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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/28121?offset=290</link>
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	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31205/yasra-reference-based-assembler</guid>
	<pubDate>Wed, 01 Mar 2017 08:32:45 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31205/yasra-reference-based-assembler</link>
	<title><![CDATA[YASRA: Reference based assembler]]></title>
	<description><![CDATA[<p>YASRA (Yet Another Short Read Assembler) performs comparative assembly of short reads using a reference genome, which can differ substantially from the genome being sequenced. Mapping reads to reference genomes makes use of LASTZ (Harris et al), a pairwise sequence aligner compatible with BLASTZ. Special scoring sets were derived to improve the performance, both in runtime and quality for 454 and Illumina sequence reads.</p>
<p>YASRA uses LASTZ (<a href="http://bx.psu.edu/miller_lab">http://bx.psu.edu/miller_lab</a> for released version and <a href="http://www.bx.psu.edu/%7Ersharris/lastz/newer">http://www.bx.psu.edu/~rsharris/lastz/newer</a> for newer version) for aligning the sequences to the reference genome. Please install LASTZ (the newest version on <a href="http://www.bx.psu.edu/%7Ersharris/lastz/newer">http://www.bx.psu.edu/~rsharris/lastz/newer</a>) and add the LASTZ binary in your executable/binary search path before installing YASRA.</p><p>Address of the bookmark: <a href="https://github.com/aakrosh/YASRA" rel="nofollow">https://github.com/aakrosh/YASRA</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42313/crbhits-from-conditional-reciprocal-best-hits-to-codon-alignments-and-kaks-in-r</guid>
	<pubDate>Wed, 11 Nov 2020 23:06:03 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42313/crbhits-from-conditional-reciprocal-best-hits-to-codon-alignments-and-kaks-in-r</link>
	<title><![CDATA[CRBHits: From Conditional Reciprocal Best Hits to Codon Alignments and Ka/Ks in R]]></title>
	<description><![CDATA[<p>CRBHits is a coding sequence (CDS) analysis pipeline in R (R Core Team, 2019). It reimplements the Conditional Reciprocal Best Hit (CRBH) algorithm crb-blast and covers all necessary steps from sequence similarity searches, codon alignments to Ka/Ks calculations and synteny. The new R package targets ecology, population and evolutionary biologists working in the field of comparative genomics.</p><p>Address of the bookmark: <a href="https://gitlab.gwdg.de/mpievolbio-it/crbhits" rel="nofollow">https://gitlab.gwdg.de/mpievolbio-it/crbhits</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/31251/bioinformatics-opening-at-icgeb-new-delhi</guid>
  <pubDate>Thu, 02 Mar 2017 04:16:36 -0600</pubDate>
  <link></link>
  <title><![CDATA[Bioinformatics opening at ICGEB NEW DELHI]]></title>
  <description><![CDATA[
<p>ICGEB NEW DELHI</p>

<p>Applications are invited for:</p>

<p>Junior Research Fellow, in a DBT funded project, is available in Translational Health Group, ICGEB, New Delhi</p>

<p>Qualifications:</p>

<p>Education: M.Sc. (preferably in Biotechnology, Life Sciences or Zoology, Chemistry, Bioinformatics). Candidates with hands on experience on GC-MS data acquisition and analysis will be given preference. Bioinformatics expertise required.</p>

<p>Fellowship: As per DBT guidelines.</p>

<p>Tenure: The position is purely on temporary basis with an initial tenure of six months and based on satisfactory performance may continue until the completion of the project.</p>

<p>Closing date for applications: 04/03/2017</p>

<p>Please send a "TWO PAGE" CV by email to:  th.icgeb@gmail.com on or before the last date.</p>

<p>Research Associate, in a DBT funded project, is available in Translational Health Group, ICGEB, New Delhi</p>

<p>Qualifications:</p>

<p>Education: Ph.D. (in Biology, Biotechnology, Chemistry, Bioinformatics). Candidates with hands on experience on GC-MS data acquisition and analysis will be given preference. </p>

<p>Fellowship: As per DBT guidelines.</p>

<p>Tenure: The position is purely on temporary basis with an initial tenure of six months and  based on satisfactory performance may continue until the completion of the project.</p>

