DEGs, or Differentially Expressed Genes, are genes whose expression levels show significant differences between two or more conditions or experimental groups. In genetics and genomics research, gene expression refers to the process by which information encoded in a gene's DNA sequence is converted into functional proteins or RNA molecules.
When studying gene expression, researchers often compare gene expression profiles between different biological samples or experimental conditions, such as healthy and diseased tissues, treated and untreated cells, or different developmental stages. By analyzing the expression levels of thousands of genes simultaneously, researchers can identify genes that are upregulated (higher expression) or downregulated (lower expression) in one condition compared to another.
Differential Gene Expression analysis is a fundamental tool for identifying genes whose expression levels significantly differ between experimental conditions or biological samples. This analysis enables us to pinpoint genes that play pivotal roles in phenotypic variation, disease development, or response to treatments. With RNA-seq, we can capture and quantify the abundance of transcripts, revealing the dynamic landscape of gene expression within a cell or tissue.
Data Preprocessing: Raw RNA-seq data contains a wealth of information but requires preprocessing steps to ensure accurate and reliable results. This includes trimming adapter sequences, filtering low-quality reads, and aligning the reads to a reference genome or transcriptome.
Read Alignment and Mapping: The next step involves mapping the processed reads to a reference genome or transcriptome. This alignment process enables the determination of the origin of each read, allowing us to associate it with specific genes or genomic regions.
Quantification of Gene Expression: Once the reads are mapped, we quantify the expression level of each gene. This can be achieved by counting the number of reads that align to each gene or by estimating transcript abundance using sophisticated algorithms.
Statistical Analysis: Statistical methods are employed to identify genes that exhibit significant changes in expression between experimental conditions. Various statistical tests, such as the negative binomial, edgeR, or DESeq2, are commonly used to assess differential gene expression.
Functional Analysis: After identifying Differentially Expressed Genes (DEGs), we delve deeper into their functional significance. By subjecting DEGs to gene ontology enrichment analysis, pathway analysis, or functional annotation, we gain insights into the biological processes, molecular functions, and pathways associated with the observed gene expression changes.
Disease Biomarker Discovery: Identification of DEGs between healthy and diseased tissues unveils potential diagnostic or prognostic biomarkers. These biomarkers aid in disease classification, patient stratification, and the development of targeted therapies, paving the way for precision medicine.
Drug Discovery and Development: DGE analysis facilitates the identification of genes responsive to specific drug treatments. By unraveling the molecular mechanisms underpinning drug response, we can optimize treatment strategies, expedite drug discovery, and develop personalized therapies tailored to individual patients.
Developmental Biology: DGE analysis provides critical insights into the genetic programs governing various stages of development. By comparing gene expression patterns during embryogenesis or tissue differentiation, we unravel the molecular events that shape organisms, advancing our understanding of developmental biology.
Environmental Stress Response: DGE analysis elucidates how genes respond to environmental stimuli, such as heat stress, chemical exposure, or pathogen infection. Unraveling the underlying molecular pathways enhances our comprehension of stress responses and enables the development of strategies to mitigate their impact.