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Neuroscience researchers are using NGS to identify variants for a new sequencing array designed for ADHD, autism, and schizophrenia studies.
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Landmark NGS study leads to a national clinical diagnostic exome sequencing platform in Singapore.
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A robust genotyping solution that’s flexible, scalable, and works from DNA to data analysis ...
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Illumina Researcher Marlem Rivera Shares Her Story
Read Article| Date | Publication | Title |
|---|---|---|
| Feb 27, 2019 | Bloomberg | A $100 Genome Within Reach, Illumina CEO Asks If World Is Ready |
| Feb 27, 2019 | Slate | Why Are We So Afraid of Each New Advance in Reproductive Technology? |
| Feb 19, 2019 | San Diego Union Tribune | San Diego biotech company teams up with doctors to offer genome sequencing to Tijuana children |