scHLAcount
scHLAcount quantifies allele-specific expression of HLA class I (HLA-A, HLA-B, HLA-C) and class II (DPA1, DPB1, DRA1, DRB1, DQA1, DQB1) genes from single-cell RNA-seq data to enable cell-type-specific and allelic-resolution studies of immune-related biology.
Key Features:
- Allele-specific HLA expression analysis: Counts molecules specific to HLA alleles in single-cell RNA-seq data for both class I and class II genes.
- Personalized reference genome: Uses an individualized reference genome to improve accuracy of allele-specific quantification.
- HLA typing and quantification: Accepts known HLA types from external methods or calls HLA types directly from the data and quantifies expression against those calls.
- Cell-type-specific detection: Enables identification of cell-type-specific allelic expression patterns across single cells, including comparisons between blood cells and tumor versus normal tissue.
- Disease-focused allelic comparisons: Detects differential allelic expression patterns between tumor and normal cells relevant to immune evasion and HLA loss-of-function analyses.
Scientific Applications:
- Cancer immunology: Characterizes how HLA allelic expression and loss contribute to tumor immune evasion.
- Transplantation medicine: Provides allele-specific expression information relevant to graft rejection and compatibility studies.
- Autoimmune disease research: Supports investigation of HLA allele-specific expression mechanisms underlying autoimmune disorders.
Methodology:
Computes allele-specific molecule counts from single-cell RNA-seq using an individualized reference genome, accepts supplied HLA types or calls HLA types from the data, and quantifies molecules against those allele calls.
Topics
Details
- License:
- MIT
- Programming Languages:
- R
- Added:
- 11/14/2019
- Last Updated:
- 12/17/2020
Operations
Publications
Darby CA, Stubbington MJT, Marks PJ, Barrio ÁM, Fiddes IT. scHLAcount: Allele-specific HLA expression from single-cell gene expression data. Unknown Journal. 2019. doi:10.1101/750612.
DOI: 10.1101/750612