NGS-CN Meeting 2024 – with AGD
NGS-CN has exciting changes in the annual meetings – from this year on, each October we’ll meet AGD colleagues in Bonn! Scientific Program is almost settled – but the registration
Bio Data Science Evening August
Our on-site Bio Data Science Evenings at University of Düsseldorf are happy to host Florian Kraft, who will discuss an important question… WHY size matters when we talk about “sequencing
Explain Podast Episode 11 is out!
Explain Podcast moves towards discussing MGI sequencing…and not only. Did you know they have the whole sequencing room available? Fancy! At the end of each episode, we now release QuickGen,
NGS Webinar July 2024
In our next webinar Natja Haag from Aachen will tell us all about pain mechanisms and how they are working on deciphering them using singlecell sequencing methods. Join us on
NGS Webinar June II 2024
This June we have not one but two NGS webinars for you! In our second webinar, Denny Popp from Leipzig, will talk about longread sequencing in clinical applications. Join us
NGS-CN Summer School 2024
Online NGS-CN Summer School “Sequencing Fundamentals & Bioinformatics” 9 – 10 September Open for everybody – don’t miss a chance to listen & ask experts!REGISTER HERE On-site NGS-CN Hands-on Training “Bioinformatics:
Explain Podast Episode 10 is out!
Season 2 of the Explain Podcast is out&about – yey! We start by discussing Bionano and Nabsys – curious tech that we’ve classified as…Genome Mapping! At the end of each
NGS Webinar June I 2024
Ana Conesa is one of the leading specialists in RNA transcript isoform sequencing. She and her partners pioneered the implementation of novel longread Sequencing technologies – both PacBio and Oxford
Bio Data Science Evening June
Our on-site Bio Data Science Evenings at University of Düsseldorf are back! 13 June | Thursday | 17:00+ at O.A.S.E. Register here and come meet fellow biodata enthusiasts on-site, learn
NGS Webinar May 2024
How much do you actually know about the heartache? Can you tell what’s the link between heartache and transcriptomics? On Thursday the 23rd May at 11:00 CEST Mirela Balan will introduce
NGS Webinar April 2024
…here comes our next NGS Webinar! On the 25th April Thursday at 11:00 CEST Prof. Dr. Stephan Ossowski will give us a glimpse on how rare disease diagnostics in complex
New funding opportunities for sequencing projects!
Great news! Deutsche Forschungsgemeinschaft (DFG) – German Research Foundation offers additional opportunities to apply for funding high sequencing costs projects together with academic sequencing institutions. Sequencing projects with costs in
Explain Podast: New episode is out now!
The last Episode of the first Season is out&about!We explore three prominent SINGLE CELL sequencing techniques using frameworks of 10x Genomics | Parse Biosciences | BD. Find it on Spotify or Deezer.
Explain special episode 3 is out!
In this Explain Podcast special episodewe explore the PhiX bacteriophage and its role in sequencing the first DNA-based genome, as well as unique molecular modifiers and something sequencing definitely always
Explain episode 4 is out!
In this Explain Podcast episode explore with us Iontorrent sequencing – how this technique works? Is it still used and where? Which ions are we talking about and where they
Exciting Update on Genomic Benchmarking!
Exciting news from our NGS-CN experts! The small variant calling benchmarking initiative by the NGS-CN and the GHGA is out and waiting for scientific feedback. Publication Link: https://doi.org/10.12688/f1000research.140344.1 Publication Highlights:
Explain episode 3 is out!
In this Explain Podcast episode explore with us – polonies, base jokers….ligation! Listen to our podcast and we’re happy to receive your feedback&questions via Email (podcast[dot]explain[at]ngs-kn[dot]de). ___The Explain Podcast is
NGS webinar speaker announcement: Ahmad Aziz
Register for our next NGS webinar on September 29th: Tandem repeats as genetic modifiers of brain function in health and disease