<p>Closing date for applications: 04/03/2017</p>

<p>Please send a "TWO PAGE" CV by email to: th.icgeb@gmail.com on or before the last date.</p>
]]></description>
</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/bookmarks/view/38389/blast-options-setting-and-defaults</guid>
	<pubDate>Mon, 10 Dec 2018 08:29:37 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/38389/blast-options-setting-and-defaults</link>
	<title><![CDATA[BLAST options, setting and defaults]]></title>
	<description><![CDATA[<p>BLAST stands for Basic Local Alignment Search Tool and was developed by Altschul et al. (1990) and significantly improved by&nbsp;<a href="http://www3.oup.co.uk/nar/Volume_25/Issue_17/freepdf/">Altschul et al. (1997).</a>&nbsp;It is a very fast search algorithm that is used to separately search protein or DNA databases. BLAST is best used for sequence similarity searching, rather than for motif searching. For searches using a query sequence of fewer than twenty residues,&nbsp;<a href="https://www.arabidopsis.org/servlets/tools/patmatch/">PatMatch</a>&nbsp;is the best choice. Another sequence alignment tool that may yield different results from BLAST, and may be useful for motif searching, is&nbsp;<a href="https://www.arabidopsis.org/cgi-bin/fasta/TAIRfasta.pl">FASTA</a>. To search nonplant datasets, try&nbsp;<a href="http://seqsim.ncgr.org/newBlast.html">NCGR BLAST</a>&nbsp;or&nbsp;<a href="http://www.ncbi.nlm.nih.gov/blast/blast.cgi?Jform=0">NCBI BLAST</a>.</p>
<p>A fairly complete on-line guide to BLAST searching can be found at the&nbsp;<a href="http://www.ncbi.nlm.nih.gov/BLAST/blast_help.html">NCBI BLAST Help Manual</a>. For a theoretical overview of BLAST, see the&nbsp;<a href="http://www.ncbi.nlm.nih.gov/BLAST/tutorial/Altschul-1.html">NCBI BLAST Course</a>. Additional information can be found in the&nbsp;<a href="https://www.arabidopsis.org/blast/aboutblast2.htm">BLAST 2.0 Release Notes</a></p>
<table border="1">
<tbody>
<tr><th>&nbsp;</th><th><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#methods">BLASTN</a></th><th><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#methods">BLASTP</a></th><th><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#methods">BLASTX</a></th><th><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#methods">TBLASTN</a></th><th><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#methods">TBLASTX</a></th><th><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#methods">PSIBLAST</a></th></tr>
<tr>
<td><a name="open" id="open"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#open"><strong>Gap opening penalty</strong></a>:<br>cost to open a gap [integer]</td>
<td align="center">default = 5</td>
<td align="center">default = 11<br>limited&nbsp;values&nbsp;are supported</td>
<td align="center">default = 11<br>limited&nbsp;values&nbsp;are supported</td>
<td align="center">default = 11<br>limited&nbsp;values&nbsp;are supported</td>
<td align="center">default = 11<br>limited&nbsp;values&nbsp;are supported</td>
<td align="center">default = 5</td>
</tr>
<tr>
<td><a name="extend" id="extend"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#extend"><strong>Gap extension penalty</strong></a>:<br>cost to extend a gap [integer]</td>
<td align="center">default = 2</td>
<td align="center">default = 1<br>a 0 in this field means to use the default</td>
<td align="center">default = 1<br>a 0 in this field means to use the default</td>
<td align="center">default = 1<br>a 0 in this field means to use the default</td>
<td align="center">default = 1<br>a 0 in this field means to use the default</td>
<td align="center">default = 2</td>
</tr>
<tr>
<td><a name="match" id="match"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#match"><strong>Nucleic match</strong></a>:<br>reward for a match in the BLAST portion of run [integer]</td>
<td align="center">default = 1</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">default = 1</td>
</tr>
<tr>
<td><a name="mismatch" id="mismatch"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#mismatch"><strong>Nucleic mismatch</strong></a>:<br>penalty for a mismatch in the blast portion of run [integer]</td>
<td align="center">default = -3</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">default = -3</td>
</tr>
<tr>
<td><strong><a name="expect" id="expect"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#expect">Expectation value</a></strong>:<br>(E) [real]</td>
<td align="center">default = 10.0</td>
<td align="center">default = 10.0</td>
<td align="center">default = 10.0</td>
<td align="center">default = 10.0</td>
<td align="center">default = 10.0</td>
<td align="center">default = 10.0</td>
</tr>
<tr>
