This two-part series will walk you through single-cell RNA sequencing (scRNA-seq) analysis starting with a matrix file or FASTQ files...

This two-part series will walk you through single-cell RNA sequencing (scRNA-seq) analysis starting with a matrix file or FASTQ files...

Discovering new genes implicated in hereditary diseases or cancer progression is challenging yet advancing rapidly due to the increase in...

This webinar will introduce users to the tools available for short reads (Illumina) as well as long reads (Oxford Nanopore,...

Discover how our new LightSpeed feature changes the world of whole genome sequencing analysis We’re excited to reveal many new...

Discover an easy way to get reproducible analyses, traceability of results and efficient bulk analysis with QIGEN CLC workflows. Stringing...

Did you know SARS-CoV-2 is shed in the feces of individuals with symptomatic or asymptomatic infection? Viral particles shed into...

Ab initio gene finding is a central step in genome analysis, which must account for the biology of the investigated...

It’s already happened: Several SARS-CoV-2 variants are upon us, lurking in various populations, bringing more uncertainty about how this pandemic...

During the current pandemic, the importance of continually monitoring viral genomes for new mutations has become fundamental to help guide...