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Hu, S. S.

Publications and source records attributed to Hu, S. S..

2 recordsLinked to original sources

HILAMA: High-dimensional multi-omic mediation analysis with latent confounding

MotivationThe increasingly available multi-omic datasets have posed both new opportunities and challenges to the development of quantitative methods for discovering novel mechanisms in biomedical research. One natural approach to analyzing such datasets is mediation analysis originated from the causal inference literature. Mediation analysis can help unravel the mechanisms through which exposure(s) exert the effect on outcome(s). However, existing methods fail to consider the case where (1) both exposures and mediators are potentially high-dimensional and (2) it is very likely that some important confounding variables are unmeasured or latent; both issues are quite common in practice. To the best of our knowledge, however, no methods have been developed to address these challenges with statistical guarantees. ResultsIn this article, we propose a new method for HIgh-dimensional LAtent-confounding Mediation Analysis, abbreviated as "HILAMA", that considers both high-dimensional exposures and mediators, and more importantly, the possible existence of latent confounding variables. HILAMA achieves false discovery rate (FDR) control under finite sample size for multiple mediation effect testing. The proposed method is evaluated through extensive simulation experiments, demonstrating its improved stability in FDR control and superior power in finite sample size compared to existing competitive methods. Furthermore, our method is applied to the proteomics-radiomics data from ADNI, identifying some key proteins and brain regions relating to Alzheimers disease. The results show that HILAMA can effectively control FDR and provide valid statistical inference for high dimensional mediation analysis with latent confounding variables. AvailabilityThe R package HILAMA is publicly available at https://github.com/Cinbo-Wang/HILAMA. Contactcinbo_w@sjtu.edu.cn

bioinformatics↗

Accurate estimation of intrinsic biases for improved analysis of chromatin accessibility sequencing data using SELMA

Genome-wide profiling of chromatin accessibility by DNase-seq or ATAC-seq has been widely used to identify regulatory DNA elements and transcription factor binding sites. However, enzymatic DNA cleavage exhibits intrinsic sequence biases that confound chromatin accessibility profiling data analysis. Existing computational tools are limited in their ability to account for such intrinsic biases and not designed for analyzing single-cell data. Here, we present Simplex Encoded Linear Model for Accessible Chromatin (SELMA), a computational method for systematic estimation of intrinsic cleavage biases from genomic chromatin accessibility profiling data. We demonstrate that SELMA yields accurate and robust bias estimation from both bulk and single-cell DNase-seq and ATAC-seq data. SELMA can utilize internal mitochondrial DNA data to improve bias estimation. We show that transcription factor binding inference from DNase footprints can be improved by incorporating estimated biases using SELMA. Furthermore, we show strong effects of intrinsic biases in single-cell ATAC-seq data, and develop the first single-cell ATAC-seq intrinsic bias correction model to improve cell clustering. SELMA can enhance the performance of existing bioinformatics tools and improve the analysis of both bulk and single-cell chromatin accessibility sequencing data.

bioinformatics↗