<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: All site bookmarks]]></title>
	<link>https://bioinformaticsonline.com/bookmarks/all?offset=620</link>
	<atom:link href="https://bioinformaticsonline.com/bookmarks/all?offset=620" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37794/mimicree2-genome-wide-forward-simulations-of-evolve-and-resequencing-studies</guid>
	<pubDate>Fri, 28 Sep 2018 09:21:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37794/mimicree2-genome-wide-forward-simulations-of-evolve-and-resequencing-studies</link>
	<title><![CDATA[MimicrEE2: Genome-wide forward simulations of Evolve and Resequencing studies]]></title>
	<description><![CDATA[<p><span>MimicrEE2, a multi-threaded Java program for genome-wide forward simulations of evolving populations. MimicrEE2 enables the convenient usage of available genomic resources, supports biological particulars of model organism frequently used in E&amp;R studies and offers a wide range of different adaptive models (selective sweeps, polygenic adaptation, epistasis). MimicrEE2 runs on any computer with Java installed. It is distributed under the GPLv3 license at&nbsp;</span><a href="https://sourceforge.net/projects/mimicree2/">https://sourceforge.net/projects/mimicree2/</a><span>.</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/mimicree2/" rel="nofollow">https://sourceforge.net/projects/mimicree2/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37788/s-plot2-creates-an-interactive-two-dimensional-heatmap-of-sequences</guid>
	<pubDate>Fri, 28 Sep 2018 05:36:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37788/s-plot2-creates-an-interactive-two-dimensional-heatmap-of-sequences</link>
	<title><![CDATA[S-plot2: creates an interactive, two-dimensional heatmap of sequences]]></title>
	<description><![CDATA[<p><span>S-plot2 creates an interactive, two-dimensional heatmap capturing the similarities and dissimilarities in nucleotide usage between genomic sequences (partial or complete). In S-plot2, whole eukaryotic chromosomes and smaller prokaryotic genomes can be efficiently compared. The tool includes functionality to extract, analyze, and automate BLAST queries of regions of interest within the heatmap. This facilitates the investigation of quickly evolving coding regions, novel coding regions, and laterally transferred elements.</span></p>
<p><span>http://www.putonti-lab.com/uploads/4/5/3/0/45307835/s-plot2_tutorial.pdf</span></p>
<p><span>http://journals.sagepub.com/doi/pdf/10.1177/1176934318797354</span></p><p>Address of the bookmark: <a href="https://bitbucket.org/lkalesinskas/splot" rel="nofollow">https://bitbucket.org/lkalesinskas/splot</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37785/haplomerger2-rebuilding-both-haploid-sub-assemblies-from-high-heterozygosity-diploid-genome-assembly</guid>
	<pubDate>Thu, 27 Sep 2018 07:08:47 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37785/haplomerger2-rebuilding-both-haploid-sub-assemblies-from-high-heterozygosity-diploid-genome-assembly</link>
	<title><![CDATA[HaploMerger2: rebuilding both haploid sub-assemblies from high-heterozygosity diploid genome assembly]]></title>
	<description><![CDATA[<p><span><span>HM2 can process any diploid assemblies, but it is especially suitable for diploid assemblies with high heterozygosity (&ge;3%), which can be difficult for other tools. This pipeline also implements flexible and sensitive assembly error detection, a hierarchical scaffolding procedure and a reliable gap-closing method for haploid sub-assemblies.</span></span></p>
<p><span>Source code, executables and the testing dataset are freely available at&nbsp;</span><a href="https://github.com/mapleforest/HaploMerger2/releases/" target="">https://github.com/mapleforest/HaploMerger2/releases/</a><span>.</span></p><p>Address of the bookmark: <a href="https://github.com/mapleforest/HaploMerger2/releases/" rel="nofollow">https://github.com/mapleforest/HaploMerger2/releases/</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37776/rhat-a-seed-and-extension-based-noisy-long-read-alignment-tool</guid>
