Evidence map›Paper›PMID 35715568›Full record

ArticleScientific reports2022

scCAN: single-cell clustering using autoencoder and network fusion.

Bang Tran, Duc Tran, Hung Nguyen, Seungil Ro, Tin Nguyen

Abstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Bang TranDepartment of Computer Science and Engineering, University of Nevada, Reno, NV, 89557, USA.
Duc TranDepartment of Computer Science and Engineering, University of Nevada, Reno, NV, 89557, USA.
Hung NguyenDepartment of Computer Science and Engineering, University of Nevada, Reno, NV, 89557, USA.
Seungil RoDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV, 89557, USA.
Tin NguyenDepartment of Computer Science and Engineering, University of Nevada, Reno, NV, 89557, USA. tinn@unr.edu.

Funding

Outreach/Diversity/Pipeline ProjectP20GM103440 · NIGMS · UNIVERSITY OF NEVADA RENO · PI Julia Petereit · 2012 to 2026
$58.0M
NIH HHS GM103440
6 · The paper itself

Abstract

Unsupervised clustering of single-cell RNA sequencing data (scRNA-seq) is important because it allows us to identify putative cell types. However, the large number of cells (up to millions), the high-dimensionality of the data (tens of thousands of genes), and the high dropout rates all present substantial challenges in single-cell analysis. Here we introduce a new method, named single-cell Clustering using Autoencoder and Network fusion (scCAN), that can overcome these challenges to accurately segregate different cell types in large and sparse scRNA-seq data. In an extensive analysis using 28 real scRNA-seq datasets (more than three million cells) and 243 simulated datasets, we validate that scCAN: (1) correctly estimates the number of true cell types, (2) accurately segregates cells of different types, (3) is robust against dropouts, and (4) is fast and memory efficient. We also compare scCAN with CIDR, SEURAT3, Monocle3, SHARP, and SCANPY. scCAN outperforms these state-of-the-art methods in terms of both accuracy and scalability. The scCAN package is available at https://cran.r-project.org/package=scCAN . Data and R scripts are available at http://sccan.tinnguyen-lab.com/.

Indexed as

Cell CommunicationSingle-Cell AnalysisCluster AnalysisExome SequencingGene Expression ProfilingSequence Analysis, RNA

Identifiers

PMID35715568
PMCPMC9206025

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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.