Seegene Inc
Contact

Complete solution for COVID-19 response

In response to the rapidly evolving COVID-19 pandemic and upcoming flu season, Seegene is committed to continuously develop and support effective tools for the fight against this global pandemic.

Complete solution for COVID-19 response


Accurate COVID-19 testing is essential for reducing the spread of SARS-CoV-2, the coronavirus that causes COVID-19, and for appropriate patient care.

Seegene’s COVID-19 solutions, which include multiple target genes for SARS-CoV-2, are multiplex real-time PCR assays intended for the detection of nucleic acids from SARS-CoV-2 in upper respiratory specimens (nasopharyngeal swab, oropharyngeal swab, aspirate and etc.) and lower respiratory specimens (sputum, bronchoalveolar lavage) from patients suspected of COVID-19. The solutions can be applied on Seegene’s All-in-One automated platform that enables high-throughput testing.




Analytes

Allplex™ 2019-nCoV Assay

  • - N gene
  • - RdRP gene
  • - E gene
  • - Internal control (IC)

Allplex™ SARS-CoV-2 Assay

  • - N gene
  • - S gene
  • - RdRP gene
  • - E gene
  • - Internal control (IC)

Allplex™ SARS-CoV-2/FluA/FluB/RSV Assay

  • - N gene
  • - S gene
  • - RdRP gene
  • - Influenza A
  • - Influenza B
  • - RSV A/B
  • - Endogenous internal control (IC)
  • - Exogenous internal control (IC)

Seegene Symposium & Exhibition

LMCE 2020
Education Workshop

COVID-19 : current prospective
solution
> View detail

ECCVID 2020
Virtual Integrated Symposium

Breakthrough of Pandemic Times: COVID-19 faces the Next Pandemic
>View detail > Official website

ECCVID 2020
Virtual Industry Learning

‘Twindemic’ Beyond the Outbreak & More
>View detail > Official website

AACC 2020
Virtual Exhibition

Complete Solution for COVID-19 Response
> Official website

Overview of product selection criteria



Expanded selectivity of syndromic test


Allplex™ SARS-CoV-2 Assay can be used alone or compatible with high multiplex respiratory essential panel for other common respiratory infections, including influenza A and B, metapneumovirus, parainfluenza virus 1/2/3/4, adenovirus, rhinovirus A/B/C and respiratory syncytial virus A/B, to provide more insights for diagnosis of symptomatic patients.


Primary screening for COVID-19, Flu and RSV

Allplex™ SARS-CoV-2/FluA/FluB/RSV Assay is designed to detect and differentiate between SARS-CoV-2, influenza A, influenza B and RSV
for primary screening during the upcoming flu season.


More reliable results using dual internal controls


- The endogenous and exogenous internal controls are designed to verify  the entire process from sample collection to nucleic acid extraction and PCR steps

- The endogenous internal control enables validating correct sampling for self-collected specimens

Increased accuracy by minimizing risks


Multiplex real-time PCR with high sensitivity and specificity by utilization of  Seegene’s proprietary technologies

Detecting N, S, RdRP and/or E target genes of SARS-CoV-2 to minimize the risk of genetic variations and allow high accuracy 

No cross-reactivity confirmed with respiratory pathogens including SARS, MERS and SARS-related viruses

Seegene OVERCOMM*
web-based statistic program

Seegene is supporting extensive clinical studies in multi-sites and multi-nation on a combined test of the most common respiratory viruses and SARS-CoV-2 from influenza like illness patient’s specimens.

It would help meet the global interests and needs for a comprehensive understanding of the syndromic test related to respiratory pathogens including SARS-CoV-2. The program is designed to simply visualize the prevalence of pathogens and demonstrate cases of multiple pathogens infection. 


*Overseas Validation Experiments for Respiratory virus & Coronavirus co-testing in Multi-center, Multi-nation

go to OVERCOMM site

Powerful automation platform

Seegene’s automated molecular diagnostic platform allows a unique streamlined workflow with quick and simple steps for detection of COVID-19.  

STARlet IVD or NIMBUS IVD

Automated Extraction & PCR Setup
> View more

CFX96TM Dx

Detection by Real-time PCR
>View more

Seegene Viewer

Automated Data Analysis
>View more

Kick your Real-time PCR up a notch!

With Seegene’s core technologies and proprietary know-hows, enhance your MDx products with incomparable performance and usability.


Oligo Design

Oligo design technology for high multiplex PCR: SG-Insilico™

Enables rapid designing of high multiplex oligos using Seegene-developed algorithms and confidential variables.


Amplification

Highly specific amplification technology for high multiplex PCR: DPO™

Allows the implementation of high multiplex diagnostics with unparalleled specificity using Seegene’s unique primer structure.


Target Detection

High multiplex target detection technology: TOCE™

Achieves accurate target signals by independently controlling multiple target signals for primer and probe annealing temperatures.


Quantitative
Detection

High multiplex target detection & quantification technology: MuDT™

Broadens capacity for high multiplex target detection & quantification by enabling analysis of multiple Ct values in a single detection channel.


Interpretation

High multiplex signal processing technology: DSP™

Enables accurate reporting of target’s positive or negative results through Seegene’s proprietary signal processing algorithms.

Note

[1] Allplex™ 2019-nCoV Assay has not been FDA cleared or approved. This test has been authorized by FDA under an emergency use authorization for use by authorized laboratories. This test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of the emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under section 564(b)(1) of the Act, 21 U.S.C. § 360bbb- 3(b)(1), unless the authorization is terminated or revoked sooner.

[2] Allplex™ SARS-CoV-2/Flu A/Flu B/RSV Assay, SARS-CoV-2 Assay and RV Essential Assay are intended for in vitro diagnostic use in Europe and not available in all countries.