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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/19633?offset=330</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31018/j-circos</guid>
	<pubDate>Fri, 17 Feb 2017 09:06:54 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31018/j-circos</link>
	<title><![CDATA[J-Circos]]></title>
	<description><![CDATA[<p>Circos plot tool (J-Circos) that is an interactive visualization tool that can plot Circos figures, as well as being able to dynamically add data to the figure, and providing information for specific data points using mouse hover display and zoom in/out functions. J-Circos uses the Java computer language to enable it to be used on most operating systems (Windows, MacOS, Linux). Users can input data into J-Circos using flat data formats, as well as from the GUI. J-Circos will enable biologists to better study more complex chromosomal interactions and fusion transcripts that are otherwise difficult to visualize from next-generation sequencing data.</p><p>Address of the bookmark: <a href="http://www.australianprostatecentre.org/research/software/jcircos" rel="nofollow">http://www.australianprostatecentre.org/research/software/jcircos</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31087/bedtools</guid>
	<pubDate>Fri, 24 Feb 2017 04:50:44 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31087/bedtools</link>
	<title><![CDATA[bedtools]]></title>
	<description><![CDATA[<p>Collectively, the&nbsp;<strong>bedtools</strong>&nbsp;utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable&nbsp;<em>genome arithmetic</em>: that is, set theory on the genome. For example,&nbsp;<strong>bedtools</strong>&nbsp;allows one to<em>intersect</em>,&nbsp;<em>merge</em>,&nbsp;<em>count</em>,&nbsp;<em>complement</em>, and&nbsp;<em>shuffle</em>&nbsp;genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF/GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g.,&nbsp;<em>intersect</em>&nbsp;two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line.</p>
<p><strong>bedtools</strong>&nbsp;is developed in the&nbsp;<a href="http://quinlanlab.org/">Quinlan laboratory</a>&nbsp;at the&nbsp;<a href="http://www.utah.edu/">University of Utah</a>&nbsp;and benefits from fantastic contributions made by scientists worldwide.</p><p>Address of the bookmark: <a href="http://bedtools.readthedocs.io/en/latest/index.html" rel="nofollow">http://bedtools.readthedocs.io/en/latest/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31137/finishersc-a-repeat-aware-and-scalable-tool-for-upgrading-de-novo-assembly-using-long-reads</guid>
	<pubDate>Mon, 27 Feb 2017 09:49:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31137/finishersc-a-repeat-aware-and-scalable-tool-for-upgrading-de-novo-assembly-using-long-reads</link>
	<title><![CDATA[FinisherSC: a repeat-aware and scalable tool for upgrading de novo assembly using long reads]]></title>
	<description><![CDATA[<p><span>FinisherSC, a repeat-aware and scalable tool for upgrading&nbsp;</span><em>de novo</em><span>&nbsp;assembly using long reads. Experiments with real data suggest that FinisherSC can provide longer and higher quality contigs than existing tools while maintaining high concordance.</span></p><p>Address of the bookmark: <a href="http://kakitone.github.io/finishingTool/" rel="nofollow">http://kakitone.github.io/finishingTool/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31343/metabat-an-efficient-tool-for-accurately-reconstructing-single-genomes-from-complex-microbial-communities</guid>
	<pubDate>Mon, 06 Mar 2017 03:44:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31343/metabat-an-efficient-tool-for-accurately-reconstructing-single-genomes-from-complex-microbial-communities</link>
	<title><![CDATA[MetaBAT:  An Efficient Tool for Accurately Reconstructing Single Genomes from Complex Microbial Communities]]></title>
	<description><![CDATA[<p>MetaBAT, An Efficient Tool for Accurately Reconstructing Single Genomes from Complex Microbial Communities</p>
<p>Grouping large genomic fragments assembled from shotgun metagenomic sequences to deconvolute complex microbial communities, or metagenome binning, enables the study of individual organisms and their interactions. Here we developed an automated metagenome binning software, called MetaBAT, which integrates empirical probabilistic distances of genome abundance and tetranucleotide frequency. Tested on both synthetic and real metagenome datasets, MetaBAT outperforms alternative methods in both accuracy and computational efficiency. Applying MetaBAT to an assembly from 1,704 human gut samples formed 1,634 genome bins (&gt;200kb) in 3 hours, where 621 genome bins are &gt;50% complete with &lt;5% contamination from other species. Further analysis shows that the quality of these genome bins approaches manually curated genomes.</p><p>Address of the bookmark: <a href="https://bitbucket.org/berkeleylab/metabat" rel="nofollow">https://bitbucket.org/berkeleylab/metabat</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31371/phenogram</guid>
	<pubDate>Tue, 07 Mar 2017 08:35:12 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31371/phenogram</link>
	<title><![CDATA[PhenoGram]]></title>
	<description><![CDATA[<p><span>With PhenoGram researchers can create chomosomal ideograms annotated with lines in color at specific base-pair locations, or colored base-pair to base-pair regions, with or without other annotation. PhenoGram allows for annotation of chromosomal locations and/or regions with shapes in different colors, gene identifiers, or other text. PhenoGram also allows for creation of plots showing expanded chromosomal locations, providing a way to show results for specific chromosomal regions in greater detail.</span></p><p>Address of the bookmark: <a href="http://ritchielab.psu.edu/software/phenogram-downloads" rel="nofollow">http://ritchielab.psu.edu/software/phenogram-downloads</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/428/five-unique-traits-of-effective-computational-biologist</guid>
	<pubDate>Thu, 11 Jul 2013 13:12:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/428/five-unique-traits-of-effective-computational-biologist</link>
	<title><![CDATA[Five unique traits of effective computational biologist]]></title>
