Neel
Bioinformatics Beginner
Our Sponsors
Related items
LRSDAY: Long-read Sequencing Data Analysis for Yeasts
By Poonam Mahapatra 2596 days agogithub.com - Long-read sequencing technologies have become increasingly popular in genome projects due to their strengths in resolving complex genomic regions. As a leading model organism with small genome size and great biotechnological importance, the budding...Comparative Genomics Data Set Including 240 Mammals Released !
By Jit 2146 days agoThe genome of 130 mammals was sequenced by a large international consortium and the data was analyzed together with 110 existing genomes to allow scientists to identify the important positions in the DNA.AMR Database !
By LEGE 853 days agogithub.com - ARG-ANNOT. PMID: 24145532 CARD. PMID: 23650175 MEGARes PMID: 27899569 NCBI BioProject: PRJNA313047 plasmidfinder PMID: 24777092 resfinder. PMID: 22782487 VFDB. PMID: 26578559 SRST2's version...What is Data Science? — A Bioinformatics Perspective
By Abhi 476 days agoIn today’s era of big biology, we’re generating more data than ever before—genomes, transcriptomes, proteomes, metabolomes, microbiomes… you name it. But raw biological data doesn’t speak for itself. Making sense of it requires more than traditional...maftools : Summarize, Analyze and Visualize MAF Files
By Neel 2112 days agowww.bioconductor.org - With advances in Cancer Genomics, Mutation Annotation Format (MAF) is being widely accepted and used to store somatic variants detected. The Cancer Genome Atlas Project has sequenced over 30 different cancers with sample size of...“One code to find them all”: a perl tool to conveniently parse RepeatMasker output files
By Poonam Mahapatra 3045 days agodoua.prabi.fr - One code to find them all is a set of perl scripts to extract useful information from RepeatMasker about transposable elements, retrieve their sequences and get some quantitative information. Assemble RepeatMasker hits into complete TE copies,...Smash: An alignment-free method to find and visualise rearrangements between pairs of DNA sequences
By Jit 3814 days agobioinformatics.ua.pt - Smash is a completely alignment-free method/tool to find and visualise genomic rearrangements. The detection is based on conditional exclusive compression, namely using a FCM (Markov model), of high context order (typically 20). For...Bioinformatics Training Material !
By BioStar 1297 days agoglittr.org - Glittr is a curated list of bioinformatics training material.All material is: In a GitHub or GitLab repository Free to use Written in markdown or similar NOTE: This list of courses is selected only based on the above criteria.There...I-PV: Interactive Protein Sequence Visualization
By Jit 3381 days agohttp://i-pv.org/ - I-PV is a interactive data visualization software designed for inspection of protein sequences and mutation information. It is mainly used for Genetics and Bioinformatics. So what exactly makes it standout? http://i-pv.org/ipv_recchromoMap-An R package for Interactive visualization and mapping of human chromosomes
By Rahul Nayak 3023 days ago Comments (1)An R package for Interactive visualization and mapping of human chromosomes
