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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31345?offset=1200</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37982/raven-a-software-suite-for-matlab-that-allows-for-semi-automated-reconstruction-of-genome-scale-models</guid>
	<pubDate>Wed, 24 Oct 2018 22:38:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37982/raven-a-software-suite-for-matlab-that-allows-for-semi-automated-reconstruction-of-genome-scale-models</link>
	<title><![CDATA[RAVEN: a software suite for Matlab that allows for semi-automated reconstruction of genome-scale models]]></title>
	<description><![CDATA[<p><span>The RAVEN (Reconstruction, Analysis and Visualization of Metabolic Networks) Toolbox 2 is a software suite for Matlab that allows for semi-automated reconstruction of genome-scale models (GEMs). It makes use of published models and/or KEGG, MetaCyc databases, coupled with extensive gap-filling and quality control features. The software suite also contains methods for visualizing simulation results and omics data, as well as a range of methods for performing simulations and analyzing the results. The software is a useful tool for system-wide data analysis in a metabolic context and for streamlined reconstruction of metabolic networks based on protein homology.</span></p><p>Address of the bookmark: <a href="https://github.com/SysBioChalmers/RAVEN" rel="nofollow">https://github.com/SysBioChalmers/RAVEN</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</guid>
	<pubDate>Tue, 14 Jun 2016 10:28:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</link>
	<title><![CDATA[Blobsplorer]]></title>
	<description><![CDATA[<p>Blobsplorer is a tool for interactive visualization of assembled DNA sequence data ("contigs") derived from (often unintentionally) mixed-species pools. It allows the simultaneous display of GC content, coverage, and taxonomic annotation for collections of contigs with a view to separating out those belonging to different taxa.</p>
<p>Blobsplorer is unlikely to be of use on its own as it requires contig data to be supplied in a format that involves considerable preprocessing (see below for a description). The easiest way to use Blobsplorer is as part of a workflow using scripts from <a href="https://github.com/blaxterlab/blobology">here</a>.</p><p>Address of the bookmark: <a href="http://nematodes.org/martin/blobsplorer/blobsplorer.html" rel="nofollow">http://nematodes.org/martin/blobsplorer/blobsplorer.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41820/shinygo-v061-gene-ontology-enrichment-analysis-more</guid>
	<pubDate>Wed, 03 Jun 2020 08:00:30 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41820/shinygo-v061-gene-ontology-enrichment-analysis-more</link>
	<title><![CDATA[ShinyGO v0.61: Gene Ontology Enrichment Analysis + more]]></title>
	<description><![CDATA[<p>2/3/2020: Now published by&nbsp;<a href="https://doi.org/10.1093/bioinformatics/btz931" target="_blank">Bioinformatics.</a></p>
<p>11/3/2019: V 0.61, Improve graphical visualization (thanks to reviewers). Interactive networks and much more.</p>
<p>5/20/2019: V.0.60, Annotation database updated to Ensembl 96. New bacterial and fungal genomes based on STRING-db! Just paste your gene list to get enriched GO terms and othe pathways for over 315 plant and animal species, based on annotation from Ensembl (Release 96), Ensembl plants (R. 43) and Ensembl Metazoa (R. 43). An additional 2031 genomes (including bacteria and fungi) are annotated based on STRING-db (v.10). In addition, it also produces KEGG pathway diagrams with your genes highlighted, hierarchical clustering trees and networks summarizing overlapping terms/pathways, protein-protein interaction networks, gene characterristics plots, and enriched promoter motifs.&nbsp;</p><p>Address of the bookmark: <a href="http://bioinformatics.sdstate.edu/go/" rel="nofollow">http://bioinformatics.sdstate.edu/go/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27845/cnidaria-fast-reference-free-phylogenomic-clustering</guid>
