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Rosario Astaburuaga-García

dblp:426/4474 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2024
0000-0003-1179-4080ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 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 › single-cell analysis › cytometry data analysis
mass cytometry data analysis
0.812024
RUCova: Removal of Unwanted Covariance in mass cytometry data · Bioinform. 2024
Bioinformatics and computational biology
single-cell analysis
0.812024
RUCova: Removal of Unwanted Covariance in mass cytometry data · Bioinform. 2024

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

principal component analysis · 0.8multivariate linear regression · 0.8
YearPublicationVenuePosition
2024 RUCova: Removal of Unwanted Covariance in mass cytometry data
abstract
MOTIVATION: High dimensional single-cell mass cytometry data are confounded by unwanted covariance due to variations in cell size and staining efficiency, making analysis, and interpretation challenging. RESULTS: We present RUCova, a novel method designed to address confounding factors in mass cytometry data. RUCova removes unwanted covariance from measured markers applying multivariate linear regression based on surrogates of sources of unwanted covariance (SUCs) and principal component analysis (PCA). We exemplify the use of RUCova and show that it effectively removes unwanted covariance while preserving genuine biological signals. Our results demonstrate the efficacy of RUCova in elucidating complex data patterns, facilitating the identification of activated signalling pathways, and improving the classification of important cell populations such as apoptotic cells. By providing a robust framework for data normalization and interpretation, RUCova enhances the accuracy and reliability of mass cytometry analyses, contributing to advances in our understanding of cellular biology and disease mechanisms. AVAILABILITY AND IMPLEMENTATION: The R package is available on https://github.com/molsysbio/RUCova. Detailed documentation, data, and the code required to reproduce the results are available on https://doi.org/10.5281/zenodo.10913464.
Rosario Astaburuaga-García, Thomas Sell, Samet Mutlu, Anja Sieber, Kirsten Lauber, Nils Blüthgen
Bioinform.1