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# Amodio_Infertility_2024
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Amodio G, Giacomini G, Boeri L, et al. **T cell exhaustion and senescence signatures characterize and differentiate infertile men**

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### 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).
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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:
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   - 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 
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      - Default Seurat settings [(NormalizeData function)](https://satijalab.org/seurat/reference/normalizedata)
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   - Scaling: 
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      - 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).
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   - 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

  
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### Directories and Files ###
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- **Script**: R scripts used for the analyses
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  - `1_PreProcessing_Data.R`: Preprocessing, cell filtering and Full object creation
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  - `2_Infertility_scRNAseq_analysis.R`: 
  - `3_SubsetAnalysis_Annotations.R`: subset analyses of T cells and cluster manual annotation
  - `4_ScoreAnalysis_TcellSubset.R`: 
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  - `5_Visualization_Export_Data.R`: 
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- **Data**: results of scRNAseq analysis: 
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