Robust reconstruction of single-cell RNA-seq data with iterative gene weight updates

被引:0
|
作者
Sheng, Yueqi [1 ]
Barak, Boaz [1 ]
Nitzan, Mor [2 ]
机构
[1] Harvard Univ, Sch Engn & Appl Sci, Boston, MA 02134 USA
[2] Hebrew Univ Jerusalem, Racah Inst Phys, Fac Med, Sch Comp Sci & Engn, IL-9190401 Jerusalem, Israel
基金
欧洲研究理事会; 以色列科学基金会;
关键词
D O I
10.1093/bioinformatics/btad253
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation Single-cell RNA-sequencing technologies have greatly enhanced our understanding of heterogeneous cell populations and underlying regulatory processes. However, structural (spatial or temporal) relations between cells are lost during cell dissociation. These relations are crucial for identifying associated biological processes. Many existing tissue-reconstruction algorithms use prior information about subsets of genes that are informative with respect to the structure or process to be reconstructed. When such information is not available, and in the general case when the input genes code for multiple processes, including being susceptible to noise, biological reconstruction is often computationally challenging. Results We propose an algorithm that iteratively identifies manifold-informative genes using existing reconstruction algorithms for single-cell RNA-seq data as subroutine. We show that our algorithm improves the quality of tissue reconstruction for diverse synthetic and real scRNA-seq data, including data from the mammalian intestinal epithelium and liver lobules. Availability and implementation The code and data for benchmarking are available at github.com/syq2012/iterative_weight_update_for_reconstruction.
引用
收藏
页码:i423 / i430
页数:8
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