!bioinformatics
@programming.devhttps://genomic.social/@mmarchin/113068708416226845
Calling everyone who works in or with a #bioinformatics core facility - we need your help! We’d like to hear your ideas on what skills core facility scientists need at different levels (I, II, III or manager). Interested in helping? Please fill in this survey by September 30th. https://docs.google.com/forms/d/e/1FAIpQLSf2P_d6nX6JmhFJtcBNX3zOQB-DuAuOMiIDc7t57tZVM4POog/viewform The results of this survey will feed into the bioinformatics core facility competency framework. Find out more: https://sites.google.com/ebi.ac.uk/bioinfocore-competencies/
2024 Galaxy Community Conference
SAVE THE DATE!
GCC 2024 will be held from June 24th–29th in Brno, Czech Republic!
See you there! #UseGalaxy2024
For more information, please visit: https://galaxyproject.org/events/gcc2024/
https://www.youtube.com/watch?v=p01s2mmsk3o
The 3 core skills to start with. Where to focus your learning depending on your level of biology expertise. 0:00 The intersection0:59 Skill 1: Python1:31 Ski...
https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-023-05438-2
Background Visualizing genome coverage is of vital importance to inspect and interpret various next-generation sequencing (NGS) data. Besides genome coverage, genome annotations are also crucial in the visualization. While different NGS data require different annotations, how to visualize genome coverage and add the annotations appropriately and conveniently is challenging. Many tools have been developed to address this issue. However, existing tools are often inflexible, complicated, lack necessary preprocessing steps and annotations, and the figures generated support limited customization. Results Here, we introduce ggcoverage, an R package to visualize and annotate genome coverage of multi-groups and multi-omics. The input files for ggcoverage can be in BAM, BigWig, BedGraph and TSV formats. For better usability, ggcoverage provides reliable and efficient ways to perform read normalization, consensus peaks generation and track data loading with state-of-the-art tools. ggcoverage provides various available annotations to adapt to different NGS data (e.g. WGS/WES, RNA-seq, ChIP-seq) and all the available annotations can be easily superimposed with ‘ + ’. ggcoverage can generate publication-quality plots and users can customize the plots with ggplot2. In addition, ggcoverage supports the visualization and annotation of protein coverage. Conclusions ggcoverage provides a flexible, programmable, efficient and user-friendly way to visualize and annotate genome coverage of multi-groups and multi-omics. The ggcoverage package is available at https://github.com/showteeth/ggcoverage under the MIT license, and the vignettes are available at https://showteeth.github.io/ggcoverage/ .
This post is a 'game' proposal. Reply with your favorite tool, if yours has been posted already, just upvote the comment.
Feel like in need of some inspiration? check tou https://github.com/topics/bioinformatics ;)
This is the place to:
Remember that this is a community we build together 🦾