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Channel: GenomeWeb - rare disease
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TargetCancer Foundation Initiates Precision Medicine Study for Rare Cancers

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NHS Wales Introduces Whole-Genome Sequencing for Critically Ill Newborns,...

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Wide Variation in Genomic Testing Utilization Across US, Report Finds

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CHOP Automates Phenotyping of Epilepsy Patients, Heralding 'EMR Genomics' Era

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GTEx Studies Provide Comprehensive Map of Genetic Regulatory Variation Across...

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Praxis Genomics Bets on Bionano Optical Maps, Sequencing to Solve Complex...

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Genome Sequencing Boosts Diagnostic Yield in Children With Unexplained...

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Centogene Reports 13 Percent Decline in Q2 Revenues

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UK Government Unveils New Genomic Healthcare Strategy

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Pacific Biosciences, Children's Mercy, Microsoft Collaborate on Rare Genetic...

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And After the Test

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Centogene Increases Full-Year Revenue Guidance; CEO Resigns

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Illumina's ExpansionHunter Software Shows Clinical Promise for STR Expansions

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PLOS Papers on Parkinson's Disease, Hirschsprung Disease, Intracranial Aneurysm

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With $50M in New Funding, Congenica Works on Platform Upgrades for Clinical...

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Putting Expanded Carrier Screening Into Practice Requires Considerations to...

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Increased Adoption of Whole-Genome Sequencing Testing Hinges on Acceptance by...

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Non-Genetics Healthcare Providers Can Effectively Return Sequencing Results,...

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Illumina, Emedgene Partner on Automated Genomic Data Interpretation

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Centogene Q3 Revenues Triple on COVID-19 Testing

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