First Peer-Reviewed Study by Mammoth Biosciences of COVID-19 Test

Mammoth Biosciences is an SF-based CRISPR diagnostic startup company. Today, it has published a peer-reviewed study, which reveals the validation of using the testing procedure to determine the presence of coronavirus in the patients.
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Mammoth Biosciences

Mammoth Biosciences

Mammoth Biosciences is an SF-based CRISPR diagnostic startup company. Today, it has published a peer-reviewed study, which reveals the validation of using the testing procedure to determine the presence of coronavirus in the patients. The study is published in Nature and shows that the performance on par with the prevailing PCR-based molecular analyzing, which is currently approved by the FDA to carry on the test to determine coronavirus in patients.

The DETECTR platform of Mammoth Biosciences is planned to have benefits over the conventional testing procedure in various ways including the reconfigurability to determine the virus since it utilizes the CRISPR to focus on a specific genetic sequence and enable a cleavage, which efficiently acts as a warning for diagnostic equipment. Generally, in a similar way, the CRISPR allows the researchers to focus on a specific portion of the DNA for alteration or removal with precision.

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The Testing and Procedure

The diagnostic of Mammoth allows the programmable, targeted matching with reference string by leading to confirmation that the RNA of this virus is present in the patient. The test, which the Mammoth is developing, has shown validated utilization under two weeks. The researchers claim that the platform is planned from ground up for quick reconfigurability to locate the virus threats. This test can deliver the result within 45 minutes, and the result will be delivered via “lateral flow strip”. It is the same sort of read-out you see with the pregnancy test that you do in your home.

It is now relatively easier to interpret. DETECTR doesn’t need a lab setting to provide results. Instead, it can be conducted with the portable heat blocks, merged with available standard reagents.

The study included 36 patients with confirmed coronavirus infections, and 42 patients had other sorts of viral respiratory problems. Importantly, the test showed 95% positive diagnostic accuracy.

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