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• • LEGE@lege

  

  LEGE published a blog post The Role of lncRNA in Bioinformatics: Unlocking the Secrets of the Genome 690 days ago

  lncRNAs are the hidden gems of the genome, and bioinformatics is the key to unearthing their full potential. As research progresses, lncRNAs could pave the way for novel diagnostics, targeted therapies, and personalized medicine, revolutionizing...
• • LEGE@lege

  

  LEGE posted a new ad in the Opportunity Postdoc in Comparative Single Cell Genomics at University of Basel 690 days ago
• • LEGE@lege

  

  LEGE created a new bio-script Methods to upgrade the Ubuntu ! 690 days ago
• • LEGE@lege

  

  LEGE posted a new ad in the Opportunity Professor/Senior Lecturer of Comparative Genomics @ University of Glasgow 691 days ago
• • BioStar@biostar

  

  BioStar answered the question How to downgrade the Perl 692 days ago

  Using Perlbrew Install Perlbrew: curl -L https://install.perlbrew.pl | bash source ~/perl5/perlbrew/etc/bashrc Install and switch to the desired Perl version: perlbrew install perl-<version> perlbrew switch...
• • BioStar@biostar

  

  BioStar posted a new ad in the ResearchLabs Rennison Lab ! 732 days ago
• • BioStar@biostar

  

  BioStar published a blog post Exploring Bioinformatics Job Websites: Your Gateway to a Thriving Career 739 days ago

  Bioinformatics is a rapidly growing field at the intersection of biology, computer science, and data analytics, with applications in healthcare, genomics, drug discovery, and more. As demand increases for skilled professionals who can manage,...
• • LEGE@lege

  

  LEGE bookmarked Variant Calling Pipeline 739 days ago

  The variantcalling.nf nextflow script will take any number of samples with paired-end reads in FASTQ format, map reads using Bowtie2, process BAM files, and finally call variants using BCFtools v1.21 and/or Freebayes v1.3.6. If part of the...

  https://github.com/Tom-Jenkins/nextflow-pipelines/blob/main/docs/variant-calling.md
• • LEGE@lege

  

  LEGE created a page Libraries or management tools for high throughput sequencing data 754 days ago

  GATB Library. The Genome Analysis Toolbox with de-Bruijn graph. A large part of tools developed by the GenScale team are based on this library.These methods enable the analysis of data sets of any size on multi-core desktop...
• • LEGE@lege

  

  LEGE created a new bio-script Install Edirect ! 755 days ago
• • LEGE@lege

  

  LEGE created a new bio-script Extract the fasta sequence using ids 755 days ago
• • LEGE@lege

  

  LEGE posted a new ad in the Opportunity Bioinformatician at QUB, UK 756 days ago
• • LEGE@lege

  

  LEGE created a page Bioinformatics Lecture Notes 757 days ago

  Study Resources for ECM3413 - Bioinformatics Contents   General Information Lecture Slides Past Exam Paper Continuous Assessments Suggested Reading List General Information This module runs in Semester 2.  It is...
• • Neel@neelam

  

  Neel posted a new ad in the ResearchLabs Chirag Lab at IISc 770 days ago
• • LEGE@lege

  

  LEGE created a new bio-script R script to add P-Values in plots ! 770 days ago
• • LEGE@lege

  

  LEGE bookmarked SVbyEye: R Package to visualize alignments between two or multiple DNA sequences 771 days ago

  R Package to visualize alignments between two or multiple DNA sequences includinga number of functionalities to facilitate processing of alignments in PAF format. SVbyEye, an open-source R package to visualize and annotate sequence-to-sequence...

  https://github.com/daewoooo/SVbyEye
• • LEGE@lege

  

  LEGE bookmarked LoVis4u: Locus Visualisation tool for comparative genomics 771 days ago

  Description LoVis4u is a bioinformatics tool for Loci Visualisation. LoVis4u, a command-line tool and Python API designed for highly customizable and fast visualisation of multiple genomic loci. LoVis4u generates vector images in...

  https://github.com/art-egorov/lovis4u
• • LEGE@lege

  

  LEGE bookmarked Figeno: Tool for plotting sequencing data along genomic coordinates. 771 days ago

  Tool for plotting sequencing data along genomic coordinates. FIGENO is a FIGure GENerator for GENOmics With figeno, you can plot various types of sequencing data along genomic coordinates. Video...

  https://github.com/CompEpigen/figeno
• • LEGE@lege

  

  LEGE posted to the wire 777 days ago

  To #uninstall #phonelink in window run it in poweshell: Get-AppxPackage Microsoft.YourPhone -AllUsers | Remove-AppxPackage
• • LEGE@lege

  

  LEGE bookmarked NGenomeSyn: an easy-to-use and flexible tool for publication-ready visualization of syntenic... 778 days ago

  NGenomeSyn: an easy-to-use and flexible tool for publication-ready visualization of syntenic relationships across multiple genomes  NGenomeSyn [multiple (N) Genome Synteny], for publication-ready visualization of syntenic relationships of...

  https://github.com/hewm2008/NGenomeSyn

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