panel for human ID

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myBaits® 95K kit

Parabon/AFDIL 95K Kinship Panel targets SNPs for kinship assessment out to 4th-degree relatives

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myBaits® Mito Kits

Long-established workhorse forensics tool for armed conflict remains identification

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myBaits® Whole Genome Enrichment (WGE) Kits

Genome-wide enrichment for IGG and other forensics applications

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If none of the above options meets your needs, our team of experts would be happy to design a myBaits Custom kit that meets your exact target specifications. Contact us today to learn more.

myBaits kits are for research use only and are not validated for diagnostic or therapeutic purposes. Daicel Arbor Biosciences does not provide accredited forensics services.

Technology

Recover genealogically-informative SNPs from challenging forensic samples

Targeted sequencing with myBaits hybridization capture is a proven and validated method for sequencing forensic DNA. With myBaits, you can retrieve high density SNP data or whole genome coverage, even from highly-degraded and low-abundance DNA sources heavily contaminated with non-human DNA. Whether targeting the mitogenome or thousands of SNPs for kinship investigation and ID validation, or a million+ SNPs for high-resolution FIGG, myBaits is the field standard for a range of forensic NGS/MPS workflows. Hybridization capture for forensics provides:

  • Increased resolution of informative sites with less sequencing compared to whole sample sequencing
  • Effective on degraded and low-abundance DNA
  • Integrates with standard NGS workflows
SNP panels
  • Hybridization capture technology vastly increases the number of targeted SNPs
  • Panels with 5K to 1M+ markers
  • Useful for kinship analysis, genetic genealogy, etc
Whole genome enrichment (WGE)
  • Genome-wide enrichment of SNPs
  • Recover as many markers as possible from complex samples; no specific markers needed
Targeted mitogenome sequencing
  • Full mitochondrial DNA sequencing
  • Beneficial when there is not enough material for other forensic methods to work

What is hybridization capture?

Hybridization capture is integrated into the overall next generation sequencing workflow immediately before sequencing on an NGS platform, such as Illumina. A fully sequenceable, barcoded/indexed NGS library (or pool of multiple libraries) is denatured, and allowed to anneal to complementary target-specific biotinylated probes/baits. These bait:library complexes are then bound to streptavidin-coated magnetic beads via the biotin on the probes, which are washed to remove non-specifically bound molecules. The remaining “enriched” library molecules are then released from the baits and amplified before sequencing.

Note! You may know the “hybridization capture” technique by another name, such as: Target enrichment, Target capture, Probe capture, SNP capture, Capture sequencing / sequence capture, Hybridization sequencing, or hyb cap

Learn more about myBaits technology: myBaits hybridization capture kits

myBaits kits are for research use only and are not validated for diagnostic or therapeutic purposes. Daicel Arbor Biosciences does not provide accredited forensics services.

Publication highlights

Forsythe, B.K., et al. (2026). Comparative Evaluation of SNP Sequencing Workflows for Identification of the Missing in Vietnam. Forensic Science International: Genetics.

Thomas, J.T., et al. (2026). Forensic Validation of the 95K SNP Panel and the Parabon Fx Forensic Analysis Platform for Identification of US Military Unknowns Using Extended Kinship Inference. Genes.

Greytak, E., et al. (2024). Investigative Genetic Genealogy for Human Remains Identification. Journal of Forensic Sciences.

Cavagnino, C., et al. (2024). Unearthing Who and Y at Harewood Cemetery and Inference of George Washington’s Y-Chromosomal Haplotype. iScience.

Cady, J., and E.M. Greytak. (2022). Whole-Genome Sequencing of Degraded DNA for Investigative Genetic Genealogy. Forensic Science International: Genetics Supplement Series.

Gorden, E.M., et al. (2022). Extended Kinship Analysis of Historical Remains Using SNP Capture. Forensic Science International: Genetics.

Lewis, E.J., et al. (2022). Nuclear DNA SNP Profiles Derived from Human Hair Shaft. Forensic Science International: Genetics Supplement Series

Tillmar, A., et al. (2021). The FORCE Panel: An All-in-One SNP Marker Set for Confirming Investigative Genetic Genealogy Leads and for General Forensic Applications. Genes.

Gorden, E.M., et al. (2021). Capture Enrichment and Massively Parallel Sequencing for Human Identification. Forensic Science International: Genetics.

Emery, M.V., et al. (2021). Whole Mitochondrial Genomes Assembled from Thermally Altered Forensic Bones and Teeth. Forensic Science International: Genetics.

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myBaits Compass 1.2M SNP Kit
This hybridization-capture kit targets ~1.2M genome-wide SNPs selected for maximum compatibility with leading FGG databases and workflows. Designed for strong kinship resolution and accurate variant calling, the panel omits ClinVar-associated SNPs and is offered in five scalable kit sizes.
myBaits WGE Human
Kit for human genome-wide enrichment, built from human genomic DNA. Caucasian, African, and Japanese options available.
myBaits Mito
Kit for enrichment of mitochondrial DNA (mtDNA). Choose from a variety of predesigned panels for different species.

Daicel Arbor Biosciences provides sensitive, proven targeted NGS solutions that:

  • Capture and sequence extremely short or damaged DNA fragments (<50 bp) that PCR-based approaches cannot access.
  • Tolerate nucleotide-level variation between reference baits and target molecules, essential for analyzing compromised forensic samples.
  • Support studies at any scale, from a single locus and the mitogenome, to hundreds to thousands of custom loci or markers, to entire nuclear genomes.
  • Include optimized protocols for forensic specimens, ensuring reliable enrichment and recovery of genetic material.

Discover how we simultaneously genotype millions of human genome-wide SNPs informative for forensic genetic genealogy (FGG) with the myBaits Compass 1.2M SNP kit and learn more about our customizable sequencing and bioinformatics services here.

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