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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/44626?offset=30</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36605/hello-python-world</guid>
	<pubDate>Mon, 14 May 2018 16:41:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36605/hello-python-world</link>
	<title><![CDATA[Hello Python World !]]></title>
	<description><![CDATA[<p>As I mentioned earlier, I will keep on posting one Python script per day to introduce you to Python programming. Whether you are an experienced programmer or not, this tutorial is intended for everyone who wishes to learn the Python programming language.</p><p>Python is a very simple language, and has a very straightforward syntax. The simplest directive in Python is the "print" directive - it simply prints out a line (and also includes a newline).</p><p>Create a file Hello.py</p><blockquote><p>print("Hello, Python World !.")</p></blockquote><p>Run</p><p>python3 Hello.py</p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/35400/zpicture-a-dynamic-blastz-alignment-visualization</guid>
	<pubDate>Tue, 30 Jan 2018 16:03:08 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/35400/zpicture-a-dynamic-blastz-alignment-visualization</link>
	<title><![CDATA[zPicture: A dynamic blastz alignment visualization]]></title>
	<description><![CDATA[<p><span>zPicture is a dynamic alignment and&nbsp;</span><span>visualization</span><span>&nbsp;tool that is based on blastz alignment program utilized by PipMaker. zPicture alignments can be automatically submitted to rVista 2.0 to identify conserved transcription factor binding sites.</span></p><p>Address of the bookmark: <a href="https://zpicture.dcode.org/" rel="nofollow">https://zpicture.dcode.org/</a></p>]]></description>
	<dc:creator>Archana Malhotra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/view/982</guid>
	<pubDate>Wed, 17 Jul 2013 15:25:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/982</link>
	<title><![CDATA[Is reference genome necessary for gene expression study in transcriptome sequencing or for variant discovery in genome sequencing?]]></title>
	<description><![CDATA[<p><span>Like in case of plant genomes where nature of genome is too complex and huge in size to accomplish complete<em> de novo</em> assembly by current sequencing technology. What would be alternate solution? Can we live in reference free world?</span></p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/3918/the-human-genome-project-video-3d-animation-introduction-low</guid>
	<pubDate>Sat, 24 Aug 2013 19:01:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/3918/the-human-genome-project-video-3d-animation-introduction-low</link>
	<title><![CDATA[The Human Genome Project Video   3D Animation Introduction Low)]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/YxoQFSBwyms" frameborder="0" allowfullscreen></iframe>]]></description>
	
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/7214/lapti-lab</guid>
  <pubDate>Thu, 12 Dec 2013 18:19:12 -0600</pubDate>
  <link></link>
  <title><![CDATA[LAPTI Lab]]></title>
  <description><![CDATA[
<p>The main theme of our research is the understanding of how genetic information is decoded from DNA into RNA and proteins. Someone may find this topic a little strange and argue that we already know how this is happening.</p>

<p>Translational recoding. </p>

<p>RNA editing. </p>

<p>Evolution of the genetic code and translation.</p>

<p>More at http://lapti.ucc.ie/research.html</p>

<p>Lab page http://lapti.ucc.ie/index.html</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/19648/mit-computational-biology-group</guid>
  <pubDate>Thu, 18 Dec 2014 14:47:01 -0600</pubDate>
  <link></link>
  <title><![CDATA[MIT Computational Biology Group]]></title>
  <description><![CDATA[
<p>My research group consists primarily of computer science graduate students and postdocs with expertise in algorithms, statistical inferences and machine learning, and sharing a passion for understanding fundamental biological problems.</p>

<p>We work in a highly interdisciplinary environment at the interface of Computer Science and Biology. Since its inception, our lab has eagerly engaged in collaborative research partnerships with biological and experimental collaborators, facilitated by our affiliation with the Broad Institute and the Computational and Systems Biology initiative (CSBi) at MIT, our participation in the Epigenome Roadmap, ENCODE, and modENCODE consortia, and by several other ongoing collaborations at MIT, Harvard, and the Harvard Medical School affiliated hospitals.</p>

