Master Python/R for Bioinformatics: Genomics, Transcriptomics & Proteomics Data in 4 weeks through hands-on, project-based online training with DSTC.
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 course bridges that gap by focusing on practical, example-driven bioinformatics using real or realistic datasets. Every participant receives a verified e-Certificate and e-Marksheet from the Deep Science & Technology Consortium.
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 course bridges that gap by focusing on practical, example-driven bioinformatics using real or realistic datasets.
1. Apply bioinformatics methods to authentic research and industry problems.
2. Produce a reproducible, portfolio-ready project you can cite in a thesis, paper, or job application.
β’ Master's and senior undergraduate students specializing in bioinformatics
β’ R&D engineers and working professionals applying bioinformatics in industry
β’ Academics and educators building research or teaching capacity in bioinformatics
β’ Tangible, reproducible bioinformatics work to show supervisors or employers.
β’ A verified e-Certificate of competency and e-Marksheet from the Deep Science & Technology Consortium.
β’ Where Python and R each genuinely have the advantage in bioinformatics
β’ Conda, renv and reproducible environments rather than a shared global install
β’ Project structure, version control and scripts over interactive one-off commands
β’ BioPython and Biostrings for sequence handling and file parsing
β’ Reading VCF and BED and using pyranges or GenomicRanges for interval work
β’ Coordinate conventions and the strand errors that silently corrupt results
β’ Count matrices, DESeq2 and the reason raw counts must not be pre-normalised
β’ Exploratory analysis with PCA and clustering before testing anything
β’ Pandas and dplyr for the reshaping most of the work actually consists of
β’ Search output, FDR at peptide and protein level, and the protein inference problem
β’ Missing values in proteomics and imputation that must be reported
β’ Normalisation and statistics on data with far fewer features than transcriptomics
β’ ggplot2 and matplotlib or seaborn for figures that survive review
β’ Volcano plots, heatmaps and MA plots read correctly
β’ R Markdown and Jupyter for an analysis someone else can rerun
| Parameter | Requirement |
|---|---|
| Covered Tool / Platform | BWA |
| Covered Tool / Platform | SAMtools |
| Covered Tool / Platform | GATK |
| Covered Tool / Platform | FastQC |
| Covered Tool / Platform | Trimmomatic |
| Covered Tool / Platform | R/Bioconductor |
| Covered Tool / Platform | IGV |
| Covered Tool / Platform | PLINK |
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