See how researchers use mRNA-Seq with the NextSeq 550 System.
Read eBook: Gene Expression and Regulation Research with RNA-Seq
See how researchers use the NextSeq 550 System for exome sequencing applications.
See how researchers can use the NextSeq 550 System to sequence small whole genomes:
A targeted deep sequencing assay identifies multi-drug-resistant tuberculosis strains responsible for silent outbreaks.
Read ArticleLandmark NGS study leads to a national clinical diagnostic exome sequencing platform in Singapore.
Read InterviewThe microenvironment surrounding tumors could tell us more about how cancer cells migrate and become drug resitant.
Read InterviewA computer scientist is expanding the reach of scRNA-Seq data through new open source technologies.
Read InterviewIn addition to sequencing, the NextSeq 550 enables microarray scanning for a broad range of applications in reproductive health, genetic health, and cancer research, including methylation analysis with the Infinium MethylationEPIC BeadChip.
Use sequence-specific hybridization to analyze genomic regions of interest.
Analyze both coding RNA and multiple forms of noncoding RNA with total RNA sequencing, for a comprehensive view of the transcriptome.
NextSeq 550 System RNA-Seq Solution
Detect both known and novel features of the RNA exome using sequence-specific capture of RNA coding regions.
Targeted resequencing focuses time, expenses, and analysis on sequencing only a subset of genes or genome regions of research interest.
Targeted gene sequencing panels contain defined probe sets focused on specific genes of interest. Both predesigned and custom panels are available.
Perform epigenetic studies with high-coverage density and flexibility enabled by sequencing-based DNA methylation analysis.
Ultra-deep sequencing of PCR amplicons enables cost-effective analysis of up to hundreds of target genomic regions in one assay.
De novo sequencing with next-generation sequencing (NGS) enables fast, accurate characterization of species without a reference genome.
Delivering Sequencing Results Quickly and at a Competitive Price
Genotyping by sequencing provides a low-cost genetic screening method to discover novel plant and animal SNPs and perform genotyping studies.
Combining chromatin immunoprecipitation (ChIP) assays with sequencing, ChIP-Seq is a powerful method for genome-wide surveys of gene regulation.
Isolate and sequence small RNA species, such as microRNA, to study the role of noncoding RNA in gene silencing and posttranscriptional regulation.
Ribosome profiling enables systematic monitoring of cellular translation processes and prediction of protein abundance.
Ribosome Profiling Enables Comprehensive Translation Analysis
Comprehensively sample genes in organisms present in a complex sample to evaluate bacterial diversity and detect unculturable microorganisms.
Next-generation sequencing offers base-by-base, genome-wide detection of chromosomal variation to complement array-based cytogenomic analysis.
Find out how to utilize RNA-Seq to discover and profile RNA-based drug response biomarkers. Access resources designed to help new users adopt this application.
Quantitatively interrogate methylation sites across the genome at single-nucleotide resolution.
Environmental DNA (eDNA) sequencing is a rapidly emerging method for studying biodiversity and monitoring ecosystem changes.
eDNA Sequencing Offers a Powerful Lens to View Changes in Biodiversity
Access the information you need—from BeadChips to library preparation for genome, transcriptome, or epigenome studies to sequencer selection, analysis, and support—all in one place. Select the best tools for your lab with our comprehensive guide designed specifically for research applications.
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