In order to explore the heterogeneity of cell genotype, phenotype, and function within a complex cell population, single-cell sequencing technologies like 10X Genomics, BD Phrapsody, and Illumina Hiseq have evolved. These technologies enable us to characterize the genome, transcriptome, and epigenomics of individual cells.
Single cell copy number variation (CNV) is a significant form of somatic aberration linked to a number of illnesses. Our robust next-generation sequencing (NGS) technologies are dependable, effective, high-scale, and high-resolution techniques for single-cell CNV analysis. They are used in numerous research fields, including tumor heterogeneity identification, cell line characterization, and neural mosaicism discovery.