	<pubDate>Sun, 23 Sep 2018 05:12:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37776/rhat-a-seed-and-extension-based-noisy-long-read-alignment-tool</link>
	<title><![CDATA[rHAT: a seed-and-extension-based noisy long read alignment tool]]></title>
	<description><![CDATA[<p><span>rHAT is a seed-and-extension-based noisy long read alignment tool. It is suitable for aligning 3rd generation sequencing reads which are in large read length with relatively high error rate, especially Pacbio's Single Molecule Read-time (SMRT) sequencing reads.</span></p><p>Address of the bookmark: <a href="https://github.com/dfguan/rHAT" rel="nofollow">https://github.com/dfguan/rHAT</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37759/pandaseq-is-a-program-to-align-illumina-reads-optionally-with-pcr-primers-embedded-in-the-sequence-and-reconstruct-an-overlapping-sequence</guid>
	<pubDate>Fri, 21 Sep 2018 10:19:52 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37759/pandaseq-is-a-program-to-align-illumina-reads-optionally-with-pcr-primers-embedded-in-the-sequence-and-reconstruct-an-overlapping-sequence</link>
	<title><![CDATA[PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the sequence, and reconstruct an overlapping sequence.]]></title>
	<description><![CDATA[<p>Development packages for zlib and libbz2 are needed, as well as a standard compiler environment. On Ubuntu, this can be installed via:</p>
<pre><code>sudo apt-get install build-essential libtool automake zlib1g-dev libbz2-dev pkg-config
</code></pre>
<p>On MacOS, the Apple Developer tools and Fink (or MacPorts or Brew) must be installed, then:</p>
<pre><code>sudo fink install bzip2-dev pkgconfig</code></pre><p>Address of the bookmark: <a href="https://github.com/neufeld/pandaseq" rel="nofollow">https://github.com/neufeld/pandaseq</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37751/kast-perform-alignment-free-k-tuple-frequency-comparisons-from-sequences</guid>
	<pubDate>Thu, 20 Sep 2018 08:56:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37751/kast-perform-alignment-free-k-tuple-frequency-comparisons-from-sequences</link>
	<title><![CDATA[KAST: Perform Alignment-free k-tuple frequency comparisons from sequences]]></title>
	<description><![CDATA[<p><span>Perform Alignment-free k-tuple frequency comparisons from sequences. This can be in the form of two input files (e.g. a reference and a query) or a single file for pairwise comparisons to be made.</span></p><p>Address of the bookmark: <a href="https://github.com/martinjvickers/KAST" rel="nofollow">https://github.com/martinjvickers/KAST</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37749/d2tools-the-toolbox-for-counting-the-frequency-of-k-tuple-from-sequencing-datasets-and-calculate-the-dissimilarity</guid>
	<pubDate>Thu, 20 Sep 2018 08:38:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37749/d2tools-the-toolbox-for-counting-the-frequency-of-k-tuple-from-sequencing-datasets-and-calculate-the-dissimilarity</link>
	<title><![CDATA[d2Tools: The toolbox for counting the frequency of k-tuple from sequencing datasets and calculate the dissimilarity]]></title>
	<description><![CDATA[<p><code>d2Tools</code>&nbsp;are the toolbox for counting the frequency of K-tuple from sequencing datasets and then calculating the pairwise dissimilarity matrix between samples with the&nbsp;<strong>d2-style</strong>(d2/d2<code>*</code>/d2S representing d2/d2Star/d2shepp, respectively) measures. Hao, Dai, Eucliean, Mahattan, and Chebyshev distance measures are also included in d2Tools.</p>
<p>Manual at&nbsp;https://code.google.com/archive/p/d2-tools/wikis/d2ToolMannual.wiki</p><p>Address of the bookmark: <a href="https://code.google.com/archive/p/d2-tools/" rel="nofollow">https://code.google.com/archive/p/d2-tools/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37746/funannotate-eukaryotic-genome-annotation-pipeline</guid>
