Accession PRJCA019122
Title Integrating Analysis of Multi-Omic data for Pathogenesis of AutismSpecturm Disorder
Relevance Medical
Data types Whole genome sequencing
Epigenomics
Exome
Variation
Genome sequencing and assembly
Organisms Homo sapiens
Description Autism is a serious neurodevelopmental disease in children. Epidemiological studies have found that the prevalence of autism has reached 1.14%. Genetic and environmental factors are two main causes. According to the highly clinical and genetic heterogeneity, the integration of multi-omics has becoming an effective approach to understanding the pathophysiology of ASD. Taking advantage of the data from whole genomics, transcriptomics, metabolomics and epiomics, we perform multi-omics analysis, trying to explore the potentially gene clusters that can be used for diagnosis and risk warning, integrating a Multi-dimension biomarker panel from a combination of non-coding variants, non-coding RNAs and metabolites, and establishing an independent large-scale cohort for validation and optimization. Theses identified gene or pathway will be selected to study how they contribute to the pathogenic mechanism of Autism by performing molecular cell experiments and gene knockout mice. This proposal, based on a multi-omic integrating analysis of high throughput sequence, will provide new insights for genetic counseling, molecular subtype classification, and pathogenic mechanism investigation in Autism.
Sample scope Multiisolate
Release date 2024-08-15
Grants
Agency program Grant ID Grant title
National Natural Science Foundation of China (NSFC) 82130043
Submitter Lu Xia (xialu0614@csu.edu.cn)
Organization Central South University
Submission date 2023-08-17

Project Data

Resource name Description