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Kara J. Mould

dblp:426/1612 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2025
—ORCID · unresolved

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 › single-cell analysis
single-cell RNA sequencing
0.912025
Simulating paired and longitudinal single-cell RNA sequencing data with rescueSim · Bioinform. 2025
Bioinformatics and computational biology
power analysis
0.312025
Simulating paired and longitudinal single-cell RNA sequencing data with rescueSim · Bioinform. 2025

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

gamma-poisson model · 0.9
YearPublicationVenuePosition
2025 Simulating paired and longitudinal single-cell RNA sequencing data with rescueSim
abstract
MOTIVATION: As single-cell RNA-sequencing (scRNA-seq) becomes more widely used in transcriptomic research, complex experimental designs, such as paired or longitudinal studies, become increasingly feasible. Paired/longitudinal scRNA-seq enables the study of transcriptomic changes over time within specific cell types, yet guidance on analytical approaches and resources for study planning, such as power analysis, remains limited. Data simulation is a valuable tool for evaluating analysis method performance and informing study design decisions, including sample size selection. Currently, most scRNA-seq simulation methods simulate cells for a single sample, thus ignoring the between-sample and between-subject variability inherent to paired/longitudinal scRNA-seq data. RESULTS: Here, we introduce rescueSim (REpeated measures Single Cell RNA-seqUEncing data SIMulation), a novel method that simulates paired/longitudinal scRNA-seq data using a gamma-Poisson framework and incorporates additional variability between samples and subjects. We demonstrate our method's ability to reproduce important data properties and demonstrate its application in study planning. AVAILABILITY AND IMPLEMENTATION: rescueSim is implemented as an R package and is available at https://github.com/ewynn610/rescueSim.
Elizabeth Wynn, Kara J. Mould, Brian Vestal, Camille M. Moore
Bioinform.2