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Eric Weine

dblp:345/6139 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2024
0009-0001-7809-1649ORCID · 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
single-cell RNA sequencing
0.812024
Accelerated dimensionality reduction of single-cell RNA sequencing data with fastglmpca · Bioinform. 2024
Bioinformatics and computational biology
count data modeling
0.212024
Accelerated dimensionality reduction of single-cell RNA sequencing data with fastglmpca · Bioinform. 2024

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

principal component analysis · 0.8parallel computing · 0.8alternating poisson regression · 0.8
YearPublicationVenuePosition
2024 Accelerated dimensionality reduction of single-cell RNA sequencing data with fastglmpca
abstract
SUMMARY: Motivated by theoretical and practical issues that arise when applying Principal component analysis (PCA) to count data, Townes et al. introduced "Poisson GLM-PCA", a variation of PCA adapted to count data, as a tool for dimensionality reduction of single-cell RNA sequencing (scRNA-seq) data. However, fitting GLM-PCA is computationally challenging. Here we study this problem, and show that a simple algorithm, which we call "Alternating Poisson Regression" (APR), produces better quality fits, and in less time, than existing algorithms. APR is also memory-efficient and lends itself to parallel implementation on multi-core processors, both of which are helpful for handling large scRNA-seq datasets. We illustrate the benefits of this approach in three publicly available scRNA-seq datasets. The new algorithms are implemented in an R package, fastglmpca. AVAILABILITY AND IMPLEMENTATION: The fastglmpca R package is released on CRAN for Windows, macOS and Linux, and the source code is available at github.com/stephenslab/fastglmpca under the open source GPL-3 license. Scripts to reproduce the results in this paper are also available in the GitHub repository and on Zenodo.
Eric Weine, Peter Carbonetto, Matthew Stephens
Bioinform.1