To make producing soft core alignments easier, we developed Core-SNP-filter, a simple and efficient tool to process SNP alignments with user-defined thresholds.
https://t.co/Vyny4agUQk
(4/4)
Do you make core genome alignments for phylogenomics? @monaltaouk and I explored how including sites with some missing data (a soft core) can improve analysis, especially for large datasets.
https://t.co/WnmQuLFkwj
(1/4)
And the benefits grow with dataset size! A 100% strict core may work fine for small datasets (e.g. ~10 genomes) but is devastating for very large ones (e.g. 1000+ genomes). A 95% soft core works well across all dataset sizes.
(3/4)
@krannich479 You can certainly give it a try, but linear sequences can be challenging for Autocycler at the moment (a focus for future development), so if your viral genome is not circular, it may not be a great fit.
New year, new assemblies!
I'm excited to announce Autocycler, my new tool for consensus assembly of long-read bacterial genomes!
It's the successor to Trycycler, designed to be faster and less reliant on user intervention.
Check it out: https://t.co/NksiyESF7u
(1/5)
Autocycler is still new and evolving. I'll continue to improve it based on your feedback. A big thank you to the alpha testers who gave me feedback before this release! Give it a try and share your thoughts.
(5/5)
However, Autocycler still allows users to manually intervene when they would like to. So it aims for the best of both worlds: either hands-off automated assemblies or hands-on curated assemblies, as the user sees fit.
(4/5)
Just had my first experience with CycloneSEQ data and shared my findings in this blog post:
https://t.co/70UrEkdC4N
How does CycloneSEQ compare to @nanopore? I looked at both read-level and consensus-level accuracy. Check it out!
If you want to try out the new --bacteria Medaka polishing option after reading Ryan's thoughts in his latest blogpost, the newest Hybacter v0.10.0 release now includes it as the default
https://t.co/YvgSurzg36
Excited to share this preprint where we’ve used genomic analysis of >3000 genomes to study Klebsiella pneumoniae in a One Health perspective 🦠🔬👩💻#OneHealth#KLEBGAP#KlebClub@IrenLohr @DrKatHolt @NORKLEBNET
@martinalexsmith@nanopore If you're assembling hac reads, then make sure to run Medaka. I've found it's much more beneficial for hac-based assemblies than for sup-based assemblies.
I finally got around to testing HERRO (https://t.co/irsWGnjpT2), the new @nanopore read correction algorithm which takes simplex ONT reads to PacBio-HiFi-level accuracy.
I was impressed! Findings are on my blog in a two-part post:
https://t.co/unWf7fIMFS
https://t.co/yEllyimky8
How low can you go? Short-read polishing of Oxford Nanopore bacterial genome assemblies. Published #OpenAccess and fee-free in #MGen using a #PublishAndRead agreement: https://t.co/DSPZ4EFUK2