<p>http://compbio.mit.edu/</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/29305/miro-mirna-omics</guid>
	<pubDate>Tue, 04 Oct 2016 14:50:48 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/29305/miro-mirna-omics</link>
	<title><![CDATA[MIRO : miRNA omics]]></title>
	<description><![CDATA[<p><span>The MIRO (the miRNA omics) pipeline is a flexible and powerful tool for the analysis of miRNA (or more generall short RNA) expression using short-read deep sequencing data. In its present implementation MIRO is especially adapted for the analysis of reads generated with the Illumina sequencing platform. MIRO allows to preprocess the Solexa-reads, map them flexibly to several reference genomes using one of four different mappers, create differential gene (miRNA) expression profiles and cluster reads using one of several algorithm. MIRO output is furthermore compatible with software such as genome browsers and miRDeep.</span></p><p>Address of the bookmark: <a href="http://seq.crg.es/download/software/Miro/" rel="nofollow">http://seq.crg.es/download/software/Miro/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34867/magic-blast-a-tool-for-mapping-large-next-generation-rna-or-dna-sequencing-runs-against-a-whole-genome-or-transcriptome</guid>
	<pubDate>Tue, 26 Dec 2017 22:23:39 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34867/magic-blast-a-tool-for-mapping-large-next-generation-rna-or-dna-sequencing-runs-against-a-whole-genome-or-transcriptome</link>
	<title><![CDATA[Magic-BLAST: a tool for mapping large next-generation RNA or DNA sequencing runs against a whole genome or transcriptome.]]></title>
	<description><![CDATA[<p>Magic-BLAST is a tool for mapping large next-generation RNA or DNA sequencing runs against a whole genome or transcriptome. Each alignment optimizes a composite score, taking into account simultaneously the two reads of a pair, and in case of RNA-seq, locating the candidate introns and adding up the score of all exons. This is very different from other versions of BLAST, where each exon is scored as a separate hit and read-pairing is ignored.</p>
<p>Magic-BLAST incorporates within the NCBI BLAST code framework ideas developed in the NCBI Magic pipeline, in particular hit extensions by local walk and jump&nbsp;<a href="http://www.ncbi.nlm.nih.gov/pubmed/26109056">(http://www.ncbi.nlm.nih.gov/pubmed/26109056)</a>, and recursive clipping of mismatches near the edges of the reads, which avoids accumulating artefactual mismatches near splice sites and is needed to distinguish short indels from substitutions near the edges.</p><p>Address of the bookmark: <a href="https://ncbi.github.io/magicblast/" rel="nofollow">https://ncbi.github.io/magicblast/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/40566/the-el-sherif-group-chair-of-developmental-biology-department-of-biology-phd-position</guid>
  <pubDate>Sun, 19 Jan 2020 10:06:37 -0600</pubDate>
  <link></link>
  <title><![CDATA[The El-Sherif Group, Chair of Developmental Biology, Department of Biology - PhD Position]]></title>
  <description><![CDATA[
<p>El-Sherif lab studies how genes are regulated to mediate patterning in Development. We use live and super-resolution imaging in addition to computational modeling to understand transcription dynamics at the single-cell level in three model systems: the fruit fly Drosophila melanogaster, the beetle Tribolium castaneum, and embryonic bodies derived from embryonic mouse stem cells.</p>

<p>In this project, you will use single-molecule techniques to label mRNA and DNA in (live and fixed) Drosophila embryos and fixed embryonic bodies. You will also use super-resolution microscopy to visualize protein condensates. Co-localization dynamics reflecting DNA-protein bindings and DNA looping events will be detected, analyzed, and used to test computational models of gene transcription.</p>

<p>Qualification:<br />MSc degree (or equivalent) in Biology, Biophysics, or Bioengineering</p>

<p>Experience in one or more of these areas: (1) molecular cloning, (2) imaging, (3) image analysis (using Matlab/Python/Java), (4) microfluidics, and (5) computational modeling.</p>

<p>How to Apply?<br />Send (1) your CV, (2) summary of research experience, and (3) email addresses of at least 2 references to ezzat.el-sherif@fau.de. Title your email ‘Transcription PhD Position’.</p>

<p>salary Grade.: E13<br />Total Time: 3 Jahre<br />Start: 01.01.2020.<br />End: 31.3.2020.</p>

<p>Address:<br />Dr. El-Sherif, Ezzat<br />Department Biologie<br />Professur für Zoologie (Entwicklungsbiologie) (Prof. Dr. Klingler)<br />Telefon 09131/85-28068, Fax 09131/85-28040, E-Mail: ezzat.el-sherif@fau.de</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/41881/hdock-server</guid>
	<pubDate>Tue, 16 Jun 2020 01:54:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/41881/hdock-server</link>
	<title><![CDATA[HDOCK SERVER]]></title>
	<description><![CDATA[<p>HDOCK SERVER</p>
<p>Protein-protein and protein-DNA/RNA docking based on a hybrid algorithm of template-based modeling and&nbsp;<em>ab initio</em>&nbsp;free docking.</p>
<p><span>The HDOCK server distinguishes itself from similar docking servers in its ability to support amino acid sequences as input and a hybrid docking strategy in which experimental information about the protein&ndash;protein binding site and small-angle X-ray scattering can be incorporated during the docking and post-docking processes.</span></p><p>Address of the bookmark: <a href="http://hdock.phys.hust.edu.cn/" rel="nofollow">http://hdock.phys.hust.edu.cn/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

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