Evidence map›Paper›PMID 35591853›Full record

ArticleFrontiers in genetics2022

NISC: Neural Network-Imputation for Single-Cell RNA Sequencing and Cell Type Clustering.

Xiang Zhang, Zhuo Chen, Rahul Bhadani, Siyang Cao, Meng Lu, Nicholas Lytal, Yin Chen, Lingling An

Abstract read
In one paragraph

Article in Frontiers in genetics, 2022. 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. Review
  2. Article
  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

8 authors.

Xiang ZhangInterdisciplinary Program in Statistics and Data Science, University of Arizona, Tucson, AZ, United States.
Zhuo ChenInterdisciplinary Program in Statistics and Data Science, University of Arizona, Tucson, AZ, United States.
Rahul BhadaniInterdisciplinary Program in Statistics and Data Science, University of Arizona, Tucson, AZ, United States.
Siyang CaoDepartment of Electrical and Computer Engineering, University of Arizona, Tucson, AZ, United States.
Meng LuInterdisciplinary Program in Statistics and Data Science, University of Arizona, Tucson, AZ, United States.
Nicholas LytalInterdisciplinary Program in Statistics and Data Science, University of Arizona, Tucson, AZ, United States.
Yin ChenCollege of Pharmacy, University of Arizona, Tucson, AZ, United States.
Lingling AnInterdisciplinary Program in Statistics and Data Science, University of Arizona, Tucson, AZ, United States.

Funding

Regulatory and Human Study Operations (RHSO) Core CU19AG065169 · NIA · UNIVERSITY OF ARIZONA · PI SCHORK, NICHOLAS JOSEPH · 2021 to 2025
$59.8M
NIA NIH HHS U19 AG065169
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) reveals the transcriptome diversity in heterogeneous cell populations as it allows researchers to study gene expression at single-cell resolution. The latest advances in scRNA-seq technology have made it possible to profile tens of thousands of individual cells simultaneously. However, the technology also increases the number of missing values, i. e, dropouts, from technical constraints, such as amplification failure during the reverse transcription step. The resulting sparsity of scRNA-seq count data can be very high, with greater than 90% of data entries being zeros, which becomes an obstacle for clustering cell types. Current imputation methods are not robust in the case of high sparsity. In this study, we develop a Neural Network-based Imputation for scRNA-seq count data, NISC. It uses autoencoder, coupled with a weighted loss function and regularization, to correct the dropouts in scRNA-seq count data. A systematic evaluation shows that NISC is an effective imputation approach for handling sparse scRNA-seq count data, and its performance surpasses existing imputation methods in cell type identification.

Indexed as

autoencoderdeep learningdropoutimputationsingle cell RNA-seq

Identifiers

PMID35591853
PMCPMC9110639

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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.