Evidence map›Paper›PMID 37106779›Full record

ArticleBiology2023

SigPrimedNet: A Signaling-Informed Neural Network for scRNA-seq Annotation of Known and Unknown Cell Types.

Pelin Gundogdu, Inmaculada Alamo, Isabel A Nepomuceno-Chamorro, Joaquin Dopazo, Carlos Loucera

Abstract read
In one paragraph

Article in Biology, 2023. 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. Pathway-guided architectures for interpretable AI in biological research.Computational and structural biotechnology journal · 2025
    Review
  3. 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

5 authors.

Pelin GundogduComputational Medicine Platform, Andalusian Public Foundation Progress and Health-FPS, 41013 Sevilla, Spain.ORCID 0000-0002-1791-9457
Inmaculada AlamoComputational Medicine Platform, Andalusian Public Foundation Progress and Health-FPS, 41013 Sevilla, Spain.ORCID 0000-0002-6295-0218
Isabel A Nepomuceno-ChamorroDpto. de Lenguajes y Sistemas Informáticos, Universidad de Sevilla, 41013 Seville, Spain.ORCID 0000-0002-4255-7160
Joaquin DopazoComputational Medicine Platform, Andalusian Public Foundation Progress and Health-FPS, 41013 Sevilla, Spain.ORCID 0000-0003-3318-120X
Carlos LouceraComputational Medicine Platform, Andalusian Public Foundation Progress and Health-FPS, 41013 Sevilla, Spain.ORCID 0000-0001-9598-6965

Funding

European Comission MLFPM2018 - Machine Learning Frontiers in Precision Medicine (813533)Instituto de Salud Carlos III IMP/0019Regional Government of Andalusia & European Social Fund PAIDI2020-DOC_00350Spanish Ministry of Science and Innovation PID2020-117954RB-C22Spanish Ministry of Science and Innovation PID2020-117979RB-I00
6 · The paper itself

Abstract

Single-cell RNA sequencing is increasing our understanding of the behavior of complex tissues or organs, by providing unprecedented details on the complex cell type landscape at the level of individual cells. Cell type definition and functional annotation are key steps to understanding the molecular processes behind the underlying cellular communication machinery. However, the exponential growth of scRNA-seq data has made the task of manually annotating cells unfeasible, due not only to an unparalleled resolution of the technology but to an ever-increasing heterogeneity of the data. Many supervised and unsupervised methods have been proposed to automatically annotate cells. Supervised approaches for cell-type annotation outperform unsupervised methods except when new (unknown) cell types are present. Here, we introduce SigPrimedNet an artificial neural network approach that leverages (i) efficient training by means of a sparsity-inducing signaling circuits-informed layer, (ii) feature representation learning through supervised training, and (iii) unknown cell-type identification by fitting an anomaly detection method on the learned representation. We show that SigPrimedNet can efficiently annotate known cell types while keeping a low false-positive rate for unseen cells across a set of publicly available datasets. In addition, the learned representation acts as a proxy for signaling circuit activity measurements, which provide useful estimations of the cell functionalities.

Indexed as

cell signalingcell-type identificationdeep learningexplainable artificial intelligencescRNA-seq

Identifiers

PMID37106779
PMCPMC10135788

What Socratic 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 Socratic graph.