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Austin Rayford

dblp:424/4601 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2025
0000-0002-6298-1591ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › omics data analysis
cell-type deconvolution
0.912025
HIDE: hierarchical cell-type deconvolution · Bioinform. 2025
Bioinformatics and computational biology
transcriptomics
0.912025
HIDE: hierarchical cell-type deconvolution · Bioinform. 2025

Methods — techniques the papers use, named apart from their topics

linear combination reconstruction · 0.9hierarchical bayesian modeling · 0.9
YearPublicationVenuePosition
2025 HIDE: hierarchical cell-type deconvolution
abstract
MOTIVATION: Cell-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. RESULTS: Here, 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. AVAILABILITY AND IMPLEMENTATION: A python implementation of HIDE is available at zenodo (doi: 10.5281/zenodo.14724906).
Dennis Völkl, Malte Mensching-Buhr, Thomas Sterr, Sarah Bolz, Andreas Schäfer 0005, Nicole Seifert, Jana Tauschke, Austin Rayford, Oddbjørn Straume, Helena U. Zacharias, Sushma Nagaraja Grellscheid, Tim Beißbarth, Michael Altenbuchinger, Franziska Görtler
Bioinform.8