<td><a name="word" id="word"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#word"><strong>Word size</strong></a>:<br>the size of the initial word that must be matched between the database and the query sequence</td>
<td align="center">default = 11</td>
<td align="center">default = 3</td>
<td align="center">default = 3</td>
<td align="center">default = 3</td>
<td align="center">default = 3</td>
<td align="center">default = 11</td>
</tr>
<tr>
<td><a name="descriptions" id="descriptions"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#descriptions"><strong>Max scores</strong></a>:<br>Number of one-line descriptions (V) [Integer]</td>
<td align="center">default = 25</td>
<td align="center">default = 25</td>
<td align="center">default = 25</td>
<td align="center">default = 25</td>
<td align="center">default = 25</td>
<td align="center">default = 25</td>
</tr>
<tr>
<td><strong><a name="alignments" id="alignments"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#alignments">Max alignments</a></strong>:<br>number of alignments to show (B) [integer]</td>
<td align="center">default = 15</td>
<td align="center">default = 15</td>
<td align="center">default = 15</td>
<td align="center">default = 15</td>
<td align="center">default = 15</td>
<td align="center">default = 15</td>
</tr>
<tr>
<td><strong>Query filter</strong>:<br>filter applied to the query sequence</td>
<td align="center">default = DUST</td>
<td align="center">default = SEG</td>
<td align="center">default = SEG</td>
<td align="center">default = SEG</td>
<td align="center">default = SEG</td>
<td align="center">default = DUST</td>
</tr>
<tr>
<td><strong><a name="gencodes" id="gencodes"></a><a href="https://www.arabidopsis.org/Blast/BLAST_help.jsp#gencodes">Query genetic code</a></strong>:<br>genetic code to be used in BLASTX translation of the query</td>
<td align="center">n/a</td>
<td align="center">n/a</td>
<td align="center">default = universal</td>
<td align="center">default = universal</td>
<td align="center">default = universal</td>
<td align="center">n/a</td>
</tr>
<tr>
<td><strong><a name="matrix" id="matrix"></a><a href="http://twod.med.harvard.edu/seqanal/matrices.html">Matrix</a></strong>:<br>substitution matrix to be used for amino acid comparisons</td>
<td align="center">no default</td>
<td align="center">default = blosum62</td>
<td align="center">default = blosum62</td>
<td align="center">default = blosum62</td>
<td align="center">default = blosum62</td>
<td align="center">no default</td>
</tr>
</tbody>
</table>
<p>Supported and Suggested&nbsp;Values&nbsp;for Gap Open and Extension in BLASTP, BLASTX, TBLASTN, and TBLASTX</p>
<table border="1">
<tbody>
<tr><th>Gaps Open</th><th>Gap Extension</th></tr>
<tr>
<td align="center">10</td>
<td align="center">1</td>
</tr>
<tr>
<td align="center">10</td>
<td align="center">2</td>
</tr>
<tr>
<td align="center">11</td>
<td align="center">1</td>
</tr>
<tr>
<td align="center">8</td>
<td align="center">2</td>
</tr>
<tr>
<td align="center">9</td>
<td align="center">2</td>
</tr>
</tbody>
</table><p>Address of the bookmark: <a href="https://www.arabidopsis.org/Blast/BLASToptions.jsp" rel="nofollow">https://www.arabidopsis.org/Blast/BLASToptions.jsp</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31382/seqmule-automated-human-exomegenome-variants-detection</guid>
	<pubDate>Tue, 07 Mar 2017 10:12:36 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31382/seqmule-automated-human-exomegenome-variants-detection</link>
	<title><![CDATA[SeqMule: Automated human exome/genome variants detection]]></title>
	<description><![CDATA[<p><span>SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its configuration file. SeqMule also has some built-in functions, such as pooling consensus calls from various callers, plotting a Venn diagram showing intersection among different callers, and downloading databases. SeqMule can be used for both Mendelian disease study and cancer genome study.</span></p><p>Address of the bookmark: <a href="http://seqmule.openbioinformatics.org/en/latest/" rel="nofollow">http://seqmule.openbioinformatics.org/en/latest/</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/view/459</guid>
	<pubDate>Thu, 11 Jul 2013 14:39:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/view/459</link>
	<title><![CDATA[Python vs Perl]]></title>
	<description><![CDATA[<p>Why bioinformatician still using Perl when Python is easy to code, good in ReXp and faster than perl?</p>]]></description>
	<dc:creator>Rahul Agarwal</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/840/junior-research-fellow-jrf</guid>
  <pubDate>Sat, 13 Jul 2013 11:17:22 -0500</pubDate>
  <link></link>
  <title><![CDATA[Junior Research Fellow (JRF)]]></title>
  <description><![CDATA[
<p>School of Biotechnology<br />Gautam Buddha University<br />Greater Noida, UP - 201310</p>

