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Researchers have characterised and analysed the unique architecture of the largest and most complex CRISPR-Cas system known to date

Researchers at the University of Copenhagen (UCPH) have characterised and analysed the unique architecture of one of the most complex […]

Studies find CRISPR gene-editing of human embryos give rise to unwanted results.

CRISPR gene-editing is a technique that allows the genomes of living organisms to be modified. Naturally, this has been looked […]

Capture the dark genome: From repeat-expansions to CRISPR unintended mutations – Webinar Summary

Tackling Disease-Related Repeat Expansion Analysis – Marzia Rossato What is the Dark Genome? The dark genome refers to parts of […]

First Point-of-Care Test for COVID-19 using CRISPR announced

Binx Health and Sherlock Biosciences have announced a partnership to develop the world’s first point-of-care diagnostic test for COVID-19 using […]

Webinar: Capture the dark genome – From repeat-expansions to CRISPR unintended mutations

Sequenced genomes retain a surprisingly large number of “dark” regions – sections that have proven difficult to characterise via short-read […]

WhopperPhage – The huge virus with CRISPR components

Huge viruses with CRISPR-Cas and translational components have been described by researchers at the University of California, Berkeley – providing […]

FoG 2020 Presentation Mike Hubank NHS England Genomics Lab Hub: Using CRISPR-CAS9 for rapid gene fusion detection

Mike Hubank, Scientific Director at NHS England Genomics Lab Hub spoke at the Festival of Genomics 2020.

FoG 2020 Presentation Ben Davies, University of Oxford: Crispr/Cas9 site-specific nucleases for the production of genetically modified disease models

Dr. Ben Davies received his PhD in molecular biology from the University of Edinburgh where he first encountered gene targeting […]

CRISPR system developed for dose-dependent gene expression

CRISPR is renowned for its precise gene-editing ability, but is gaining ground in alternative applications; namely the control of selected […]

Improved methods for CRISPR homology-directed repair using Alt-R HDR enhancer and ssDNA donors with optimized design

CRISPR-Cas proteins introduce double-stranded breaks (DSBs) at targeted genomic loci. These are repaired by endogenous cellular pathways such as non-homologous […]