High-Order Correlation Integration for Single-Cell or Bulk RNA-seq Data Analysis
Quantifying or labeling the sample type with high quality is a challenging task, which is a key step for understanding complex diseases. Reducing noise pollution to data and ensuring the extracted intrinsic patterns in concordance with the primary data structure are important in sample clustering an...
Main Authors: | Hui Tang, Tao Zeng, Luonan Chen |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2019-04-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fgene.2019.00371/full |
Similar Items
-
Interpreting Functional Impact of Genetic Variations by Network QTL for Genotype–Phenotype Association Study
by: Kai Yuan, et al.
Published: (2022-01-01) -
Identifying Critical States of Complex Diseases by Single-Sample Jensen-Shannon Divergence
by: Jinling Yan, et al.
Published: (2021-06-01) -
c-CSN: Single-cell RNA Sequencing Data Analysis by Conditional Cell-specific Network
by: Lin Li, et al.
Published: (2021-04-01) -
RDAClone: Deciphering Tumor Heterozygosity through Single-Cell Genomics Data Analysis with Robust Deep Autoencoder
by: Jie Xia, et al.
Published: (2021-11-01) -
Systems biology intertwines with single cell and AI
by: Yong Wang, et al.
Published: (2019-05-01)