Life science technology company PacBio (NASDAQ:PACB), a developer of advanced sequencing solutions, and microbiome research and discovery specialist Intus Bio announced on Friday the launch of GutID, the first commercial human gut health test powered by PacBio's HiFi sequencing technology and Intus Bio's Titan-1 platform.
GutID is designed to provide a comprehensive and accurate analysis of the gut microbiome, including strain-level identification of both beneficial and pathogenic bacteria.
The test utilises PacBio's long-read sequencing technology, enabling high-resolution analysis of the microbiome and delivering robust and repeatable results.
GutID is targeted at individuals seeking to understand and improve their gut health, and is particularly beneficial for those with conditions such as irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD).
The test involves a simple at-home sample collection and provides users with a detailed report, including a microbiome health score and personalised recommendations.
Relay Therapeutics wins FDA breakthrough status for zovegalisib in breast cancer treatment
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Valneva and Instituto Butantan launch pilot chikungunya vaccination campaign in Brazil
Lupin launches Dasatinib tablets in US market
WuXi Biologics enters into licence and research service agreement with Vertex Pharmaceuticals
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Astrazeneca Imfinzi perioperative regimen gains positive EU CHMP opinion in early gastric cancer
I Peace generates human iPS cells from NKT cells and offers them for research use
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
AstraZeneca agrees obesity and type 2 diabetes collaboration with CSPC
Ascletis Pharma Inc reports topline results from Phase III open-label study of denifanstat
Innovative Molecules GmbH completes Phase 1 clinical development programme for adibelivir
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA