Difference between revisions of "PyNAST"
(→version information fix)
(→resource info https://github.com/biocore/pynast link has been added)
|Line 45:||Line 45:|
Revision as of 14:05, 24 April 2020
alignment of short DNA sequences
The package provices a reimplementation of the Nearest Alignment Space Termination tool in Python. It was prepared for next generation sequencers.
Given a set of sequences and a template alignment, PyNAST will align the input sequences against the template alignment, and return a multiple sequence alignment which contains the same number of positions (or columns) as the template alignment. This facilitates the analysis of new sequences in the context of existing alignments, and additional data derived from existing alignments such as phylogenetic trees. Because any protein or nucleic acid sequences and template alignments can be provided, PyNAST is not limited to the analysis of 16s rDNA sequences.
Debian: Andreas Tille <firstname.lastname@example.org>
11 August 2014
License: Modified BSD License (also known as New or Revised BSD)
Leaders and contributors
|PyNAST Development Team||contact|
Resources and communication
|Debian (Ref) (R)||https://tracker.debian.org/pkg/pynast|
|VCS Repository Webview||https://github.com/biocore/pynast|
Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.3 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts. A copy of the license is included in the page “GNU Free Documentation License”.
The copyright and license notices on this page only apply to the text on this page. Any software or copyright-licenses or other similar notices described in this text has its own copyright notice and license, which can usually be found in the distribution or license text itself.