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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44900?offset=130</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/22569/reverse-complement-problem-solved-with-perl</guid>
	<pubDate>Tue, 09 Jun 2015 23:37:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/22569/reverse-complement-problem-solved-with-perl</link>
	<title><![CDATA[Reverse Complement Problem Solved with Perl]]></title>
	<description><![CDATA[<p>Question at http://rosalind.info/problems/1b/</p><p>#Find the reverse complement of a DNA string.<br />#Given: A DNA string Pattern.<br />#Return: Pattern, the reverse complement of Pattern.<br /><br />use strict;<br />use warnings;<br /><br />my $string="AAAACCCGGT";<br />my $finalString="";<br />my %hash = (<br />&nbsp;&nbsp; &nbsp;"C" =&gt; "G", <br />&nbsp;&nbsp; &nbsp;"A" =&gt; "T", <br />&nbsp;&nbsp; &nbsp;"T" =&gt; "A", <br />&nbsp;&nbsp; &nbsp;"G" =&gt; "C",<br />);<br /><br />for (my $aa=0; $aa&lt;=(length($string)-1); $aa++) {<br />&nbsp;&nbsp; &nbsp;my $char=substr $string, $aa, 1;<br />&nbsp;&nbsp; &nbsp;#print $hash{$char};<br />&nbsp;&nbsp; &nbsp;$finalString="$hash{$char}"."$finalString";<br />}<br /><br />print $finalString;<br />print "\n";</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/22961/bioscripts</guid>
	<pubDate>Sun, 28 Jun 2015 07:46:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/22961/bioscripts</link>
	<title><![CDATA[BioScripts]]></title>
	<description><![CDATA[<p>You are requested to please bookmark collection of bioinformatics tools, scripts, codes that can be pieced together in a very easy and flexible manner to perform both simple and complex bioinformatics tasks.</p>
<p>The next-generation sequencing included whole genome sequencing(WGS), transcriptome sequencing (whole cDNA sequencing, RNA-seq), digital gene expression sequencing (Tag-Seq), ChIP-Seq, and so on. And there are many sequencing platform to generate sequece, as well know Sanger/ABi(the frist generation), Solexa/illumina, SOLiD/ABi, 454/Roche. But thier sequence format is different, also they have different error type. High quality data is very important for further analysis or data mining. There are many pipeline for raw sequence quality analysis and control with few of process for reporting reads quality statistical details, trimming, filtering, and error correction. Please bookmarks them for the benefits of bioinformatics community.</p>
<p>https://code.google.com/p/biowiki/</p>
<p>https://code.google.com/p/ngs-pipeline/source/browse/#svn%2Ftrunk</p>
<p>NGSand Perl scripts https://code.google.com/hosting/search?q=NGS+perl&amp;projectsearch=Search+projects</p>
<p>NGS and Python scripts https://code.google.com/hosting/search?q=NGS+Python&amp;projectsearch=Search+projects</p><p>Address of the bookmark: <a href="https://code.google.com/hosting/search?q=bioinformatics&amp;sa=Search" rel="nofollow">https://code.google.com/hosting/search?q=bioinformatics&amp;sa=Search</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31278/metapred2cs</guid>
	<pubDate>Fri, 03 Mar 2017 05:15:07 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31278/metapred2cs</link>
	<title><![CDATA[MetaPred2CS]]></title>
	<description><![CDATA[<p style="text-align: justify;"><strong>MetaPred2CS Web server&nbsp;</strong>is a meta-predictor based on&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/17160063">Support Vector Machine (SVM)</a>&nbsp;that combines 6 individual sequence based protein-protein interaction prediction methods to predict&nbsp;<strong>prokaryotic two-component system&nbsp;</strong>protein-protein interactions (PPIs). The methods implemented in MetaPred2CS are 2 co-evolutionary methods:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/11933068">in-silico two hybrid (i2h)</a>&nbsp;and&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/11707606">mirror tree (MT)</a>&nbsp;methods and 4 genomics context based methods:&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/15947018">phylogenetic profiling (PP)</a>,&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/10573422">gene fusion (GF)</a>,&nbsp;<a href="http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.0030043">gene neighbourhood (GN)</a>&nbsp;and and&nbsp;<a href="http://www.ploscompbiol.org/article/info%3Adoi%2F10.1371%2Fjournal.pcbi.0030043">gene operon methods (GO)</a>.</p>
