<![CDATA[BOL: Related items]]> https://bioinformaticsonline.com/related/41734?offset=250 https://bioinformaticsonline.com/bookmarks/view/36360/dendropy-a-python-library-for-phylogenetic-computing Mon, 23 Apr 2018 05:49:50 -0500 https://bioinformaticsonline.com/bookmarks/view/36360/dendropy-a-python-library-for-phylogenetic-computing <![CDATA[DendroPy: a Python library for phylogenetic computing]]> DendroPy is a Python library for phylogenetic computing. It provides classes and functions for the simulation, processing, and manipulation of phylogenetic trees and character matrices, and supports the reading and writing of phylogenetic data in a range of formats, such as NEXUS, NEWICK, NeXML, Phylip, FASTA, etc. Application scripts for performing some useful phylogenetic operations, such as data conversion and tree posterior distribution summarization, are also distributed and installed as part of the libary. DendroPy can thus function as a stand-alone library for phylogenetics, a component of more complex multi-library phyloinformatic pipelines, or as a scripting “glue” that assembles and drives such pipelines.

The primary home page for DendroPy, with detailed tutorials and documentation, is at:

DendroPy is also hosted in the official Python repository:

Requirements and Installation

DendroPy 4.x runs under Python 3 (all versions > 3.1) and Python 2 (Python 2.7 only).

You can install DendroPy by running:

 

More information is available here:

Address of the bookmark: https://pypi.org/project/DendroPy/

]]> Seema Singh https://bioinformaticsonline.com/bookmarks/view/38646/visnetwork-an-r-package-for-network-visualization-using-visjs-javascript-library Wed, 09 Jan 2019 11:00:32 -0600 https://bioinformaticsonline.com/bookmarks/view/38646/visnetwork-an-r-package-for-network-visualization-using-visjs-javascript-library <![CDATA[visNetwork: an R package for network visualization, using vis.js javascript library]]>

visNetwork is an R package for network visualization, using vis.js javascript library (http://visjs.org/). All remarks and bugs are welcome on github : https://github.com/datastorm-open/visNetwork.

Features

Based on htmlwidgets, so :

  • compatible with shiny, R Markdown documents, and RStudio viewer

The package proposes all the features available in vis.js API, and even more with special features for R :

  • easy to use
  • custom shapes, styles, colors, sizes, …
  • works smooth on any modern browser for up to a few thousand nodes and edges
  • interactivity controls (highlight, collapsed nodes, selection, zoom, physics, movement of nodes, tooltip, events, …)
  • visualize rpart tree

Address of the bookmark: https://datastorm-open.github.io/visNetwork/

]]> Jit https://bioinformaticsonline.com/bookmarks/view/35420/telomerehunter Fri, 02 Feb 2018 04:23:59 -0600 https://bioinformaticsonline.com/bookmarks/view/35420/telomerehunter <![CDATA[TelomereHunter]]> TelomereHunter is a tool for estimating telomere content from human whole-genome sequencing data. It is designed to take BAM files from a tumor and a matching control sample as input. However, it is also possible to run TelomereHunter with one input file. TelomereHunter extracts and sorts telomeric reads from the input sample(s). For the estimation of telomere content, GC biases are taken into account. Finally, the results of TelomereHunter are visualized in several diagrams.

TelomereHunter is available for download at the following address: https://pypi.python.org/pypi/telomerehunter/

Address of the bookmark: http://www.dkfz.de/en/applied-bioinformatics/telomerehunter/telomerehunter.html

]]> Jit https://bioinformaticsonline.com/bookmarks/view/37602/indexcov-fast-coverage-quality-control-for-whole-genome-sequencing Wed, 29 Aug 2018 09:20:46 -0500 https://bioinformaticsonline.com/bookmarks/view/37602/indexcov-fast-coverage-quality-control-for-whole-genome-sequencing <![CDATA[Indexcov: fast coverage quality control for whole-genome sequencing]]> indexcov, an efficient estimator of whole-genome sequencing coverage to rapidly identify samples with aberrant coverage profiles, reveal large-scale chromosomal anomalies, recognize potential batch effects, and infer the sex of a sample. Indexcov is available at https://github.com/brentp/goleft under the MIT license.

Address of the bookmark: https://github.com/brentp/goleft

]]> Jit https://bioinformaticsonline.com/bookmarks/view/41996/wgd%E2%80%94simple-command-line-tools-for-the-analysis-of-ancient-whole-genome-duplications Thu, 23 Jul 2020 05:49:45 -0500 https://bioinformaticsonline.com/bookmarks/view/41996/wgd%E2%80%94simple-command-line-tools-for-the-analysis-of-ancient-whole-genome-duplications <![CDATA[wgd—simple command line tools for the analysis of ancient whole-genome duplications]]> wgd is a easy to use command-line tool for KS distribution construction named wgd. The wgd suite provides commonly used KS and colinearity analysis workflows together with tools for modeling and visualization, rendering these analyses accessible to genomics researchers in a convenient manner.

https://academic.oup.com/bioinformatics/article/35/12/2153/5162749

Address of the bookmark: https://github.com/arzwa/wgd

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