Your browser doesn't support javascript.
loading
scEWE: high-order element-wise weighted ensemble clustering for heterogeneity analysis of single-cell RNA-sequencing data.
Huang, Yixiang; Jiang, Hao; Ching, Wai-Ki.
Afiliación
  • Huang Y; School of Mathematics, Renmin University of China, No. 59 Zhong guancun Street, 100872, Beijing, China.
  • Jiang H; School of Mathematics, Renmin University of China, No. 59 Zhong guancun Street, 100872, Beijing, China.
  • Ching WK; Department of Mathematics, The University of Hong Kong, Pokfulam Road, Hong Kong.
Brief Bioinform ; 25(3)2024 Mar 27.
Article en En | MEDLINE | ID: mdl-38701413
ABSTRACT
With the emergence of large amount of single-cell RNA sequencing (scRNA-seq) data, the exploration of computational methods has become critical in revealing biological mechanisms. Clustering is a representative for deciphering cellular heterogeneity embedded in scRNA-seq data. However, due to the diversity of datasets, none of the existing single-cell clustering methods shows overwhelming performance on all datasets. Weighted ensemble methods are proposed to integrate multiple results to improve heterogeneity analysis performance. These methods are usually weighted by considering the reliability of the base clustering results, ignoring the performance difference of the same base clustering on different cells. In this paper, we propose a high-order element-wise weighting strategy based self-representative ensemble learning framework scEWE. By assigning different base clustering weights to individual cells, we construct and optimize the consensus matrix in a careful and exquisite way. In addition, we extracted the high-order information between cells, which enhanced the ability to represent the similarity relationship between cells. scEWE is experimentally shown to significantly outperform the state-of-the-art methods, which strongly demonstrates the effectiveness of the method and supports the potential applications in complex single-cell data analytical problems.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Análisis de Secuencia de ARN / Análisis de la Célula Individual Límite: Humans Idioma: En Revista: Brief Bioinform Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Análisis de Secuencia de ARN / Análisis de la Célula Individual Límite: Humans Idioma: En Revista: Brief Bioinform Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: China