<p>&nbsp;http://metapred2cs.ibers.aber.ac.uk/</p><p>Address of the bookmark: <a href="https://github.com/martinjvickers/MetaPred2CS" rel="nofollow">https://github.com/martinjvickers/MetaPred2CS</a></p>]]></description>
	<dc:creator>Manisha Mishra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27847/anvio</guid>
	<pubDate>Thu, 16 Jun 2016 18:15:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27847/anvio</link>
	<title><![CDATA[Anvio]]></title>
	<description><![CDATA[<p>In a nutshell</p>
<p>Anvi&rsquo;o is an analysis and visualization platform for &lsquo;omics data.</p>
<p>Please find the methods paper here: https://peerj.com/articles/1319/</p>
<p>Anvi&rsquo;o would not have been possible without the help of many people who directly or indirectly contributed to its development. Here is the acknowledgements section of our methods paper</p>
<p><span>An analysis and visualization platform for 'omics data</span><span>&nbsp;</span><span><a href="http://merenlab.org/projects/anvio">http://merenlab.org/projects/anvio</a></span></p>
<p><span>Paper&nbsp;https://peerj.com/articles/1839/</span></p><p>Address of the bookmark: <a href="https://github.com/meren/anvio" rel="nofollow">https://github.com/meren/anvio</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/28199/genome-workbench-2107</guid>
	<pubDate>Fri, 01 Jul 2016 12:09:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/28199/genome-workbench-2107</link>
	<title><![CDATA[Genome Workbench 2.10.7]]></title>
	<description><![CDATA[<p>Genome Workbench 2.10.7 is here! New features include added support for local custom BLAST databases and improvements to Tree View.</p><p>For the full list of features, improvements and fixes, see the release notes:<a href="https://ncbi.nlm.nih.gov/tools/gbench/releasenotes" target="_blank">https://ncbi.nlm.nih.gov/tools/gbench/releasenotes</a></p><p>New Features</p><ul>
<li>BLAST Tool: added support for local custom BLAST databases</li>
<li>Graphical Sequence View: added log scaling option for graph tracks</li>
<li>Generic Table View:&nbsp;<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial17">new tutorial</a>&nbsp;added</li>
</ul><p>Bug Fixes and Improvements</p><ul>
<li>Project Tree View: Genomic Collections/Assemblies now show accessions, not just names</li>
<li>Tree View: layout updated to better accommodate nodes of different sizes</li>
<li>Table Import Dialog (MacOS): fixed issue with table visibility</li>
<li>Fixed bug where different molecules IDs in GenBank could resolve to the same sequence</li>
<li>Graphical Sequence View: fixed issue where sequence track was not shown for some sequences</li>
<li>Graphical Sequence View: fixed protein coloration methods</li>
<li>Graphical Sequence View: improved rendering of Markers to better indicate boundaries and produce higher quality PDF images</li>
<li>Create Gene Model tool: fixed scenario when gene model tool failed with local sequences</li>
<li>Search View: ORF Finder &ndash; fixed incorrect protein lengths</li>
<li>Fixed bug with not opening project file (.gbp) on a click</li>
<li>Fixed issues in GVF import</li>
<li>Fixed BLAST Search tool against NCBI databases not working</li>
<li>Fixed tblastn (protein BLAST) not working in standalone mode</li>
<li>Fixed GTF export failure</li>
</ul>]]></description>
	<dc:creator>Gudiya Pal</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28415/scarpa</guid>
	<pubDate>Wed, 13 Jul 2016 07:59:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28415/scarpa</link>
	<title><![CDATA[Scarpa]]></title>
	<description><![CDATA[<p><strong>Scarpa</strong>&nbsp;is a stand-alone scaffolding tool for NGS data. It can be used together with virtually any genome assembler and any NGS read mapper that supports SAM format. Other features include support for multiple libraries and an option to estimate insert size distributions from data. Scarpa is available free of charge for academic and commercial use under the GNU General Public License (GPL).</p>
