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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/37835?offset=450</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38199/pacasus-correction-of-palindromes-in-long-reads-from-pacbio-and-nanopore</guid>
	<pubDate>Mon, 12 Nov 2018 05:26:48 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38199/pacasus-correction-of-palindromes-in-long-reads-from-pacbio-and-nanopore</link>
	<title><![CDATA[Pacasus: Correction of palindromes in long reads from PacBio and Nanopore]]></title>
	<description><![CDATA[<p><br>Tool for detecting and cleaning PacBio / Nanopore long reads after whole genome amplification. Check the poster from the Revolutionizing Next-Generation Sequencing (2nd edition) conference in the source folder:&nbsp;<a href="https://github.com/swarris/Pacasus/blob/master/vib2017.pdf">https://github.com/swarris/Pacasus/blob/master/vib2017.pdf</a>.</p>
<p>The prepint version is found on&nbsp;<a href="http://www.biorxiv.org/content/early/2017/08/09/173872">http://www.biorxiv.org/content/early/2017/08/09/173872</a></p>
<p>It uses the pyPaSWAS framework for sequence alignment (<a href="https://github.com/swarris/pyPaSWAS">https://github.com/swarris/pyPaSWAS</a>)</p><p>Address of the bookmark: <a href="https://github.com/swarris/Pacasus" rel="nofollow">https://github.com/swarris/Pacasus</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40754/understanding-your-reads-and-mapping</guid>
	<pubDate>Wed, 29 Jan 2020 06:29:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40754/understanding-your-reads-and-mapping</link>
	<title><![CDATA[Understanding your reads and mapping !]]></title>
	<description><![CDATA[<p>One of the best tutorial for beginners ...</p>
<p>https://bioinformatics-core-shared-training.github.io/cruk-summer-school-2017/Day1/Session4-seqIntro.html</p><p>Address of the bookmark: <a href="https://bioinformatics-core-shared-training.github.io/cruk-summer-school-2017/Day1/Session4-seqIntro.html" rel="nofollow">https://bioinformatics-core-shared-training.github.io/cruk-summer-school-2017/Day1/Session4-seqIntro.html</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/43954/elgg-installation-steps</guid>
	<pubDate>Wed, 07 Sep 2022 00:43:53 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/43954/elgg-installation-steps</link>
	<title><![CDATA[Elgg Installation steps !]]></title>
	<description><![CDATA[<p>Elgg is an open source social networking engine that allows the creation of social environments such as campus social networks and internal collaborative platforms for organizations. Elgg offers a number of social networking features including microblogging, messaging, file-sharing and groups. This tutorial will guide you through the process of installing Elgg on a Ubuntu 18.04 VPS.</p><h2 id="Prerequisites">Prerequisites</h2><ul>
<li>A fresh Vultr Cloud Compute instance with Ubuntu 18.04 and root access.</li>
</ul><h2 id="Step_1__Install_Apache__MySQL__and_PHP">Step 1: Install Apache, MySQL, and PHP</h2><p>Elgg requires MySQL, PHP, and a web server. Before you can install Elgg, you will need to install the Apache web server, MySQL, and PHP.</p><p>Update the repository list.</p><pre><code>apt-get update
</code></pre><p>Install the Apache web server.</p><pre><code>apt-get install apache2 -y
</code></pre><p>Install MySQL.</p><pre><code>apt-get install mysql-server -y
</code></pre><p>Complete the MySQL installation by executing the following command.</p><pre><code>/usr/bin/mysql_secure_installation
</code></pre><p>During the installation, you will be asked to enter a root password. Enter a secure password. This will be the MySQL root password.</p><pre><code>Would you like to setup VALIDATE PASSWORD plugin? [Y/N] N
New password: password
Re-enter new password: password
Remove anonymous users? [Y/N] Y
Disallow root login remotely? [Y/N] Y
Remove test database and access to it? [Y/N] Y
Reload privilege tables now? [Y/N] Y
