» Articles » PMID: 31743345

ADAPTS: Automated Deconvolution Augmentation of Profiles for Tissue Specific Cells

Overview
Journal PLoS One
Date 2019 Nov 20
PMID 31743345
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Immune cell infiltration of tumors and the tumor microenvironment can be an important component for determining patient outcomes. For example, immune and stromal cell presence inferred by deconvolving patient gene expression data may help identify high risk patients or suggest a course of treatment. One particularly powerful family of deconvolution techniques uses signature matrices of genes that uniquely identify each cell type as determined from single cell type purified gene expression data. Many methods from this family have been recently published, often including new signature matrices appropriate for a single purpose, such as investigating a specific type of tumor. The package ADAPTS helps users make the most of this expanding knowledge base by introducing a framework for cell type deconvolution. ADAPTS implements modular tools for customizing signature matrices for new tissue types by adding custom cell types or building new matrices de novo, including from single cell RNAseq data. It includes a common interface to several popular deconvolution algorithms that use a signature matrix to estimate the proportion of cell types present in heterogenous samples. ADAPTS also implements a novel method for clustering cell types into groups that are difficult to distinguish by deconvolution and then re-splitting those clusters using hierarchical deconvolution. We demonstrate that the techniques implemented in ADAPTS improve the ability to reconstruct the cell types present in a single cell RNAseq data set in a blind predictive analysis. ADAPTS is currently available for use in R on CRAN and GitHub.

Citing Articles

Cell-type deconvolution for bulk RNA-seq data using single-cell reference: a comparative analysis and recommendation guideline.

Xu X, Li R, Mo O, Liu K, Li J, Hao P Brief Bioinform. 2025; 26(1).

PMID: 39899596 PMC: 11789683. DOI: 10.1093/bib/bbaf031.


Oncolytic immunotherapy with nivolumab in muscle-invasive bladder cancer: a phase 1b trial.

Li R, Villa N, Yu X, Johnson J, Borjas G, Dhillon J Nat Med. 2024; 31(1):176-188.

PMID: 39521884 DOI: 10.1038/s41591-024-03324-9.


Multi-omics reveal immune microenvironment alterations in multiple myeloma and its precursor stages.

Cheng Y, Sun F, Alapat D, Wanchai V, Mery D, Siegel E Blood Cancer J. 2024; 14(1):194.

PMID: 39505839 PMC: 11541562. DOI: 10.1038/s41408-024-01172-x.


An optimized pipeline for high-throughput bulk RNA-Seq deconvolution illustrates the impact of obesity and weight loss on cell composition of human adipose tissue.

Ahn C, Divoux A, Zhou M, Seldin M, Sparks L, Whytock K bioRxiv. 2024; .

PMID: 39386599 PMC: 11463495. DOI: 10.1101/2024.09.23.614489.


Characterization of driver mutations identifies gene signatures predictive of prognosis and treatment sensitivity in multiple myeloma.

Li J, Parthasarathy A, Kannappan A, Arsang-Jang S, Dong J, Cheng C Oncologist. 2024; 29(11):e1552-e1564.

PMID: 39250742 PMC: 11639189. DOI: 10.1093/oncolo/oyae244.


References
1.
Newman A, Steen C, Liu C, Gentles A, Chaudhuri A, Scherer F . Determining cell type abundance and expression from bulk tissues with digital cytometry. Nat Biotechnol. 2019; 37(7):773-782. PMC: 6610714. DOI: 10.1038/s41587-019-0114-2. View

2.
Gaujoux R, Seoighe C . CellMix: a comprehensive toolbox for gene expression deconvolution. Bioinformatics. 2013; 29(17):2211-2. DOI: 10.1093/bioinformatics/btt351. View

3.
Erkkila T, Lehmusvaara S, Ruusuvuori P, Visakorpi T, Shmulevich I, Lahdesmaki H . Probabilistic analysis of gene expression measurements from heterogeneous tissues. Bioinformatics. 2010; 26(20):2571-7. PMC: 2951082. DOI: 10.1093/bioinformatics/btq406. View

4.
Bianchi G, Munshi N . Pathogenesis beyond the cancer clone(s) in multiple myeloma. Blood. 2015; 125(20):3049-58. PMC: 4432002. DOI: 10.1182/blood-2014-11-568881. View

5.
Lahdesmaki H, Shmulevich L, Dunmire V, Yli-Harja O, Zhang W . In silico microdissection of microarray data from heterogeneous cell populations. BMC Bioinformatics. 2005; 6:54. PMC: 1274251. DOI: 10.1186/1471-2105-6-54. View