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Project-based courses in NGS, RNA-Seq, variant calling, Python, R, Linux and computational drug discovery — taught with the same datasets working researchers use. Self-paced, lifetime access, certificate on completion.
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Real pipelines on real research datasets — not toy examples.
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Built by working bioinformaticians, kept current with the field.
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Loved by learners
“This course really helped me get comfortable with R for bioinformatics, especially when it comes to building and automating pipelines for repetitive data tasks. The practical examples made the tedious parts of data processing feel much more manageable and even a bit…”
“I took this course to get hands-on with whole exome sequencing analysis, and it really delivered. The Linux command line work felt intimidating at first, but the step-by-step guidance made the variant calling process clear and manageable. By the end, I felt…”
“This course gave me a solid foundation for handling biological data and running sequence alignments. I really liked how the hands-on exercises made the evolutionary analysis concepts click, even though I started with zero bioinformatics experience. Definitely recommend it to anyone looking…”