How to get started with data analysis

How to take your data analysis further

How to get started with nanopore sequencing and plan your experiment

Understanding File Formats in Bioinformatics: VCF and gVCF

Decoding the epigenome with Oxford Nanopore real-time methylation detection

Webinar: RNA-Seq Basics with Oxford Nanopore Technologies and CyVerse Tools

How to run your sequencing device and get started with data analysis

How to download sequencing data from SRA NCBI using windows SRA tool kit ?

Illumina Sequencing Overview: Library Prep to Data Analysis | Webinar | Ambry Genetics

The Beginner's Guide to RNA-Seq - #ResearchersAtWork Webinar Series

How to analyse your data with EPI2ME

Sanger Sequencing Data Analysis

5 genomics file formats you must know

A Guide to Next Generation Sequencing Basics and Terminologies | Bioinformatics 101

How to load a PromethION Flow Cell

Nanopore MinION starter-pack video

Matt Attreed: How to generate assemblies and call variants

Learn about Illumina's Next-Generation Sequencing Workflow

RNA Sequencing - Building a FASTQ to BAM pipeline

WGS Variant Calling: Variant calling with GATK - Part 1 | Detailed NGS Analysis Workflow

Epigenetics 2 - DNA methylation and Bisulfite Sequencing