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  • Bukowski
    replied
    Some minION sequencing?

    There's nothing wrong with that number of contigs from a 2x250 MiSeq run.

    Leave a comment:


  • szy0931
    replied
    Thak you very much!
    I have one set paired (2 x250) Illumnia MiSeq data from Salmonella.
    They look good by FastaQC
    I did Unicycler assembling but I did not get a whole genome.
    The longest contig is 446213 and totally I got 59 contigs longer than 500 bp.
    What can I do next?

    Leave a comment:


  • Bukowski
    replied
    Yes, because it acts as an optimiser for Spades.. which is perfectly happy with just short read data.

    Leave a comment:


  • szy0931
    started a topic Unicycler

    Unicycler

    I know Unicycler is specialised for bacterial genome assembling from hybrid of short and long reads.
    But, is Unicycler also good for bacterial genome assembling only from short reads such as from Illumina MiSeq

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  • SEQadmin2
    Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
    by SEQadmin2



    CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

    Despite this, “CRISPR helped turn genome editing from a specialized technique into
    ...
    07-31-2026, 11:01 AM

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