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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/14215?offset=210</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30130/scaffmatch</guid>
	<pubDate>Tue, 13 Dec 2016 10:23:56 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30130/scaffmatch</link>
	<title><![CDATA[ScaffMatch]]></title>
	<description><![CDATA[<p>caffMatch is a novel scaffolding tool based on Maximum-Weight Matching able to produce high-quality scaffolds from NGS data (reads and contigs). The tool is written in Python 2.7. It also includes a bash script wrapper that calls aligner in case one needs to first map reads to contigs (instead of providing .sam files).</p>
<p>The arguments accepted by ScaffMatch are:</p>
<p>&nbsp; -w) Working directory -- this is the directory where ScaffMatch files are stored. These are .sam files produced after mapping reads to contigs and the resulting scaffolds file `scaffolds.fa` fasta file;</p>
<p>&nbsp; -c) Contig fasta file;</p>
<p>&nbsp; -m) Command line argument with no options. It is used when .sam files are used instead of reads .fastq files. Do not use this option if you provide reads files;</p>
<p>&nbsp; -1) (Comma separated list of) either .fastq or .sam file(s) corresponding to the first read of the read pair;</p>
<p>&nbsp; -2) (Comma separated list of) either .fastq or .sam file(s) corresponding to the second read of the read pair;</p>
<p>&nbsp; -i) (Comma separated list of) insert size(s) of the library(-ies);</p>
<p>&nbsp; -s) (Comma separated list of) library(-ies) standard deviation(s) of insert size(s);</p>
<p>&nbsp; -t) Bundle threshold. Pairs of contigs supported by number of read pairs less than the value of this argument are discarded. Optional argument, by default it is equal to 5;</p>
<p>&nbsp; -g) Matching heuristics: use `max_weight` for Maximum Weight Matching heuristics with the Insertion step, use `backbone` for Maximum Weight Matching heuristics without the Insertion step, use `greedy` for Greedy Matching heuristics;</p>
<p>&nbsp; -l) Log file - where to store the logs. Optional argument. By default, stdout is used.</p><p>Address of the bookmark: <a href="http://alan.cs.gsu.edu/NGS/?q=content/scaffmatch" rel="nofollow">http://alan.cs.gsu.edu/NGS/?q=content/scaffmatch</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30153/e-mem-efficient-computation-of-maximal-exact-matches</guid>
	<pubDate>Thu, 15 Dec 2016 09:30:43 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30153/e-mem-efficient-computation-of-maximal-exact-matches</link>
	<title><![CDATA[E-MEM: Efficient computation of Maximal Exact Matches]]></title>
	<description><![CDATA[<p>E-MEM is a C++/OpenMP program designed to efficiently compute MEMs between large genomes. See the README file for instructions on how to use E-MEM.&nbsp;<br><br>E-MEM source code</p>
<p>The source code can be downloaded&nbsp;<a href="http://www.csd.uwo.ca/~ilie/E-MEM/e-mem.zip">here</a>.&nbsp;<br><br>If you use E-MEM, please cite:</p>
<ul>
<li>N. Khiste, L. Ilie, E-MEM: Efficient computation of Maximal Exact Matches for very large genomes,&nbsp;<a href="http://bioinformatics.oxfordjournals.org/content/31/4/509.short">Bioinformatics</a>&nbsp;<strong>31</strong>(4) (2015) 509 -- 514.</li>
</ul>
<p>For any questions, please contact Lucian Ilie:&nbsp;<a href="mailto:ilie@uwo.ca">ilie@uwo.ca</a>&nbsp;</p><p>Address of the bookmark: <a href="http://www.csd.uwo.ca/~ilie/E-MEM/" rel="nofollow">http://www.csd.uwo.ca/~ilie/E-MEM/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30212/pear</guid>
	<pubDate>Mon, 19 Dec 2016 09:28:30 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30212/pear</link>
	<title><![CDATA[PEAR]]></title>
	<description><![CDATA[<p><strong>PEAR</strong>&nbsp;is an ultrafast, memory-efficient and highly accurate pair-end read merger. It is fully parallelized and can run with as low as just a few kilobytes of memory.</p>
<p>PEAR evaluates all possible paired-end read overlaps and without requiring the target fragment size as input. In addition, it implements a statistical test for minimizing false-positive results. Together with a highly optimized implementation, it can merge millions of paired end reads within a couple of minutes on a standard desktop computer.</p><p>Address of the bookmark: <a href="http://sco.h-its.org/exelixis/web/software/pear/doc.html" rel="nofollow">http://sco.h-its.org/exelixis/web/software/pear/doc.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30236/pyscaf</guid>
