Luke Hickey

@Luke_Hickey

Senior Director of Strategic Marketing at PacBio & MBA BerkeleyHaas

San Francisco Bay Area, CA
Vrijeme pridruživanja: ožujak 2009.

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  1. proslijedio/la je Tweet

    Human Pangenome Reference Consortium announces data freeze of HG002 for assembly bench marking and evaluation purposes. , , , HG002-Data Freeze v1.0: Github:

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  2. proslijedio/la je Tweet
    20. stu 2019.

    "Structural Variant Calling: The Long and Short of it" just out . Highlighting the great promise of and long read for SV inference. Great collaboration by and students from

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    10. stu 2019.

    Greatly enjoyed the meeting! My slides are up at for anyone interested in my talk on long-read transcriptomics

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    11. stu 2019.

    Submit your proposal today! Only 250 words or less standing between you & the chance to advance understanding of & disease w/ SMRT Sequencing

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  5. 30. lis 2019.

    California Life Science Institute (CLSI) event honoring Rich Lyons and his new position as Chief Innovation and Entrepreneurship Officer at UC Berkeley. He led with Haas DLP’s in his interview for the new position.

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  6. 28. lis 2019.

    Long-read human WGS on the Sequel II System — latest run from Univ of Washington yielded >500 Gb raw data with >35 Gbps of HiFi data (~10-fold coverage) from just one SMRT Cell 8M. Congrats on the excellent results!

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  7. 18. lis 2019.
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  8. 16. lis 2019.

    Shawn Levy, Hudson Alpha, planning complimentary long-read sequencing of ~7,000 human genomes for All of Us for common SV discovery.

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  9. 16. lis 2019.

    Naomichi Matsumoto announces special long-read sequencing issue of the Journal of Human Genetics, Jan 2020

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  10. 16. lis 2019.

    NM it’s now time to use long read sequencing for these types of diseases [repeat expansion disorders]

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  11. 16. lis 2019.

    Naomichi Matsumoto from using long-read WGS of WES negative cases to identify pathogenic Structural Variants

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    16. lis 2019.

    Full house at our workshop highlighting the Sequel II System for accurate & affordable long-read sequencing of human genomes. FOMO? Sign up to get the recording:

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    16. lis 2019.

    Existing long read variant calling methods can catch SVs, but many miss other variants. See how enabled to & co to comprehensively cover SNVs & CNVs in this poster Chat with them live at 3 p.m., poster 1068

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    14. lis 2019.

    In New Tibetan Genome Assembly, Variants for Living at Altitude and the Imprint of Archaic DNA from the blog

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  15. 26. ruj 2019.
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    7. ruj 2019.

    Hoischen: new HiFi data yields best quality genome seen so far!

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  18. 6. ruj 2019.

    I see DNA everywhere 🧬! Real picture of a light in a cafe

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    12. kol 2019.

    Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome via . De novo genome assembly produced a contiguous and accurate genome with a contig N50 of >15 Mb & concordance of 99.997%

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  20. proslijedio/la je Tweet
    4. ožu 2019.

    We need more diversity in genomic databases - otherwise, is imprecise. Our CSO Jonas Korlach pens an important piece for

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