Irina Voineagu

dblp:279/9947 · DBLP profile ↗
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3ranked-venue papers
0as first author
2since 2021 · last 2021
0000-0003-4162-3872ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 3 · 2 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
2 papers
Bioinformatics and computational biology · 100%
Computer graphics and multimedia
1 paper
Visualization and visual analytics · 100%

Topics — the 6 heaviest of 7, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genomics
0.512021
NeuroCirc: an integrative resource of circular RNA expression in the human brain · Bioinform. 2021
Bioinformatics and computational biology
transcriptomics
0.512021
NeuroCirc: an integrative resource of circular RNA expression in the human brain · Bioinform. 2021
Bioinformatics and computational biology › network bioinformatics › biological network analysis
network visualization
0.412020
TDAview: an online visualization tool for topological data analysis · Bioinform. 2020
Bioinformatics and computational biology
topological data analysis
0.412020
TDAview: an online visualization tool for topological data analysis · Bioinform. 2020
Bioinformatics and computational biology › neuroscience
neuroinformatics
0.112021
NeuroCirc: an integrative resource of circular RNA expression in the human brain · Bioinform. 2021
Visualization and visual analytics
biological data visualization
0.112020
TDAview: an online visualization tool for topological data analysis · Bioinform. 2020

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

mapper algorithm · 0.9
YearPublicationVenuePosition
2021 Supervised application of internal validation measures to benchmark dimensionality reduction methods in scRNA-seq data
abstract
A typical single-cell RNA sequencing (scRNA-seq) experiment will measure on the order of 20 000 transcripts and thousands, if not millions, of cells. The high dimensionality of such data presents serious complications for traditional data analysis methods and, as such, methods to reduce dimensionality play an integral role in many analysis pipelines. However, few studies have benchmarked the performance of these methods on scRNA-seq data, with existing comparisons assessing performance via downstream analysis accuracy measures, which may confound the interpretation of their results. Here, we present the most comprehensive benchmark of dimensionality reduction methods in scRNA-seq data to date, utilizing over 300 000 compute hours to assess the performance of over 25 000 low-dimension embeddings across 33 dimensionality reduction methods and 55 scRNA-seq datasets. We employ a simple, yet novel, approach, which does not rely on the results of downstream analyses. Internal validation measures (IVMs), traditionally used as an unsupervised method to assess clustering performance, are repurposed to measure how well-formed biological clusters are after dimensionality reduction. Performance was further evaluated over nearly 200 000 000 iterations of DBSCAN, a density-based clustering algorithm, showing that hyperparameter optimization using IVMs as the objective function leads to near-optimal clustering. Methods were also assessed on the extent to which they preserve the global structure of the data, and on their computational memory and time requirements across a large range of sample sizes. Our comprehensive benchmarking analysis provides a valuable resource for researchers and aims to guide best practice for dimensionality reduction in scRNA-seq analyses, and we highlight Latent Dirichlet Allocation and Potential of Heat-diffusion for Affinity-based Transition Embedding as high-performing algorithms.
Forrest C. Koch, Gavin J. Sutton, Irina Voineagu, Fatemeh Vafaee
Briefings Bioinform.3
2021 NeuroCirc: an integrative resource of circular RNA expression in the human brain
abstract
MOTIVATION: CircRNAs are covalently closed RNA molecules that are particularly abundant in the brain. While circRNA expression data from the human brain is rapidly accumulating, integration of large-scale datasets remains challenging and time-consuming, and consequently an integrative view of circRNA expression in the human brain is currently lacking. RESULTS: NeuroCirc is a web-based resource that allows interactive exploration of multiple types of circRNA data from the human brain, including large-scale expression datasets, circQTL data and circRNA expression across neuronal differentiation and cellular maturation time-courses. NeuroCirc also allows users to upload their own circRNA expression data and explore it in the integrative platform, thereby supporting circRNA prioritization for experimental validation and functional studies. AVAILABILITY AND IMPLEMENTATION: NeuroCirc is freely available at: https://voineagulab.github.io/NeuroCirc/. The source code and user documentation are available at: https://github.com/Voineagulab/NeuroCirc. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Kieran Walsh, Akira Gokool, Hamid Alinejad-Rokny, Irina Voineagu
Bioinform.4
2020 TDAview: an online visualization tool for topological data analysis
abstract
SUMMARY: TDAview is an online tool for topological data analysis (TDA) and visualization. It implements the Mapper algorithm for TDA and provides extensive graph visualization options. TDAview is a user-friendly tool that allows biologists and clinicians without programming knowledge to harness the power of TDA. TDAview supports an analysis and visualization mode in which a Mapper graph is constructed based on user-specified parameters, followed by graph visualization. It can also be used in a visualization only mode in which TDAview is used for visualizing the data properties of a Mapper graph generated using other open-source software. The graph visualization options allow data exploration by graphical display of metadata variable values for nodes and edges, as well as the generation of publishable figures. TDAview can handle large datasets, with tens of thousands of data points, and thus has a wide range of applications for high-dimensional data, including the construction of topology-based gene co-expression networks. AVAILABILITY AND IMPLEMENTATION: TDAview is a free online tool available at https://voineagulab.github.io/TDAview/. The source code, usage documentation and example data are available at TDAview GitHub repository: https://github.com/Voineagulab/TDAview.
Kieran Walsh, Mircea A. Voineagu, Fatemeh Vafaee, Irina Voineagu
Bioinform.4