Illumina, IDX-PI-1004-192, Kit D, indices PI501-8, PI701-12

Name: Kit D, indices PI501-8, PI701-12
Brand: Illumina
SKU: IDX-PI-1004-192

Kit D, indices PI501-8, PI701-12

Catalog Number: IDX-PI-1004-192

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Category

NGS Library Preparation Kits

TagsSequencing kits Library preparation kits

Description

Overview
The Pillar oncoReveal BRCA1 & BRCA2 + CNV Panel targets BRCA1/2 mutations and copy number variations. The assay uses proprietary Stem Loop Inhibition-Mediated amplification (SLIMamp) technology, a tiled amplicon-based library prep chemistry for efficient single-tube target enrichment.
Maintain control of samples and results with single-tube, tiled amplification that can be performed in-house by any NGS lab
Achieve variant detection as low as 1% VAF without UIDs, even with limited DNA input or poor sample quality
Improve lab efficiency and reduce “no calls”, repeat testing and difficult interpretation decisions
< 8 hours from DNA to sequencer

Example workflow
Pillar oncoReveal BRCA1 & BRCA2 + CNV Panel
MiSeq i100 Series
MiSeq System
NextSeq 550 System
Illumina Connected Insights

Panel specifications
Pillar oncoReveal BRCA1 & BRCA2 Plus CNV Panel specifications for the detection of DNA variants from BRCA 1 and BRCA2.
Pillar® oncoReveal™ BRCA1 & BRCA2 + CNV Panel (24 reactions)
HDA-BR-1003-24
Pillar® oncoReveal™ BRCA1 & BRCA2 + CNV Panel (24 reactions) View less
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Indices PI501-8, PI701-4 (32 combinations, 96 reactions)
IDX-PI-1001-96
Indices PI501-8, PI701-4 (32 combinations, 96 reactions) View less
Kit D, indices PI501-8, PI701-12
IDX-PI-1004-192
Kit D, indices PI501-8, PI701-12 View less
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Specifications

General

Content specifications	Covers full coding gene sequence, plus flanking intronic regions (10bp)
Instruments	MiSeq System , NextSeq 550 System , MiSeqDx in Research Mode , NextSeq 550Dx in Research Mode , MiSeq i100 System , MiSeq i100 Plus System
Method	Targeted DNA sequencing , Amplicon sequencing
Nucleic acid type	DNA
Specialized sample types	Blood, Low-input samples, FFPE tissue
Species category	Human
Technology	Sequencing
Variant class	Somatic variants, Germline variants, Single nucleotide variants (SNVs), Insertions-deletions (indels), Copy number variants (CNVs)

Ordering

Notice

Unless otherwise stated, the minimum order amount is USD 1,000.
For orders below USD 1,000, an additional handling fee may apply, or we may arrange local delivery / local handover where available.
All quotations are subject to final confirmation, including product availability, lead time, batch information, shipping cost, and applicable export or handling requirements.
For quotation requests, please send an RFQ from website or contact:

[email protected]

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