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
The PicoPLEX Gold Single Cell DNA-Seq Kit is the preferred technology for detecting aneuploidies in embryo biopsies, characterizing the heterogeneity of cancer tissues, profiling circulating immune cells, and more.
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 FLEX 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
Incorporating unique molecular identifiers (UMIs), ThruPLEX Tag-Seq FLEX offers added power in correcting for polymerase and sequencing errors—key advantages when detecting low-frequency variants.
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