</code></pre><p>Install PHP 7.2, as well as the PHP modules required by Elgg.</p><pre><code>apt-get install php7.2 libapache2-mod-php7.2 php7.2-common php7.2-sqlite3 php7.2-curl php7.2-intl php7.2-mbstring php7.2-xmlrpc php7.2-mysql php7.2-gd php7.2-xml php7.2-cli php7.2-zip -y
</code></pre><h2 id="Step_2__Create_a_MySQL_database_for_Elgg">Step 2: Create a MySQL database for Elgg</h2><p>Elgg will require a MySQL database. Log into the MySQL console.</p><pre><code>mysql -u root -p
</code></pre><p>When prompted for a password, enter the MySQL root password you set in step 1. Once you are logged in to the MySQL console, create a new database.</p><pre><code>CREATE DATABASE elgg;
</code></pre><p>Create a new MySQL user and grant it privileges to the newly created database. You can replace&nbsp;<code>username</code>&nbsp;and&nbsp;<code>password</code>&nbsp;with the username and password of your choice.</p><pre><code>GRANT ALL PRIVILEGES on elgg.* to 'username'@'localhost' identified by 'password';
FLUSH PRIVILEGES;
</code></pre><p>Exit the MySQL console.</p><pre><code>exit
</code></pre><h2 id="Step_3__Download_and_Install_Elgg">Step 3: Download and Install Elgg</h2><p>Download the latest version of Elgg.</p><pre><code>cd /var/www/html
rm -r index.html
wget https://elgg.org/download/elgg-2.3.7.zip
</code></pre><p>Unzip the downloaded archive and move the files to the root of the Apache web server.</p><pre><code>apt install unzip
unzip elgg-2.3.7.zip
mv ./elgg-2.3.7/* . &amp;&amp; rm elgg-2.3.7.zip &amp;&amp; rm -r elgg-2.3.7
</code></pre><p>Create a data directory for Elgg.</p><pre><code>sudo mkdir -p /var/www/html/data
</code></pre><p>Set the appropriate file permissions.</p><pre><code>sudo chown -R www-data:www-data /var/www/html/
sudo chmod -R 755 /var/www/html/
</code></pre><h2 id="Step_4__Configure_Apache_for_Elgg">Step 4: Configure Apache for Elgg</h2><p>Elgg requires the Apache rewrite module. Enable the Apache rewrite module.</p><pre><code>sudo a2enmod rewrite
</code></pre><p>Create an Apache configuration file for the Elgg installation.</p><pre><code>sudo nano /etc/apache2/sites-available/elgg.conf
</code></pre><p>Paste the following snippet to the file, replacing&nbsp;<code>example.com</code>&nbsp;with your own domain name.</p><pre><code>&lt;VirtualHost *:80&gt;
     DocumentRoot /var/www/html/
     ServerName example.com
     &lt;Directory /var/www/html/&gt;
          Options FollowSymlinks
          AllowOverride All
          Require all granted
     &lt;/Directory&gt;
     ErrorLog ${APACHE_LOG_DIR}/error.log
     CustomLog ${APACHE_LOG_DIR}/access.log combined
&lt;/VirtualHost&gt;
</code></pre><p>Enable the configuration and restart the Apache server.</p><pre><code> sudo a2ensite elgg.conf
 sudo systemctl restart apache2.service</code></pre>]]></description>
	<dc:creator>Abhi</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</guid>
	<pubDate>Thu, 29 Aug 2013 15:05:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4099/sequencing-solutions-to-world-health</link>
	<title><![CDATA[Sequencing Solutions to World Health]]></title>
	<description><![CDATA[<p>"<em>New technology that quickly, easily and economically reveals the genomes of viruses and pathogens transforms public health and medicine."</em></p>
<p><strong>Source</strong>: Life technologies</p><p>Address of the bookmark: <a href="http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264" rel="nofollow">http://www.lifetechnologies.com/global/en/home/communities-social/blog/blogs/sequencing-solutions-to-world-health.html?cid=social_blogseries_20130829_11098264</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/2726/comparison-of-short-read-de-novo-alignment-algorithms</guid>
	<pubDate>Wed, 21 Aug 2013 07:56:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/2726/comparison-of-short-read-de-novo-alignment-algorithms</link>
	<title><![CDATA[Comparison of Short Read De Novo Alignment Algorithms]]></title>
