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Udemy – Bioinformatics: Learn NGS Data Analysis From Scratch 2025-6

Updated August 10, 2026 1.98 GB
Udemy – Bioinformatics: Learn NGS Data Analysis From Scratch 2025-6

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Descriptions

Bioinformatics: Learn NGS Data Analysis From Scratch, Become a Bioinformatics Pro with Hands-On NGS Data Analysis Skills! Next-Generation Sequencing (NGS) is transforming healthcare, research, and biotechnology. With bioinformatics expertise now essential for biologists, clinicians, and researchers, this Udemy course empowers you to analyse human genomic data like a pro using the GATK pipeline (Genome Analysis Toolkit). Master industry-standard workflows to process FASTQ files, call variants, annotate VCFs, and unlock insights for personalised medicine, cancer genomics, and rare disease research. Bioinformatics is critical for interpreting NGS data and standing out in academia, pharma, or clinical labs. No prior coding experience is needed; you will learn end-to-end NGS analysis for human genomes (WGS/WES) and follow best practices endorsed by the Broad Institute for accurate, reproducible results. Analyse real datasets, annotate variants with Funcotator, and build a portfolio for job applications. The course covers bioinformatics basics for biologists, NGS technologies and data formats, GATK pipeline steps, VCF file mastery, and Funcotator for VCF annotation. You will work with downloadable workflows, practice datasets, and receive a certificate of completion. The course is focused on human genomic data (WGS/WES); microbial workflows are not covered.

What you’ll learn

  • You will learn the fundamentals of Molecular Biology From Genotype to Phenotype
  • You will installation of Linux in Windows (WSL) and fundamentals of bash scripting
  • You will learn about the FASTQ and FASTA file formats
  • You will learn the installation of tools for Variant Calling in Linux
  • You will learn the GATK best practice pipeline for Variant calling starting from FASTQ to VCF
  • You will learn the structure of VCF file and understanding of its information
  • You will learn about Annotations of Variants present in FASTQ file using Funcotator
  • You will learn the sorting of Annotated VCF file to take clinical decisions
  • You will learn how to leverage the open source software to analyze the NGS data

Who this course is for

  • Beginner in field of Biology
  • Beginners in field of Bioinformatics
  • Beginners in molecular diagnostics
  • Data scientists interested to understand genomic (DNA) data
  • Researcher pursing their carrier in Molecular biology, Biochemistry and Biotechnology

Specificatoin of Bioinformatics: Learn NGS Data Analysis From Scratch

  • Publisher : Udemy
  • Teacher : Naeem Mahmood Ashraf
  • Language : English
  • Level : Beginner
  • Number of Course : 68
  • Duration : 4 hours and 21 minutes

Content of Bioinformatics: Learn NGS Data Analysis From Scratch

Bioinformatics_ Learn NGS Data Analysis From Scratch

Requirements

  • No prior knowledge of programming is needed.
  • Fundamental knowledge of Molecular Biology is needed but not mandatory. You will learn some essential molecular biology knowledge in first module of course.
  • Fundamentals of Bioinformatics is needed but not mandatory. You will learn most of its part related to NGS data analysis in course
  • In online teaching, it’s always hard to engage the students. Therefore we have designed this course keeping the psychology of students in view. Usually, students start to lose their interest when they are stuck in a complex concept that’s why We tried to move from simple to complex easily and understandably.

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Bioinformatics_ Learn NGS Data Analysis From Scratch

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Subtitle : English

Quality: 720

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File size

1.98 GB