QuantideX® NGS DNA Hotspot 21 Kit

The QuantideX® NGS DNA Hotspot 21 Kit (RUO) is a next generation sequencing (NGS) research tool that interrogates 46 hotspot regions (amplicons) within 21 genes that are commonly mutated in a number of solid and hematological malignancies.  The kit detects over 1,500 known variants, including single nucleotide variants (SNVs), insertions/deletions (indels), and structural rearrangements.  Leveraging our proprietary NGS-in-a-Box™ workflow and Sample-Aware™ bioinformatics quality control solutions, this kit provides a simple, robust, and reliable NGS assay for the routine investigation of these genomic variants.

Features & Benefits

The QuantideX NGS DNA Hotspot 21 Kit combines Asuragen’s unique NGS-in-a-Box™ solution with a streamlined testing workflow to enable unprecedented NGS workflow efficiency and high sensitivity at low input amounts from precious FFPE samples.

Reduced Complexity
Assay incorporates sample-to-data solutions in a unique NGS-in-a-Box™ configuration

  • Detects >1,500 variants from commonly mutated genomic regions across multiple tumor types
  • End-to-end kitted solution
  • Fully integrated data analysis pipeline

Optimized Workflow
Provides operational efficiencies to reduce testing costs, hands-on and total turnaround time

  • Reduced labor required for library preparation
  • Improved turnaround time enables higher throughput
  • Common workflow across portfolio streamlines training & implementation

Quality Performance
Highly sensitive assay with integrated, Sample-Aware™ bioinformatics software and built-in quality checks to minimize erroneous results and sample failures

  • Highly sensitive detection of DNA-based variants
  • Low input (~20ng) of DNA from FFPE
  • Sample-Aware™ bioinformatics analysis and sample quality control

Product Description

Relevant Content
The QuantideX NGS DNA Hotspot 21 Kit detects over 1,500 genomic variants as reported in the Catalogue of Somatic Mutations in Cancer (COSMIC) Database within 21 genes, representing approximately 80% of known variants within these targets.

Table 1: Mutation coverage of QuantideX NGS DNA Hotspot 21 Kit

 

Table 2: Clinical relevance of covered mutations


1NCCN Clinical Practice Guidelines
*Includes gastric, pancreatic, glicomas, sarcomas, and other tumor types

A Fully Integrated Workflow
A unique NGS-in-a-Box™ configuration offers a simplified and fully integrated NGS workflow with cGMP-manufactured reagents, components and controls ready to use.

 

Includes:

  • An internal quality control kit to measure the absolute copy number of amplifiable DNA and reports PCR inhibition
  • Gene-specific PCR primers and Master Mix reagents
  • Dual-index barcodes for sample multiplexing
  • Library purification and quantification reagents
  • Integrated data analysis and reporting software (QuantideX NGS Reporter)

 


Rapid & Efficient
Adopt and run NGS-based analysis with minimum investment of time and resources, regardless of NGS experience and infrastructure.

  • Fully integrated workflow reduces complexity and ensures reliable reagent quality
  • Push-button analysis & reporting makes bioinformatics easy and efficient, regardless of experience level
  • Integrated kit reduces overall workflow time

 


Performance Data

Highly Sensitive and Accurate Detection of DNA Mutations

 

QuantideX® NGS Reporter

Push-button analytics & reporting suite – Set-up-and-go workflow designed for easy installation and implementation, right out of the box.

Operates on a standard desktop computer – Install locally on a desktop computer using Windows® operating system.  No prior bioinformatics experience or large server environments required.

Comprehensive– Full bioinformatics and reporting of variants (SNVs, Indels), and standard QC metrics are automatically calculated.

Integrates Sample-Aware – Bioinformatics with integrated functional template copy number analysis dramatically reduces false-call rates.

Ordering

Product Name Number of Reactions Catalog Number
QuantideX NGS DNA Hotspot 21 Kit* 48 46108

T 1.877.777.1874 | 512.681.5200
F 512.681.5202
E orders@asuragen.com

*For Research Use Only. Not for use in Diagnostic procedures.

