Phase Genomics’ ultra-long-range genome sequencing technology and computational tools empower scientists to address some of today’s most pressing health and environmental challenges.
Identify and characterize all major types of chromosomal abnormalities with a single, high-resolution assay to better understand the genetic basis of cancer and inherited diseases.
Read MoreDeconvolute complex metagenomic samples; discover new species, strains and genes; attribute mobile genetic elements to their hosts; study the human microbiome, infectious disease, antibiotic resistance and gene function.
Read MoreConstruct high-quality, chromosome-scale reference genomes; resolve haplotypes and polyploidy; compare and study gene structure, function and interactions; understand biology and evolution to conserve and protect biodiversity.
Read MoreJoin a growing community of scientists who are using proximity genome mapping to enrich genomic data sets and accelerate discovery in life sciences, medicine, and agriculture.
Reach out to discover how Phase Genomics can enhance your research.
Thousands of scientists throughout the world apply Phase Genomics’ technology to drive new innovations and therapeutic discoveries at leading academic and research organizations and biopharmaceutical firms.