HPE DSI 400
Data Science Courses
Prerequisites
Participants should have a basic understanding of biology or genetics. Previous experience with programming or the UNIX/Linux command-line environment is beneficial but not required.
Description
This special topics course introduces participants to the fundamentals of bioinformatics and the computational analysis of next-generation sequencing (NGS) data. Bioinformatics integrates computational methods, statistical techniques, and biological sciences to analyze and interpret large-scale biological datasets. Advances in NGS technologies have transformed modern genomics and biomedical research by enabling rapid, high-throughput sequencing of genetic material.
The course provides both theoretical foundations and practical experience in bioinformatics workflows commonly used in genomics research. Through a combination of lectures, demonstrations, and hands-on laboratory exercises, participants will learn the principles of NGS data processing, analysis, and interpretation using contemporary bioinformatics tools and computational methods.
Topics covered include sequencing technologies, biological data formats, quality control (QC) and preprocessing of sequencing data, sequence alignment and read mapping, variant discovery and variant calling workflows, functional annotation, and interpretation of genomic variants. Participants will also gain exposure to commonly used bioinformatics software, command-line tools, and computational workflows used in modern genomics pipelines.
Emphasis is placed on practical data analysis skills and reproducible computational workflows that can be applied to real-world biological and biomedical research projects. Participants will work with example datasets and develop the ability to perform foundational NGS analyses independently.
Upon successful completion of the course, participants will be able to:
- Understand the foundational principles of bioinformatics and genomics data analysis
- Explain the workflow of next-generation sequencing data processing
- Perform quality assessment and preprocessing of sequencing datasets
- Conduct sequence alignment and read mapping analyses
- Execute basic variant calling and annotation workflows
- Interpret genomic analysis results in biological research contexts
- Utilize bioinformatics software and command-line tools for NGS analysis
This course is intended for students, researchers, and professionals interested in genomics, computational biology, biomedical research, and data-driven life sciences applications.
Mandatory Policies
Attendance: Regular class attendance, participation, and engagement in coursework are important contributors to student success. Grades (Pass/Fail) will not be assigned to students who fail to attend at least 12 hours of synchronous instruction. Absences may be excused as provided in the Excused Absence Policies included in the current UH Course Catalog.
Recording of Class: Students may not record all or part of class, livestream all or part of class, or make/distribute screen captures, without advanced written consent of the instructor. Classes may be recorded by the instructor. Students may use instructor’s recordings for their own studying and note-taking. Instructor’s recordings are not authorized to be shared with anyone without the prior written approval of the instructor.