Polygenic Risk Scores Could Become Useful Tools in the Physician's...

Customer Interview

Polygenic Risk Scores Could Become Useful Tools in the Physician's...

Researchers perform large GWAS studies with the Global Screening Array to identify disease-associated DNA risk loci and develop PRSs for clinical...

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NGS Identifies Rare Disease Variants in Infants with Undiagnosed...

Customer Interview

NGS Identifies Rare Disease Variants in Infants with Undiagnosed...

Landmark NGS study leads to a national clinical diagnostic exome sequencing platform in Singapore.

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The Clinical Value of NIPT

Customer Videos

The Clinical Value of NIPT

Learn how noninvasive prenatal testing (NIPT) is making an impact around the world. Hear from the staff at AMES discuss how NIPT, particularly...

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Sequencing

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Microarrays

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Illumina Sequencers Help Characterize and Control Coronavirus

NGS accelerating viral identification and control measures

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Single-Cell RNA Sequencing

Generating RNA libraries from ultra-low-input samples

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Simplify Rare Variant Analysis and Interpretation

Call, prioritize, and report on variants from one interface

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Employee Story

Learn what bioengineers do and why Erin chose this field

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