实验描述
This study is aimed to decipher the gene expression patterns that exist across the different cell cycle stages at level of individual cells and their inherent heterogeneity. Conventional studies in yeast and human cells have shown coordination between gene expression and cell-cycle. However such a study for mouse ES cells (mES) and their differentiation has not been performed at a single cell level. In this study, we obtain pure mES cells from different cell cycle stages using FACS and apply single cell RNA-sequencing using the Fluidigm C1 system. This work will decipher and unravel the transcriptional patterns that coordinated with cell cycle progression at a single cell level.
样本属性
developmental stage
embryonic stem cell line
sample description
AB2.2 Rex1-GFP cells. Asynchronous cells stained with 5uM Hoechst staining and sN/Ap frozen on 9/2/2014. RN/A extraction done by Sequencing facility, AB2.2 Rex1-GFP cells. Cells sorted using 5uM Hoechst staining for G1 phase and sN/Ap frozen on 9/2/2014. RN/A extraction done by Sequencing facility, AB2.2 Rex1-GFP cells. Cells sorted using 5uM Hoechst staining for G2M phase and sN/Ap frozen on 9/2/2014. RN/A extraction done by Sequencing facility, AB2.2 Rex1-GFP cells. Cells sorted using 5uM Hoechst staining for S phase and sN/Ap frozen on 9/2/2014. RN/A extraction done by Sequencing facility, mRNAseq Nextera library made from AB2.2 Rex1-GFP. Cells sorted using 5uM Hoechst staining for G1 phase and lysed on 5/12/2013, mRNAseq Nextera library made from AB2.2 Rex1-GFP. Cells sorted using 5uM Hoechst staining for G1 phase and lysed on 6/12/2013, mRNAseq Nextera library made from AB2.2 Rex1-GFP. Cells sorted using 5uM Hoechst staining for G2M phase and lysed on 5/12/2013, mRNAseq Nextera library made from AB2.2 Rex1-GFP. Cells sorted using 5uM Hoechst staining for S phase and lysed on 6/12/2013