QIAGEN QIAseq Targeted DNA Ultra (12)

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 Molecular Indices (UMIs), they enable precise, error-correc

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Product Name	Description	Item#	QTY
QIAGEN QIAseq Targeted DNA Ultra UDI	Set D (96) used for multiplexed Next-Generation Sequencing (NGS) library preparation on Illumina platforms. It utilizes unique dual-index (UDI) primers to mitigate index hopping, enabling high-accuracy, low-frequency variant detection (down to 0.1% V	2927-334195	EA
QIAGEN QIAseq Targeted DNA Ultra (96)	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 (UMIs) and dual-barcoded adapters for ultra-sensitiv	2927-334055	EA
QIAGEN QIAseq Targeted DNA Ultra UDI	Set B (96) used for high-throughput, Next-Generation Sequencing (NGS) library preparation, specifically designed for molecular barcoding and identification of up to 96 DNA samples on Illumina platforms. It enables precise, target-enriched sequencing,	2927-334175	EA
QIAGEN QIAseq Targeted DNA Ultra UDI	(96) designed for high-throughput NGS library preparation, enabling ultra-sensitive detection of low-frequency variants (down to 0.1%) in DNA, particularly cfDNA. They utilize Unique Dual Indexes (UDI) to eliminate index hopping and Unique Molecular	2927-334151	EA
QIAGEN QIAseq Targeted DNA Ultra UDI	Set A (96) used to generate library prep indices for targeted next-generation sequencing (NGS) of DNA on Illumina platforms. It enables high-accuracy, multiplexed identification of variants, including somatic mutations, SNVs, and CNVs, in cancer rese	2927-334165	EA

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QIAGEN QIAseq Targeted DNA Ultra (12)

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