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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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For fast and efficient preparation of DNA libraries for use in NGS applications
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For research use, clinical reporting or clinical diagnostic purposes
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A high-performance computing solution for mapping reads to a reference and de novo assembly of next-generation sequencing data.
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For advanced DNA, RNA, and protein analyses
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For flexible next-generation sequencing data analysis
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CLC Genomics Cloud Engine
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For analyzing, comparing, and visualizing next-generation sequencing data
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ANNOVAR
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For identifying disease-causing variants from human whole genome, exome and gene panel next-generation sequencing studies
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For modeling, analyzing, and understanding complex 'omics data
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