Bernhard Bein

@bernhardbein.bsky.social

PhD student in comparative genomics @ Senckenberg and Goethe University Frankfurt

Absolute tour de force led by @ymalovichko.bsky.social, with contributions from many in the lab @leonhilgers.bsky.social @xuelingyi.bsky.social @mich-albertini.bsky.social Alejandro Gonzales-Irribarren, Evgeny Leushkin and many others Check #TOGA2 out: github.com/hillerlab/TO...

GitHub - hillerlab/TOGA2: TOGA2: A faster, more versatile successor of Tool to infer Orthologs from Genome Alignments

TOGA2: A faster, more versatile successor of Tool to infer Orthologs from Genome Alignments - hillerlab/TOGA2

github.com

Michael Hiller@hillermich.bsky.social · 2mo ago

The #TOGA2 preprint is now at www.biorxiv.org/content/10.6.... Describes the new method and the comparative genomics resource (annotations, orthologs, gene losses/dups, retrogenes and more) generated using a total of 9420 TOGA2 runs for 2173 vertebrate genome assemblies.

For those interested in PacBio's SPRQ-Nx chemistry and reusable SMRT Cells: in the Genome of Sweden project, we moved from 2 to 3 acquisitions per SMRT Cell in June. The results are impressive—we’re now approaching 400 Gb HiFi yield from a single SMRT Cell!

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I've always been fascinated with biodiversity, dreaming of discovering new species. That dream has finally come true: We found two new crab species tugged away in small streamlets in Guangdong! This journey started 7 years ago, huge thanks to Chao for taking me along! 🦀 🦀 🦀 doi.org/10.6620/ZS.2...

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Our paper on foldback artifacts in long-read sequencing is now published in BMC Genomics! We introduce Breakinator to flag foldback and chimeric artifacts across library types, sequencers, and chemistries. Paper: link.springer.com/article/10.1... With Matthew Meyerson and @lh3lh3.bsky.social

Detecting foldback artifacts in long-reads - BMC Genomics

Long-read sequencing data is useful for detecting large and complex structural variations; however, technical artifacts can lead to false structural variant calls. In our analyses, we became aware of ...

link.springer.com

Say hello to Nallo - our Nextflow pipeline for long-read WGS analysis!👋 It handles both ONT and PacBio data and we’re using this for rare disease and population projects in Sweden. A big team effort by Felix Lenner, Anders Jemt et al.🧬💻 academic.oup.com/bioinformati...

Nallo: a Nextflow pipeline for comprehensive human long-read genome analysis

AbstractMotivation. Long-read sequencing (LRS) is increasingly used for human medical research and clinical diagnostics, due to its capacity to generate co

academic.oup.com

The last chapter of my PhD is finally out !!!! In the same species, on neighboring islands, we see radically different warning colors emerge. Evolution in action: Selection-driven color variation in the aposematic strawberry poison frog, Oophaga pumilio: Current Biology www.cell.com/current-biol...

Selection-driven color variation in the aposematic strawberry poison frog, Oophaga pumilio

Aguilar-Gómez et al. use exome sequencing of 347 strawberry poison frogs to uncover the genetic basis of color variation. They identify that kit, ttc39b, and bco1 underlie blue-red, yellow-red, and gr...

cell.com