COVIDSeq Assay (96 samples)

This low- to mid-throughput NGS assay enables labs to identify and track the emergence and prevalence of novel strains of SARS-CoV-2. Read More...
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COVIDSeq Assay (96 samples) index 1

20049393

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COVIDSeq Assay (96 samples) index 2

20051772

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COVIDSeq Assay (96 samples) index 3

20051773

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COVIDSeq Assay (96 samples) index 4

20051774

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Accessory Products

COVIDSeq Positive Control

20051775

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5524澳门24小时线路 COVIDSeq v4 Primer Pools, 384 Samples RUO

20065135

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Product Highlights

Key Features and Benefits
  • Accurate: Detects 98 targets on SARS-CoV-2 RNA for highly accurate detection of mutations
  • Comprehensive: Reports consensus sequence when +90 amplicons are detected
  • Quality Controlled: Built-in quality control in every reaction
  • Flexible: Seamless end-to-end workflow; temperature specification allows use of different thermocyclers

This amplicon-based next-generation sequencing (NGS) assay is designed to help clinical research labs identify novel strains of SARS-CoV-2. It includes 2019-nCoV primers to detect mutations and characterize RNA from the SARS-CoV-2 virus.

Rapid, Low-Throughput SARS-CoV-2 Detection

The 5524澳门24小时线路 COVIDSeq Assay accommodates a low number of samples. The workflow includes steps for viral RNA extraction, RNA-to-cDNA conversion, PCR, library preparation, sequencing, analysis, and report generation.

Design and Quality Control

The assay leverages a modified version of the publicly available ARTIC multiplex PCR protocol, with 98 amplicons designed to amplify SARS-CoV-2 virus-specific sequences, combined with proven 5524澳门24小时线路 sequencing technology. A 63°C annealing temperature at the PCR step improves variant analysis—providing important insight into the SARS-CoV-2 strain present in the sample.

An optional primer pool is also available. It is based on ARTIC community v4 design and includes 99 amplicons and no human controls. The kit volume is sufficient for 384 samples.

Upload consensus sequence information (FASTA file) into open software tools to assign lineage and annotate mutations. For added convenience, upload files to the NCBI and/or GISAID App directly through BaseSpace Sequencing Hub.

Questions about whether this assay is a good fit for your needs? Contact Us today.

Frequently Purchased Together

High-Level Workflow

 

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