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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/27331?offset=1240</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34488/scripts-for-the-analysis-of-hgt-in-genome-sequence-data</guid>
	<pubDate>Wed, 29 Nov 2017 16:44:10 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34488/scripts-for-the-analysis-of-hgt-in-genome-sequence-data</link>
	<title><![CDATA[Scripts for the analysis of HGT in genome sequence data.]]></title>
	<description><![CDATA[<p><span>Scripts for the analysis of HGT in genome sequence data</span></p><p>Address of the bookmark: <a href="https://github.com/reubwn/hgt" rel="nofollow">https://github.com/reubwn/hgt</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/19580/internship-program-for-bioinformatics-biotechnology-mba-mca-no-of-vacancy-5</guid>
  <pubDate>Mon, 15 Dec 2014 08:11:02 -0600</pubDate>
  <link></link>
  <title><![CDATA[Internship Program for Bioinformatics / Biotechnology / MBA / MCA (No. Of Vacancy: 5)]]></title>
  <description><![CDATA[
<p>ArrayGen is offering an Internship Program for Post graduate Bioinformatics / Biotechnology / MBA / MCA students and professionals. ArrayGen Technologies provide an excellent opportunity to gain research experience and explore if a scientific career is right for you. Currently we offer positions to outstanding students interested in Next Generation Sequencing (NGS) data analysis or marketing or software development. Applications are accepted throughout the year. Accepted students will be notified through email.</p>
]]></description>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/36711/ancestral-sequence-reconstruction-steps</guid>
	<pubDate>Fri, 18 May 2018 08:28:26 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/36711/ancestral-sequence-reconstruction-steps</link>
	<title><![CDATA[Ancestral sequence reconstruction steps !]]></title>
	<description><![CDATA[<div><strong>Ancestral sequence reconstruction</strong>&nbsp;(<strong>ASR</strong>) &ndash; also known as&nbsp;<strong>ancestral gene</strong>/<strong>sequence reconstruction</strong>/<strong>resurrection</strong>&nbsp;&ndash; is a technique used in the study of&nbsp;molecular evolution. The method consists of the synthesis of an ancestral&nbsp;gene&nbsp;and expression of the corresponding ancestral&nbsp;protein.&nbsp;<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-thornton-1"></a>The idea of protein 'resurrection' was suggested in 1963 by Pauling and Zuckerkandl.<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-2"></a>&nbsp;Some early efforts were made in the eighties-nineties, led by the laboratory of&nbsp;Steven A. Benner, showing the potential of this technique &ndash; one that only started to be fulfilled in the post-genomic era.<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-3"></a>&nbsp;Thanks to the improvement of algorithms and of better sequencing and synthesis techniques, the method was developed further in the early 2000s to allow the resurrection of a greater variety of and much more ancient genes.<a href="https://en.wikipedia.org/wiki/Ancestral_sequence_reconstruction#cite_note-4"></a>&nbsp;Over the last decade, ancestral protein resurrection has developed as a strategy to reveal the mechanisms and dynamics of protein evolution.&nbsp;</div><div>&nbsp;</div><div>BEAST is the best way to predict the ancestral structure. but, I suggest following steps?</div><div>&nbsp;</div><div>1- Alignments "Mafft -&nbsp;<a href="https://www.researchgate.net/deref/http%3A%2F%2Fmafft.cbrc.jp%2Falignment%2Fsoftware%2Fsource.html" target="_blank">http://mafft.cbrc.jp/alignment/software/source.html</a>"</div><div>mafft --maxiterate 1000 --reorder --thread 24 --genafpair Dataset.fasta &gt; Dataset_Alig.fasta</div><div>&nbsp;</div><div>2- Your dataset has a good phylogenetic signal, is possible to perform with Tree-Puzzle "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fwww.tree-puzzle.de" target="_blank">http://www.tree-puzzle.de</a>";</div><div>&nbsp;</div><div id="yui_3_14_1_1_1526649596608_1443">3 - This dataset which the saturation index, I perform with "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fdambe.bio.uottawa.ca%2Fdambe.asp" target="_blank">http://dambe.bio.uottawa.ca/dambe.asp</a>";</div><div>&nbsp;</div><div>4- Has evidence of possible recombination in your dataset, the evaluate if this presence or absence, because this may to influence the grouping of clades, I perform with</div><div>---recombination</div><div>&nbsp;</div><div>4.1- Phi-test, implemented in SplitTree4"<a href="https://www.researchgate.net/deref/http%3A%2F%2Fwww.splitstree.org" target="_blank">http://www.splitstree.org</a>", (.nex file)</div><div>&nbsp;</div><div>4.2- GARD deployed in webserver in the DataMonkey "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fwww.datamonkey.org%2F" target="_blank">http://www.datamonkey.org/</a>" - turning to the amino acid seaview -&gt; view proteins -&gt; save as ...) Ideally do a tree-based groups.