	<pubDate>Thu, 16 Jun 2016 17:55:17 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27845/cnidaria-fast-reference-free-phylogenomic-clustering</link>
	<title><![CDATA[CNIDARIA: fast, reference-free phylogenomic clustering]]></title>
	<description><![CDATA[<p>Motivation: Identification of biological specimens is a major requirement for a range of applications. Reference-free methods analyse unprocessed sequencing data without relying on prior knowledge, but these do not scale to arbitrarily large genomes and arbitrarily large phylogenetic distances.</p>
<p>Results: We present Cnidaria, a practical tool for clustering genomic and transcriptomic data with no limitation on ge-nome size or phylogenetic distances. We successfully simultaneously clustered 169 genomic and transcriptomic datasets from 4 kingdoms, achieving 100% accuracy at supra-species level and 78% accuracy for species level.</p>
<p>Availability and Implementation: Cnidaria is written in C++ and Python and is available at http://www.ab.wur.nl/cnidaria.</p>
<p>Contact: Saulo Aflitos - sauloal@gmail.com</p>
<p>Supplementary information: Supplementary data are available at Bioinformatics online.</p><p>Address of the bookmark: <a href="https://github.com/sauloal/cnidaria/wiki" rel="nofollow">https://github.com/sauloal/cnidaria/wiki</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44188/understanding-go-analysis</guid>
	<pubDate>Wed, 08 Feb 2023 04:22:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44188/understanding-go-analysis</link>
	<title><![CDATA[Understanding GO analysis]]></title>
	<description><![CDATA[<p>The confusion about gene ontology and gene ontology analysis can start right from the term itself. There are actually two different entities that are commonly referred to as gene ontology or &ldquo;GO&rdquo;:</p>
<ol>
<li>the&nbsp;<span>ontology itself</span>, which is a set of terms with their precise definitions and defined relationships between them, and</li>
<li>the&nbsp;<span>associations between gene products and GO terms</span>, which are used to capture the existing knowledge about what each gene is known to do.</li>
</ol>
<p>But the term gene ontology, or GO, is commonly used to refer to both, which is sometimes a source of potential confusion. In order to avoid this, here we will use the term &ldquo;GO ontology&rdquo; to describe the set of terms and their hierarchical structure and &ldquo;GO annotations&rdquo; to describe the set of associations between genes and GO terms.</p>
<p>There are 3 types of terms, or domains if you wish, in the gene ontology:</p>
<ul>
<li>Biological Processes (BP)</li>
<li>Molecular Functions (MF)</li>
<li>Cellular Components (CC)</li>
</ul><p>Address of the bookmark: <a href="https://advaitabio.com/faq-items/understanding-gene-ontology/" rel="nofollow">https://advaitabio.com/faq-items/understanding-gene-ontology/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27959/darkhorse</guid>
	<pubDate>Wed, 22 Jun 2016 05:37:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27959/darkhorse</link>
	<title><![CDATA[DarkHorse]]></title>
	<description><![CDATA[<p><em>DarkHorse</em>&nbsp;is a bioinformatic method for rapid, automated identification and ranking of phylogenetically atypical proteins on a genome-wide basis. It works by selecting potential ortholog matches from a reference database of amino acid sequences, then using these matches to calculate a lineage probability index (LPI) score for each genome protein.</p>
<p>LPI scores are inversely proportional to the phylogenetic distance between database match sequences and the query genome. These scores are useful not only for large-scale<em>de novo</em>&nbsp;predictions of horizontally transferred proteins, but can also serve as an independent quality control test for potential horizontal transfer candidates identified by alternative methods, especially those based on nucleic acid signatures. Candidates having high LPI scores are unlikely to have been horizontally transferred, since they are highly conserved among closely related organisms.</p>
