The Illumina Long Read Applications Ecosystem is a group of partnerships dedicated to ensuring the delivery of high quality data for a fully featured genome, including phasing, detection of structural variants, and de novo assembly of all species. We believe that the combination of our core sequencing technology, along with our partners’ linked-read preps, assembly protocols and analysis pipelines, will enable Illumina to bring advanced long read applications solutions to the market today.
10x Genomics Chromium genome and exome products, making phasing and structural variant information accessible to our human health researchers.
Learn MoreDovetail Genomics assembly service (full assembly and assembly improvements) for a wide range of genomes, leveraging its Chicago library prep and proprietary analysis pipeline.
Learn MoreNRGene DeNovoMagic analysis product, delivering computational tools to facilitate optimal trait discovery for seed companies, animal breeders, and academia.
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