DNA-seq
Our ThruPLEX and PicoPLEX DNA-Seq library kits enable the generation of high-complexity NGS libraries from a variety of challenging sample types such as cell-free DNA, formalin-fixed paraffin-embedded (FFPE) DNA, and extremely low-input samples.
Our kits and their applications are described in detail in the technical notes and other resources listed below.
Whole genome amplification (WGA)
Single-cell DNA-seq for variant detection
Accurate and reproducible profiling of CNVs, SNVs, indels, and other small structural variants.
Whole genome amplification for variant detection
Single-cell whole genome amplification for CNV and SNV detection.
DNA-seq
DNA-seq from low-volume sample inputs
High-quality NGS libraries from low-input DNA samples.
Whole-exome sequencing
High-quality NGS libraries for whole-exome sequencing from low-input DNA samples.
Plasma-seq for cell-free DNA-seq
High-quality NGS libraries from cell-free DNA and RNA samples.
DNA-seq from FFPE samples
High-quality NGS libraries from FFPE samples.
ThruPLEX HV: DNA-seq for cfDNA and FFPE
High-quality NGS libraries from FFPE and cell-free DNA.
ThruPLEX HV PLUS: DNA-seq for cfDNA and FFPE
High-quality NGS libraries from FFPE and cell-free DNA, now with enzymatic fragmentation.
Comparison note: ThruPLEX HV vs NEBNext Ultra II
Learn how ThruPLEX HV compares to other end-to-end library prep systems.
Comparison note: ThruPLEX HV PLUS vs KAPA HyperPlus and NEBNext Ultra II FS
Learn how ThruPLEX HV PLUS compares to other end-to-end library prep systems.
ChIP-seq for epigenetic profiling
High-quality NGS libraries from limited amounts of ChIP DNA.
DNA-seq with molecular tags for rare variant detection
DNA-seq for FFPE and cell-free DNA featuring UMIs to enable detection of low-frequency mutations.
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