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  • Combined Small RNA and mRNA Library Prep

    The NEXTFLEX® Combo-Seq™ mRNA/miRNA kit enables the user to generate mRNA and small RNA libraries in a single workflow using 5 ng – 100 ng of total RNA inputs, without requiring upfront rRNA depletion or poly(A) selection. The kit utilizes patented and patent-pending technology allowing the construction of a library from both mRNA and small RNA from a single input. Like the NEXTFLEX® small RNA-seq kit v3, the NEXTFLEX® Combo-Seq™ mRNA/miRNA library preparation kit utilizes adapters with randomized ends to greatly reduce bias compared to standard small RNA library preparation protocols. This allows a more accurate representation of small RNA in the starting material. Adapter-dimer reducing techniques built into the protocol enables gel-free workflow from inputs as low as 5 ng of total RNA. As a result, the kit is streamlined from start-to-finish and automated on the Sciclone® G3 NGS/NGSx workstations. Additionally, unique dual index barcode primers, included in the kit, prevent sample mis-assignment on Illumina® NovaSeq®, MiSeq®, and HiSeq® 2000/2500 platforms.
    For research use only. Not for use in diagnostic procedures.

Latest Articles

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  • seqadmin
    Advancing Precision Medicine for Rare Diseases in Children
    by seqadmin




    Many organizations study rare diseases, but few have a mission as impactful as Rady Children’s Institute for Genomic Medicine (RCIGM). “We are all about changing outcomes for children,” explained Dr. Stephen Kingsmore, President and CEO of the group. The institute’s initial goal was to provide rapid diagnoses for critically ill children and shorten their diagnostic odyssey, a term used to describe the long and arduous process it takes patients to obtain an accurate...
    12-16-2024, 07:57 AM
  • seqadmin
    Recent Advances in Sequencing Technologies
    by seqadmin



    Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.

    Long-Read Sequencing
    Long-read sequencing has seen remarkable advancements,...
    12-02-2024, 01:49 PM

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