QuantideX® NGS DNA Hotspot 21 Kit

The QuantideX® NGS DNA Hotspot 21 Kit is an in vitro diagnostic, next-generation sequencing (NGS) panel for the detection of clinically relevant variants across a multitude of tumor types, including non-small cell lung cancer, colorectal cancer, and melanoma.  The kit screens for over 1,500 known genomic variants, including single nucleotide variants (SNVs), insertions/deletions (indels), and structural rearrangements, many of which are treatable with novel therapies, inform on patient management, or are the subject of further clinical evaluation.  Leveraging our proprietary NGS-in-a-Box™ workflow and Sample-Aware™ bioinformatics quality control solutions, the panel provides a robust and reliable NGS solution for the identification of clinically relevant targets you and your clinicians can trust.

Features & Benefits

The QuantideX NGS DNA Hotspot 21 Kit combines Asuragen’s unique NGS-in-a-Box™ solution with a streamlined testing workflow to enable unprecedented NGS workflow efficiency and high sensitivity at low input amounts from precious FFPE samples.

Reduced Complexity

Assay incorporates sample-to-data solutions in a unique NGS-in-a-Box™ configuration

  • Detects >1,500 variants from commonly mutated genomic regions across multiple tumor types
  • End-to-end kitted solution
  • Fully integrated data analysis pipeline
Optimized Workflow

Provides operational efficiencies to reduce testing costs, hands-on and total turnaround time

  • Reduced labor required for library preparation
  • Improved turnaround time enables higher throughput
  • Common workflow across portfolio streamlines training & implementation
Quality Performance

Highly sensitive assay with integrated, Sample-Aware™ bioinformatics software and built-in quality checks to minimize erroneous results and sample failures

  • Highly sensitive detection of DNA-based variants
  • Low input (~20ng) of DNA from FFPE
  • Sample-Aware™ bioinformatics analysis and sample quality control

Product Description

Relevant Content

The QuantideX NGS DNA Hotspot 21 Kit detects over 1,500 genomic variants as reported in the Catalogue of Somatic Mutations in Cancer (COSMIC) Database within 21 genes, representing approximately 80% of known variants within these targets.  Several of these variants are associated with approved therapies, while others are currently in trials to clarify their clinical significance.

Table 1: Mutation coverage of QuantideX NGS DNA Hotspot 21 Kit

Table 2: Clinical relevance of covered mutations

1NCCN Clinical Practice Guidelines
*Includes gastric, pancreatic, glicomas, sarcomas, and other tumor types

Fully Integrated Workflow
A unique NGS-in-a-Box™ configuration offers a simplified and fully integrated NGS workflow with cGMP-manufactured reagents, components and controls ready to use.

 

 

Includes:

  • An internal quality control kit to measure the absolute copy number of amplifiable DNA and reports PCR inhibition
  • Gene-specific PCR primers and Master Mix reagents
  • Dual-index barcodes for sample multiplexing
  • Library purification and quantification reagents
  • Integrated data analysis and reporting software (QuantideX NGS Reporter)

 

Rapid & Efficient

Adopt and run NGS-based analysis with minimum investment of time and resources, regardless of NGS experience and infrastructure.

  • Fully integrated workflow reduces complexity and ensures reliable reagent quality
  • Push-button analysis & reporting makes bioinformatics easy and efficient, regardless of experience level
  • Integrated kit reduces overall workflow time

Performance Data

Highly Sensitive and Accurate Detection of DNA Mutations

 

 

 

 

QuantideX® NGS Reporter

 

Push-button analytics & reporting suite – Set-up-and-go workflow designed for easy installation and implementation, right out of the box.

Operates on a standard desktop computer – Install locally on a desktop computer using Windows® operating system.  No prior bioinformatics experience or large server environments required.

Comprehensive – Full bioinformatics and reporting of variants (SNVs, Indels) and standard QC metrics are automatically calculated.

Integrates Sample-Aware – bioinformatics with integrated functional template copy number analysis dramatically reduces false-call rates.

Ordering

Product Name Number of Reactions Catalog Number
QuantideX NGS DNA Hotspot 21 Kit* 48 76044

T 1.877.777.1874 | 512.681.5200
F 512.681.5202
E orders@asuragen.com

*For Research Use Only. Not for use in Diagnostic procedures.

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