Evidence map›Paper›PMID 39110511›Full record

ArticleBioinformatics (Oxford, England)2024

Accelerated dimensionality reduction of single-cell RNA sequencing data with fastglmpca.

Eric Weine, Peter Carbonetto, Matthew Stephens

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Eric WeineLaboratory for Information and Decision Systems, Massachusetts Institute of Technology, Cambridge, MA 02139, United States.ORCID 0009-0001-7809-1649
Peter CarbonettoDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, United States.
Matthew StephensDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, United States.

Funding

Genome analysis: statistical methods and applicationsR01HG002585 · NHGRI · UNIVERSITY OF WASHINGTON · PI MATTHEW STEPHENS · 2002 to 2026
$8.4M
NHGRI NIH HHS R01 HG002585NIH HHS R01HG002585
6 · The paper itself

Abstract

summaryMotivated 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.

Indexed as

AlgorithmsSequence Analysis, RNASingle-Cell AnalysisSoftwareHumansPrincipal Component Analysis

Identifiers

PMID39110511
PMCPMC11322042

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.