Our new e-course on statistics for MS-based proteomics data analysis is now online. Learn the basics and how to document your analyses in fully reproducible reports using R/RStudio or our shinyApp: https://t.co/CLTuUO66Uc
Why would we only care about differences in the **average** gene expression in a scRNA-seq DE analysis? 🤔
We present a framework to jointly test for differences in average gene expression and gene DETECTION. Extra hypothesis tested, no extra cost!
https://t.co/1V7EKNswyk
Clustering algorithms report clusters even when none exist. In single-cell RNA-Seq pipelines, novel cell types are often identified by clustering algorithms. Expanding on Kimes et al.'s work, we introduce significance analysis for single-cell RNA-Seq data: https://t.co/ut1kPjKVCM
Fast differential usage, aberrant splicing and expression analysis that scales to large RNA-seq data compendia? Check @Alex_Segers_ preprint to see how juggling offsets unlocks bulk RNA-seq tools for these applications. Great collaboration with @elfridedebaere lab and @RAREMED1
First day of the 4-day BePA Proteomics Summer School @ VIB starting with interesting talks on Proteomics applications and the DOs and DONTs of sample preparation
👉👉 https://t.co/zL3peCo99Z
#proteomics#tech#training#summerschool
DeepLC is out in @naturemethods! Our LC retention time prediction tool for any modification has already shown substantial impact on the analysis of DIA data, proteogenomics, PSM validation, rescoring PSMs... Definitely give it a try for your application! https://t.co/UadyHSbC0e
Excited to announce that I'm now an Associate Editor for Reproducibility at the Journal of the American Statistical Association 👩💻
🔖 https://t.co/s9JoAmP8g2
👀 Want to know more? Check out the JASA Reproducibility Guide: https://t.co/3r7ajr3AM0
Open modification search engine ionbot has the potential to cause a paradigm shift in the proteomics field. Amalgamation of multiple research lines over a decade in the @compomics group that led up to this moment: https://t.co/bi8hp0byeq
Do you like Multi Omics Factor Analysis ? Check out MUON spearheaded by @gtcaa - a software framework that makes multi omics data analysis easy and fun. preprint: https://t.co/WwFUCPLEmJ
Credit to all the methods and software MUON builds on, in particular scanpy!
msqrob2 for robust DE analysis of MS-based proteomics is finally available in bioconductor. Thx to all contributors @LudgerGoeminne, Adriaan sticker, @MilanMlft, @lgatt0, & @OllyMCrook https://t.co/vex8sIsrLx
*satuRn* is published at @F1000Research! *satuRn* is an R software package for studying differential transcript usage in large (sc-)RNA-seq datasets.
Key features:
- High performance
- Fast
- Accurate FDR control
- Direct transcript-level inference
https://t.co/sdPwzreDPk
Bioconductor 3.13 is Released!! Thank you to all developers and community members for contributing to the project. See full release announcement: https://t.co/TVyB7z3XRw #rstats@Bioconductor
🥳I'm so excited to say that it is finally time to enjoy a GeneTonic - now in preprint format 🎉🎉🎉
https://t.co/sdW2XZnagh
@AnnekathrinLudt joined the team to deliver a whole set of new features, now it is even easier to combine *all* elements from DE and enrichment 🥃🍹🍸🍺
In our newest paper, we profiled a 48-h diel transcriptome of the benthic diatom Seminavis robusta. Our analysis revealed very high levels of rhythmicity, oscillating lincRNAs, 12-h periodic genes, exciting potential new cell wall genes and much more!
Fast and memory-efficient code for performing PCA on Pearson residuals from sparse single cell RNA-Seq data.
1.3 million x 1,000 gene matrix can be done in under 50 seconds on 32GB MacBook.
Starting to add optimized functions for most common tasks here: https://t.co/3PWOyPZhf6
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL) https://t.co/8JUSLtQKAs #bioRxiv
Ooh this looks like a way better method of skimming literature than my current method of bookmarking anything interesting on twitter and then never being able to find it again...