Single-Cell Transcriptomics
Please, contact us to discuss how we can be of assistance in achieving your project goals or to receive a quote for your project.
Single-cell RNA sequencing (scRNA-seq) captures transcriptomic profiles of individual cells, revealing cellular heterogeneity hidden in bulk analyses. HPCBio can perform analyses that will
- Transform your raw FASTQ files to cell-specific gene counts, quality-filtered to remove empty droplets, dying cells (high mitochondrial %), and doublets,
- Normalize and visualize data to assess the global structure of cell populations,
- Cluster cells with similar transcriptional profiles into putative cell types or states, and
- Perform cell type annotation using known marker genes, automated reference-based tools, or differential expression between clusters.
Follow-Up Analyses:
- Trajectory / Pseudotime Analysis – Infer developmental or differentiation paths (Monocle 3, scVelo for RNA velocity)
- Cell–Cell Communication – Infer ligand-receptor interactions between cell types (CellChat, NicheNet, LIANA)
- Gene Regulatory Networks – Reconstruct transcription factor regulons (SCENIC/pySCENIC)
- Multi-omics Integration – Joint analysis with ATAC-seq, proteomics, or spatial data (Seurat v5, MOFA+, WNN)
- Spatial Transcriptomics – Map gene expression in tissue context (Visium, Xenium, MERFISH + Squidpy/Giotto)
- Compositional Analysis – Test changes in cell type proportions across conditions (scCODA, propeller)
- Gene Set / Pathway Scoring – Score cells for pathway activity (AUCell, decoupleR, GSVA)
- Perturbation Analysis – Model transcriptional responses to genetic or drug perturbations (scGen, CellOracle)
We have experience with tools such as:
- The 10x Genomics pipeline (Cell Ranger, Loupe Browser)
- Curio Bioscience data workflow
- Parse Bioscience data workflow
- alevin-fry / STARsolo / Kallisto|bustools – alignment and quantification
- Seurat –scRNA-seq analysis
- Scanpy– Python equivalent of Seurat
- scDblFinder / DoubletFinder– Doublet detection and removal
- Harmony / scVI / BBKNN– Batch correction and data integration across samples
- CellTypist / SingleR– Automated reference-based cell type annotation
- edgeR – Differential gene expression testing