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A new crop modification technique relies on a spray that introduces bioactive molecules into plant cells through their leaves.
Researchers have developed a test to screen for three rare genetic disorders simultaneously in newborns, enabling earlier diagnosis and treatment.
The Earlham Institute has boosted its capability in high-fidelity long-read sequencing to support the Earth BioGenome Project.
The lab will make available the latest in DNA sequencing, array platforms and data analysis tools, all supported by specialist scientific expertise.
A new type of COVID-19 test could help streamline the process of identifying COVID-19 cases, tracking SARS-CoV-2 variants and detecting co-infecting viruses.
Merck has launched its CRISPR inhibition (CRISPRi) whole-genome libraries and pools to complement its suite of genome-editing products and technologies.
Public health laboratories will aim to sequence the virus genomes of all positive COVID-19 tests in Australia and track COVID-19 using genomics across the country.
The TruePrime Single Cell Whole Genome Amplification Kit from 4basebio uses a novel method to achieve genome amplification from single or just a few cells.
Blood cancer patients at Melbourne's Epworth HealthCare and Peter MacCallum Cancer Centre now have access to circulating tumour DNA (ctDNA) genomic testing.
UK scientists have pioneered a new method for profiling the microbiome of preterm babies that can significantly speed up the identification of infections and indicate more effective treatments.
By combining single-cell analysis techniques with machine learning algorithms, researchers have developed a method to 'fingerprint' human cells.
scATAC-seq technology provides unprecedented opportunity to study the impact of epigenetic changes on development and disease.
Phase Genomics applies Hi-C and other proximity-ligation methods to enable chromosome-scale genome assembly and metagenomic deconvolution, as well as analysis of structural genomic variation and genome architecture.