	<description><![CDATA[<p>Excellent article to introduce different sequencing methods along with tools for de novo assembly of sequencing reads and their relevant references.</p>
<p>Title:&nbsp;<strong>Comparison of Short Read De Novo Alignment Algorithms&nbsp;</strong></p>
<p>Author<strong>: Nikhil Gopal</strong></p><p>Address of the bookmark: <a href="http://biochem218.stanford.edu/Projects%202011/Gopal%202011.pdf" rel="nofollow">http://biochem218.stanford.edu/Projects%202011/Gopal%202011.pdf</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/4208/latest-paper-on-comparison-of-mapping-tools</guid>
	<pubDate>Tue, 03 Sep 2013 18:00:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/4208/latest-paper-on-comparison-of-mapping-tools</link>
	<title><![CDATA[Latest paper on comparison of mapping tools]]></title>
	<description><![CDATA[<p>A. Hatem, D. Bozdag, A. E. Toland, U. V. Catalyurek "Benchmarking short sequence mapping tools" BMC Bioinformatics, 14(1):184, 2013.</p>
<p>http://bmi.osu.edu/hpc/software/benchmark/</p>
<p><a href="http://bmi.osu.edu/hpc/software/pmap/pmap.html">http://bmi.osu.edu/hpc/software/pmap/pmap.html</a></p>
<p>Other similiar papers:</p>
<p><a href="http://online.liebertpub.com/doi/pdf/10.1089/cmb.2012.0022">http://online.liebertpub.com/doi/pdf/10.1089/cmb.2012.0022</a></p>
<p><a href="http://bioinformatics.oxfordjournals.org/content/28/24/3169">http://bioinformatics.oxfordjournals.org/content/28/24/3169</a></p>
<p>Some new Mapping tool links:<a href="http://bmi.osu.edu/hpc/software/benchmark/"></a></p>
<p><strong>GSNAP</strong></p>
<p><a href="http://research-pub.gene.com/gmap/"></a><a href="http://research-pub.gene.com/gmap/">http://research-pub.gene.com/gmap/</a></p>
<p><strong>RMAP</strong></p>
<p><a href="http://rulai.cshl.edu/rmap/"></a><a href="http://rulai.cshl.edu/rmap/">http://rulai.cshl.edu/rmap/</a></p>
<p><strong>mrsFAST</strong></p>
<p><a href="http://mrsfast.sourceforge.net/Home"></a><a href="http://mrsfast.sourceforge.net/Home">http://mrsfast.sourceforge.net/Home</a></p>
<p><a href="http://sourceforge.net/projects/mrsfast/files/mrsfast-ultra-3.1.0/">http://sourceforge.net/projects/mrsfast/files/mrsfast-ultra-3.1.0/</a></p>
<p><strong>BFAST</strong></p>
<p><a href="http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page">http://sourceforge.net/apps/mediawiki/bfast/index.php?title=Main_Page</a></p>
<p><strong>SHRiMP (for&nbsp;AB SOLiD color-space reads)</strong></p>
<p><a href="http://compbio.cs.toronto.edu/shrimp/">http://compbio.cs.toronto.edu/shrimp/</a></p>
<p><strong>RazerA 3</strong></p>
<p><a href="http://www.seqan.de/projects/razers/">http://www.seqan.de/projects/razers/</a></p><p>Address of the bookmark: <a href="http://www.biomedcentral.com/1471-2105/14/184" rel="nofollow">http://www.biomedcentral.com/1471-2105/14/184</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/9400/largest-genome-sequenced</guid>
	<pubDate>Fri, 21 Mar 2014 13:57:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/9400/largest-genome-sequenced</link>
	<title><![CDATA[Largest Genome Sequenced]]></title>
	<description><![CDATA[<p>The enormous size of the <strong>loblolly pine genome</strong> having <strong>22 billion base pairs</strong> compared to only 3 billion in the human genome. In other words, it is&nbsp;<strong>seven times</strong> larger than a human&rsquo;s and also the largest and the most complete&nbsp;<strong>conifer<a href="http://en.wikipedia.org/wiki/Pinophyta" target="_blank"></a></strong>&nbsp;genome ever sequenced.</p>
<p><strong>Related Paper:</strong></p>
<p>http://genomebiology.com/2014/15/3/R59/abstract</p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://www.news.ucdavis.edu/search/news_detail.lasso?id=10859" rel="nofollow">http://www.news.ucdavis.edu/search/news_detail.lasso?id=10859</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/10243/new-rna-seq-tool</guid>
	<pubDate>Fri, 25 Apr 2014 10:59:04 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/10243/new-rna-seq-tool</link>
