QIAGEN

used for high-efficiency, NGS-based, target enrichment of DNA (including cfDNA, FFPE, and low-quality samples) to detect mutations like SNVs, indels, and CNVs. They utilize Unique Molecular Indices...

used for ultra-sensitive, targeted next-generation sequencing (NGS) to detect low-frequency variants like SNVs, indels, and CNVs (down to 0.1% VAF) from challenging samples. Utilizing Unique...

Panel containing all reagents for 96-sample multimodal DNA and RNA sequencing reactions. QIAGEN

used to facilitate efficient DNA binding and precise size selection of NGS library fragments, working alongside QIAseq Beads. It is designed for magnetic bead-based cleanup and size selection steps...

used for constructing NGS libraries from DNA, specifically for targeted enrichment and high-accuracy detection of variants (SNVs, indels, CNVs) in solid/hematologic tumors, germline mutations, and...

used to sequence libraries generated with QIAseq Targeted DNA Panels on Illumina instruments. This primer ensures proper binding to the UMI-containing, targeted DNA libraries, allowing for accurate,...

used for NGS-based detection, quantification, and discovery of known and novel gene fusions and splicing variants in RNA, particularly for cancer research. It employs molecular barcodes (UMIs) to...

conv kit RI (12) Genomics / NGS. designed for NGS-based detection, quantification, and identification of known and novel gene fusions, particularly in cancer research. Utilizing UMI-based digital RNA...

(96) Genomics / NGS. used for unique dual indexing (UDI) in Illumina NGS library preparation, enabling up to 96-sample multiplexing per set to prevent index hopping and improve accuracy. It is...

(384) Genomics / NGS. used for multiplexing up to 96 samples (or part of a 384-sample set) for Next-Generation Sequencing (NGS) on Illumina platforms. It provides unique dual-indexed adapters to...

(384) Genomics / NGS. used for multiplexing up to 96 DNA samples per sequencing run on Illumina platforms, specifically with QIAseq Targeted DNA Panels. This kit, containing 384 indices, enables...

(96) Genomics / NGS. used for unique dual indexing (UDI) of up to 96 DNA or RNA libraries, specifically enabling high-throughput NGS on Illumina platforms. It mitigates index hopping, ensures...