Know More about Single-Cell Sequencing to Achieve More Biology Findings

SHIRLEY, NY - Nov 5, 2014 - As cell is the basic unit of biology, more and more scientists are trying to separate, study and compare cells. At present, single-cell sequencing is most frequently used in tumor research.

According to the introduction by scientists from CD Genomics, we can know that single-cell genomics will help to uncover cell lineage relationships, single-cell transcriptomics will supplant the coarse notion of marker-based cell types; and single-cell epigenomics and proteomics will allow the functional states of individual cells to be analyzed.

Application Flow

About the application flow, we contain the following parts: profiling scarce clinical samples, measuring intra-tumor heterogeneity and guiding chemotherapy, cancer cells evolution analysis during tumor progression, as well as pre-implantation genetic diagnosis (PGD).

Features and Benefits

A researcher from CD Genomics told us the major benefits of Single-Cell Sequencing in CD Genomics’ labs.  He said, “[We] can get the highest throughput since we have unprecedented parallel processing of up to 96 single cells per run. Besides, it is the easiest method to use within less than three hours total hands-on time, working directly from single cells, with no RNA fragmentation and purification step. For many newly established offices, it is much affordable amounting to one-eighth the cost of other library preparation system.”

CD Genomics’s Single-Cell Sequencing conference focuses on the links between cell variation in tissues and organ function and further elucidates the origins of diseases. Scientists will concentrate on its development and achieve more findings with this unique technique.

For more detailed information, please visit CD Genomics homepage at http://www.cd-genomics.com.

Contact Information
Tel: 1-631-626-9181
Fax: 1-631-614-7828
Email: info@cd-genomics.com