	<description><![CDATA[<p>Bioinformatics research is driven by large set of software, scripts, and tools to analyse gigantic biological data. Being a great biological programmer or bioinformatician involves more than writing code that works. The biological programmers who rise to the top ranks of their profession are not only good programmer but also expert in biological stuff. Moreover, In order to be a good and effective biological programmer, you need to possess a combination of traits that allow your computational as well as biological skill, experience, and knowledge to produce working code. There are some technically skilled biological programmers who will never be effective because they lack the other important traits needed. Here are top five traits that are necessary to become a great biological programmer.</p><p><strong>1. Learn and get updated</strong></p><p>Some of the bad biological programmers only learn new technical or non-technical things when it&rsquo;s absolutely necessary. The good biological programmers learn new technical skills proactively. But great biological programmers not only learn new technical skills on their own but also learn non-technical skills, and have an open mind to sources of knowledge that others may shut out.</p><p>In other concrete term, the bad biological programmer learn Perl's regular expression when they started a project on comparative genomics; the good biological programmer learned it a year before because it looked interesting; and the great biological programmer also read about the BioPerl packages, genomics, DNA string, genomic theories, or some similar course of study so that they could understand the results and explain it biologically.</p><p><strong>2. Not a merely coder!!!</strong></p><p>I often encountered with biological programmer who call themself a hard-core computer programmer and avoid biology. I can almost guarantee that if you are one of them then you are not doing research but merely writing "dry" codes.</p><p>According to my supervisor most of the computational biologist, don't know what they are doing biologically. Even they struggle to explain their own programs output and results. Therefore, It is highly advisable to learn basic of biology which can assist you to explain the result and understand your discovery. Always remember you are a researcher not a coder.</p><p><strong>3. Be Social with biologist</strong></p><p>The computational biologist spends most of the time in from of computers, writing codes. They always think their job is to produce working codes, not technical research perfections. But, they are completely wrong. You should not forget that apart from your computational skills you also need some biologist, other than your supervisor, to explain and make you understand the complex biological mechanism.</p><p>I highly recommend your to interact with biotech researchers and learn how do they explain their one graph (which they generally produce after one year of work) biologically. Remember, the origin of your research project is complex biological phenomenon, which is more complex than that of your limited programming rules.</p><p><strong>4. Do not search, research for answers</strong></p><p>Researching for answers means more than typing several keywords into a search engine or posting a question at Stack Overflow or the BioStars forums. I have entered problems into search engines that generate no results, and every question I posted on Stack Overflow or the BioStars forums never got anything resembling an answer, yet I solved the issues and moved on. I&rsquo;m not a magician &mdash; I just know how to find answers or discover root causes.</p><p>Many problems are situational, and if you depend on search engines and forums, you can waste a lot of time going down a rabbit hole and possibly never getting a solution. Learn to perform root cause analysis, learn enough about the underlying system to look for other clues and solutions, and learn to take a long distance view of an issue before deep diving into it.</p><p><strong>5. Love and defend your research</strong></p><p>You cannot rise to the top in this research profession without loving your work. There are some very good &ldquo;it&rsquo;s just a job&rdquo; biological programmers (I&rsquo;ve been one at times), but if that is your outlook, you won&rsquo;t be willing to do whatever it takes to succeed. This idea gets a lot of folks in a huff, because they feel it is a personal insult. &ldquo;I&rsquo;m a good programmer, but I have other priorities and can&rsquo;t make work my life.&rdquo; I understand completely; I have other priorities too. As much as I hate to say it, when I am passionate about my work, I am willing (though not eager) to abandon my other priorities to finish the job. It is not an insult to say that if you aren&rsquo;t willing to pull out all the stops you can&rsquo;t be the best, it is a fact.</p><p>You must be passionate about more than programming &mdash; you must also be excited about your research, the tools and technology you are using, and so on. I have seen very good and even great biological programmers operating at mediocre levels because something was not a good fit, such as they hated the project or were using a technology they disliked. Therefore, like your research project and get excited about your discoveries. You have not only to discover but also defend your finding with scientific words.</p><p>Thanks to all of you for reading.</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31568/pacbio-long-reads-compatible-software-and-tools</guid>
	<pubDate>Wed, 15 Mar 2017 14:19:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31568/pacbio-long-reads-compatible-software-and-tools</link>
	<title><![CDATA[Pacbio Long Reads Compatible Software and Tools]]></title>
	<description><![CDATA[<p>The following software packages are known to be compatible with PacBio&reg; data, in addition to PacBio's own SMRT&reg; Analysis suite. All packages are believed to be open source or freely available for non-commercial use. See the individual project sites for up-to-date license information. A separate page lists&nbsp;<a href="http://pacb.com/community/partner_program/current_partners/">commercial software</a>.</p>
<p>Know of any other open source software for PacBio data?&nbsp;<a href="mailto:devnet@pacificbiosciences.com">Email us</a>.</p>
<p>Software categories:</p>
<ul>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#denovo">De novo assembly</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#svdetection">Structural Variations Detection</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#aligners">Reference-based alignment</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#variants">Consensus and variant calling</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#RNA">RNA analysis</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#basemods">Epigenetic base modifications and methylation</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#barcoding">Barcoding</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#browsers">Genome Browsers</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#qc">Run QC</a></li>
<li><a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software#frameworks">Frameworks and APIs</a></li>
</ul><p>Address of the bookmark: <a href="https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software" rel="nofollow">https://github.com/PacificBiosciences/DevNet/wiki/Compatible-Software</a></p>]]></description>
	<dc:creator>Archana Malhotra</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/851/the-institute-for-molecular-bioscience-imb-bailey-lab</guid>
  <pubDate>Sun, 14 Jul 2013 11:53:08 -0500</pubDate>
  <link></link>
  <title><![CDATA[The Institute for Molecular Bioscience (IMB), Bailey Lab]]></title>
  <description><![CDATA[
<p>Pattern recognition and computational biology</p>

