Results for "Standalone"
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UCSC Genome Browser and Blat software !
This directory contains Genome Browser and Blat application binaries built for standalone command-line use on various supported Linux and UNIX platforms. To determine which set of binar...2987 days ago
- ...ytoscape files to visualize transcript evidence that suggests adjacency between scaffolds and contigs. Software requirements BLAT (tested with Standalone BLAT v. 32×1). Source B...
2799 days ago
- CLgenomics is a standalone desktop software specifically designed for bacterial genome analysis. This program has a powerful multi-genome browser, which enables rapid and respons...
2608 days ago
- A tool for converting for recovering synteny blocks from multiple alignment (in MAF fromat) This tool is a standalone version of Ragout module [http://fenderglass.github./Ragout]
2532 days ago
RNAcon: web-server for the prediction and classification of non-coding RNAs
...of ncRNAs into different classes. The structural information based graph properties were used for the development of prediction model. The standalone version (Linux-based command-...2472 days ago
DFAST: a flexible prokaryotic genome annotation pipeline for faster genome publication
...cessed since its first launch in 2016. Here, we present a newly implemented background annotation engine for DFAST, which is also available as a standalone command-line program. The new...2352 days ago
RITA: Rapid identification of high-confidence taxonomic assignments for metagenomic data
RITA is a standalone software package and Web server for taxonomic assignment of metagenomic sequence reads. By combining homology predictions from BLAST or UBLAST with compos...2339 days ago
CAMSA :: a tool for Comparative Analysis and Merging of Scaffold Assemblies
CAMSA – is a tool for Comparative Analysis and Merging of Scaffold Assemblies, distributed both as a standalone software package and as Python library und...2308 days ago
ETE 3: Reconstruction, Analysis, and Visualization of Phylogenomic Data
ETE v3, featuring numerous improvements in the underlying library of methods, and providing a novel set of standalone tools to perform common tasks in comparative genomics and phylogene...2255 days ago
- BFC is a standalone high-performance tool for correcting sequencing errors from Illumina sequencing data. It is specifically designed for high-coverage whole-genome human dat...
2154 days ago
