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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/8382?offset=1230</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26993/lastz</guid>
	<pubDate>Mon, 18 Apr 2016 04:41:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26993/lastz</link>
	<title><![CDATA[LASTZ]]></title>
	<description><![CDATA[<p>LASTZ is a program for aligning DNA sequences, a pairwise aligner. Originally designed to handle sequences the size of human chromosomes and from different species, it is also useful for sequences produced by NGS sequencing technologies such as Roche 454.</p>
<p>More at http://www.bx.psu.edu/~rsharris/lastz/</p>
<p>Thesis: http://www.bx.psu.edu/~rsharris/rsharris_phd_thesis_2007.pdf</p><p>Address of the bookmark: <a href="http://www.bx.psu.edu/~rsharris/lastz/" rel="nofollow">http://www.bx.psu.edu/~rsharris/lastz/</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/24762/postdoctoral-fellowship-in-bioinformatics-at-pesolelab</guid>
  <pubDate>Thu, 01 Oct 2015 07:20:48 -0500</pubDate>
  <link></link>
  <title><![CDATA[Postdoctoral Fellowship in Bioinformatics at pesolelab]]></title>
  <description><![CDATA[
<p>Job Description: Bioinformatics postdoc positions are available in the area of genomics with main focus on exome and RNAseq technologies by ultra high-throughput sequencing platforms. Successful applicants should have the following qualities:</p>

<p>1) demonstrated experience in Bioinformatics research,<br />2) programing experience (python and/or R, C and C++ are very welcome),<br />3) knowledge of Linux/Unix environment,<br />4) experience in handling deep-seq data,<br />5) highly motivated and hard working, and<br />6) interested to work with a multi-disciplinary team combining bioinformatics, genomics, computational biology approaches with experimental biology.</p>

<p>Our research interest covers different areas of bioinformatics and genomics in order to achieve a deeper understanding of gene and genome structure and function (please look at our PubMed publications for more details about our research http://www.ncbi.nlm.nih.gov/pubmed/?term=pesole+g).</p>

<p>Interested applicants should email the curriculum vitae to Prof. Graziano Pesole at graziano.pesole@uniba.it or Dr. Ernesto Picardi at Ernesto.picardi@uniba.it.</p>

<p>Start date: immediate</p>

<p>Duration: up to 24 months<br />Contact Person (Referent): Ernesto Picardi<br />Ref. E-Mail: ernesto.picardi@uniba.it<br />Tel: +390805443308<br />Fax: +390805443317</p>

<p>Group Web Page: http://www.pesolelab.it/</p>
]]></description>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/25323/project-fellow-positions-at-csir-ihbt-palampur</guid>
  <pubDate>Tue, 01 Dec 2015 05:45:58 -0600</pubDate>
  <link></link>
  <title><![CDATA[Project Fellow Positions at CSIR-IHBT Palampur]]></title>
  <description><![CDATA[
<p>Walk-in-Interview is scheduled to be held on the date as mentioned below for selection of Suitable candidates in the following areas under the different Sponsored/CSIR Networked Projects on purely temporary basis for the duration of the project(s) or till completion of projects whichever is earlier:</p>

<p>Sponsored/CSIR Networked Project:<br /> (i) Genomics and Informatics Solutions for Integrating Biology (GENESIS)" [BSC-0121] (up to March, 2017).<br />(ii) Profiling and characterization of early phase differential mi-RNA (s) responsible for downstream developmen of insulin resistance in hMSC derived adipocytes. (GAP-0188) [up to 31.03.2018].</p>

<p>Position:       	Project Fellow (2 position)<br />Age :           	28 years as on 18.12.15<br />Salary :        	Rs.12,000/- P.M.<br />			Rs.14,000/- P.M.<br />                	as per the funds provisions in the respective projects.<br />Eligibility Criteria :  1st Class B. Tech. in Bioinformatics/ Computational Biology<br />						OR<br />			M.Sc. in Bioinformatics/ Computational Biology with 55% marks<br />						OR<br />			M.Tech. in Bioinformatics/ Computational Biology with 55% marks<br />						OR<br />			M.Sc. in any field of Life Science with Diploma in Bioinformatics</p>