<p>Applications are invited for one position of Junior Research Fellow (JRF) in a Department of Biotechnology (DBT) sponsored research project entitled “Design, synthesis and evaluation of potent aminopeptidase inhibitors for malarial therapy” under the supervision of Dr. Shakti Sahi.</p>

<p>The monthly fellowship of JRF will be Rs 12,000/- plus HRA as per the University rules.</p>

<p>Essential Qualification: Master degree in any discipline of Life Science with NET qualified.</p>

<p>Desirable Qualification: Preference will be given to candidates having research experience in in silico drug designing/Bioinformatics.</p>

<p>Interested candidates may send their resume to undersigned on or before 14th July 2013 by post-mail/e-mail shaktis@gbu.ac.in or shaktisahi@gmail.com. No TA and DA will be paid for appearing for the interview. Dr. Shakti Sahi (Principle Investigator)</p>

<p>Advertisement:<br />www.gbu.ac.in/Recruitment/JRF_Advt_DBTProject_Shakt</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/31881/gbtools-interactive-visualization-of-metagenome-bins-in-r</guid>
	<pubDate>Sun, 26 Mar 2017 15:41:31 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/31881/gbtools-interactive-visualization-of-metagenome-bins-in-r</link>
	<title><![CDATA[gbtools: Interactive Visualization of Metagenome Bins in R]]></title>
	<description><![CDATA[<p><span>We have developed gbtools, a software package that allows users to visualize metagenomic assemblies by plotting coverage (sequencing depth) and GC values of contigs, and also to annotate the plots with taxonomic information. Different sets of annotations, including taxonomic assignments from conserved marker genes or SSU rRNA genes, can be imported simultaneously; users can choose which annotations to plot. Bins can be manually defined from plots, or be imported from third-party binning tools and overlaid onto plots, such that results from different methods can be compared side-by-side. gbtools reports summary statistics of bins including marker gene completeness, and allows the user to add or subtract bins with each other.&nbsp;</span></p>
<p><span>Tool at&nbsp;https://github.com/kbseah/genome-bin-tools</span></p><p>Address of the bookmark: <a href="http://journal.frontiersin.org/article/10.3389/fmicb.2015.01451/full" rel="nofollow">http://journal.frontiersin.org/article/10.3389/fmicb.2015.01451/full</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/847/nedelec-lab</guid>
  <pubDate>Sat, 13 Jul 2013 17:38:55 -0500</pubDate>
  <link></link>
  <title><![CDATA[Nedelec Lab]]></title>
  <description><![CDATA[
<p>Location :European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.</p>

<p>Our long-term research objective is to understand microtubule organization in living cells, with an emphasis on mitosis. We develop in-vitro assays, quantitative image analysis and cytosim, a computer simulation to study cellular architecture from a mechanistic angle, modeling the interactions of microtubules and related proteins such as molecular motors. In the past, we combined simulations and experiments to study microtubule self-organization, and the mechanical stability of two interacting asters. More recently, we looked at the focusing of mitotic fibers, the formation of antiparallel arrays of microtubules in fission yeast and the spindle positionning in C. elegans.<br />We are supported by BioMS, an initiative in Systems Biology, and involved in Cell networks.</p>

<p>Link: http://www.cytosim.org</p>
]]></description>
</item>

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