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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37230?offset=240</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35543/genometools-the-versatile-open-source-genome-analysis-software</guid>
	<pubDate>Wed, 07 Feb 2018 10:44:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35543/genometools-the-versatile-open-source-genome-analysis-software</link>
	<title><![CDATA[GenomeTools: The versatile open source genome analysis software]]></title>
	<description><![CDATA[<p>The&nbsp;<em>GenomeTools</em>&nbsp;genome analysis system is a&nbsp;<a href="http://genometools.org/license.html">free</a>&nbsp;collection of bioinformatics&nbsp;<a href="http://genometools.org/tools.html">tools</a>&nbsp;(in the realm of genome informatics) combined into a single binary named&nbsp;<em>gt</em>. It is based on a C library named &ldquo;libgenometools&rdquo; which consists of several modules.</p>
<p>If you are interested in gene prediction, have a look at&nbsp;<a href="http://genomethreader.org/" title="GenomeThreader gene prediction        software"><em>GenomeThreader</em></a>.</p><p>Address of the bookmark: <a href="http://genometools.org/" rel="nofollow">http://genometools.org/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38462/egad-ultra-fast-functional-analysis-of-gene-networks</guid>
	<pubDate>Fri, 14 Dec 2018 04:10:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38462/egad-ultra-fast-functional-analysis-of-gene-networks</link>
	<title><![CDATA[EGAD: Ultra-fast functional analysis of gene networks]]></title>
	<description><![CDATA[<p><span>With the EGAD (Extending &lsquo;Guilt-by-Association&rsquo; by Degree) package, we present a series of highly efficient tools to calculate functional properties in networks based on the guilt-by-association principle. These allow rapid controlled comparisons and analyses. Two of the core features are: a function prediction algorithm which is fully vectorized (neighbor_voting), allowing network characterization across even thousands of functional groups to be accomplished in minutes in cross-validation and an analytic determination of the optimal prior to guess candidates genes across multiple functional sets (calculate_multifunc, auc_multifunc).</span></p><p>Address of the bookmark: <a href="https://github.com/sarbal/EGAD" rel="nofollow">https://github.com/sarbal/EGAD</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/40882/troyanskaya-lab</guid>
  <pubDate>Tue, 04 Feb 2020 06:40:36 -0600</pubDate>
  <link></link>
  <title><![CDATA[Troyanskaya Lab]]></title>
  <description><![CDATA[
<p>The goal of our research is to interpret and distill this complexity through accurate analysis and modeling of molecular pathways, particularly those in which malfunctions lead to the manifestation of disease. We are inventing integrative methods for systems-level pathway modeling through integrative analysis of genome-scale datasets. We apply these approaches in studying challenging biological problems, such as how pathways function in diverse cell types and how they change dynamically.</p>

<p>https://function.princeton.edu/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41475/proteoclade-a-taxonomic-toolkit-for-multi-species-and-metaproteomic-analysis</guid>
	<pubDate>Wed, 18 Mar 2020 14:27:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41475/proteoclade-a-taxonomic-toolkit-for-multi-species-and-metaproteomic-analysis</link>
	<title><![CDATA[ProteoClade: A taxonomic toolkit for multi-species and metaproteomic analysis]]></title>
	<description><![CDATA[<p>ProteoClade is a Python library for&nbsp;<span>taxonomic-based annotation and quantification of bottom-up proteomics data</span>. It is designed to be user-friendly, and has been optimized for speed and storage requirements.</p>
<p>ProteoClade helps you analyze two general categories of experiments:</p>
<ol>
<li>
<p><span><em>Targeted Database</em>&nbsp;Searches:</span>&nbsp;Experiments in which a limited number of species are defined ahead of time, such as those involving Patient-Derived Xenografts (PDXs) or host-pathogen interactions. Reference protein sequence databases are used for targeted searches (ex: using Mascot, MaxQuant).</p>
</li>
<li>
<p><span><em>De Novo</em>&nbsp;Searches:</span>&nbsp;Experiments in which the organisms are unspecified ahead of time or involve samples of high taxonomic complexity. Mass spectra are analyzed in the absence of a reference database (ex: using PEAKS, PepNovo).</p>
</li>
</ol>
<p>ProteoClade scales from two organisms to every organism in UniProt. Please&nbsp;<a href="https://proteoclade.readthedocs.io/">refer to the complete documentation at proteoclade.readthedocs.io</a>&nbsp;for installation, a user's guide, and examples.</p>
