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Using NGS to Study Rare Undiagnosed Genetic Disease

Customer Interview

Using NGS to Study Rare Undiagnosed Genetic Disease

Whole-exome and transcriptome sequencing prove beneficial in uncovering mutations and pathways associated with rare disease.

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Using Analytics to Improve Cancer Diagnosis and Therapy Selection

Customer Interview

Using Analytics to Improve Cancer Diagnosis and Therapy Selection

Developing and automating best-practice workflows that make analyzing, processing, and disseminating genomic data accessible to researchers...

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Sandip Patel, MD: Comprehensive Genomic Profiling

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Sandip Patel, MD: Comprehensive Genomic Profiling

Sandip Patel, MD, from UCSD Moores Cancer Center provides his point of view on Comprehensive Genomic Profiling (CGP), as an approach for assessing...

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Sequencing

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Microarrays

Analyze genetic variation on any scale

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Shining a light on genomic healthcare for all

Announcing SPARK—a global genomics forum by Illumina. April 26—27, 2021

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Illumina Stranded Total RNA Prep with Ribo-Zero Plus

Study the coding and non-coding transcriptome with unparalleled flexibility

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NovaSeq 6000 Reagent Kits v1.5

Improved Q30 score, support for UMIs, extended shelf life, and support for Illumina DNA PCR-Free Library Prep

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Employee Story

Clinical lab manager Rita walks you through her day

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