
Whole-Genome Sequencing (WGS) - Illumina
What is whole-genome sequencing? Whole-genome sequencing (WGS) is a comprehensive method for analyzing entire genomes. Genomic information has been instrumental in …
Human Whole-Genome Sequencing - Illumina
Our three-step human whole-genome sequencing workflow provides a fully featured, rapid solution for labs. The resulting WGS delivers high-quality insights across the entire genome for …
Next-Generation Sequencing (NGS) | Explore the technology
Next-generation sequencing, in contrast, makes large-scale whole-genome sequencing (WGS) accessible and practical for the average researcher. It enables scientists to analyze the entire …
Illumina DNA PCR-Free Prep | For sensitive WGS applications
Illumina DNA PCR-Free Prep offers a rapid and flexible workflow for preparing libraries for use in sensitive whole-genome sequencing applications, such as human whole-genome sequencing …
Whole Genome vs Exome Sequencing - Illumina
Learn about the critical differences between whole-genome and whole-exome sequencing and when to use each method to efficiently make your next discoveries.
DNA Library Preparation - Illumina
Human WGS with Illumina DNA Prep Library prep from blood, saliva, or genomic DNA that provides uniform coverage for human whole-genome sequencing (WGS).
Long-Read Sequencing Technology | For challenging genomes
With advanced NGS data analysis, short-read sequencing can generate whole-genome variant calls with outstanding accuracy. In addition, a small fraction of genomic regions can benefit …
NGS Workflow Steps | Illumina sequencing workflow
The next-generation sequencing workflow contains three basic steps: library preparation, sequencing, and data analysis.
Why more clinical labs are turning to whole-genome sequencing …
Apr 4, 2024 · This year, Illumina announced collaborations with Johnson & Johnson Innovative Medicine and Bristol Myers Squibb to innovate on our MRD research assay, currently under …
Sequencing Read Length | How to calculate NGS read length
Learn how to choose the right read length for your next-generation sequencing run.