NGS (next generation sequencing) has made it possible for researchers to gather vast amounts of genomic sequencing data, which has a broad range of applications. NGS enables labs to:
- Rapidly sequence whole genomes
- Discover novel RNA variants
- Deeply sequence target regions
- Sequence cancer samples
- Analyze epigenetic modifications
- Sequence exomes
- Study the human microbiome
- Identify and isolate genes responsible for certain diseases
- Understand how organisms are affected by altered expression of genetic variants
- Uncover mutations and pathways associated with rare genetic diseases
- Provide the correct copy of a defective gene for gene therapy
- Explore the tumor microenvironment and study gene expression patterns to better understand drug resistance and metastasis