<p><a href="https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1007741">https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1007741</a></p><p>Address of the bookmark: <a href="https://github.com/HeldLab/ProteoClade" rel="nofollow">https://github.com/HeldLab/ProteoClade</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/43447/rna-seq-workflow-gene-level-exploratory-analysis-and-differential-expression</guid>
	<pubDate>Sat, 09 Oct 2021 07:59:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/43447/rna-seq-workflow-gene-level-exploratory-analysis-and-differential-expression</link>
	<title><![CDATA[RNA-seq workflow: gene-level exploratory analysis and differential expression]]></title>
	<description><![CDATA[<p><span>Here we walk through an end-to-end gene-level RNA-seq differential expression workflow using Bioconductor packages. We will start from the FASTQ files, show how these were quantified to the reference transcripts, and prepare gene-level count datasets for downstream analysis. We will perform exploratory data analysis (EDA) for quality assessment and to explore the relationship between samples, perform differential gene expression analysis, and visually explore the results.</span></p><p>Address of the bookmark: <a href="http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html" rel="nofollow">http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/43999/tools-for-differential-expression-analysis</guid>
	<pubDate>Tue, 08 Nov 2022 03:40:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/43999/tools-for-differential-expression-analysis</link>
	<title><![CDATA[Tools for Differential expression analysis]]></title>
	<description><![CDATA[<p><span>apeglm</span>&nbsp;-&nbsp;<a href="https://bioconductor.org/packages/release/bioc/html/apeglm.html" target="_blank">https://bioconductor.org/packages/release/bioc/html/apeglm.html</a></p><p><span>ashr</span>&nbsp;-&nbsp;<a href="https://github.com/stephens999/ashr" target="_blank">https://github.com/stephens999/ashr</a>,&nbsp;<a href="https://cran.r-project.org/web/packages/ashr/index.html" target="_blank">https://cran.r-project.org/web/packages/ashr/index.html</a></p><p><span>consensusDE</span>&nbsp;-&nbsp;<a href="https://bioconductor.org/packages/release/bioc/html/consensusDE.html" target="_blank">https://bioconductor.org/packages/release/bioc/html/consensusDE.html</a></p><p><span>DESeq2</span>&nbsp;-&nbsp;<a href="https://bioconductor.org/packages/release/bioc/html/DESeq2.html" target="_blank">https://bioconductor.org/packages/release/bioc/html/DESeq2.html</a></p><p><span>edgeR</span>&nbsp;-&nbsp;<a href="https://bioconductor.org/packages/release/bioc/html/edgeR.html" target="_blank">https://bioconductor.org/packages/release/bioc/html/edgeR.html</a></p><p><span>limma</span>&nbsp;-&nbsp;<a href="https://kasperdanielhansen.github.io/genbioconductor/html/limma.html" target="_blank">https://kasperdanielhansen.github.io/genbioconductor/html/limma.html</a>&nbsp;&nbsp;<a href="https://bioconductor.org/packages/release/bioc/html/limma.html" target="_blank">https://bioconductor.org/packages/release/bioc/html/limma.html</a></p><p><span>MetaCycle</span>&nbsp;-&nbsp;<a href="https://cran.r-project.org/web/packages/MetaCycle/index.html" target="_blank">https://cran.r-project.org/web/packages/MetaCycle/index.html</a>,&nbsp;<a href="https://github.com/gangwug/MetaCycle" target="_blank">https://github.com/gangwug/MetaCycle</a></p><p><span>RUVSeq</span>&nbsp;-&nbsp;<a href="https://bioconductor.org/packages/release/bioc/html/RUVSeq.html" target="_blank">https://bioconductor.org/packages/release/bioc/html/RUVSeq.html</a></p><p><span>SARTools</span>&nbsp;-&nbsp;<a href="https://github.com/PF2-pasteur-fr/SARTools" target="_blank">https://github.com/PF2-pasteur-fr/SARTools</a></p><p><span>tximport</span>&nbsp;-&nbsp;<a href="https://github.com/mikelove/tximport" target="_blank">https://github.com/mikelove/tximport</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44561/bactopia-a-flexible-pipeline-for-complete-analysis-of-bacterial-genomes</guid>
	<pubDate>Sat, 08 Jun 2024 16:25:08 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44561/bactopia-a-flexible-pipeline-for-complete-analysis-of-bacterial-genomes</link>
	<title><![CDATA[Bactopia: a flexible pipeline for complete analysis of bacterial genomes]]></title>
	<description><![CDATA[<p>Bactopia is a flexible pipeline for complete analysis of bacterial genomes. The goal of Bactopia is process your data with a broad set of tools, so that you can get to the fun part of analyses quicker!</p>
<p>Bactopia was inspired by&nbsp;<a href="https://staphopia.github.io/">Staphopia</a>, a workflow we (Tim Read and myself) released that is targeted towards&nbsp;<em>Staphylococcus aureus</em>&nbsp;genomes. Using what we learned from Staphopia and user feedback, Bactopia was developed from scratch with usability, portability, and speed in mind from the start.</p>
