HudsonAlpha Institute for Biotechnology

Leveraging over 25+ years of genomics experience, HudsonAlpha offers full-service short-read and long-read sequencing workflows for better resolution and in-depth genomic analysis. Ideal for detecting repeat expansions, structural rearrangements, and complex haplotypes in rare disease research, oncology, and population genomics. 🧬 HMW extraction, PacBio Revio HiFi sequencing, and advanced bioinformatics 📊 Structural variant, INDEL, and phasing analyses included 👨🔬 Managed in-house by our experienced genomic scientists and PhDs High-resolution genomic data for high-impact discoveries. Get your custom quote today.

Reference-based genomic services often miss population-specific variation. HudsonAlpha’s KhufuPAN constructs a custom founder-based pangenome graph that removes reference bias and improves the detection of structural variants and allelic diversity. Increase marker discovery accuracy and enhance trait resolution across diverse populations. It’s high-resolution data built for real-world breeding. 🎯 Request your custom quote.

From sample to insight, HudsonAlpha provides full-service sequencing tailored to your research. Whether you’re studying rare disease or scaling a population cohort, we deliver HiFi data built for precision medicine. 🧬 PacBio Revio-based HiFi sequencing 📊 15–25 kb HiFi reads for improved variant calling 👩🔬 Scientific collaboration with our PhDs and genomics experts With 25+ years of experience sequencing human genomes, we deliver results you can trust. Get your custom quote.

Capture structural variants, phasing, and repeat expansions with HiFi data from HudsonAlpha’s full-service sequencing center. Our end-to-end PacBio Revio workflows support population genomics, rare disease discovery, and oncology research. ✅ Long-read HiFi sequencing with >99.9% accuracy 📊 Custom reports for variant calling and biomarker validation 👩🔬 Expert support from our PhDs and computational biologists with 25+ years of experience Turn technically challenging genomes into usable genomic data. Get your custom quote.

Having trouble getting actionable insights from generic reference genomes? A single reference genome hides too much variation, but pangenomes help you uncover trait-relevant markers you can trust. With HudsonAlpha’s KhufuPAN, you’ll identify structural variants and allelic diversity across your population with a custom founder-based pangenome graph. Get better data for better breeding decisions. 🎯 Request your custom quote.

Don’t miss out on critical variants. With KhufuPAN, we build a custom pangenome graph from your founders, eliminating reference bias and capturing population-specific diversity. Discover structural variants and trait-linked markers that standard references overlook, and drive your research forward. 🎯 Get your custom quote.