</div><div>&nbsp;</div><div>4.3- RDP4 for download and installation on Windows in "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fweb.cbio.uct.ac.za%2F~darren%2Frdp.html" target="_blank">http://web.cbio.uct.ac.za/~darren/rdp.html</a>"</div><div>&nbsp;</div><div>4.4- Hyphy (Mac, Windows, Linux) in "<a href="https://www.researchgate.net/deref/http%3A%2F%2Fhyphy.org%2Fw%2Findex.php%2FDownload" target="_blank">http://hyphy.org/w/index.php/Download</a>"</div><div>&nbsp;</div><div>4.5- Path-o-Gen (temporal structure of a tree input file -&gt; arquivo.tre)</div><div>These steps above, I call of pre-processing to inferences phylogenetic...</div><div>&nbsp;</div><div>5- Perform phylogenetic tree, used Bayesian Inference with Molecular Clock, but is necessary Clock Testing:</div><div>&nbsp;</div><div>- This step is performed with program Beast (Beauti, Beast and TreeAnnotator), and Tracer_v1.5 more FigTree to inspection.</div><div>&nbsp;</div><div>- Tutorials:&nbsp;<a href="https://www.researchgate.net/deref/http%3A%2F%2Fbeast.bio.ed.ac.uk%2Ftutorials" target="_blank">http://beast.bio.ed.ac.uk/tutorials</a></div><div>- Downloads:&nbsp;<a href="https://www.researchgate.net/deref/http%3A%2F%2Fbeast.bio.ed.ac.uk%2Fdownloads" target="_blank">http://beast.bio.ed.ac.uk/downloads</a></div>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/19792/irishgrid-irish-grid-mapping-system</guid>
	<pubDate>Fri, 26 Dec 2014 07:53:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/19792/irishgrid-irish-grid-mapping-system</link>
	<title><![CDATA[irishgrid: Irish Grid Mapping System]]></title>
	<description><![CDATA[<p>Perl module for creating geographic 10km-square maps using either SVG or PNG (with GD library) output format.</p>
<p>Originally design to map the location of objects in a 10 km map IrishGrid includes:</p>
<ul>
<li>native support of the Irish Grid System (see <a href="http://www.osi.ie/">http://www.osi.ie/</a>)</li>
<li>optimize for speed (there's as less as possible data to conversion)</li>
<li>customized color functions</li>
</ul>
<p>https://code.google.com/p/irishgrid/downloads/detail?name=irishgrid.pl</p><p>Address of the bookmark: <a href="https://code.google.com/p/irishgrid/" rel="nofollow">https://code.google.com/p/irishgrid/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37962/wtdbg2-a-de-novo-sequence-assembler-for-long-noisy-reads-produced-by-pacbio-or-oxford-nanopore</guid>
	<pubDate>Fri, 19 Oct 2018 08:48:43 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37962/wtdbg2-a-de-novo-sequence-assembler-for-long-noisy-reads-produced-by-pacbio-or-oxford-nanopore</link>
	<title><![CDATA[Wtdbg2: a de novo sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore]]></title>
	<description><![CDATA[<p><span>Wtdbg2 is a&nbsp;</span><em>de novo</em><span>&nbsp;sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore Technologies (ONT). It assembles raw reads without error correction and then builds the consensus from intermediate assembly output. Wtdbg2 is able to assemble the human and even the 32Gb&nbsp;</span><a href="https://www.nature.com/articles/nature25458">Axolotl</a><span>&nbsp;genome at a speed tens of times faster than&nbsp;</span><a href="https://github.com/marbl/canu">CANU</a><span>&nbsp;and&nbsp;</span><a href="https://github.com/PacificBiosciences/FALCON">FALCON</a><span>while producing contigs of comparable base accuracy.</span></p><p>Address of the bookmark: <a href="https://github.com/ruanjue/wtdbg2" rel="nofollow">https://github.com/ruanjue/wtdbg2</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/23536/teaching-assistant-at-svims</guid>
  <pubDate>Fri, 31 Jul 2015 10:15:16 -0500</pubDate>
  <link></link>
  <title><![CDATA[Teaching Assistant at SVIMS]]></title>
  <description><![CDATA[
<p>Eligible candidates are invited for a walk-in-interview for recruitment of Teaching Assistant in the Department of Bioinformatics on 8.08.2015 at 10 A.M. in the Committee Hall, SVIMS, Tirupati. The candidates have to attend with all original certificates of qualification, experience on the date of interview. The engagement will be made purely on adhoc basis for a period of 6 months and it can be terminated at any time without notice or without assigning any reason thereof. This is purely an adhoc appointment and the candidate will not have any right to claim permanent benefits of any kind.</p>

