“End-to-End RNA-Seq Data Analysis With Python-Based Pipeline” is a comprehensive course designed to equip learners with the skills and knowledge
Tag: ngs
Cancer Genomics: NGS (Whole Exome Sequencing) Variant Calling Using Linux
Cancer genomics is a rapidly evolving field that utilizes next-generation sequencing (NGS) technologies to better understand the genetic basis of
Cancer Genomics: NGS (Whole Genome Sequencing) Variant Calling Using Linux
In the field of cancer genomics, the analysis of NGS/whole genome data has become an integral part of cancer research.
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Python
Hands-on: NGS (Whole Exome Sequencing) Variant Calling Using Python The primary goal of this course is to thoroughly equip students
Hands-on: NGS (Whole Genome Sequencing) Variant Calling for Microbial Genomics
Hands-on NGS (Whole Genome Sequencing) Variant Calling for Microbial Genomics Microbes, also known as microorganisms, are found all around us and
Command-line Based Practical RNA-Seq Data Analysis With Linux & R (Subscription)
Command-line Based Practical RNA-Seq Data Analysis With Linux & R
Hands-on Practical RNA-Seq Data Analysis With Galaxy
If you’ve ever been curious about understanding the inner workings of RNA-Seq and Next-Generation Sequencing (NGS) technologies, this comprehensive course
