Evidence map›Paper›PMID 31068142›Full record

ArticleBMC genomics2019

scNPF: an integrative framework assisted by network propagation and network fusion for preprocessing of single-cell RNA-seq data.

Wenbin Ye, Guoli Ji, Pengchao Ye, Yuqi Long, Xuesong Xiao, Shuchao Li, Yaru Su, Xiaohui Wu

Abstract read
In one paragraph

Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
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.

Wenbin YeDepartment of Automation, Xiamen University, Xiamen, 361005, China.
Guoli JiDepartment of Automation, Xiamen University, Xiamen, 361005, China.
Pengchao YeDepartment of Automation, Xiamen University, Xiamen, 361005, China.
Yuqi LongSoftware Quality Testing Engineering Research Center, China Electronic Product Reliability and Environmental Testing Research Institute, Guangzhou, 510610, China.
Xuesong XiaoDepartment of Automation, Xiamen University, Xiamen, 361005, China.
Shuchao LiDepartment of Automation, Xiamen University, Xiamen, 361005, China.
Yaru SuCollege of Mathematics and Computer Science, Fuzhou University, Fuzhou, 350116, China.
Xiaohui WuDepartment of Automation, Xiamen University, Xiamen, 361005, China. xhuister@xmu.edu.cn.

Funding

National Natural Science Foundation of China 61673323National Natural Science Foundation of China 61871463
6 · The paper itself

Abstract

backgroundSingle-cell RNA-sequencing (scRNA-seq) is fast becoming a powerful tool for profiling genome-scale transcriptomes of individual cells and capturing transcriptome-wide cell-to-cell variability. However, scRNA-seq technologies suffer from high levels of technical noise and variability, hindering reliable quantification of lowly and moderately expressed genes. Since most downstream analyses on scRNA-seq, such as cell type clustering and differential expression analysis, rely on the gene-cell expression matrix, preprocessing of scRNA-seq data is a critical preliminary step in the analysis of scRNA-seq data.

resultsWe presented scNPF, an integrative scRNA-seq preprocessing framework assisted by network propagation and network fusion, for recovering gene expression loss, correcting gene expression measurements, and learning similarities between cells. scNPF leverages the context-specific topology inherent in the given data and the priori knowledge derived from publicly available molecular gene-gene interaction networks to augment gene-gene relationships in a data driven manner. We have demonstrated the great potential of scNPF in scRNA-seq preprocessing for accurately recovering gene expression values and learning cell similarity networks. Comprehensive evaluation of scNPF across a wide spectrum of scRNA-seq data sets showed that scNPF achieved comparable or higher performance than the competing approaches according to various metrics of internal validation and clustering accuracy. We have made scNPF an easy-to-use R package, which can be used as a versatile preprocessing plug-in for most existing scRNA-seq analysis pipelines or tools.

conclusionsscNPF is a universal tool for preprocessing of scRNA-seq data, which jointly incorporates the global topology of priori interaction networks and the context-specific information encapsulated in the scRNA-seq data to capture both shared and complementary knowledge from diverse data sources. scNPF could be used to recover gene signatures and learn cell-to-cell similarities from emerging scRNA-seq data to facilitate downstream analyses such as dimension reduction, cell type clustering, and visualization.

Indexed as

Gene Expression RegulationGene Regulatory NetworksGenome, HumanSoftwareTranscriptomeAlgorithmsGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansSingle-Cell AnalysisCell type clusteringDropout imputationNetwork propagationSimilarity measurementSingle cell RNA-sequencing

Identifiers

PMID31068142
PMCPMC6505295

What OpenQuestion 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 OpenQuestion graph.