<p>Bactopia uses&nbsp;<a href="https://www.nextflow.io/">Nextflow</a>&nbsp;to manage the workflow, allowing for support of many types of environments (e.g. cluster or cloud). Bactopia allows for the usage of many public datasets as well as your own datasets to further enhance the analysis of your sequencing. Bactopia only uses software packages available from&nbsp;<a href="https://bioconda.github.io/">Bioconda</a>&nbsp;and&nbsp;<a href="https://conda-forge.org/">Conda-Forge</a>&nbsp;to make installation as simple as possible for&nbsp;<em>all</em>&nbsp;users.</p>
<p>To highlight the use of&nbsp;<a href="https://bactopia.github.io/latest/full-guide/">Bactopia</a>&nbsp;and&nbsp;<a href="https://bactopia.github.io/latest/bactopia-tools/">Bactopia Tools</a>, we performed an analysis of 1,664 public&nbsp;<em>Lactobacillus</em>&nbsp;genomes, focusing on&nbsp;<em>Lactobacillus crispatus</em>, a species that is a common part of the human vaginal microbiome. The results from this analysis are published in mSystems under the title:&nbsp;<em><a href="https://doi.org/10.1128/mSystems.00190-20">Bactopia: a flexible pipeline for complete analysis of bacterial genomes</a></em></p>
<p><a href="https://bactopia.github.io/latest/assets/bactopia-workflow.png"><img src="https://bactopia.github.io/latest/assets/bactopia-workflow.png" alt="Bactopia Workflow" style="border: 0px;"></a></p><p>Address of the bookmark: <a href="https://bactopia.github.io/latest/" rel="nofollow">https://bactopia.github.io/latest/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39728/patterns-a-modeling-tool-dedicated-to-biological-network-modeling</guid>
	<pubDate>Fri, 26 Jul 2019 01:11:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39728/patterns-a-modeling-tool-dedicated-to-biological-network-modeling</link>
	<title><![CDATA[Patterns: a modeling tool dedicated to biological network modeling]]></title>
	<description><![CDATA[<p>It is designed to work with <strong>patterned data</strong>. Famous examples of problems related to patterned data are:</p>
<ul>
<li>recovering <strong>signals</strong> in networks after a <strong>stimulation</strong> (cascade network reverse engineering),</li>
<li>analysing <strong>periodic signals</strong>.</li>
</ul><p>Address of the bookmark: <a href="https://github.com/fbertran/Patterns" rel="nofollow">https://github.com/fbertran/Patterns</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/8481/des-higgins-visualizing-multiple-sequence-alignments</guid>
	<pubDate>Wed, 26 Feb 2014 00:50:08 -0600</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/8481/des-higgins-visualizing-multiple-sequence-alignments</link>
	<title><![CDATA[Des Higgins: Visualizing Multiple Sequence Alignments]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/IQkOK3dsWs4" frameborder="0" allowfullscreen></iframe>Copyright Broad Institute, 2013. All rights reserved.
Des Higgins (http://www.bioinf.ucd.ie) gives a very entertaining introduction to the visualization of multiple sequence alignment, and to his widely-used Clustal tool. He highlights the emerging challenge of managing alignments with a very large number of sequences, and presents several approaches to this challenge, including faster algorithms and abstract views of clusters of alignments. This talk was presented at VIZBI 2011, an international conference series on visualizing biological data (http://www.vizbi.org) funded by NIH & EMBO.

For information about data visualization efforts at the Broad Institute, please visit:
http://www.broadinstitute.org/node/1363/]]></description>
	
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/19090/deeptools</guid>
	<pubDate>Sat, 08 Nov 2014 15:02:08 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/19090/deeptools</link>
	<title><![CDATA[deepTools]]></title>
	<description><![CDATA[<p>deepTools addresses the challenge of handling the large amounts of data that are now routinely generated from DNA sequencing centers. To do so, deepTools contains useful modules to process the mapped reads data to create coverage files in standard bedGraph and bigWig file formats. By doing so, deepTools allows the creation of normalized coverage files or the comparison between two files (for example, treatment and control). Finally, using such normalized and standardized files, multiple visualizations can be created to identify enrichments with functional annotations of the genome.<br /><br />Publicaton: http://nar.oxfordjournals.org/content/early/2014/05/05/nar.gku365.full<br /><br />Source Code and Wiki: https://github.com/fidelram/deepTools/wiki<br /><br />Galaxy Tool Shed repository: http://toolshed.g2.bx.psu.edu/view/bgruening/deeptools<br /><br />and example Galaxy workflows: http://toolshed.g2.bx.psu.edu/view/bgruening/deeptools_workflows</p>]]></description>
	<dc:creator>Martin Jones</dc:creator>
</item>

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