#Karrieremontag: 🧬🌲 Mit #eDNA für mehr #Biodiversität!

Forsche am Thünen-Institut für #Forstgenetik im Projekt EDNA-Lab. Dein Einsatzort wird unter anderem das neue Landschaftslabor EiLT sein:
👉 Nimm eDNA-Proben.
👉 Extrahiere eDNA, etwa aus Regenwasser oder Mulm.
👉 Führe PCR-Reaktionen durch.
👉 Etabliere und optimiere Metabarcoding-Analysen.
👉 Und mehr.
https://t1p.de/Thuenen_Job200

#Forstwissenschaften #Biologie #Waldökosysteme #UmweltDNA #NextGenerationSequencing #Molekularbiologie

🧬 Can DNA molecules become the most reliable “hard drives” ever created?

🔗 Pantheon-DNA: Versatile encoding-decoding system with integrated adaptive NGS preprocessing algorithms for DNA data storage. Computational and Structural Biotechnology Journal, DOI: https://doi.org/10.1016/j.csbj.2025.09.002

📚 CSBJ: https://www.csbj.org/

#DNA #DataStorage #ComputationalBiology #Bioinformatics #DataScience #NextGenerationSequencing #SyntheticBiology #Genomics #MolecularData

Next Generation Sequencing: A Brief Guide to NGS Technology!

Explore how Next-Generation Sequencing (NGS) is evolving genomics. Get to know about the key benefits of NGS technology in medicine.

Keep Reading On Here: https://rb.gy/n3m362

#genetictesting #nextgenerationsequencing #generationsequencing #dnasequencing #healthcare

Next Generation Sequencing Technology: Key Benefits & Features

Explore how Next-Generation Sequencing (NGS) is evolving genomics. Get to know about the key benefits of NGS technology in medicine.

Per SIN e SICP importante la diagnosi pre e post-natale per le cardiopatie congenite

#Cardiologia #NextGenerationSequencing

https://trendsanita.it/malformazioni-cardiache-alla-base-anche-fattori-genetici/

Malformazioni cardiache: alla base anche fattori genetici

Per SIN e SICP importante la diagnosi pre e post-natale per le cardiopatie congenite

In #NextGenerationSequencing news, $ONTTF Oxford @nanopore presented results for 31 Dec 2022: Oxford Nanopore Technologies plc
Final results for the year ended 31 December 2022
Strong underlying1 LSRT revenue growth of 30% in 2022, driven by innovation and customer acquisition;
The NovaSeq X is the natural step forward from the NovaSeq 6000 systems for Illumina, considering what the company has based their Next-Generation Sequencing strategy in ever-increase in throughput by increasing the number of clusters in flow cells and incresing the speed of
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RT @albertvilella
In #NextGenerationSequencing news, $ILMN Illumina finally announced the availability and pricing for their Infinity Long Reads solution. At…
https://twitter.com/AlbertVilella/status/1637031289063612418
Tweet / Twitter

Twitter

Morgan MacKenzie's (overwhelmingly) and yours truly review just published 👇

An Introduction to #Nanopore #Sequencing: Past, Present, and Future Considerations https://www.mdpi.com/2140596 #mdpimicromachines

#nextgenerationsequencing #ngs

An Introduction to Nanopore Sequencing: Past, Present, and Future Considerations

There has been significant progress made in the field of nanopore biosensor development and sequencing applications, which address previous limitations that restricted widespread nanopore use. These innovations, paired with the large-scale commercialization of biological nanopore sequencing by Oxford Nanopore Technologies, are making the platforms a mainstay in contemporary research laboratories. Equipped with the ability to provide long- and short read sequencing information, with quick turn-around times and simple sample preparation, nanopore sequencers are rapidly improving our understanding of unsolved genetic, transcriptomic, and epigenetic problems. However, there remain some key obstacles that have yet to be improved. In this review, we provide a general introduction to nanopore sequencing principles, discussing biological and solid-state nanopore developments, obstacles to single-base detection, and library preparation considerations. We present examples of important clinical applications to give perspective on the potential future of nanopore sequencing in the field of molecular diagnostics.

MDPI
In #NextGenerationSequencing news, Nava Whiteford @[email protected] has been writing about the sensitivity of qPCR vs DNA Sequencing in a series of substack posts.
This has become more relevant in recent years with the aim of detecting SARS-CoV-2 material in COVID19 patients.
In #NextGenerationSequencing news, more details of the new $200/genome pricing of Element Bio @[email protected] AVITI instruments and reagents. at 100 flowcells per quarter, it's a 2xAVITI system and $460/genome, and at 230+ flowcells/quarter, it's $200/genome with 3-5 AVITI systems.
In #NextGenerationSequencing news, $ILMN Illumina announced a product of their old array technology to assay methylation marks in a panel of >285k CpGs of the mouse genome. https://emea.illumina.com/products/by-type/microarray-kits/infinium-mouse-methylation.html
Infinium Mouse Methylation BeadChip | High-resolution epigenetic analyses of mouse strains

Features > 285k markers across the methylome for high-resolution epigenetic analyses of diverse murine strains.