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biology/bio-1.5.0 (Score: 0.2108313)
Integrated environment for Bioinformatics written in Ruby
BioRuby project aims to implement integrated environment for Bioinformatics by using Ruby.
biology/samtools-1.3.1 (Score: 0.2108313)
Tools for manipulating next-generation sequencing data
Samtools implements various utilities for post-processing alignments in the SAM, BAM, and CRAM formats, including indexing, variant calling (in conjunction with bcftools), and a simple alignment viewer.
biology/seaview-4.6 (Score: 0.2108313)
Multiple DNA/protein sequence alignment editor
SeaView is a multiple sequence alignment editor. You can align DNA/protein sequences from several organisms, and find out their relative postions in phylogenic tree. Once SeaView is installed, you can open the on-line help window through the 'Help' button to learn how to use SeaView. Example mase files can be found at: ftp://pbil.univ-lyon1.fr/pub/mol_phylogeny/seaview/
biology/seqtools-4.43.0 (Score: 0.2108313)
Tools for visualising sequence alignments
A suite of tools for visualising sequence alignments. Blixem is an interactive browser of pairwise alignments that have been stacked up in a "master-slave" multiple alignment; it is not a 'true' multiple alignment but a 'one-to-many' alignment. Belvu is a multiple sequence alignment viewer and phylogenetic tool. It has an extensive set of user-configurable modes to color residues by conservation or by residue type, and some basic alignment editing capabilities. Dotter is a graphical dot-matrix program for detailed comparison of two sequences. Every residue in one sequence is compared to every residue in the other, with one sequence plotted on the x-axis and the other on the y-axis.
biology/slclust-2010.02.02 (Score: 0.2108313)
Single-linkage clustering with Jaccard similarity
Slclust is a utility that performs single-linkage clustering with the option of applying a Jaccard similarity coefficient to break weakly bound clusters into distinct clusters.
biology/ssaha-3.1c (Score: 0.2108313)
Very fast matching and alignment of DNA sequences
SSAHA is a software tool for very fast matching and alignment of DNA sequences. It stands for Sequence Search and Alignment by Hashing Algorithm. It achieves its fast search speed by converting sequence information into a `hash table' data structure, which can then be searched very rapidly for matches. SSAHA: a fast search method for large DNA databases (2001). Ning Z, Cox AJ, Mullikin JC. Genome Res. 11: 1725-9. PMID: 11591649
biology/tRNAscan-SE-1.23 (Score: 0.2108313)
Improved tool for transfer RNA detection
tRNAscan-SE was written in the PERL (version 5.0) script language. Input consists of DNA or RNA sequences in FASTA format. tRNA predictions are output in standard tabular or ACeDB format. tRNAscan-SE does no tRNA detection itself, but instead combines the strengths of three independent tRNA prediction programs by negotiating the flow of information between them, performing a limited amount of post-processing, and outputting the results in one of several formats.
biology/treeviewx-0.5.1s20100823 (Score: 0.2108313)
Phylogenetic tree viewer
TreeView X is program to display phylogenetic trees on Unix-like platforms. It can read and display NEXUS and Newick format tree files (such as those output by PAUP*, ClustalX, TREE-PUZZLE, and other programs). It has a subset of the functionality of the version of TreeView available for the Mac Classic and Windows (it is roughly equivalent to version 0.95 of TreeView).
biology/trimmomatic-0.35 (Score: 0.2108313)
Flexible read trimming tool for Illumina NGS data
Trimmomatic performs a variety of useful trimming tasks for illumina NGS paired-end and single ended data.
biology/ugene-1.22.0 (Score: 0.2108313)
Free, open-source, cross-platform bioinformatics toolkit
Unipro UGENE is multiplatform, open-source software with the main goal of assisting molecular biologists without much expertise in bioinformatics to manage, analyze, and visualize their data. UGENE integrates widely used bioinformatics tools within one common user interface. UGENE toolkit supports multiple biological data formats and allows the retrieval of data from remote data sources. It provides visualization modules for biological objects such as annotated genome sequences, Next Generation Sequencing (NGS) assembly data, multiple sequence alignments, phylogenetic trees, and 3D structures.
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