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  • pacbio
    Member
    • Sep 2011
    • 91

    1/30 Webinar: Amplicon Sequencing: High-fidelity Long-read Sequencing with Confidence

    Amplicon sequencing requires the highest quality, accuracy, and throughput to be cost effective. With PacBio amplicon sequencing, you do not need to compromise on quality, accuracy, or throughput to be cost effective.

    High-throughput amplicon sequencing using Single Molecule, Real-Time (SMRT) Sequencing and the Sequel System allows you to easily and cost effectively generate high-fidelity, long reads (>99% single-molecule read accuracy and >99.999% consensus accuracy) from amplicons ranging in size from several hundred base pairs to 20 kb.

    This webinar will explore:
    • Latest advances in SMRT Sequencing performance for detection of all variant types even in difficult to sequence regions of the genome
    • Multiplexing options to increase throughput and improve efficiency
    • Examples of amplicon sequencing of clinically relevant targets


    Speakers:
    Cheryl Heiner, Principal Scientist, PacBio
    Lori Aro, Sr. Director Clinical Genomics, PacBio

    Register for January 30: 9 AM PST/12:00 PM EST/ 5:00 PM GMT
    Register for January 30/January 31: 5 PM PST/ 9 AM CST (Jan. 31)/ 10 AM JST (Jan. 31)/ 12 PM AEDT (Jan. 31)

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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