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 rare disease”? 14 August | Wednesday | 17:00 at O.A.S.E. Forum Register HERE and come meet fellow biodata enthusiasts on-site, learn something new & have… Continue reading Bio Data Science Evening August
Category: science
Explain Podcast 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, where hosts shortly discuss one term from Genetics. This time it’s about introns and exons! Let’s keep the conversation going – choose the platform where… Continue reading Explain Podcast Episode 11 is out!
Explain Podcast 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 episode, we now release a new subsection QuickGen, where hosts shortly discuss one term from Genetics. This time it’s about transposons or…JUMPING GENES! Let’s keep… Continue reading Explain Podcast Episode 10 is out!
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 something new & have a great time together! After the lecture we’ll enjoy networking get-together with pizza&drinks! Organized by the West German Genome Center. Supported… Continue reading Bio Data Science Evening June
Exciting Update on Genomic Benchmarking!
Exciting news from our WGGC 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: Delve into this pioneering work and stay at the forefront of genomic benchmarking!
Method of the Year 2022: long-read sequencing
LRS was selected as the method of the year 2022 by Nature Methods! This highlights the success of LRS in unraveling the dark regions of the human genome as part of the Telomere to Telomere (T2T) Consortium as well as for another organism. Cite this article & find out more: Method of the Year 2022:… Continue reading Method of the Year 2022: long-read sequencing