Organs from the female reproductive tract (FRT) in C57BL/6 mice were sampled. Experimental timepoints were 3 months old mice across all four estrus phases, pregnant (decidualized) and aged (18 months, acyclic) mice. A total of 483,611 cells were sequenced using the 10X Chromium Gene Expression technology.
In-depth analyses of gene expression patterns, transcription factor activity and cell-to-cell communcation are found at the following links or via the navigation bar on top of the page
Download links to raw and processed data can be found here.
DEG analysis was performed using a multi-level generalised negative binomial
regression model with random intercept. Normalised gene counts were used as the
dependent variable, while estrus cycle phases were used as the independent variable,
and sample label as random effect. Model was fitted gene-wise for each cell
subpopulation.
To explore DEGs please select organ, cell type, contrast and significance threshold
Hovering the cursor on genes shows their identiy, p-value and log2-fold change in a tooltip. Click and drag around genes to zoom in. Double click to zoom out again.
Using the search box, you can highlight genes of interest and show detailed per-gene results in a table or use the checkbox to show all significant genes.
DEG analysis was performed using a multi-level generalised negative binomial regression
model with random intercept. Normalised gene counts were used as the dependent variable,
while age was used as the independent variable, and sample label as random effect. Model
was fitted gene-wise for each cell subpopulation.
To explore DEGs please select organ, cell type, contrast and significance threshold
Hovering the cursor on genes shows their identiy, p-value and log2-fold change in a tooltip. Click and drag around genes to zoom in. Double click to zoom out again.
Using the search box, you can highlight genes of interest and show detailed per-gene results in a table or use the checkbox to show all significant genes.
For each organ of the mouse female reproductive tract, we determined how gene expression changes in fibroblasts across the four phases of the estrus cycle. This panel shows the normalized expression values (Z-scores) for genes of selected pathways, or individual genes.
Z-scores of estimated activity scores of targets of transcription factors in fibroblasts
in cycling mice. Results were generated using the Single-Cell Regulatory Network Inference and Clustering (SCENIC) method.
Hovering the cursor on tiles of the heatmap shows detailed properties. Click and drag around areas of the heatmap to zoom in.
Double click to zoom out again.
Log2-fold changes of estimated activity scores of transcription
factors in fibroblasts of old mice compared to fibroblasts from young mice.
Results were generated using the Single-Cell Regulatory Network Inference and Clustering (SCENIC) method.
Hovering the cursor on tiles of the heatmap shows detailed properties. Click and drag around areas of the heatmap to zoom in.
Double click to zoom out again.
Z-scores of ligand-receptor products averaged across phases.
Ligand expression is averaged across all cell-types; receptors are
in selected cell types only.
The X-axis shows the organ label and the Y-axis shows the ligand-receptor pairs or ligand-receptor-complex pairs.
To explore cell-to-cell communication scores please select cell type and
ligand.
Hovering the cursor on tiles of the heatmap shows detailed properties. Click and drag around areas of the heatmap to zoom in.
Double click to zoom out again.
Log2-fold changes of ligand-receptor products in old mice compared to
young mice. Ligand expression is averaged across all cell-types; receptors
are in selected cell types only.
The X-axis shows the organ label and the Y-axis shows the ligand-receptor pairs or ligand-receptor-complex pairs.
To explore cell-to-cell communication scores please select cell type and
ligand.
Hovering the cursor on tiles of the heatmap shows detailed properties. Click and drag around areas of the heatmap to zoom in.
Double click to zoom out again.