Every cancer insight you can imagine, & then some. A cancer-free future starts with a transformative view of the methylome, genome, & transcriptome – all from a single platform. With our unique multiomics toolkit, never see cancer the same way again. https://t.co/qSxcj1i5o7
Hereditary cancer testing shouldn’t leave gaps. With the Oxford Nanopore hereditary cancer panel, examine 258 cancer genes in one assay and detect SNVs, CNVs, pseudogenes & methylation — transforming how we understand hereditary cancer risk. https://t.co/AfKxjUThU8
As we continue the countdown to #Nanoporeconf, who remembers Helen Gunter’s talk from London Calling 2024? Her work accelerated the development of mRNA vaccines, demonstrating the opportunities for direct RNA sequencing.
Find out more: https://t.co/ecBnyR1aiA
In our upcoming webinar, discover how #nanopore technology rapidly identifies viral respiratory pathogens. With simple end-to-end workflows, you'll learn how to generate all the data you need to inform a public health response.
"https://t.co/YuqPG5sQVG
Nanopore sequencing overcomes the limitations of Sanger, tackling complex DNA regions like high-GC content and tandem repeats. Check out this blog to learn why @markwbudde calls it a ‘game changer’, making plasmid verification faster and more reliable.
https://t.co/CeeqBJJDMm
High-quality meets complete.
Short reads often miss critical genomic information. This brochure shows how long #nanopore reads can sequence complex regions, such as repeats, to produce high-quality microbial genomes.
Read here: https://t.co/ekRAB4gjHl
🌱 ¿Tu proyecto trabaja por la conservación de la biodiversidad? ¡Esta convocatoria es para ti! 📣
Únete a la Iniciativa Darwin, un programa británico🇬🇧 que ofrece financiación a proyectos de conservación y reducción de la pobreza.
Postúlate aquí 👉🏽 https://t.co/p1HbfxgeG4
In this webinar, Etienne Raimondeau will share an overview of the point and click EPI2ME workflows available to investigate genetic variation and methylation simultaneously, perform de novo assembly & examine the transcriptome of cancer.
Register here: https://t.co/MVMaDbS6yK
See what you're missing.
Hear how @MishaKolmogorov has developed an efficient and scalable workflow that generates state-of-the art small and structural variant calls, and de novo assemblies, from a single PromethION Flow Cell.
Register here: https://t.co/ofVeKYARMC
Try our new DNA Markers & Ladders Selection Tool to find the best one for your needs. This tool provides a quick and easy way to find your perfect ladder match from NEB!
Link https://t.co/RKVmsWCkQy
El 15/12/1860 nació Niels Ryberg Finsen, Premio Nobel de Medicina en 1903 por su contribución al tratamiento de enfermedades, especialmente lupus vulgar, con radiación lumínica concentrada
Llevamos a cabo los cursos precongreso Entomovirología: Trabajo de campo en Quebrada Valencia, Sierra Nevada de Santa Marta y Secuenciación de virus usando nanoporos en el marco del X Simposio Colombiano de #Virología@BiovIntCIAT_esp
El 16/11/1999 falleció Daniel Nathans, Premio Nobel de Medicina compartido en 1978 por el descubrimiento de las enzimas de restricción y su aplicación a problemas de genética molecular