	<pubDate>Mon, 19 Dec 2016 14:20:33 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30236/pyscaf</link>
	<title><![CDATA[pyScaf]]></title>
	<description><![CDATA[<p>pyScaf orders contigs from genome assemblies utilising several types of information:</p>
<ul>
<li>paired-end (PE) and/or mate-pair libraries (<a href="https://github.com/lpryszcz/pyScaf#ngs-based-scaffolding">NGS-based mode</a>)</li>
<li>long reads (<a href="https://github.com/lpryszcz/pyScaf#scaffolding-based-on-long-reads">NGS-based mode</a>)</li>
<li>synteny to the genome of some related species (<a href="https://github.com/lpryszcz/pyScaf#reference-based-scaffolding">reference-based mode</a>)</li>
</ul>
<p>Scaffolding&nbsp;</p>
<p>In reference-based mode, pyScaf uses synteny to the genome of closely related species in order to order contigs and estimate distances between adjacent contigs.</p>
<p>Contigs are aligned globally (end-to-end) onto reference chromosomes, ignoring:</p>
<ul>
<li>matches not satisfying cut-offs (<code>--identity</code>&nbsp;and&nbsp;<code>--overlap</code>)</li>
<li>suboptimal matches (only best match of each query to reference is kept)</li>
<li>and removing overlapping matches on reference.</li>
</ul>
<p>In preliminary tests, pyScaf performed superbly on simulated heterozygous genomes based on&nbsp;<em>C. parapsilosis</em>&nbsp;(13 Mb; CANPA) and&nbsp;<em>A. thaliana</em>&nbsp;(119 Mb; ARATH) chromosomes, reconstructing correctly all chromosomes always for CANPA and nearly always for ARATH (<a href="https://www.dropbox.com/sh/bb7lwggo40xrwtc/AAAZ7pByVQQQ-WhUXZVeJaZVa/pyScaf?dl=0">Figures in dropbox</a>,&nbsp;<a href="https://docs.google.com/spreadsheets/d/1InBExy-qKDLj-upd8tlPItVSKc4mLepZjZxB31ii9OY/edit#gid=2036953672">CANPA table</a>,&nbsp;<a href="https://docs.google.com/spreadsheets/d/1InBExy-qKDLj-upd8tlPItVSKc4mLepZjZxB31ii9OY/edit#gid=1920757821">ARATH table</a>).<br>Runs took ~0.5 min for CANPA on&nbsp;<code>4 CPUs</code>&nbsp;and ~2 min for ARATH on&nbsp;<code>16 CPUs</code>.</p>
<p><span>Important remarks:</span></p>
<ul>
<li>Reduce your assembly before (fasta2homozygous.py) as any redundancy will likely break the synteny.</li>
<li>pyScaf works better with contigs than scaffolds, as scaffolds are often affected by mis-assemblies (no&nbsp;<em>de novo assembler</em>&nbsp;/ scaffolder is perfect...), which breaks synteny.</li>
<li>pyScaf works very well if divergence between reference genome and assembled contigs is below 20% at nucleotide level.</li>
<li>pyScaf deals with large rearrangements ie. deletions, insertion, inversions, translocations.&nbsp;<span>Note however, this is experimental implementation!</span></li>
<li>Consider closing gaps after scaffolding.</li>
</ul><p>Address of the bookmark: <a href="https://github.com/lpryszcz/pyScaf" rel="nofollow">https://github.com/lpryszcz/pyScaf</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30304/mcscan</guid>
	<pubDate>Thu, 22 Dec 2016 03:53:58 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30304/mcscan</link>
	<title><![CDATA[MCscan]]></title>
	<description><![CDATA[<p><span>MCscan is a computer program that can simultaneously scan multiple genomes to identify homologous chromosomal regions and subsequently align these regions using genes as anchors. This is the toolset for generating the synteny correspondences in&nbsp;</span><a href="http://chibba.agtec.uga.edu/duplication">Plant Genome Duplication Database</a><span>. It is intended as an easy-to-use and quick way to identify conserved gene arrays both within the same genome and across different genomes.</span></p>
<p><span>More at&nbsp;http://chibba.agtec.uga.edu/duplication/mcscan/</span></p><p>Address of the bookmark: <a href="http://chibba.agtec.uga.edu/duplication/mcscan/" rel="nofollow">http://chibba.agtec.uga.edu/duplication/mcscan/</a></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31105/understanding-pacbio</guid>
	<pubDate>Fri, 24 Feb 2017 10:17:36 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31105/understanding-pacbio</link>
	<title><![CDATA[Understanding PacBio]]></title>
	<description><![CDATA[<p>This tutorial includes resources for learning more about PacBio data and bioinformatics analysis, and includes content suitable for both beginners and experts. Below are links to training modules (webinars and PowerPoint presentations) to help you get started with your data processing, as well as information for specialized applications.</p>
<p>Training Resources:</p>
