Single-cell genomics is the study of the genome and transcriptome at the single-cell level. With the development of high-throughput sequencing technology, single-cell genomics has also developed rapidly, and various applications of sequencing technology in single-cell genomics are emerging. CD Genomics enables the functional identification and classification of cells at the single-cell level, thus providing useful information for future developments in medicine and biology.
Functions
1. By traditional bulk RNA-seq methods, cell-to-cell differences are missed and cellular heterogeneity can be completely masked
2. Single cell RNA-Seq opens a whole new field in biology by allowing the study of cell-to-cell transcriptome heterogeneity.
3. Examines thousands of cells per sample through cell-by-cell 3' end counting of mRNA transcripts.
4. Enables identification of rare cell types, analysis of cellular heterogeneity, and understanding of individual cell states and cellular responses to environmental signals and conditions.
1. Analyze transcriptomes on a cell-by-cell with Chromium Single Cell 3' Solution
2. Samples: Single cell suspension; total RNA; tissue (for nuclei isolation).
3. To ensure high-quality results Dead Cell Removal has optimized
4. High-Throughput 10× Genomics Chromium Single Cell RNA-Seq: process 100's to 10,000's of single cells in a single 7-minute Chromium Instrument run.
5. To ensure high-quality results Dead Cell Removal has optimized
CD Genomics offers you 10× Genomics Chromium System based single cell genomics services that can solve problems that ordinary genomics cannot. If this is of interest to you, please contact us directly for details.
For research use only, not intended for any clinical use.
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