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Use these components in ATAC-Seq experiments to analyze chromatin accessibility
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Provides accurate, ultra-rapid secondary analysis of sequencing data
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RNA-Seq and HLA typing are increasing the power and efficiency of a target discovery platform
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Illumina to collaborate with the Frederick National Laboratory for Cancer Research
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Deadline for 2020 Agricultural Greater Good Initiative grant applications is December 6
Discover how genetic variants and PRS could enable more effective treatment of genetic conditions.
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Assay targeting multiple somatic variant types from plasma, including TMB and MSI
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Learn how noninvasive prenatal testing (NIPT) is making an impact around the world.
Consortium aims to expand access to clinical whole-genome sequencing for genetic diseases
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
Oligonucleotide (oligo) sequences of Illumina adapters used in Nextera, TruSeq, TruSight, and AmpliSeq for Illumina library prep kits. This information is provided for use with Illumina instruments only.
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Jun 13, 2019