	<pubDate>Wed, 19 Sep 2018 07:47:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37746/funannotate-eukaryotic-genome-annotation-pipeline</link>
	<title><![CDATA[funannotate: Eukaryotic Genome Annotation Pipeline]]></title>
	<description><![CDATA[<p><span>Funannotate is a genome prediction, annotation, and comparison software package. It was originally written to annotate fungal genomes (small eukaryotes ~ 30 Mb genomes), but has evolved over time to accomodate larger genomes. The impetus for this software package was to be able to accurately and easily annotate a genome for submission to NCBI GenBank. Existing tools (such as Maker) require significant manually editing to comply with GenBank submission rules, thus funannotate is aimed at simplifying the genome submission process.</span></p><p>Address of the bookmark: <a href="https://github.com/nextgenusfs/funannotate" rel="nofollow">https://github.com/nextgenusfs/funannotate</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37737/rebaler-program-for-conducting-reference-based-assemblies-using-long-reads</guid>
	<pubDate>Tue, 18 Sep 2018 07:52:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37737/rebaler-program-for-conducting-reference-based-assemblies-using-long-reads</link>
	<title><![CDATA[Rebaler: program for conducting reference-based assemblies using long reads.]]></title>
	<description><![CDATA[<p>Rebaler is a program for conducting reference-based assemblies using long reads. It relies mainly on&nbsp;<a href="https://github.com/lh3/minimap2">minimap2</a>&nbsp;for alignment and&nbsp;<a href="https://github.com/isovic/racon">Racon</a>&nbsp;for making consensus sequences.</p>
<p>I made Rebaler for bacterial genomes (specifically for the task of&nbsp;<a href="https://github.com/rrwick/Basecalling-comparison">testing basecallers</a>). It should in principle work for non-bacterial genomes as well, but I haven't tested it.</p><p>Address of the bookmark: <a href="https://github.com/rrwick/Rebaler" rel="nofollow">https://github.com/rrwick/Rebaler</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37732/making-2d-hilbert-curve</guid>
	<pubDate>Mon, 17 Sep 2018 05:43:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37732/making-2d-hilbert-curve</link>
	<title><![CDATA[Making 2D Hilbert Curve]]></title>
	<description><![CDATA[<p><a href="https://en.wikipedia.org/wiki/Hilbert_curve">Hilbert curve</a>&nbsp;is a type of space-filling curves that folds one dimensional axis into a two dimensional space, but still keeps the locality. It has advantages to visualize data with long axis in following two aspects:</p>
<ol>
<li>greatly improve resolution of the visualization fron n to&nbsp;<span><span><span><span><span><span><span>&radic;</span></span><span><span><span><span>n</span></span></span></span></span></span></span></span><span>n</span></span>;</li>
<li>easy to visualize clusters because generally data points in the axis will also be close in the 2D space.</li>
</ol>
<p>This package aims to provide an easy and flexible way to visualize data through Hilbert curve. The implementation and example figures are based on following sources:</p>
<ul>
<li><a href="http://mkweb.bcgsc.ca/hilbert/">http://mkweb.bcgsc.ca/hilbert/</a></li>
<li><a href="http://corte.si/posts/code/hilbert/portrait/index.html">http://corte.si/posts/code/hilbert/portrait/index.html</a></li>
<li><a href="http://bioconductor.org/packages/devel/bioc/html/HilbertVis.html">http://bioconductor.org/packages/devel/bioc/html/HilbertVis.html</a></li>
</ul><p>Address of the bookmark: <a href="https://bioconductor.org/packages/devel/bioc/vignettes/HilbertCurve/inst/doc/HilbertCurve.html" rel="nofollow">https://bioconductor.org/packages/devel/bioc/vignettes/HilbertCurve/inst/doc/HilbertCurve.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

</channel>
</rss>