<p>See the&nbsp;<a href="http://compbio.cs.toronto.edu/hapsembler/hapsembler-2.21_manual.pdf">user manual</a>&nbsp;or the&nbsp;<a href="http://compbio.cs.toronto.edu/hapsembler/scarpa_paper.pdf">paper</a>&nbsp;for more information about Scarpa. Click&nbsp;<a href="http://compbio.cs.toronto.edu/hapsembler/ScarpaSupplementary.pdf">here</a>&nbsp;for the supplementary material.</p><p>Address of the bookmark: <a href="http://compbio.cs.toronto.edu/hapsembler/scarpa.html" rel="nofollow">http://compbio.cs.toronto.edu/hapsembler/scarpa.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31100/vaguevelvet-assembler-graphical-front-end</guid>
	<pubDate>Fri, 24 Feb 2017 08:56:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31100/vaguevelvet-assembler-graphical-front-end</link>
	<title><![CDATA[VAGUE:Velvet Assembler Graphical Front End]]></title>
	<description><![CDATA[<p>VAGUE is a vague acronym for "Velvet Assembler Graphical Front End", which means it is a GUI for the Velvet <em>de novo</em> assembler. The command line version of Velvet can be complicated for beginners to use, but VAGUE makes it clear and simple</p>
<p>More at&nbsp;http://www.vicbioinformatics.com/software.vague.shtml</p><p>Address of the bookmark: <a href="http://www.vicbioinformatics.com/software.vague.shtml" rel="nofollow">http://www.vicbioinformatics.com/software.vague.shtml</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28842/repeatmodeler</guid>
	<pubDate>Thu, 18 Aug 2016 09:57:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28842/repeatmodeler</link>
	<title><![CDATA[RepeatModeler]]></title>
	<description><![CDATA[<p><span>RepeatModeler is a de-novo repeat family identification and modeling package. At the heart of RepeatModeler are two de-novo repeat finding programs ( RECON and RepeatScout ) which employ complementary computational methods for identifying repeat element boundaries and family relationships from sequence data. RepeatModeler assists in automating the runs of RECON and RepeatScout given a genomic database and uses the output to build, refine and classify consensus models of putative interspersed repeats.</span></p><p>Address of the bookmark: <a href="http://www.repeatmasker.org/RepeatModeler.html" rel="nofollow">http://www.repeatmasker.org/RepeatModeler.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28884/tgnet</guid>
	<pubDate>Wed, 24 Aug 2016 05:36:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28884/tgnet</link>
	<title><![CDATA[TGNet]]></title>
	<description><![CDATA[<p><span>Recent technological progress has greatly facilitated&nbsp;</span><em>de novo</em><span>&nbsp;genome sequencing. However,&nbsp;</span><em>de novo</em><span>&nbsp;assemblies consist in many pieces of contiguous sequence (contigs) arranged in thousands of scaffolds instead of small numbers of chromosomes. Confirming and improving the quality of such assemblies is critical for subsequent analysis.&nbsp;</span></p>
<p>Visualization and quality assessment of de novo genome assemblies</p>
<p>Citation</p>
<p>This software is fully described in the paper:<br>Riba-Grognuz, Keller, Falquet, Xenarios &amp; Wurm (2011) Visualization and quality assessment of de novo genome assemblies.</p>
<p>In brief, our scripts create Cytoscape files to visualize transcript evidence that suggests adjacency between scaffolds and contigs.</p>
<p>Software requirements</p>
<p>BLAT (tested with Standalone BLAT v. 32&times;1). Source Binaries .<br>Cytoscape (tested with versions 2.7.0, 2.8.2)<br>a UNIX machine (tested on Mac OS X 10.6 and CentOS 4.6)</p><p>Address of the bookmark: <a href="https://github.com/ksanao/TGNet" rel="nofollow">https://github.com/ksanao/TGNet</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28915/useful-bioinformatics-tools</guid>
	<pubDate>Mon, 29 Aug 2016 04:08:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28915/useful-bioinformatics-tools</link>
	<title><![CDATA[Useful Bioinformatics Tools]]></title>
	<description><![CDATA[<p>Collections of few handy tools for bioinformatician</p>
<p>http://molbiol-tools.ca/Convert.htm</p><p>Address of the bookmark: <a href="http://molbiol-tools.ca/Convert.htm" rel="nofollow">http://molbiol-tools.ca/Convert.htm</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>

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