# Amodio_Infertility_2024 Amodio G, Giacomini G, Boeri L, et al. **T cell exhaustion and senescence signatures characterize and differentiate infertile men** ### Single-Cell RNA Sequencing Analysis ### **scRNAseq** (from 10X Genomics) analysis of CD3+ T cells purified from the peripheral blood of men diagnosed with oligo-astheno-teratozoospermia (OAT, n=4), idiopathic non-obstructive azoospermia (iNOA, n=6), and a control group (FER, n=5). scRNAseq analysis was performed using a standard [Seurat](https://satijalab.org/seurat/) pipeline that includes the following steps starting from a minimal object after loading of 10X data to markers identification: - Preprocessing and cell filtering - Each sample was pre-processed and cells with mitochondrial RNA percentages higher than 10 and a number of features <1200 or >6000, were filtered out. - Normalization - Default Seurat settings [(NormalizeData function)](https://satijalab.org/seurat/reference/normalizedata) - Scaling: - Data was regressed out by passing UMI count, the percentage of mitochondrial genes, the difference between the cell cycle phases scores, as described in the Seurat [vignette](https://satijalab.org/seurat/articles/cell_cycle_vignette.html#alternate-workflow-1). - Dimensionality reduction and Harmony batch removal: - A principal component analysis (PCA) with 100 principal components (PCs) was performed and a UMAP-representation as well as clusters were computed on the top 55 components (orig.ident as batch variable) - Clustering - Markers identification - Cluster annotation: - Intra-cluster comparisons ### Directories and Files ### - **Script**: R scripts used for the analyses - `1_PreProcessing_Data.R`: Preprocessing, cell filtering and Full object creation - `2_Infertility_scRNAseq_analysis.R`: - `3_SubsetAnalysis_Annotations.R`: subset analyses of T cells and cluster manual annotation - `4_ScoreAnalysis_TcellSubset.R`: - `5_Visualization_Export_Data.R`: - **Data**: results of scRNAseq analysis: