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Ross F. Laidlaw

dblp:425/2691 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2025
0009-0006-9559-7218ORCID · 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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
gene expression dynamics
0.912025
TrAGEDy - trajectory alignment of gene expression dynamics · Bioinform. 2025
Bioinformatics and computational biology › single-cell analysis
single-cell transcriptomics
0.912025
TrAGEDy - trajectory alignment of gene expression dynamics · Bioinform. 2025
Bioinformatics and computational biology › single-cell analysis
single-cell RNA sequencing
0.312025
TrAGEDy - trajectory alignment of gene expression dynamics · Bioinform. 2025

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

trajectory alignment · 0.9
YearPublicationVenuePosition
2025 TrAGEDy - trajectory alignment of gene expression dynamics
abstract
MOTIVATION: Single-cell transcriptomics sequencing is used to compare different biological processes. However, often, those processes are asymmetric which are difficult to integrate. Current approaches often rely on integrating samples from each condition before either cluster-based comparisons or analysis of an inferred shared trajectory. RESULTS: We present Trajectory Alignment of Gene Expression Dynamics (TrAGEDy), which allows the alignment of independent trajectories to avoid the need for error-prone integration steps. Across simulated datasets, TrAGEDy returns the correct underlying alignment of the datasets, outperforming current tools which fail to capture the complexity of asymmetric alignments. When applied to real datasets, TrAGEDy captures more biologically relevant genes and processes, which other differential expression methods fail to detect when looking at the developments of T cells and the bloodstream forms of Trypanosoma brucei when affected by genetic knockouts. AVAILABILITY AND IMPLEMENTATION: TrAGEDy is freely available at https://github.com/No2Ross/TrAGEDy, and implemented in R.
Ross F. Laidlaw, Emma M. Briggs, Keith R. Matthews, Amir Madany Mamlouk, Richard McCulloch, Thomas D. Otto
Bioinform.1