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Vrijeme pridruživanja: lipanj 2015.

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  1. Prikvačeni tweet

    We are excited to be attending , the largest forum for Precision Medicine in the country. See how is empowering genomic innovations in the precision health journey, visit us at booth C2123. Click here to see a complete list of our talks:

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  2. From questions to insights, learn more about 's expanded TruSight™ Oncology portfolio at , booth C2123. Click here to dive deeper into TruSight™ Oncology 500:

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  3. Thank you for joining us at Find out more:

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  4. Visit booth C2123& learn about our new high-throughput oncology solution, TruSight™ Oncology 500 High-Throughput, coming soon. W/ sample batching flexibility, you will be able perform more samples per run on the NovaSeq™ 6000. Dive deeper:

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  5. attendees did you know: the expanded TruSight™ Oncology 500 Portfolio enables flexibility to analyze from tissue and liquid biopsy? Visit booth C2123 to learn more. Click here to dive deeper:

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  6. Save precious sample, time and costs. Consolidate solid tumor analysis by covering all biomarkers in guidelines and clinical trials, in a single assay on the NextSeq™ 550 and 550Dx platforms. Visit boothC2123to learn more. Dive deeper here:

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  7. Enable accurate solid tumor classification using methylation arrays. Visit booth C2123, to speak to an team member today. Click here to learn more about our microarray kits:

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  8. Take cancer from uncertainty to insights. Expanding the TruSight™ Oncology 500 Portfolio has enabled flexibility to analyze from tissue and liquid biopsy. attendees can learn more at booth C2123. For more now, click here:

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  9. Where ever you are in your precision health journey, is empowering genomic innovations that will meet your needs. Visit booth C2123 to learn more. Click here to dive deeper:

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  10. Address the needs of oncology today and tomorrow. Achieve efficiencies through test consolidation and gain highly confident results. attendees can dive deeper at the booth C2123. Click here to learn more about our product highlights:

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  11. attendees did you know you can use DRAGEN's secondary analysis to call small variants, copy number variants (CNVs), structural variants, mitochondrial variants, repeat expansions, & more? Visit booth C2123 to learn more. Dive deeper:

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  12. Comprehensive Genomic Profiling (CGP) is driving a new standard of care. CGP identifies actionable biomarkers that help optimize treatment. Learn about CGP at booth C2123, the team is waiting. Click here to dive deeper:

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  13. Don’t forget to join our workshop today in Salle Descartes, 12:45 - 13:45: "Comprendre les maladies génétiques, de la recherche aux applications cliniques."

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  14. Unlock larger tissue sample batch sizes and detect biomarkers in circulating tumor DNA liquid biopsy. Learn more about the flexibility of the NovaSeq™ portfolio at booth C2123. Click here to dive deeper:

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  15. Attending ? Join 's VP of Human Resources, , for an in-depth talk on Workplace Genomics. Talk starts at 330pm, Track 5. Click here to learn more about careers at :

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  16. NextSeq™ 550Dx, the next level in diagnostic power for the clinical lab. attendees visit booth C2123 and elevate your understanding of this powerful instrument. Click here to learn more:

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  17. Learn more about NGS Workflow For Clinical Diagnostics Applications at . 's Mark Van Oene will be speaking on the panel starting at 1pm, Track 4. Click here to diver deeper:

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  18. Don't miss 's as he sits down with  for a fireside chat at . Join us at 1130am, Track 2.  Click here to learn more:

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  19. Join 's  at as he discusses creating a sustainable genomic testing service with in healthcare systems that improves outcomes. Talk starts at 2pm, Track 2.  Click here to learn more:

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  20. Odgovor korisniku/ci

    Come by the booth at to see our latest benchtop sequencer

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  21. DRAGEN™ is a cost-effective solution that offers ultra-rapid secondary analysis of sequencing data, accurate data, & robust speed. Discover more at booth C2123. Click here to review the specs:

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