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Rayford, A.

Publications and source records attributed to Rayford, A..

2 recordsLinked to original sources

HIDE: Hierarchical cell-type Deconvolution

MotivationCell-type deconvolution is a computational approach to infer cellular distributions from bulk transcriptomics data. Several methods have been proposed, each with its own advantages and disadvantages. Reference based approaches make use of archetypic transcriptomic profiles representing individual cell types. Those reference profiles are ideally chosen such that the observed bulks can be reconstructed as a linear combination thereof. This strategy, however, ignores the fact that cellular populations arise through the process of cellular differentiation, which entails the gradual emergence of cell groups with diverse morphological and functional characteristics. ResultsHere, we propose Hierarchical cell-type Deconvolution (HIDE), a cell-type deconvolution approach which incorporates a cell hierarchy for improved performance and interpretability. This is achieved by a hierarchical procedure that preserves estimates of major cell populations while inferring their respective subpopulations. We show in simulation studies that this procedure produces more reliable and more consistent results than other state-of-the-art approaches. Finally, we provide an example application of HIDE to explore breast cancer specimens from TCGA. AvailabilityA python implementation of HIDE is available at zenodo (doi:10.5281/zenodo.14724906). Supplementary informationSupplementary material is available at Bioinformatics online.

bioinformatics↗

Deconvolution of omics data in Python with Deconomix -- cellular compositions, cell-type specific gene regulation, and background contributions

BackgroundGene expression profiles derived from heterogeneous bulk samples contain signals from various cell populations. Cell-type deconvolution approaches are computational tools to reverse engineer the composition of bulks in term of cell populations. Accurate estimates of cell compositions are crucial for identifying cell populations relevant for disease. Moreover, analyses, such as the identification of differentially expressed genes, can be confounded by cellular composition, as differences in gene expression may arise from both variations in cellular composition and gene regulation. ResultsWe present Deconvolution of omics data (Deconomix) - a comprehensive toolbox for the cell-type deconvolution of bulk transcriptomics data, available as a Python package and standalone graphical user interface. Deconomix stands apart from competing solutions with rich functionality and highly efficient implementations. It facilitates (A) the inference of cellular compositions from bulk transcriptomics data, (B) the machine learning-based optimization of gene weights to resolve small cell populations and to disentangle phenotypically related cells, (C) the inference of background contributions which otherwise would deteriorate cell-type deconvolution, and (D) population estimates of cell-type specific gene regulation. To showcase the application of Deconomix, we present a case study on breast cancer data from TCGA, highlighting subtype-specific cellular compositions and cell-type-specific gene-regulatory programs. ConclusionWe present Deconomix, a comprehensive Python package including a graphical user interface for the inference of cellular compositions, cell-type-specific gene regulation, and background contributions from bulk transcriptomics data. O_TEXTBOXKey PointsO_LIDeconomix optimizes gene weights to disentangle small cell populations and phenotypically related cells. C_LIO_LIDeconomix estimates cell compositions, unknown background contributions and cell-type specific gene regulation from bulk transcriptomics data. C_LIO_LIA Python package is available as code repository and installable via PyPI [1]. C_LIO_LIA standalone graphical user interface is available as code repository [2]. C_LIO_LIAn exemplary analysis of a breast cancer case study is provided as tutorial [3]. C_LI C_TEXTBOX

bioinformatics↗