MOCHA's advanced statistical modeling of scATAC-seq data enables functional genomic inference in large human cohorts.
Samir Rachid ZaimMark-Phillip PebworthImran McGrathLauren Y OkadaMorgan WeissJulian ReadingJulie L CzartoskiTroy R TorgersonM Juliana McElrathThomas F BumolPeter J SkeneXiao-Jun LiPublished in: Nature communications (2024)
Single-cell assay for transposase-accessible chromatin using sequencing (scATAC-seq) is being increasingly used to study gene regulation. However, major analytical gaps limit its utility in studying gene regulatory programs in complex diseases. In response, MOCHA (Model-based single cell Open CHromatin Analysis) presents major advances over existing analysis tools, including: 1) improving identification of sample-specific open chromatin, 2) statistical modeling of technical drop-out with zero-inflated methods, 3) mitigation of false positives in single cell analysis, 4) identification of alternative transcription-starting-site regulation, and 5) modules for inferring temporal gene regulatory networks from longitudinal data. These advances, in addition to open chromatin analyses, provide a robust framework after quality control and cell labeling to study gene regulatory programs in human disease. We benchmark MOCHA with four state-of-the-art tools to demonstrate its advances. We also construct cross-sectional and longitudinal gene regulatory networks, identifying potential mechanisms of COVID-19 response. MOCHA provides researchers with a robust analytical tool for functional genomic inference from scATAC-seq data.
Keyphrases
- single cell
- rna seq
- high throughput
- genome wide
- cross sectional
- transcription factor
- gene expression
- dna damage
- endothelial cells
- minimally invasive
- public health
- quality control
- sars cov
- coronavirus disease
- big data
- machine learning
- climate change
- deep learning
- induced pluripotent stem cells
- mass spectrometry
- risk assessment
- data analysis