Evidence map›Paper›PMID 37243667›Full record

ArticleBioinformatics (Oxford, England)2023

IndepthPathway: an integrated tool for in-depth pathway enrichment analysis based on single-cell sequencing data.

Sanghoon Lee, Letian Deng, Yue Wang, Kai Wang, Maureen A Sartor, Xiao-Song Wang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sanghoon LeeUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15232, United States.
Letian DengUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15232, United States.
Yue WangUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15232, United States.
Kai WangDepartment of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.
Maureen A SartorDepartment of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0001-6155-5702
Xiao-Song WangUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA 15232, United States.ORCID 0000-0002-2570-7139

Funding

Strategic Vision & Impact on Environmental HealthP30ES017885 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Dana Dolinoy · 2011 to 2026
$21.3M
CHARACTERIZATION OF RECURRENT ADJACENT GENE TRANSLOCATIONS IN BREAST CANCERR01CA183976 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, XIAOSONG · 2014 to 2019
$1.6M
Integrative Consig: NLK as Attractive Drug Target for Intractable Breast CancerR01CA181368 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, XIAOSONG · 2014 to 2018
$1.6M
Characterization of EPHA3 intragenic rearrangements in high-grade serous carcinoma progression and recurrenceR21CA237964 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, XIAOSONG · 2020 to 2021
$402k
NCI NIH HHS R01 CA181368NCI NIH HHS R01 CA183976NCI NIH HHS R21 CA237964NIEHS NIH HHS P30 ES017885
6 · The paper itself

Abstract

motivationSingle-cell sequencing enables exploring the pathways and processes of cells, and cell populations. However, there is a paucity of pathway enrichment methods designed to tolerate the high noise and low gene coverage of this technology. When gene expression data are noisy and signals are sparse, testing pathway enrichment based on the genes expression may not yield statistically significant results, which is particularly problematic when detecting the pathways enriched in less abundant cells that are vulnerable to disturbances.

resultsIn this project, we developed a Weighted Concept Signature Enrichment Analysis specialized for pathway enrichment analysis from single-cell transcriptomics (scRNA-seq). Weighted Concept Signature Enrichment Analysis took a broader approach for assessing the functional relations of pathway gene sets to differentially expressed genes, and leverage the cumulative signature of molecular concepts characteristic of the highly differentially expressed genes, which we termed as the universal concept signature, to tolerate the high noise and low coverage of this technology. We then incorporated Weighted Concept Signature Enrichment Analysis into an R package called "IndepthPathway" for biologists to broadly leverage this method for pathway analysis based on bulk and single-cell sequencing data. Through simulating technical variability and dropouts in gene expression characteristic of scRNA-seq as well as benchmarking on a real dataset of matched single-cell and bulk RNAseq data, we demonstrate that IndepthPathway presents outstanding stability and depth in pathway enrichment results under stochasticity of the data, thus will substantially improve the scientific rigor of the pathway analysis for single-cell sequencing data. AVAILABILITY AND IMPLEMENTATION: The IndepthPathway R package is available through: https://github.com/wangxlab/IndepthPathway.

Indexed as

Single-Cell AnalysisSoftwareExome SequencingGene Expression ProfilingSequence Analysis, RNA

Identifiers

PMID37243667
PMCPMC10275909

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.