<p>Selection Procedure : 	Walk In Interview </p>

<p>Date :			18 Dec , 2015<br />Time :			10:00 A.M.<br />Venue : 		CSIR-IHBT Palampur (H.P.)</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26559/microscope</guid>
	<pubDate>Fri, 04 Mar 2016 05:26:31 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26559/microscope</link>
	<title><![CDATA[Microscope]]></title>
	<description><![CDATA[<p>Microscope Platform user documentation.</p>
<p>The MicroScope platform is available at this URL:</p>
<p><a href="https://www.genoscope.cns.fr/agc/microscope">https://www.genoscope.cns.fr/agc/microscope</a></p><p>Address of the bookmark: <a href="http://microscope.readthedocs.org/en/latest/index.html" rel="nofollow">http://microscope.readthedocs.org/en/latest/index.html</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26363/flo</guid>
	<pubDate>Wed, 10 Feb 2016 10:52:32 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26363/flo</link>
	<title><![CDATA[flo]]></title>
	<description><![CDATA[<p>flo - same species annotations lift over pipeline</p>
<p>Lift over is the process of transferring annotations from one genome assembly to another. Usually lift over is done because there is a new, improved genome assembly for the species and good quality annotations (maybe manually curated or experimentally verified) are available on the old assembly.</p>
<p>The idea is simple: align the new assembly with the old one (e.g., with BLAT), process the alignment data to define how a coordinate or coordinate range on the old assembly should be transformed to the new assembly (e.g., as a chain file), transform the coordinates (e.g., with liftOver).</p>
<p>&nbsp;</p>
<p>https://github.com/wurmlab/flo</p><p>Address of the bookmark: <a href="https://github.com/wurmlab/flo" rel="nofollow">https://github.com/wurmlab/flo</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26414/advanced-bash-scripting-guide</guid>
	<pubDate>Thu, 18 Feb 2016 04:50:51 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26414/advanced-bash-scripting-guide</link>
	<title><![CDATA[Advanced Bash-Scripting Guide]]></title>
	<description><![CDATA[<p>This tutorial assumes no previous knowledge of scripting or programming, yet progresses rapidly toward an intermediate/advanced level of instruction <em>. . . all the while sneaking in little nuggets of <span>UNIX</span>&reg; wisdom and lore</em>. It serves as a textbook, a manual for self-study, and as a reference and source of knowledge on shell scripting techniques. The exercises and heavily-commented examples invite active reader participation, under the premise that <tt><strong>the only way to really learn scripting is to write scripts</strong></tt>.</p>
<p>This book is suitable for classroom use as a general introduction to programming concepts.</p>
<p>More at http://tldp.org/LDP/abs/html/</p><p>Address of the bookmark: <a href="http://tldp.org/LDP/abs/html/" rel="nofollow">http://tldp.org/LDP/abs/html/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27113/picard</guid>
	<pubDate>Fri, 29 Apr 2016 08:21:54 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27113/picard</link>
	<title><![CDATA[Picard]]></title>
	<description><![CDATA[<p>Picard is a set of command line tools for manipulating high-throughput sequencing (HTS) data and formats such as SAM/BAM/CRAM and VCF. These file formats are defined in the <a href="http://samtools.github.io/hts-specs/">Hts-specs</a> repository. See especially the <a href="http://samtools.github.io/hts-specs/SAMv1.pdf">SAM specification</a> and the <a href="http://samtools.github.io/hts-specs/VCFv4.3.pdf">VCF specification</a>.</p>
<p>Note that the information on this page is targeted at end-users. For developers, the source code, building instructions and implementation/development resources are available on <a href="https://github.com/broadinstitute/picard">GitHub</a>.</p>
<p>The Picard toolkit is open-source under the <a href="https://tldrlegal.com/license/mit-license">MIT license</a> and free for all uses.</p>
<p>Enjoy!</p><p>Address of the bookmark: <a href="http://broadinstitute.github.io/picard/" rel="nofollow">http://broadinstitute.github.io/picard/</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26909/sequence-assembly-with-mira-4</guid>
	<pubDate>Wed, 06 Apr 2016 08:21:22 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26909/sequence-assembly-with-mira-4</link>
