Its been a while but last weekend I finally got to sail again a race.
The best view when finishing a race :)
Fritz Sedlazeck
Xinchang Zheng
You can join us at the end of Nov if you want to learn how to analyse SVs
www.physalia-courses.org/courses-work...
The guy in the middle might be a reference :)
Last year we had participants from around the world. Its a great open event to get to know new people and new tricks every year :) .
Join us at our 8th Hackathon @bcmhgsc.bsky.social !
Registration:
forms.gle/N4FDxuq34g5J...
Dates: 25-28th Aug 2026
Location: Hybrid (online + in Houston)
We are going to work on #bioinformatics problems that will be reported in F1000 publication. Come and join us!
@dcgenomics.bsky.social
Fritz Sedlazeck
Sensational #ASHG event on detecting variants, including Structural Variants, from long reads learning.ashg.org/products/unc...
@sedlazeck.bsky.social @bcmhouston.bsky.social
Fritz Sedlazeck
Registrations are now open for the 4th edition of the Structural Variant detection course! with @sedlazeck.bsky.social & Luis Paulin!
Learn short & long-read workflows, assembly & mapping methods, SV filtering, QC, population VCFs & much more
www.physalia-courses.org/courses-work...
Structural variant calling using Sniffles2 www.nature.com/articles/s41...
Congratulations to Luis and @sedlazeck.bsky.social
BCM Human Genome Sequencing Center
Physalia-courses@Online
Physalia-courses@Online
Physalia-courses@Online
Today we kicked off the #ComparativeGenomics course with @sedlazeck.bsky.social & Ingo Ebersberger!
On Day 1, we’re covering de novo assembly strategies, best practices, and quality control for genome assemblies.
Last seats available! 🚨
Join our #ComparativeGenomics course with @sedlazeck.bsky.social & @Ingo Ebersberger and learn how to analyse, compare, and interpret genomes using modern bioinformatics approaches. Don’t miss it—registration is closing soon!
@nanoporetech.com @pacbio.bsky.social
Physalia-courses@Online
Physalia-courses@Online
30 November - 2 December 2026 To foster international participation, this course will be held online
Sniffles2 is an open-source software for reliable detection of structural variants (50 bp and upward) from long-read sequencing. Sniffles2 is able to call variants over a wide variant allele fraction ...