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For isolation of high-molecular-weight genomic DNA
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For parallel processing of up to 12 samples during nucleic acid isolation using magnetic beads
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For RNA library construction from single cells for Illumina sequencing applications
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For DNA library construction from single cells for Illumina sequencing applications
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For highly uniform whole genome amplification (WGA) from single cells or limited sample material
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For whole transcriptome amplification of total RNA or mRNA from single cells
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For parallel whole genome and whole transcriptome amplification from cells and limited samples
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For enhancing functionalities of CLC Genomics Workbench, Biomedical Genomics Workbench, and CLC Server solutions
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For use with the GeneRead Library Quant System
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For targeted enrichment of a customizable gene panel using any of 570 laboratory-verified primer sets prior to NGS
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For targeted enrichment of a customized set of genes or genomic regions specific for your NGS needs
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For qPCR-enabled quantification of NGS libraries before sequencing
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For fast and efficient preparation of DNA libraries for use in NGS applications
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For quick and reliable removal of DNA fragments <150 bp for library preparation in NGS applications
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For targeted enrichment of biologically and clinically relevant panels using any of 15 laboratory-verified primer sets prior to NGS
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For analyzing and interpreting real-time PCR or NGS data
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For fast and efficient preparation of DNA libraries for use in NGS applications
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For fast and efficient preparation of DNA libraries for use in NGS applications
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For fast and efficient preparation of DNA libraries for use in NGS applications
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