	<title><![CDATA[Sequence assembly with MIRA 4]]></title>
	<description><![CDATA[<p>MIRA is a multi-pass DNA sequence data assembler/mapper for whole genome and EST/RNASeq projects. MIRA assembles/maps reads gained by</p>
<div>
<ul>
<li>
<p>electrophoresis sequencing (aka Sanger sequencing)</p>
</li>
<li>
<p>454 pyro-sequencing (GS20, FLX or Titanium)</p>
</li>
<li>
<p>Ion Torrent</p>
</li>
<li>
<p>Solexa (Illumina) sequencing</p>
</li>
<li>
<p>(in development) Pacific Biosciences sequencing</p>
</li>
</ul>
</div>
<p>into contiguous sequences (called <span><em>contigs</em></span>). One can use the sequences of different sequencing technologies either in a single assembly run (a <span><em>true hybrid assembly</em></span>) or by mapping one type of data to an assembly of other sequencing type (a <span><em>semi-hybrid assembly (or mapping)</em></span>) or by mapping a data against consensus sequences of other assemblies (a <span><em>simple mapping</em></span>).</p>
<p>The MIRA acronym stands for <span><strong>M</strong></span>imicking <span><strong>I</strong></span>ntelligent <span><strong>R</strong></span>ead <span><strong>A</strong></span>ssembly and the program pretty well does what its acronym says (well, most of the time anyway). It is the Swiss army knife of sequence assembly that I've used and developed during the past 14 years to get assembly jobs I work on done efficiently - and especially accurately. That is, without me actually putting too much manual work into it.</p>
<p>More at http://mira-assembler.sourceforge.net/docs/DefinitiveGuideToMIRA.html</p><p>Address of the bookmark: <a href="http://mira-assembler.sourceforge.net/docs/DefinitiveGuideToMIRA.html" rel="nofollow">http://mira-assembler.sourceforge.net/docs/DefinitiveGuideToMIRA.html</a></p>]]></description>
	<dc:creator>Priya Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26972/understanding-fastqc-output</guid>
	<pubDate>Fri, 15 Apr 2016 05:47:40 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26972/understanding-fastqc-output</link>
	<title><![CDATA[Understanding Fastqc Output]]></title>
	<description><![CDATA[<p>Understanding Following table and graphs</p>
<ol>
<li>Duplication level</li>
<li>kmer profile</li>
<li>per base GC content</li>
<li>per base N content</li>
<li>per base quality</li>
<li>per base sequence content</li>
<li>per sequence GC content</li>
<li>per sequence quality</li>
<li>sequence length distribution</li>
</ol>
<p>More at http://www.bioinformatics.babraham.ac.uk/projects/fastqc/Help/3%20Analysis%20Modules/</p><p>Address of the bookmark: <a href="http://www.bioinformatics.babraham.ac.uk/projects/fastqc/Help/3%20Analysis%20Modules/" rel="nofollow">http://www.bioinformatics.babraham.ac.uk/projects/fastqc/Help/3%20Analysis%20Modules/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27090/canu-assembling-large-genomes-with-single-molecule-sequencing-and-locality-sensitive-hashing</guid>
	<pubDate>Tue, 26 Apr 2016 11:38:10 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27090/canu-assembling-large-genomes-with-single-molecule-sequencing-and-locality-sensitive-hashing</link>
	<title><![CDATA[CANU: Assembling Large Genomes with Single-Molecule Sequencing and Locality Sensitive Hashing.]]></title>
	<description><![CDATA[<p>Canu is a fork of the&nbsp;<a href="http://wgs-assembler.sourceforge.net/wiki/index.php?title=Main_Page" title="Celera Assembler">Celera Assembler</a>&nbsp;designed for high-noise single-molecule sequencing (such as the PacBio RSII or Oxford Nanopore MinION). The software is currently alpha level, feel free to use and report issues encountered.</p>
<p>Canu is a hierachical assembly pipeline which runs in four steps:</p>
<ul>
<li>Detect overlaps in high-noise sequences using&nbsp;<a href="https://github.com/marbl/MHAP" title="MHAP">MHAP</a></li>
<li>Generate corrected sequence consensus</li>
<li>Trim corrected sequences</li>
<li>Assemble trimmed corrected sequences</li>
</ul>
<p>Read the&nbsp;<a href="http://canu.readthedocs.org/" title="docs">documentation</a></p>
<p>New release https://github.com/marbl/canu/releases</p><p>Address of the bookmark: <a href="https://github.com/marbl/canu" rel="nofollow">https://github.com/marbl/canu</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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