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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/36830?offset=460</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36852/mcmctree-a-phylogenetic-program-for-bayesian-estimation-of-species-divergence-times</guid>
	<pubDate>Sat, 02 Jun 2018 07:40:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36852/mcmctree-a-phylogenetic-program-for-bayesian-estimation-of-species-divergence-times</link>
	<title><![CDATA[MCMCTREE: a phylogenetic program for Bayesian estimation of species divergence times]]></title>
	<description><![CDATA[<p><a href="http://abacus.gene.ucl.ac.uk/software/paml.html" target="_blank">MCMCTREE</a><span>&nbsp;is a phylogenetic program for Bayesian estimation of species divergence times using soft fossil constraints under various molecular clock models. This is part of the&nbsp;</span><a href="http://abacus.gene.ucl.ac.uk/software/paml.html" target="_blank">PAML</a><span>&nbsp;package. In this tutorial I will analyze an easy example modified from dataset of&nbsp;</span><a href="http://www.ncbi.nlm.nih.gov/pubmed/20551041" target="_blank">Inoue et al. (2010)</a><span>. Here we conduct a commonly used time estimation method, "Approximate Likelihood Method", for the datasets including more than 10 species.</span></p><p>Address of the bookmark: <a href="http://www.fish-evol.com/mcmctreeExampleVert6/text1Eng.html" rel="nofollow">http://www.fish-evol.com/mcmctreeExampleVert6/text1Eng.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/38625/croco-a-program-to-detect-potential-cross-contaminations-in-hts-assembled-transcriptomes-using-expression-level-quantification</guid>
	<pubDate>Mon, 07 Jan 2019 18:17:44 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38625/croco-a-program-to-detect-potential-cross-contaminations-in-hts-assembled-transcriptomes-using-expression-level-quantification</link>
	<title><![CDATA[CroCo: A program to detect potential cross contaminations in HTS assembled transcriptomes using expression level quantification]]></title>
	<description><![CDATA[<p>CroCo is a program to detect cross contamination events in assembled transcriptomes using sequencing reads to determine the true origin of every transcripts.<br>Such cross contaminations can be expected if several RNA-Seq experiments were prepared during the same period at the same lab, or by the same people, or if they were processed or sequenced by the same sequencing service facility.<br>Our approach first determines a subset of transcripts that are suspiciously similar across samples using a pairwise BLAST procedure. CroCo then combine all transcriptomes into a metatranscriptome and quantifies the "expression level" of all transcripts successively using every sample read data (e.g. several species sequenced by the same lab for a particular study) while allowing read multi-mappings.<br>Several mapping tools implemented in CroCo can be used to estimate expression level (default is RapMap).<br>This information is then used to categorize each transcript in the following 5 categories :</p>
<p><br>clean: the transcript origin is from the focal sample.</p>
<p>cross contamination: the transcript origin is from an alien sample of the same experiment.</p>
<p>dubious: expression levels are too close between focal and alien samples to determine the true origin of the transcript.</p>
<p>low coverage: expression levels are too low in all samples, thus hampering our procedure (which relies on differential expression) to confidently assign it to any category.</p>
<p>over expressed: expression levels are very high in at least 3 samples and CroCo will not try to categorize it. Indeed, such a pattern does not correspond to expectations for cross contaminations, but often reflect highly conserved genes such as ribosomal gene, or external contamination shared by several samples (e.g. Escherichia coli contaminations).</p><p>Address of the bookmark: <a href="https://gitlab.mbb.univ-montp2.fr/mbb/CroCo" rel="nofollow">https://gitlab.mbb.univ-montp2.fr/mbb/CroCo</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40214/gooey-turn-almost-any-python-command-line-program-into-a-full-gui-application-with-one-line</guid>
	<pubDate>Fri, 01 Nov 2019 00:29:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40214/gooey-turn-almost-any-python-command-line-program-into-a-full-gui-application-with-one-line</link>
	<title><![CDATA[Gooey: Turn (almost) any Python command line program into a full GUI application with one line]]></title>
	<description><![CDATA[<p><span>Turn (almost) any Python command line program into a full GUI application with one line</span></p>
<p>The easiest way to install Gooey is via&nbsp;<code>pip</code></p>
<pre><code>pip install Gooey 
</code></pre>
<p>Alternatively, you can install Gooey by cloning the project to your local directory</p>
<pre><code>git clone https://github.com/chriskiehl/Gooey.git
</code></pre>
<p>run&nbsp;<code>setup.py</code></p>
<pre><code>python setup.py install</code></pre><p>Address of the bookmark: <a href="https://github.com/chriskiehl/Gooey" rel="nofollow">https://github.com/chriskiehl/Gooey</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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