Studying the variability in molecular alterations in single cells, the differential expression of transcripts which inevitably leads to variability at the protein level, and the interaction between the cells and their microenvironment, provides a deeper understanding of the biological mechanisms that contribute to disease and how they can be regulated. The challenge, however, is getting sufficient sample to serve as input for your single cell sequencing applications, while avoiding sequence bias.
Our solutions for your single cell next-generation sequencing (single-cell NGS) workflow combine robustness, and sensitivity to deliver exceptional data quality. Whether you need whole genome libraries with comprehensive coverage and high sequence fidelity for single cell NGS or highly uniform whole genome amplification from single cells, our solutions can help you advance your research.