	<title><![CDATA[New RNA Seq tool]]></title>
	<description><![CDATA[<p>"<span>By removing the time-consuming step of read mapping, the authors reported, Sailfish able to provide quantification estimates 20&ndash;30 times faster than current methods without loss of accuracy."</span></p>
<p><span>Tool link:</span></p>
<p><span>http://www.cs.cmu.edu/~ckingsf/software/sailfish/</span></p>
<p><span></span></p><p>Address of the bookmark: <a href="http://www.genengnews.com/gen-news-highlights/lightweight-algorithms-sail-through-rna-sequencing-data/81249765/" rel="nofollow">http://www.genengnews.com/gen-news-highlights/lightweight-algorithms-sail-through-rna-sequencing-data/81249765/</a></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/10966/genxpro-gmbh</guid>
	<pubDate>Thu, 22 May 2014 07:18:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/10966/genxpro-gmbh</link>
	<title><![CDATA[GenXPro GmbH]]></title>
	<description><![CDATA[<p><strong>GenXPro</strong>&nbsp;GMbH is service provider for entire spectrum of nucleotide-based information&nbsp;of any biological sample. By combining intelligent data reduction techniques and&nbsp;latest next generation sequencing technologies, our service portfolio provides most accurate and cost efficient solutions for&nbsp;transcriptomic-, genomic- or epigenomic research.</p><p><span><span><strong><span>GENXPRO GMBH</span>,&nbsp;</strong></span></span><span>ALTENH&Ouml;FERALLEE 3,&nbsp;</span><span>60438 FRANKFURT MAIN,&nbsp;</span><span>GERMANY</span></p><p><span><span><strong>Website</strong></span>:&nbsp;<a href="http://www.genxpro.info/products_and_services/"></a><a href="http://www.genxpro.info/products_and_services/">http://www.genxpro.info/products_and_services/</a></span></p><p><span><strong>PHONE</strong>: +49 (0)69- 95 73 97 10,&nbsp;FAX: +49 (0)69- 95 73 97 06</span></p><p><span>EMAIL: info@genxpro.de</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/13415/genomics-and-sequencing-approach-for-identification-of-biomarkers-to-assess-the-efficacy-of-tgf-%CE%B2ri-inhibitors-of-liver-cancer-in-vivo</guid>
	<pubDate>Tue, 05 Aug 2014 13:55:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/13415/genomics-and-sequencing-approach-for-identification-of-biomarkers-to-assess-the-efficacy-of-tgf-%CE%B2ri-inhibitors-of-liver-cancer-in-vivo</link>
	<title><![CDATA[Genomics and sequencing approach for identification of biomarkers to assess the efficacy of TGF-βRI inhibitors (of liver cancer) in vivo]]></title>
	<description><![CDATA[<p>Liver cancer is third leading cause of deaths and fourth most frequent occuring cancer worldwide. There are multiple signaling pathways responsible for causing cancer amongst which TGFb is most important cytokine whose signaling pathway promote cancer. However, main problem is to cure this cancer at late stage where we still have no treatment strategy to tackle this deadly cancer. &nbsp;Hence we need to find out new therapeutic target. One way is to look the relationships between mRNA, methylation and miRNA data of patients with different pathological conditions (cancer vs control either with inhibitor/not). MiRNA is small RNA molecules known to inhibit mRNA expression of particular gene by binding improperly to 3'UTR region of a gene and hence block binding of TF /translation of gene. CpG regions is known to located at promoter region of gene (5' UTR) and usually hypomethylated which allow to gene to transcribe and translate however sometime this region become hyper-methylated thats prevent expression of host gene. Thus , integration of these three data reveal new targets and pathways important for causing or preventing cancer and also reveal biomarker thats check the effects of inhibitor on signaling pathway underlying liver cancer.</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/13415" length="26423" type="image/jpeg" />
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