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  • pacbio
    Member
    • Sep 2011
    • 91
    #1

    Webinar: Smoking Out Structural Variants in the Cannabis Genome

    Join our speakers as they share the latest advances in cannabis genomics, including: (1) How PacBio long-read sequencing enables high-quality genomics research in plants, (2) High-quality annotation of the cannabis reference genome using full-length transcript sequencing, and (3) New insights into cannabinoid synthesis across different types of cannabis plants.

    Register to attend: https://programs.pacificbiosciences....9-04-17/3zbk5f
    Tags: None
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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.
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  • SEQadmin2
    Nine Things a Sample Prep Scientist Thinks About Before Sequencing
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    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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