Evidence map›Paper›PMID 38974799›Full record

ArticleNAR genomics and bioinformatics2024

Fast clustering and cell-type annotation of scATAC data using pre-trained embeddings.

Nathan J LeRoy, Jason P Smith, Guangtao Zheng, Julia Rymuza, Erfaneh Gharavi, Donald E Brown, Aidong Zhang, Nathan C Sheffield

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2024. 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.

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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

8 authors.

Nathan J LeRoyCenter for Public Health Genomics, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0000-0002-7354-7213
Jason P SmithCenter for Public Health Genomics, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0000-0002-2688-0988
Guangtao ZhengDepartment of Computer Science, School of Engineering, University of Virginia, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0000-0002-1287-4931
Julia RymuzaCenter for Public Health Genomics, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0009-0009-2762-9048
Erfaneh GharaviCenter for Public Health Genomics, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0000-0003-4444-2751
Donald E BrownSchool of Data Science, University of Virginia, Charlottesville, VA 22904, USA.ORCID https://orcid.org/0000-0002-9140-2632
Aidong ZhangDepartment of Biomedical Engineering, School of Medicine, University of Virginia, Charlottesville, VA 22904, USA.ORCID https://orcid.org/0000-0001-9723-3246
Nathan C SheffieldCenter for Public Health Genomics, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID https://orcid.org/0000-0001-5643-4068

Funding

Single-Cell Epigenomics, Transcriptomics, and Bioinformatics CoreP50DK096373 · NIDDK · UNIVERSITY OF VIRGINIA · PI PATRICIO E. RAY · 2012 to 2026
$13.8M
A modular data analysis ecosystem using portable encapsulated projectsR35GM128636 · NIGMS · UNIVERSITY OF VIRGINIA · PI SHEFFIELD, NATHAN · 2018 to 2022
$1.9M
Novel methods for large-scale genomic interval comparisonR01HG012558 · NHGRI · UNIVERSITY OF VIRGINIA · PI SHEFFIELD, NATHAN · 2022 to 2025
$1.8M
Interdisciplinary Training in Systems & Biomolecular Data ScienceT32GM145443 · NIGMS · UNIVERSITY OF VIRGINIA · PI Kevin A Janes, Jason Papin · 2022 to 2026
$1.5M
NHGRI NIH HHS R01 HG012558NIDDK NIH HHS P50 DK096373NIGMS NIH HHS R35 GM128636NIGMS NIH HHS T32 GM145443
6 · The paper itself

Abstract

Data from the single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq) are now widely available. One major computational challenge is dealing with high dimensionality and inherent sparsity, which is typically addressed by producing lower dimensional representations of single cells for downstream clustering tasks. Current approaches produce such individual cell embeddings directly through a one-step learning process. Here, we propose an alternative approach by building embedding models pre-trained on reference data. We argue that this provides a more flexible analysis workflow that also has computational performance advantages through transfer learning. We implemented our approach in scEmbed, an unsupervised machine-learning framework that learns low-dimensional embeddings of genomic regulatory regions to represent and analyze scATAC-seq data. scEmbed performs well in terms of clustering ability and has the key advantage of learning patterns of region co-occurrence that can be transferred to other, unseen datasets. Moreover, models pre-trained on reference data can be exploited to build fast and accurate cell-type annotation systems without the need for other data modalities. scEmbed is implemented in Python and it is available to download from GitHub. We also make our pre-trained models available on huggingface for public use. scEmbed is open source and available at https://github.com/databio/geniml. Pre-trained models from this work can be obtained on huggingface: https://huggingface.co/databio.

Identifiers

PMID38974799
PMCPMC11224678

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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.