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High-throughput technologies like next-generation sequencing and mass spectrometry generate massive volumes of omics data. To turn this raw information into meaningful biological insights, researchers must be comfortable with scripting, data wrangling, and analysis workflows in Python and R. This workshop bridges that gap by focusing on practical, example-driven bioinformatics using real or realistic datasets.
Participants will learn how to import, clean, explore, and analyze genomics, transcriptomics, and proteomics data using widely adopted libraries and packages. Topics include sequence data handling, basic alignment/annotation outputs, gene expression analysis, simple differential expression pipelines, and basic visualization (heatmaps, PCA, volcano plots). The emphasis is on hands-on coding, reproducible workflows, and interpreting results in a biological context.
This workshop aims to train participants in using Python and R for practical bioinformatics analysis across genomics, transcriptomics, and proteomics datasets. It focuses on data handling, preprocessing, visualization, and basic statistical and machine-learning workflows for high-throughput omics data. Through hands-on sessions, participants will learn how to work with FASTA/FASTQ, count matrices, differential expression data, and proteomics tables. The goal is to build confidence in using open-source tools and scripting to solve real biological questions.
02/07/2026
IST 7:00 PM
02/07/2026 – 02/09/2026
IST 8:00 PM
Dr Harishchander Anandaram is an Assistant Professor at Centre for Excellence in Computational Engineering and Networking, Amrita Vishwa Vidyapeetham, Coimbatore, Tamil Nadu, India. He received his Ph.D. Degree in Bioengineering from Sathyabama Institute of Science and Technology, Chennai, in 2020. . . .
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