<p>1. Remuneration : Rs. 12000/- per month (consolidated)</p>

<p>2. Qualification : M.Sc./M.Tech. Bioinformatics (preference will be given to the candidates with BINC / NET / GATE / Bioinformatics DBT-Traineeship / Studentship and teaching experience)</p>

<p>3. Place of work : Department of Bioinformatics, SVIMS, Tirupati</p>

<p>4. No. of Position : One</p>

<p>Terms and conditions:</p>

<p>1. Candidates are required to submit the Biodata, attested copies of relevant certificates in support of their age, educational qualification, experience etc., before the interview committee, SVIMS University, Tirupati.<br />2. No TA / DA will be paid for attending the interview.<br />3. Interim enquiries will not be entertained.<br />4. The maximum age limit for Teaching Assistant is 34 years as on 8th August, 2015.<br />5. The tenure of will be further extended subject to performance of the incumbent.</p>

<p>Advertisement: http://svimsbic.org/Teaching_Assistant_B.I._2015.pdf</p>
]]></description>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/39689/msaprobs-parallel-and-accurate-multiple-sequence-alignment</guid>
	<pubDate>Tue, 09 Jul 2019 23:58:44 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/39689/msaprobs-parallel-and-accurate-multiple-sequence-alignment</link>
	<title><![CDATA[MSAProbs - Parallel and accurate multiple sequence alignment]]></title>
	<description><![CDATA[<p><strong>MSAProbs</strong><span>&nbsp;is a well-established state-of-the-art multiple sequence alignment algorithm for protein sequences. The design of MSAProbs is based on a combination of pair hidden Markov models and partition functions to calculate posterior probabilities. Assessed using the popular benchmarks: BAliBASE, PREFAB, SABmark and OXBENCH, MSAProbs achieves statistically significant accuracy improvements over the existing top performing aligners, including ClustalW, MAFFT, MUSCLE, ProbCons and Probalign. In addition, MSAProbs is optimized for shared-memory CPUs by employing a multi-threaded design, and further parallelized for distributed-memory systems using MPI to overcome high memory overhead barrier and achieve good parallel and data-size scalability.</span></p><p>Address of the bookmark: <a href="http://msaprobs.sourceforge.net/homepage.htm#latest" rel="nofollow">http://msaprobs.sourceforge.net/homepage.htm#latest</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/view/19838</guid>
	<pubDate>Sat, 27 Dec 2014 13:30:15 -0600</pubDate>
	<link>https://bioinformaticsonline.com/view/19838</link>
	<title><![CDATA[Interview with a bioinformatician series ...]]></title>
	<description><![CDATA[<p>The aim of this series to interviews some notable bioinformaticians to get their views on various aspects of bioinformatics research. Hopefully these answers will prove useful to others in the field, especially to those who are just starting their bioinformatics careers.<br /><br />This series will be available at BOL every fortnight.<br /><br /><br /><br /></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40212/kalign-fast-multiple-sequence-alignment-program-for-biological-sequences</guid>
	<pubDate>Fri, 01 Nov 2019 00:20:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40212/kalign-fast-multiple-sequence-alignment-program-for-biological-sequences</link>
	<title><![CDATA[Kalign: fast multiple sequence alignment program for biological sequences.]]></title>
	<description><![CDATA[<p><span>Kalign is a fast multiple sequence alignment program for biological sequences.</span></p>
<p>Align sequences and output the alignment in MSF format:</p>
<pre><code>kalign -i BB11001.tfa -f msf  -o out.msf
</code></pre>
<p>Align sequences and output the alignment in clustal format:</p>
<pre><code>kalign -i BB11001.tfa -f clu -o out.clu
</code></pre>
<p>Re-align sequences in an existing alignment:</p>
<pre><code>kalign -i BB11001.msf  -o out.afa
</code></pre>
<p>Reformat existing alignment:</p>
<pre><code>kalign -i BB11001.msf -r afa -o out.afa</code></pre><p>Address of the bookmark: <a href="https://github.com/TimoLassmann/kalign" rel="nofollow">https://github.com/TimoLassmann/kalign</a></p>]]></description>
	<dc:creator>BioStar</dc:creator>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/19992/binc-examination-2015</guid>
	<pubDate>Mon, 29 Dec 2014 12:23:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/news/view/19992/binc-examination-2015</link>
	<title><![CDATA[BINC examination 2015 !!!]]></title>
	<description><![CDATA[<p>Pondicherry University,Puducherry,on behalf of Department of Biotechnology, Government of India, will conduct the BINC examination in 2015. The objective of this examination is to certify bioinformatics professionals, trained formally as well as self-trained.Registration for BINC examination 2015 will open soon.</p><p>Pondicherry University Puducherry has been identified as a nodal agency by the Department of Biotechnology, Govt. of India to coordinate this examination along with nine centres namely, Pune University, Pune; Anna University, Chennai; Calcatta University (WBUT) Kolkata; Institute of Bioinformatics &amp; Applied Biotechnology, Bangalore; North-Eastern Hill University, Shillong, University of Hyderabad, Hyderabad; University of Kerala, Thiruvananthapuram; Jawaharlal Nehru University, New Delhi and Assam Agricultural University, Guwahati.</p><p>In the BINC 2013 examination,17 candidates were certified. DBT has agreed to fund Research fellowships for all the BINC qualified Indian nationals to pursue Ph.D. in Indian Institutes/Universities. Note that the candidate must possess a postgraduate degree(or equivalent) &amp; meet the criteria of the institutes/universities in order to avail research fellowship. In addition, cash prize of Rs. 10,000/- will be awarded to the top 10 BINC qualifiers.<br /><br /></p><p>More at http://210.212.230.224:9999/BINC/</p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
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