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scHLAcount: Allele-specific HLA expression from single-cell gene expression data

scHLAcount: Allele-specific HLA expression from single-cell gene expression data

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2282307655

scHLAcount: Allele-specific HLA expression from single-cell gene expression data

About this item

Full title

scHLAcount: Allele-specific HLA expression from single-cell gene expression data

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2019-08

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Studies in bulk RNA sequencing data suggest cell-type and allele-specific expression of the human leukocyte antigen (HLA) genes. These loci are extremely diverse and they function as part of the major histocompatibility complex (MHC) which is responsible for antigen presentation. Mutation and or misregulation of expression of HLA genes has implications in diseases, especially cancer. Immune responses to tumor cells can be evaded through HLA loss of function. However, bulk RNA-seq does not fully disentangle cell type specificity and allelic expression. Here we present scHLAcount, a workflow for computing allele-specific molecule counts of the HLA genes in single cells an individualized reference. We demonstrate that scHLAcount can be used to find cell-type specific allelic expression of HLA genes in blood cells, and detect different allelic expression patterns between tumor and normal cells in patient biopsies. scHLAcount is available at https://github.com/10XGenomics/scHLAcount. Footnotes * https://github.com/10XGenomics/scHLAcount...

Alternative Titles

Full title

scHLAcount: Allele-specific HLA expression from single-cell gene expression data

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2282307655

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2282307655

Other Identifiers

E-ISSN

2692-8205

DOI

10.1101/750612