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  • pacbio
    Member
    • Sep 2011
    • 91

    Live Webinar 4/29 & 4/30: Gain New Insights in Genome and Transcriptome Research

    Hear from PacBio CSO Jonas Korlach as he discusses the scientific value of greater than 10 kb, unbiased sequencing reads for an expanding range of applications. SMRT Sequencing technology has rapidly advanced in read lengths, throughput and adoption in the past year – Dr. Korlach will review published work from a variety of researchers utilizing these new capabilities.

    Tuesday, April 29 @ 5:00 PM, PST
    Wednesday, April 30 @ 8:00 AM, PST

    Full webinar details

    Benefits of attending the webinar:
    • Hear how SMRT Sequencing brings new insights to applications, such as: full-length transcript sequencing, de novo genome assembly, and targeted sequencing for minor-variant detection and haplotype phasing.
    • Learn about recently published studies enabled by SMRT Sequencing in many different research areas.
    • Find out how the current performance specifications for the PacBio® RS II system (read length, accuracy, uniformity and base-modification detection) can add a new dimension to your research

    For the most recent publications and latest information on PacBio, vist our blog
  • pacbio
    Member
    • Sep 2011
    • 91

    #2
    Recording of webinar now available

    A recording of the webinar is now available - enjoy!

    Comment

    Latest Articles

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    • GATTACAT
      Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
      by GATTACAT
      Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
      07-01-2026, 11:43 AM
    • SEQadmin2
      Nine Things a Sample Prep Scientist Thinks About Before Sequencing
      by SEQadmin2


      I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.

      Here are nine questions we think about, in roughly the order they matter, before...
      06-18-2026, 07:11 AM

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