Rezultati pretraživanja
  1. 15. sij

    On-instrument CCS on Sequel II coming in 2020!

  2. 1. velj

    Registration is now open for - April 28-30. Join us, & the SMRT community for three days of engaging science & networking in the Netherlands. Featuring: Preview agenda & register:

  3. 16. sij

    1/ My attempt to summarize some of the cool discussions that came out of the after yesterday. Chime in to correct me

    Prikaži ovu nit
  4. 15. sij

    . very excited about the complementarity of StrandSeq for allowing chromosomal separation (enabling phased assembly) of long reads

  5. 15. sij

    . : chormosomal clustering for phased assembly using HiFi + StrandSeq. Workflow below.

  6. 15. sij

    explaining why phasing matters at , can't remember who I was talking to about phasing at but basically this matters.

  7. 15. sij

    . : Nighthawk phases bubbles, fast and accurate

  8. 15. sij

    At meeting and someone's phone goes off with the Pokémon go music. Gotta catchem all!

  9. 15. sij

    THIS! As de novo genome assemblies get better, it’s important to make sure you’re measuring quality in the right ways.

  10. 15. sij

    Nice to see the breadth of easy to use tools for various applications of sequencing.

  11. 15. sij

    Tzvetana Kerelska from kicking off this year’s developer’s conference by reminding us of all the improvements made in the last year.

  12. 23. pro 2019.

    Just a heads up for users, I will be at and in San Diego in January. Not presenting but if you want to ask questions in person or get some ideas/help on pipelines, feel free to message me to meetup. Or if you see me, just say hi.

  13. 12. pro 2019.
    Odgovor korisnicima i sljedećem broju korisnika:

    Looking forward to the great science at . Thanks for including me.

  14. 10. pro 2019.

    Looking forward to on the 15th. Expecting great discussions + updates from . Also meeting some friends , , + finding new ones. Chances are the flamingos are also there.. ;)

  15. 25. stu 2019.

    Hey tweeps! We have a few speaking slots open for developers conference Wed after . If you have a new method that uses reads, let me know!

  16. 12. velj 2019.

    Slides for my lightning talk on detecting small variants in long reads are here: Better late than never, right?

    Prikaži ovu nit
  17. 16. sij 2019.

    Fantastic discussions about current issues and future needs in the analysis of more and better data for both DNA and RNA.

  18. 16. sij 2019.

    AR: Why do we need more human references? Because there’s a lot of variation out there that isn’t represented in our references.

  19. 16. sij 2019.

    Arang Rhie from NHGRI closes out the lightning talks with her work on assembling human genomes and with resolves haplotypes.

  20. 16. sij 2019.

    . on haplotype resolved human genomes

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