OmniEdge Scientific
Comprehensive
Beginner to Advanced

Bioinformatics Skill Development Workshop: From Programming to NGS Analysis

Bioinformatics Skill Development Workshop: From Programming to NGS Analysis

A comprehensive workshop designed to take you from Zero Programming to advanced Structural Bioinformatics and Next-Generation Sequencing (NGS) analysis.

  • Section I: Data Analysis Using R and R-Studio
  • Section II: Python, Biopython, and Molecular Docking
  • Section III: Next-Generation Sequencing (NGS) Analysis

Course Overview

Join the next generation of researchers combining Biology, AI, and Innovation. This workshop provides hands-on experience using Linux-based environments and industry-standard bioinformatics tools to solve real-world genomic and structural challenges.


What You Will Learn

Section I: Data Analysis Using R

  • Data Wrangling: Import, clean, and reshape real-world datasets using the tidyverse.
  • Statistical Analysis: Perform hypothesis testing (t-tests, ANOVA), normality assessments, and post-hoc tests like Tukey HSD and DMRT.
  • Visualization: Create publication-ready and interactive plots using ggplot2 and Plotly.
  • Multivariate Exploration: Run PCA and cluster analysis for complex biological datasets.

Section II: Python & Structural Bioinformatics

  • Programming Foundations: Learn to store, manipulate, and process DNA, RNA, and protein data.
  • Biopython Workflows: Automate sequence retrieval from NCBI, perform BLAST searches, and construct phylogenetic trees.
  • Structural Analysis: Parse PDB files to analyze hydrophobicity and B-factors, and perform RMSD superimpositions.
  • Drug Discovery: Understand the fundamentals of Molecular Docking, ligand preparation, and result interpretation.

Section III: Next-Generation Sequencing (NGS)

  • Linux Mastery: Set up and navigate a Linux environment using WSL (Windows Subsystem for Linux).
  • Quality Control: Assess raw sequencing data using FastQC and perform read trimming.
  • Genome Assembly & Alignment: Assemble reads using SPAdes and align them to reference genomes using BWA and SAMtools.
  • Variant Calling: Understand the principles of identifying genetic variations and interpreting VCF files.

Capstone Project

Bring your skills together by performing a complete structural and sequence analysis of a target protein. This includes integrating sequence retrieval, BLAST analysis, structural parsing, and visualization into a single automated workflow.


Key Tools & Packages Covered

  • Languages: R, Python, Linux Shell.
  • R Packages: dplyr, ggplot2, tidyr, rstatix, car, pheatmap, FactoMineR.
  • Python Libraries: Biopython, Pandas, NumPy, Matplotlib.
  • NGS Tools: FastQC, SPAdes, BWA, SAMtools.
Lessons
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