Mechanisms and Heritability
of Genetic Disorders
Have an exponential impact on genetic health by deciphering underlying genomic heterogeneity and heritability with our Chromium Solutions.
To truly understand disease mechanisms, heritability, and the development of therapies, we need access to more genomic information. Our Chromium Genome and Exome solutions use the power of Linked-Reads to construct long-range information from short-reads and provide access to more variants than any
other solution on the market today.
10x Advantages in Genetic Health
Reliably Interrogate Unmappable Regions
Analyze more of the genome by accessing medically relevant regions that are unmappable with only short-reads, such as those located in NGS dead zones, for a more complete understanding of human health and disease.
Resolve Haplotypes for an Improved Understanding of Disease Inheritance
Identify changes that occur on maternal or paternal haplotypes and confidently call variants in cis or trans to better decipher the mechanisms underlying inherited disorders.
Consolidate Multiple Assays into one Low-input Assay
Get access to more variants by detecting SNVs and CNVs, as well as balanced and complex structural variants, in a single, comprehensive assay that requires only 1 ng of DNA input.
Complete Solutions, from Sample Prep to Analysis
A simplified and fully automatable workflow, along with cutting-edge and intuitive software, gives you the tools to effortlessly and rapidly find answers to your complex biological questions.
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