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GenBank release 257.0 is now available! This release has 25.10 trillion bases and 3.69 billion records.

https://practical-stats-med-r.netlify.app/

More likely you have error in config file.  Go to /etc/apache2 and run the test $ apache2ctl configtest I will report the error line in your config file. 

abc@ubuntu:/var/www/html$ sudo systemctl restart apache2Job for apache2.service failed because the control process exited with error code.See "systemctl status apache2.service" and "journalctl -xe" for details.

There are numerous genome assembly tools available, each with its strengths and weaknesses. Here is a list of some widely used genome assembly tools as of my last update in September 2021: SPAdes: An assembler specifically designed for...

Before applying to Ph.D. positions in bioinformatics, it's essential to prepare yourself thoroughly to increase your chances of success. Here are some key areas to focus on: 1. Academic Preparation: Ensure you have a strong foundation in...

Creating a bootable Linux OS drive involves creating a bootable installation media (such as a USB flash drive) from the Linux distribution's ISO file. The process can vary slightly depending on your operating system (Windows, macOS, or Linux). Here...

Whether you should buy a Chromebook for bioinformatics work depends on several factors, including the specific bioinformatics tasks you need to perform, your workflow, and your overall computing needs. Chromebooks can be a cost-effective option for...

Validating a genome assembly is crucial to ensure its accuracy and completeness. Several methods can be employed to assess the quality of a genome assembly. Here are some of the best methods commonly used in the field: Benchmarking against a...

Assembly and Genome record pages now redirect to new NCBI Datasets pages.

Bioinformatics is an interdisciplinary field that combines biology, computer science, statistics, and mathematics to analyze and interpret biological data. It plays a crucial role in advancing our understanding of biological processes, enabling...

Working with SARS-CoV-2 data, especially data related to human subjects, often involves sensitive information and potential privacy concerns. The need for ethical clearance or approval depends on the specific context and the nature of the research...

Metabuli 분리 improves metagenomic read classification through metamers, DNA-AA k-mers, to be sensitive and specific, recovering 99% and 98% of DNA or AA classifiers.   Metabuli is metagenomic classifier that jointly analyze both DNA and amino...

This tutorial describes the usage of homologizer to phase gene copies into polyploid subgenomes. The tutorial is an abbreviated version of a soon-to-be published paper in Methods in Molecular Biology. Please see that paper for many more...

The Genome Context Viewer (GCV) is a web-app that visualizes genomic context data provided by third party services. Specifically, it uses functional annotations as a unit of search and comparison. By adopting a common set of annotations, data-store...

g:Convert enables to convert between various gene, protein, microarray probe and numerous other types of namespaces. We provide at least 40 types of IDs for more than 60 species. The 98 different namespaces supported for human include Ensembl,...

Proksee is an expert system for genome assembly, annotation and visualization. To begin using Proksee, provide a complete genome sequence, sequencing reads or a CGView/Proksee map JSON file.

https://hplgit.github.io/bioinf-py/doc/pub/html/main_bioinf.html #Learn #Python #Bioinformatics