Evidence map›Paper›PMID 39502448›Full record

ReviewBioinformatics and biology insights2024

Approaches for Benchmarking Single-Cell Gene Regulatory Network Methods.

Karamveer, Yasin Uzun

Abstract readReview
In one paragraph

Review in Bioinformatics and biology insights, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
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

2 authors.

KaramveerDepartment of Pediatrics, The Pennsylvania State University College of Medicine, Hershey, PA, USA.ORCID https://orcid.org/0000-0002-5339-3317
Yasin UzunDepartment of Pediatrics, The Pennsylvania State University College of Medicine, Hershey, PA, USA.ORCID https://orcid.org/0000-0003-3478-3499

Funding

Integrated frameworks for single-cell epigenomics based transcriptional regulatory networksR35GM150616 · NIGMS · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Yasin Uzun · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM150616
6 · The paper itself

Abstract

Gene regulatory networks are powerful tools for modeling genetic interactions that control the expression of genes driving cell differentiation, and single-cell sequencing offers a unique opportunity to build these networks with high-resolution genomic data. There are many proposed computational methods to build these networks using single-cell data, and different approaches are used to benchmark these methods. However, a comprehensive discussion specifically focusing on benchmarking approaches is missing. In this article, we lay the GRN terminology, present an overview of common gold-standard studies and data sets, and define the performance metrics for benchmarking network construction methodologies. We also point out the advantages and limitations of different benchmarking approaches, suggest alternative ground truth data sets that can be used for benchmarking, and specify additional considerations in this context.

Indexed as

benchmarkingepigenomicsGene regulatory networksground truthsingle-cell genomics

Identifiers

PMID39502448
PMCPMC11536393

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.