<ul>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Bioinformatics-Workshop">Bioinformatics Workshop (Webinars)</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Bioinformatics-Training-Slides">Bioinformatics Training Slides</a></li>
</ul>
<p>Specialized Applications:</p>
<ul>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/De-Novo-Assembly">De Novo Assembly</a></li>
<li><a href="https://github.com/PacificBiosciences/cDNA_primer/wiki">Transcriptome analysis</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Base-modification-analysis">Base Modification Analysis</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Barcoding">Barcoding</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Data-Analysis-Tools">Data Analysis Tools</a></li>
<li><a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki/Minor-Variants-and-Phasing-Analysis">Minor Variants and Phasing Analysis</a></li>
</ul><p>Address of the bookmark: <a href="https://github.com/PacificBiosciences/Bioinformatics-Training/wiki" rel="nofollow">https://github.com/PacificBiosciences/Bioinformatics-Training/wiki</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30973/abacas</guid>
	<pubDate>Thu, 16 Feb 2017 12:15:55 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30973/abacas</link>
	<title><![CDATA[ABACAS]]></title>
	<description><![CDATA[<p><span>ABACAS is intended to rapidly contiguate (align, order, orientate) , visualize and design primers to close gaps on shotgun assembled contigs based on a reference sequence. It uses MUMmer to find alignment positions and identify syntenies of assembly contigs against the reference. The output is then processed to generate a pseudomolecule taking overlaping contigs and gaps in to account. MUMmer's alignment generating programs, Nucmer and Promer are used followed by the 'delta-filter' utility function. Users could also run tblastx on contigs that are not used to generate the pseudomolecule.&nbsp;</span></p><p>Address of the bookmark: <a href="http://abacas.sourceforge.net/Manual.html#9._Colour_code" rel="nofollow">http://abacas.sourceforge.net/Manual.html#9._Colour_code</a></p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31014/sockeye</guid>
	<pubDate>Fri, 17 Feb 2017 08:51:16 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31014/sockeye</link>
	<title><![CDATA[sockeye]]></title>
	<description><![CDATA[<p>This sockeye&nbsp;software uses the Ensembl database project to import sequence and annotation information from several eukaryotic species. A user can additionally import their own custom sequence and annotation data. Individual annotation objects are displayed in Sockeye by using custom 3D models. Ensembl-derived and imported sequences can be analyzed by using a suite of multiple and pair-wise alignment algorithms. The results of these comparative analyses are also displayed in the 3D environment of Sockeye. By using the Java3D API to visualize genomic data in a 3D environment, we are able to compactly display cross-sequence comparisons. This provides the user with a novel platform for visualizing and comparing genomic feature organization.</p><p>Address of the bookmark: <a href="http://www.bcgsc.ca/platform/bioinfo/software/sockeye/releases/1.3" rel="nofollow">http://www.bcgsc.ca/platform/bioinfo/software/sockeye/releases/1.3</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31302/multi-metagenome-assembly</guid>
	<pubDate>Fri, 03 Mar 2017 10:14:18 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31302/multi-metagenome-assembly</link>
	<title><![CDATA[Multi-metagenome assembly]]></title>
	<description><![CDATA[<p>This project contains scripts and tutorials on how to assemble individual microbial genomes from metagenomes, as described in:</p>
<p>Genome sequences of rare, uncultured bacteria obtained by differential coverage binning of multiple metagenomes<br><br>Mads Albertsen, Philip Hugenholtz, Adam Skarshewski, Gene W. Tyson, K&aring;re L. Nielsen and Per .H. Nielsen</p>
<p>Nature Biotechnology 2013, doi:&nbsp;<a href="http://www.nature.com/nbt/journal/vaop/ncurrent/abs/nbt.2579.html">10.1038/nbt.2579</a></p><p>Address of the bookmark: <a href="https://github.com/MadsAlbertsen/multi-metagenome" rel="nofollow">https://github.com/MadsAlbertsen/multi-metagenome</a></p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/31520/research-associate-openings-at-iasri-india</guid>
  <pubDate>Fri, 10 Mar 2017 03:53:03 -0600</pubDate>
  <link></link>
  <title><![CDATA[Research Associate openings at IASRI, India]]></title>
  <description><![CDATA[
<p>Research Associate (RA) Two (2) </p>

