Expand cancer insights at the genome-wide and single cell level using 10x Genomics’ Chromium Solutions.
Our product offerings support multiple cancer research areas—from single nucleotide and structural variant detection to single cell whole transcriptome gene expression analysis of thousands of individual cells, including paired, full-length T- and B-cell immune repertoire profiling. Our cancer solutions will allow you to answer questions that you have never before thought possible.
10x Advantages in Cancer Research
Unmask Tumor Heterogeneity
The inherent heterogeneity of cancer cell populations, including the diversity of normal, malignant, immune, and other cellular gene expression profiles of common and rare cell types, can be uncovered and analyzed at an astounding resolution.
Map the Immune Response
Elucidate tumor infiltrating lymphocyte phenotypes and clonal antigen recognition within the tissue microenvironment, and research molecular and cellular responses to novel immunotherapies derived from single cell genomics’ discoveries.
Better Characterization of Mutations in Cancer Susceptibility Genes
Accurately detect and resolve ambiguous variants, while maintaining haplotype information.
Consolidate Multiple Assays into One Low-input Assay
Get a more accurate view of the cancer genomic landscape by detecting SNVs, 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 workflow, along with cutting-edge and intuitive software, gives you the tools to effortlessly and rapidly complete your investigations.
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