Evidence map›Paper›PMID 33355120›Full record

ArticleScience advances2020

Predicting transcription factor binding in single cells through deep learning.

Laiyi Fu, Lihua Zhang, Emmanuel Dollinger, Qinke Peng, Qing Nie, Xiaohui Xie

Abstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Modeling strategies forBioinformatics advances · 2026
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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.

Laiyi FuSystems Engineering Institute, School of Electronic and Information Engineering, Xi'an Jiaotong University, Xi'an, Shannxi 710049, China.ORCID 0000-0001-9086-3982
Lihua ZhangDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0001-7841-5562
Emmanuel DollingerDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.ORCID 0000-0002-2562-7980
Qinke PengSystems Engineering Institute, School of Electronic and Information Engineering, Xi'an Jiaotong University, Xi'an, Shannxi 710049, China.
Qing NieDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA. qnie@uci.edu xhx@uci.edu.ORCID 0000-0002-8804-3368
Xiaohui XieDepartment of Computer Science, University of California, Irvine, Irvine, CA 92697, USA. qnie@uci.edu xhx@uci.edu.ORCID 0000-0002-5479-6345

Funding

Shared Resource Core: Single Cell AnalysisU54CA217378 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI VAN ETTEN, RICHARD A. · 2018 to 2022
$9.7M
UCI P30 Skin Center Systems Biology CoreP30AR075047 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI ANDERSEN, BOGI, GANESAN, ANAND K · 2019 to 2025
$5.1M
Multiscale Models of Wound Cell Plasticity for RegenerationU01AR073159 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI DAI, XING, NIE, QING · 2018 to 2022
$3.5M
Mentor Training to enhance mentorship in an interdisciplinary training programT32GM136624 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Arthur D Lander, Qing Nie · 2020 to 2026
$3.1M
Mammary basal/stem cell plasticity and regulationR01GM123731 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI DAI, XING · 2017 to 2020
$1.9M
NCI NIH HHS U54 CA217378NIAMS NIH HHS P30 AR075047NIAMS NIH HHS U01 AR073159NIGMS NIH HHS R01 GM123731NIGMS NIH HHS T32 GM136624
6 · The paper itself

Abstract

Characterizing genome-wide binding profiles of transcription factors (TFs) is essential for understanding biological processes. Although techniques have been developed to assess binding profiles within a population of cells, determining them at a single-cell level remains elusive. Here, we report scFAN (single-cell factor analysis network), a deep learning model that predicts genome-wide TF binding profiles in individual cells. scFAN is pretrained on genome-wide bulk assay for transposase-accessible chromatin sequencing (ATAC-seq), DNA sequence, and chromatin immunoprecipitation sequencing (ChIP-seq) data and uses single-cell ATAC-seq to predict TF binding in individual cells. We demonstrate the efficacy of scFAN by both studying sequence motifs enriched within predicted binding peaks and using predicted TFs for discovering cell types. We develop a new metric "TF activity score" to characterize each cell and show that activity scores can reliably capture cell identities. scFAN allows us to discover and study cellular identities and heterogeneity based on chromatin accessibility profiles.

Identifiers

PMID33355120
PMCPMC11206197

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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.