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Today's complex genomic research questions demand a depth of information beyond the capacity of traditional DNA sequencing technologies. With its unprecedented throughput, scalability, and speed, next-generation sequencing (NGS) enables researchers to study biological systems at a level never before possible.
The updated Illumina NGS Methods Guide contains all of the information you need—from genome, transcriptome, or epigenome library preparation to sequencer selection, analysis, and support—all in one place. Select the best tools for your lab with our comprehensive catalog designed specifically for research applications.
The Guide includes information on how to:
- Rapidly sequence whole genomes
- Zoom in to deeply sequence target regions
- Utilize RNA sequencing to discover novel RNA variants and splice sites, or precisely quantify mRNAs for gene expression analysis
- Analyze genome-wide methylation or DNA-protein interactions
- Study microbial diversity in humans or in the environment
Complete the form to download your guide and navigate your road to NGS results.
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