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Illumina

Illumina

Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological functions. The company also provides sequencing and array-based solutions for genetic analysis, as well as genotyping, NIPT and whole-genome sequencing services for government laboratories, hospitals, an ...
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About Illumina

Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological functions. The company also provides sequencing and array-based solutions for genetic analysis, as well as genotyping, NIPT and whole-genome sequencing services for government laboratories, hospitals, and reference laboratories, among others.

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NGS System
NextSeq 550Dx

The NextSeq 550Dx is a FDA-regulated and CE-IVD marked next-generation sequencing (NGS) system with dual boot functionality, and includes a diagnostic mode (Dx mode) and a research mode, providing the flexibility to perform both clinical research and develop a range of IVD assays on a single instrument. It offers a validated high-throughput platform for large clinical laboratories, and fully-integrated onboard analysis software with modular software architecture to support current and future assays.
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NGS Test
MiSeqDx Cystic Fibrosis 139-Variant Assay

The MiSeqDx Cystic Fibrosis 139-Variant Assay is an FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to detect 139 CFTR variants. It provides a fully integrated molecular CF testing solution on the MiSeqDx instrument and includes all index primers and reagents needed for library preparation, sample multiplexing, and sequencing in a single kit.
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Reagents
MiSeqDx Universal Kit

The MiSeqDx Universal Kit is a validated, FDA-cleared amplicon sequencing solution that enables clinical laboratories to develop their own next-generation sequencing (NGS) assays for use on the FDA-cleared MiSeqDx instrument. It allows molecular diagnostics labs to develop assays using oligonucleotide probes designed on their own and provides a quick and easy to perform automated workflow to potentially minimize human error.
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Clinical Laboratory

NGS System
NextSeq 550Dx

The NextSeq 550Dx is a FDA-regulated and CE-IVD marked next-generation sequencing (NGS) system with dual boot functionality, and includes a diagnostic mode (Dx mode) and a research mode, providing the flexibility to perform both clinical research and develop a range of IVD assays on a single instrument. It offers a validated high-throughput platform for large clinical laboratories, and fully-integrated onboard analysis software with modular software architecture to support current and future assays.
More details

NGS Test
MiSeqDx Cystic Fibrosis 139-Variant Assay

The MiSeqDx Cystic Fibrosis 139-Variant Assay is an FDA-cleared in vitro diagnostic (IVD) next-generation sequencing test designed to detect 139 CFTR variants. It provides a fully integrated molecular CF testing solution on the MiSeqDx instrument and includes all index primers and reagents needed for library preparation, sample multiplexing, and sequencing in a single kit.
More details

Reagents
MiSeqDx Universal Kit

The MiSeqDx Universal Kit is a validated, FDA-cleared amplicon sequencing solution that enables clinical laboratories to develop their own next-generation sequencing (NGS) assays for use on the FDA-cleared MiSeqDx instrument. It allows molecular diagnostics labs to develop assays using oligonucleotide probes designed on their own and provides a quick and easy to perform automated workflow to potentially minimize human error.
More details

Clinical NGS System
MiSeqDx System

The MiSeqDx System is the first FDA-cleared next-generation sequencing (NGS) platform for in vitro diagnostic (IVD) testing that provides accurate, reliable data for screening and diagnostic testing, including assays for cystic fibrosis testing. Designed specifically for clinical laboratories, it delivers a broad range of sequencing applications and provides an easy-to-use, automated workflow for obtaining comprehensive and reliable DNA sequencing results.
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