<p>Ph.D. in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent or Master’s in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent with 4 years or 5 years of Bachelor’s degree having 1st Division or 60% marks or equivalent overall grade point average, with at least two years of research experience as evidenced from fellowship/ associateship/ training/ other engagements. </p>

<p>Knowledge in System Biology/ Statistical and computational Genomics/ Bioinformatics <br />Knowledge in computer programming, LINUX OS. <br />Expertise in use of R/other Bioinformatics software </p>

<p>More at http://iasri.res.in/employment/2017/cabin_advertisement_RA_SRF_YP_Mar2017.pdf</p>

<p>Phenomics of Moisture Deficit Stress Tolerance and Nitrogen Use December 31, 2019 </p>

<p>Research Associate (RA) Two (2) </p>

<p>Ph.D. in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent or System Administrator/ Computer expert for database development, development of phenome data bank and virtual phenomics facility, data archiving and Efficiency in Rice and Wheat-Phase II (Funded by National Agricultural Science Fund, ICAR) Master’s in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent with 4 years or 5 years of Bachelor’s degree having 1st Division or 60% marks or equivalent overall grade point average, with at least two years of research experience as evidenced from fellowship/ associateship/ training/ other engagements. maintenance; Development of image analysis algorithms, APIs and IAPs. </p>

<p>Knowledge in System Biology/ Statistical and computational Genomics/ Bioinformatics <br />Knowledge of programming in LINUX/R/Perl/JAVA/PHP/JSP and use of various software &amp; tools. <br />December 31, 2019 </p>

<p>Ph.D. in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science / Computer Application or equivalent or Master’s in Bioinformatics/ Agricultural Statistics/ Statistics/ Computer Science/ Computer Application or equivalent with 4 years or 5 years of Bachelor’s degree having 1st Division or 60% marks or equivalent overall grade point average, with at least two years of research experience as evidenced from fellowship/ associateship/ training/ other engagements. </p>

<p>Knowledge of Statistical and Computational Genomics/ Bioinformatics. <br />Knowledge of programming in LINUX/R/Perl/JAVA/PHP/JSP and use of various software &amp; tools. <br />March 31, 2020</p>
]]></description>
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