<p>One unique and powerful feature of the DarkHorse HGT Candidate database is the opportunity to explore the phylogenetic background of potential HGT donors as well as recipients. The breadth of the database allows not only query sequences, but also their database match partners to be evaluated for sequence similarity or novelty compared to taxonomically related organisms.</p>
<p><em>DarkHorse</em>&nbsp;is configurable for varying degrees of phylogenetic granularity and protein sequence conservation. Users should consult the&nbsp;<a href="http://darkhorse.ucsd.edu/#references">references</a>&nbsp;cited below for a complete explanation of parameter selection and result interpretation. A brief&nbsp;<a href="http://darkhorse.ucsd.edu/tutorial.html">tutorial</a>&nbsp;page is also available on-line.</p><p>Address of the bookmark: <a href="http://darkhorse.ucsd.edu/download.html" rel="nofollow">http://darkhorse.ucsd.edu/download.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44620/diy-transcriptomics</guid>
	<pubDate>Wed, 31 Jul 2024 01:19:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44620/diy-transcriptomics</link>
	<title><![CDATA[DIY Transcriptomics]]></title>
	<description><![CDATA[<p><span>A semester-long course covering best practices for the analysis of high-throughput sequencing data from gene expression (RNA-seq) studies, with a primary focus on empowering students to be independent in the use of lightweight and open-source software using the R programming language and the Bioconductor suite of packages. This course follows a hybrid format in which online lectures are paired with in-person labs where students participate in hands-on, live coding exercises using real &lsquo;omic datasets. The course is focused on datasets and topics central to infectious disease research, immunology, and One-Health, but the concepts and approaches covered are applicable to any genomic study.</span></p>
<p>https://diytranscriptomics.com</p><p>Address of the bookmark: <a href="https://diytranscriptomics.com" rel="nofollow">https://diytranscriptomics.com</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/27965/cheatsheet-for-linux</guid>
	<pubDate>Wed, 22 Jun 2016 07:55:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/27965/cheatsheet-for-linux</link>
	<title><![CDATA[Cheatsheet for Linux !!]]></title>
	<description><![CDATA[<p>Linux Commands Cheat Sheet<br /><br />&nbsp;&nbsp;&nbsp; File System<br /><br />&nbsp;&nbsp;&nbsp; ls &mdash; list items in current directory<br /><br />&nbsp;&nbsp;&nbsp; ls -l &mdash; list items in current directory and show in long format to see perimissions, size, an modification date<br /><br />&nbsp;&nbsp;&nbsp; ls -a &mdash; list all items in current directory, including hidden files<br /><br />&nbsp;&nbsp;&nbsp; ls -F &mdash; list all items in current directory and show directories with a slash and executables with a star<br /><br />&nbsp;&nbsp;&nbsp; ls dir &mdash; list all items in directory dir<br /><br />&nbsp;&nbsp;&nbsp; cd dir &mdash; change directory to dir<br /><br />&nbsp;&nbsp;&nbsp; cd .. &mdash; go up one directory<br /><br />&nbsp;&nbsp;&nbsp; cd / &mdash; go to the root directory<br /><br />&nbsp;&nbsp;&nbsp; cd ~ &mdash; go to to your home directory<br /><br />&nbsp;&nbsp;&nbsp; cd - &mdash; go to the last directory you were just in<br /><br />&nbsp;&nbsp;&nbsp; pwd &mdash; show present working directory<br /><br />&nbsp;&nbsp;&nbsp; mkdir dir &mdash; make directory dir<br /><br />&nbsp;&nbsp;&nbsp; rm file &mdash; remove file<br /><br />&nbsp;&nbsp;&nbsp; rm -r dir &mdash; remove directory dir recursively<br /><br />&nbsp;&nbsp;&nbsp; cp file1 file2 &mdash; copy file1 to file2<br /><br />&nbsp;&nbsp;&nbsp; cp -r dir1 dir2 &mdash; copy directory dir1 to dir2 recursively<br /><br />&nbsp;&nbsp;&nbsp; mv file1 file2 &mdash; move (rename) file1 to file2<br /><br />&nbsp;&nbsp;&nbsp; ln -s file link &mdash; create symbolic link to file<br /><br />&nbsp;&nbsp;&nbsp; touch file &mdash; create or update file<br /><br />&nbsp;&nbsp;&nbsp; cat file &mdash; output the contents of file<br /><br />&nbsp;&nbsp;&nbsp; less file &mdash; view file with page navigation<br /><br />&nbsp;&nbsp;&nbsp; head file &mdash; output the first 10 lines of file<br /><br />&nbsp;&nbsp;&nbsp; tail file &mdash; output the last 10 lines of file<br /><br />&nbsp;&nbsp;&nbsp; tail -f file &mdash; output the contents of file as it grows, starting with the last 10 lines<br /><br />&nbsp;&nbsp;&nbsp; vim file &mdash; edit file<br /><br />&nbsp;&nbsp;&nbsp; alias name 'command' &mdash; create an alias for a command<br />&nbsp;&nbsp;&nbsp; System<br /><br />&nbsp;&nbsp;&nbsp; shutdown &mdash; shut down machine<br /><br />&nbsp;&nbsp;&nbsp; reboot &mdash; restart machine<br /><br />&nbsp;&nbsp;&nbsp; date &mdash; show the current date and time<br /><br />&nbsp;&nbsp;&nbsp; whoami &mdash; who you are logged in as<br /><br />&nbsp;&nbsp;&nbsp; finger user &mdash; display information about user<br /><br />&nbsp;&nbsp;&nbsp; man command &mdash; show the manual for command<br /><br />&nbsp;&nbsp;&nbsp; df &mdash; show disk usage<br /><br />&nbsp;&nbsp;&nbsp; du &mdash; show directory space usage<br /><br />&nbsp;&nbsp;&nbsp; free &mdash; show memory and swap usage<br /><br />&nbsp;&nbsp;&nbsp; whereis app &mdash; show possible locations of app<br /><br />&nbsp;&nbsp;&nbsp; which app &mdash; show which app will be run by default<br />&nbsp;&nbsp;&nbsp; Process Management<br /><br />&nbsp;&nbsp;&nbsp; ps &mdash; display your currently active processes<br /><br />&nbsp;&nbsp;&nbsp; top &mdash; display all running processes<br /><br />&nbsp;&nbsp;&nbsp; kill pid &mdash; kill process id pid<br /><br />&nbsp;&nbsp;&nbsp; kill -9 pid &mdash; force kill process id pid<br />&nbsp;&nbsp;&nbsp; Permissions<br /><br />&nbsp;&nbsp;&nbsp; ls -l &mdash; list items in current directory and show permissions<br /><br />&nbsp;&nbsp;&nbsp; chmod ugo file &mdash; change permissions of file to ugo - u is the user's permissions, g is the group's permissions, and o is everyone else's permissions. The values of u, g, and o can be any number between 0 and 7.<br /><br />&nbsp;&nbsp;&nbsp; 7 &mdash; full permissions<br /><br />&nbsp;&nbsp;&nbsp; 6 &mdash; read and write only<br /><br />&nbsp;&nbsp;&nbsp; 5 &mdash; read and execute only<br /><br />&nbsp;&nbsp;&nbsp; 4 &mdash; read only<br /><br />&nbsp;&nbsp;&nbsp; 3 &mdash; write and execute only<br /><br />&nbsp;&nbsp;&nbsp; 2 &mdash; write only<br /><br />&nbsp;&nbsp;&nbsp; 1 &mdash; execute only<br /><br />&nbsp;&nbsp;&nbsp; 0 &mdash; no permissions<br /><br />&nbsp;&nbsp;&nbsp; chmod 600 file &mdash; you can read and write - good for files<br /><br />&nbsp;&nbsp;&nbsp; chmod 700 file &mdash; you can read, write, and execute - good for scripts<br /><br />&nbsp;&nbsp;&nbsp; chmod 644 file &mdash; you can read and write, and everyone else can only read - good for web pages<br /><br />&nbsp;&nbsp;&nbsp; chmod 755 file &mdash; you can read, write, and execute, and everyone else can read and execute - good for programs that you want to share<br />&nbsp;&nbsp;&nbsp; Networking<br /><br />&nbsp;&nbsp;&nbsp; wget file &mdash; download a file<br /><br />&nbsp;&nbsp;&nbsp; curl file &mdash; download a file<br /><br />&nbsp;&nbsp;&nbsp; scp user@host:file dir &mdash; secure copy a file from remote server to the dir directory on your machine<br /><br />&nbsp;&nbsp;&nbsp; scp file user@host:dir &mdash; secure copy a file from your machine to the dir directory on a remote server<br /><br />&nbsp;&nbsp;&nbsp; scp -r user@host:dir dir &mdash; secure copy the directory dir from remote server to the directory dir on your machine<br /><br />&nbsp;&nbsp;&nbsp; ssh user@host &mdash; connect to host as user<br /><br />&nbsp;&nbsp;&nbsp; ssh -p port user@host &mdash; connect to host on port as user<br /><br />&nbsp;&nbsp;&nbsp; ssh-copy-id user@host &mdash; add your key to host for user to enable a keyed or passwordless login<br /><br />&nbsp;&nbsp;&nbsp; ping host &mdash; ping host and output results<br /><br />&nbsp;&nbsp;&nbsp; whois domain &mdash; get information for domain<br /><br />&nbsp;&nbsp;&nbsp; dig domain &mdash; get DNS information for domain<br /><br />&nbsp;&nbsp;&nbsp; dig -x host &mdash; reverse lookup host<br /><br />&nbsp;&nbsp;&nbsp; lsof -i tcp:1337 &mdash; list all processes running on port 1337<br />&nbsp;&nbsp;&nbsp; Searching<br /><br />&nbsp;&nbsp;&nbsp; grep pattern files &mdash; search for pattern in files<br /><br />&nbsp;&nbsp;&nbsp; grep -r pattern dir &mdash; search recursively for pattern in dir<br /><br />&nbsp;&nbsp;&nbsp; grep -rn pattern dir &mdash; search recursively for pattern in dir and show the line number found<br /><br />&nbsp;&nbsp;&nbsp; grep -r pattern dir --include='*.ext &mdash; search recursively for pattern in dir and only search in files with .ext extension<br /><br />&nbsp;&nbsp;&nbsp; command | grep pattern &mdash; search for pattern in the output of command<br /><br />&nbsp;&nbsp;&nbsp; find file &mdash; find all instances of file in real system<br /><br />&nbsp;&nbsp;&nbsp; locate file &mdash; find all instances of file using indexed database built from the updatedb command. Much faster than find<br /><br />&nbsp;&nbsp;&nbsp; sed -i 's/day/night/g' file &mdash; find all occurrences of day in a file and replace them with night - s means substitude and g means global - sed also supports regular expressions<br />&nbsp;&nbsp;&nbsp; Compression<br /><br />&nbsp;&nbsp;&nbsp; tar cf file.tar files &mdash; create a tar named file.tar containing files<br /><br />&nbsp;&nbsp;&nbsp; tar xf file.tar &mdash; extract the files from file.tar<br /><br />&nbsp;&nbsp;&nbsp; tar czf file.tar.gz files &mdash; create a tar with Gzip compression<br /><br />&nbsp;&nbsp;&nbsp; tar xzf file.tar.gz &mdash; extract a tar using Gzip<br /><br />&nbsp;&nbsp;&nbsp; gzip file &mdash; compresses file and renames it to file.gz<br /><br />&nbsp;&nbsp;&nbsp; gzip -d file.gz &mdash; decompresses file.gz back to file<br />&nbsp;&nbsp;&nbsp; Shortcuts<br /><br />&nbsp;&nbsp;&nbsp; ctrl+a &mdash; move cursor to beginning of line<br /><br />&nbsp;&nbsp;&nbsp; ctrl+f &mdash; move cursor to end of line<br /><br />&nbsp;&nbsp;&nbsp; alt+f &mdash; move cursor forward 1 word<br /><br />&nbsp;&nbsp;&nbsp; alt+b &mdash; move cursor backward 1 word</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/44900/pegas-a-comprehensive-bioinformatic-solution-for-pathogenic-bacterial-genomic-analysis</guid>
	<pubDate>Mon, 01 Sep 2025 01:18:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/44900/pegas-a-comprehensive-bioinformatic-solution-for-pathogenic-bacterial-genomic-analysis</link>
	<title><![CDATA[PeGAS: A Comprehensive Bioinformatic Solution for Pathogenic Bacterial Genomic Analysis]]></title>
	<description><![CDATA[<p><span>This is PeGAS, a powerful bioinformatic tool designed for the seamless quality control, assembly, and annotation of Illumina paired-end reads specific to pathogenic bacteria. This tool integrates state-of-the-art open-source software to provide a streamlined and efficient workflow, ensuring accurate insights into the genomic makeup of pathogenic microbial strains.</span></p>
<p><span><img src="https://github.com/liviurotiul/PeGAS/raw/main/Features.png" alt="image" style="border: 0px;"></span></p><p>Address of the bookmark: <a href="https://github.com/liviurotiul/PeGAS" rel="nofollow">https://github.com/liviurotiul/PeGAS</a></p>]]></description>
	<dc:creator>LEGE</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28168/sam-flags</guid>
	<pubDate>Wed, 29 Jun 2016 15:38:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28168/sam-flags</link>
	<title><![CDATA[SAM flags]]></title>
	<description><![CDATA[<p>Decoding SAM flags</p>
<p>This utility makes it easy to identify what are the properties of a read based on its SAM flag value, or conversely, to find what the SAM Flag value would be for a given combination of properties.</p>
<p>To decode a given SAM flag value, just enter the number in the field below. The encoded properties will be listed under Summary below, to the right.</p><p>Address of the bookmark: <a href="https://broadinstitute.github.io/picard/explain-flags.html" rel="nofollow">https://broadinstitute.github.io/picard/explain-flags.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>

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