|
Week - 1 |
Introduction to Genomic Data Analysis
Content:
• Definition and scope of genomic data analysis
• The role of genomic approaches in molecular biology
• Concepts of genome, transcriptome, epigenome, and metagenome
• Use of omics technologies in biomedical research
• Basic concepts in genomic data analysis
• Relationship between experimental data and bioinformatics analysis
• Developing biological questions for genomic data analysis
|
|
Week - 2 |
Genomic Data Generation Technologies
Content:
• Introduction to next-generation sequencing technologies
• Short-read and long-read sequencing approaches
• Overview of Illumina, Ion Torrent, PacBio, and Oxford Nanopore technologies
• DNA-seq, RNA-seq, ChIP-seq, ATAC-seq, metagenomics, and single-cell sequencing data types
• Targeted panels, exome sequencing, and whole-genome sequencing
• Advantages and limitations of sequencing platforms
• Selection of technology according to the research question
|
|
Week - 3 |
Genomic Experimental Design and Sample Planning
Content:
• Developing research questions and hypotheses in genomic studies
• Determination of sample groups
• Selection of control groups
• Biological and technical replicates
• Randomization and batch effect
• Sample size and statistical power
• Effects of DNA/RNA quality criteria on experimental design
• Planning clinical and biological metadata
|
|
Week - 4 |
Raw Data Formats and Data Organization
Content:
• FASTQ, FASTA, SAM, BAM, CRAM, BED, GTF/GFF, and VCF file formats
• Concepts of reads, base quality, Phred score, and Q-score
• Reference genome and genome annotation files
• File naming and folder organization
• Preparation of metadata files
• Distinction between raw data, processed data, and analysis outputs
• Data storage, backup, and traceability in genomic studies
|
|
Week - 5 |
Raw Data Quality Control and Preprocessing
Content:
• Principles of quality control in raw sequencing data
• Interpretation of FastQC and MultiQC outputs
• Per-base sequence quality
• GC content
• Adapter contamination
• Duplication level
• Overrepresented sequences
• Read trimming and filtering
• Overview of Cutadapt, Trimmomatic, and similar tools
• Interpretation of quality control reports in the experimental context
|
|
Week - 6 |
Reference Genome Alignment and Alignment Evaluation
Content:
• Principles of alignment to the reference genome
• Differences between DNA-seq and RNA-seq alignment
• Overview of alignment tools such as BWA, Bowtie2, HISAT2, and STAR
• Mapping rate, properly paired reads, insert size, and coverage
• Structure of SAM/BAM files
• Basic operations using SAMtools
• Marking PCR duplicates
• Alignment errors and the impact of low-quality alignment on results
|
|
Week - 7 |
Variant Calling Analyses
Content:
• Differences between germline and somatic variant calling
• Detection of SNVs and indels
• Concepts of coverage, allele depth, and variant allele frequency
• Overview of the GATK workflow
• Variant calling quality metrics
• Causes of false-positive and false-negative variant calls
• Introduction to CNV and structural variant analyses
• Technical limitations in variant calling
|
|
Week - 8 |
Variant Annotation and Clinical/Biological Interpretation
Content:
• Interpretation of VCF files
• Concept of variant annotation
• Annotation at gene, transcript, and protein levels
• Prediction of functional effects
• Evaluation of population frequency
• ClinVar, gnomAD, dbSNP, OMIM, and COSMIC databases
• Overview of annotation tools such as VEP, ANNOVAR, and SnpEff
• Variant prioritization strategies
• Basic principles in germline and somatic variant interpretation
|
|
Week - 9 |
Introduction to RNA-seq Data and Gene Expression Analysis
Content:
• Basic principles of RNA-seq technology
• Total RNA-seq, mRNA-seq, and small RNA-seq approaches
• RNA quality control and RIN value
• Concepts of read count, transcript abundance, and expression matrix
• Gene-level and transcript-level analyses
• Overview of STAR, HISAT2, featureCounts, Salmon, and kallisto approaches
• Concept of normalization
• Differences between TPM, FPKM, and raw counts
|
|
Week - 10 |
Differential Gene Expression Analysis
Content:
• Concept of differential gene expression
• Expression comparison between experimental groups
• Overview of DESeq2, edgeR, and limma-voom approaches
• Log2 fold change, p-value, and adjusted p-value
• Multiple testing correction
• Interpretation of volcano plots, MA plots, and heatmaps
• Biological interpretation of upregulated and downregulated genes
• Batch effects and confounding factors in differential expression analysis
|
|
Week - 11 |
Functional Annotation, Pathway Analysis, and Systems Biology
Functional Annotation, Pathway Analysis, and Systems Biology |
|
Week - 12 |
Genomic Data Visualization and Reporting
Content:
• Principles of genomic data visualization
• PCA plots, volcano plots, heatmaps, bar plots, and scatter plots
• Visual evaluation of genomic variants using IGV
• Coverage plots and genome browser usage
• UCSC Genome Browser and Ensembl Genome Browser
• Preparation of publication-quality figures
• Preparation of analysis reports
• Communicating bioinformatics analysis results to experimental biologists
|
|
Week - 13 |
Biomedical Applications of Genomic Data Analysis
Content:
• Genomic data analysis in inherited diseases
• Cancer genomics and somatic variant analysis
• Discovery of transcriptomic biomarkers
• Pharmacogenomic data analysis
• Infectious diseases and metagenomic analysis
• Liquid biopsy and cfDNA analyses
• Personalized medicine applications
• Clinical genomic reporting approaches
• Use of genomic data in translational research
|
|
Week - 14 |
Ethical Principles, Data Security, Reproducibility, and Student Presentations
Content:
• Ethical principles in genomic data analysis
• Personal genetic data and privacy
• Informed consent
• Data sharing and open science
• FAIR data principles
• Reproducibility in genomic analyses
• Pipeline documentation and version control
• Artificial intelligence-supported genomic data analysis
• Student project presentations
• General course evaluation
|