We propose TWO-SIGMA-G, a competitive gene set test for scRNA-seq data. TWO-SIGMA-G uses a mixed-effects regression model based on our previously published TWO-SIGMA to test for differential expression at the gene-level. This regression-based model provides flexibility and rigor at the gene-level in (1) handling complex experimental designs, (2) accounting for the correlation between biological replicates and (3) accommodating the distribution of scRNA-seq data to improve statistical inference. Moreover, TWO-SIGMA-G uses a novel approach to adjust for inter-gene-correlation (IGC) at the set-level to control the set-level false positive rate. Simulations demonstrate that TWO-SIGMA-G preserves type-I error and increases power in the presence of IGC compared with other methods. Application to two datasets identified HIV-associated interferon pathways in xenograft mice and pathways associated with Alzheimer's disease progression in humans.
TWO-SIGMA-G: a new competitive gene set testing framework for scRNA-seq data accounting for inter-gene and cell-cell correlation.
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作者:Van Buren Eric, Hu Ming, Cheng Liang, Wrobel John, Wilhelmsen Kirk, Su Lishan, Li Yun, Wu Di
| 期刊: | Briefings in Bioinformatics | 影响因子: | 7.700 |
| 时间: | 2022 | 起止号: | 2022 May 13; 23(3):bbac084 |
| doi: | 10.1093/bib/bbac084 | ||
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