Next-generation sequencing key visual
Using NGS for cancer genotyping applications
For isolation of genomic, mitochondrial, bacterial, parasite or viral DNA
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For simultaneous purification of genomic DNA and total RNA (including small RNAs) from formalin-fixed, paraffin-embedded tissue sections
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For simultaneous purification of DNA and RNA from cells and tissues
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For simultaneous purification of genomic DNA and total RNA, including miRNA, from cells and difficult-to-lyse tissue
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For automated purification of nucleic acids from up to 14 human, forensic, or molecular diagnostics samples
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For automated purification of DNA from 1–6 samples or 1–14 samples per run
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For purification of up to 500 µg genomic DNA from whole blood
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For purification of DNA from tissues fixed and stabilized in PAXgene Tissue Containers
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For isolation of free-circulating DNA and RNA from human plasma or serum
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For purification of up to 12 µg genomic, mitochondrial, or viral DNA from blood and related body fluids
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For purification of genomic DNA from formalin-fixed paraffin-embedded tissues
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For fully integrated automation of complete workflows, from sample preparation to assay setup
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For highly uniform whole genome amplification (WGA) from single cells or limited sample material
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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 targeted enrichment of a customized set of genes or genomic regions specific for your NGS needs
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For fully automated sample prep using QIAGEN spin-column kits
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For fast and efficient preparation of DNA libraries for use in NGS applications
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For DNA library construction from single cells for Illumina sequencing applications
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For fully automated sample prep using QIAGEN spin-column kits
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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 qPCR-enabled quantification of NGS libraries
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For use with the GeneRead Library Quant System
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For effortless DNA and RNA analysis
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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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