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Pengchao Ye

dblp:210/2153 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2020
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis › single-cell data preprocessing
dropout imputation
0.412020
scHinter: imputing dropout events for single-cell RNA-seq data with limited sample size · Bioinform. 2020
Bioinformatics and computational biology › single-cell analysis › single-cell RNA sequencing
single-cell RNA-seq analysis
0.412020
scHinter: imputing dropout events for single-cell RNA-seq data with limited sample size · Bioinform. 2020
Bioinformatics and computational biology
transcriptomics
0.412020
scHinter: imputing dropout events for single-cell RNA-seq data with limited sample size · Bioinform. 2020

Methods — techniques the papers use, named apart from their topics

synthetic minority over-sampling · 0.4hierarchical framework · 0.4ensemble distance · 0.4
YearPublicationVenuePosition
2020 scHinter: imputing dropout events for single-cell RNA-seq data with limited sample size
abstract
MOTIVATION: Single-cell RNA-sequencing (scRNA-seq) is fast and becoming a powerful technique for studying dynamic gene regulation at unprecedented resolution. However, scRNA-seq data suffer from problems of extremely high dropout rate and cell-to-cell variability, demanding new methods to recover gene expression loss. Despite the availability of various dropout imputation approaches for scRNA-seq, most studies focus on data with a medium or large number of cells, while few studies have explicitly investigated the differential performance across different sample sizes or the applicability of the approach on small or imbalanced data. It is imperative to develop new imputation approaches with higher generalizability for data with various sample sizes. RESULTS: We proposed a method called scHinter for imputing dropout events for scRNA-seq with special emphasis on data with limited sample size. scHinter incorporates a voting-based ensemble distance and leverages the synthetic minority oversampling technique for random interpolation. A hierarchical framework is also embedded in scHinter to increase the reliability of the imputation for small samples. We demonstrated the ability of scHinter to recover gene expression measurements across a wide spectrum of scRNA-seq datasets with varied sample sizes. We comprehensively examined the impact of sample size and cluster number on imputation. Comprehensive evaluation of scHinter across diverse scRNA-seq datasets with imbalanced or limited sample size showed that scHinter achieved higher and more robust performance than competing approaches, including MAGIC, scImpute, SAVER and netSmooth. AVAILABILITY AND IMPLEMENTATION: Freely available for download at https://github.com/BMILAB/scHinter. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Pengchao Ye, Wenbin Ye 0002, Congting Ye, Shuchao Li, Lishan Ye, Guoli Ji
Bioinform.1