<p>MEME Suite software development; gene expression; mathematical modelling; gene regulation and transcription</p>

<p>Specialization:<br />Pattern recognition and modelling in computational biology</p>

<p>Link @ http://www.imb.uq.edu.au/tim-bailey</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/32190/dbg2olcefficient-assembly-of-large-genomes-using-long-erroneous-reads-of-the-third-generation-sequencing-technologies</guid>
	<pubDate>Wed, 19 Apr 2017 10:09:51 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/32190/dbg2olcefficient-assembly-of-large-genomes-using-long-erroneous-reads-of-the-third-generation-sequencing-technologies</link>
	<title><![CDATA[DBG2OLC:Efficient Assembly of Large Genomes Using Long Erroneous Reads of the Third Generation Sequencing Technologies]]></title>
	<description><![CDATA[<p>DBG2OLC:Efficient Assembly of Large Genomes Using Long Erroneous Reads of the Third Generation Sequencing Technologies</p>
<p>Our work is published in Scientific Reports:</p>
<p>Ye, C. et al. DBG2OLC: Efficient Assembly of Large Genomes Using Long Erroneous Reads of the Third Generation Sequencing Technologies. Sci. Rep. 6, 31900; doi: 10.1038/srep31900 (2016).</p>
<p><a href="http://www.nature.com/articles/srep31900">http://www.nature.com/articles/srep31900</a></p>
<p>The manual can be downloaded from:</p>
<p><a href="https://github.com/yechengxi/DBG2OLC/raw/master/Manual.docx">https://github.com/yechengxi/DBG2OLC/raw/master/Manual.docx</a></p>
<p>To use precompiled versions,please go to:</p>
<p><a href="https://github.com/yechengxi/DBG2OLC/tree/master/compiled">https://github.com/yechengxi/DBG2OLC/tree/master/compiled</a></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="https://github.com/yechengxi/DBG2OLC" rel="nofollow">https://github.com/yechengxi/DBG2OLC</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/6420/studentship-and-traineeship-university-of-madras</guid>
  <pubDate>Sat, 16 Nov 2013 19:27:40 -0600</pubDate>
  <link></link>
  <title><![CDATA[STUDENTSHIP and TRAINEESHIP @ University of Madras]]></title>
  <description><![CDATA[
<p>Bioinformatics Infrastructure Facility<br />University of Madras<br />Chennai 600 025</p>

<p>Applications are invited for the STUDENTSHIP and TRAINEESHIP vacancies to carry out project/research work in the DBT - Bioinformatics Infrastructure Facility with consolidated stipend of Rs.5,000/- per month.</p>

<p>Essential Qualification</p>

<p>Student Trainee: Those who have completed M.Sc., Bioinformatics/Biophysics/Life sciences or Pursuing M.Tech., Bioinformatics/Biotechnology</p>

<p>Duration : 3-4 Months</p>

<p>Student Trainee: Those who are pursuing M.Sc Bioinformatics/Biophysics/ Life sciences/others</p>

<p>Duration : 2-3 Months</p>

<p>Mail your CV on or before 25th November 2013 to shirai2011@gmail.com and hard copy to "Dr. D. Velmurugan, Professor &amp; Head, CAS in Crystallography and Biophysics, University of Madras, Guindy Campus, Chennai 600 025". Also, the applicants are requested to attend the interview on 29th November, 2013 at 11 A.M.</p>

<p>Advertisement:</p>

<p>www.unom.ac.in/uploads/announcements/bifadvertisement_20131114080003_23240.pdf</p>
]]></description>
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