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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/42166?offset=1380</link>
	<atom:link href="https://bioinformaticsonline.com/related/42166?offset=1380" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27331/andi</guid>
	<pubDate>Fri, 13 May 2016 05:16:35 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27331/andi</link>
	<title><![CDATA[Andi]]></title>
	<description><![CDATA[<p>This is the <code>andi</code> program for estimating the evolutionary distance between closely related genomes. These distances can be used to rapidly infer phylogenies for big sets of genomes. Because <code>andi</code> does not compute full alignments, it is so efficient that it scales even up to thousands of bacterial genomes.</p>
<p>This readme covers all necessary instructions for the impatient to get <code>andi</code> up and running. For extensive instructions please consult the <a href="https://github.com/EvolBioInf/andi/blob/master/andi-manual.pdf">manual</a>.</p>
<p>More at https://github.com/evolbioinf/andi/</p><p>Address of the bookmark: <a href="http://bioinformatics.oxfordjournals.org/content/early/2015/01/13/bioinformatics.btu815.full" rel="nofollow">http://bioinformatics.oxfordjournals.org/content/early/2015/01/13/bioinformatics.btu815.full</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27475/polyphen-2-prediction-of-functional-effects-of-human-nssnps</guid>
	<pubDate>Mon, 23 May 2016 02:27:25 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27475/polyphen-2-prediction-of-functional-effects-of-human-nssnps</link>
	<title><![CDATA[PolyPhen-2: Prediction of functional effects of human nsSNPs]]></title>
	<description><![CDATA[<p><strong>PolyPhen-2</strong> (<strong>Poly</strong>morphism <strong>Phen</strong>otyping v<strong>2</strong>) is a tool which predicts possible impact of an amino acid substitution on the structure and function of a human protein using straightforward physical and comparative considerations.</p><p>Address of the bookmark: <a href="http://genetics.bwh.harvard.edu/pph2/" rel="nofollow">http://genetics.bwh.harvard.edu/pph2/</a></p>]]></description>
	<dc:creator>Anjana</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27440/stampy</guid>
	<pubDate>Fri, 20 May 2016 19:13:32 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27440/stampy</link>
	<title><![CDATA[Stampy]]></title>
	<description><![CDATA[<p><strong>Stampy&nbsp;</strong><span>is a package for the mapping of short reads from illumina sequencing machines onto a reference genome. It's recommended for most workflows, including those for genomic resequencing, RNA-Seq and Chip-seq. Stampy excels in the mapping of reads containing that contain sequence variation relative to the reference, in particular for those containing insertions or deletions.</span></p><p>Address of the bookmark: <a href="http://www.well.ox.ac.uk/project-stampy" rel="nofollow">http://www.well.ox.ac.uk/project-stampy</a></p>]]></description>
	<dc:creator>Abhi</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27461/maftools</guid>
	<pubDate>Sat, 21 May 2016 22:40:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27461/maftools</link>
	<title><![CDATA[mafTools]]></title>
	<description><![CDATA[<p><span>Bioinformatics tools for dealing with Multiple Alignment Format (MAF) files.</span></p><p>Address of the bookmark: <a href="https://github.com/dentearl/mafTools" rel="nofollow">https://github.com/dentearl/mafTools</a></p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/27473/project-assistantjunior-research-fellow-position-at-centre-of-biomedical-research-sanjay-gandhi-postgraduate-institute-of-medical-sciences-campus-lucknow</guid>
  <pubDate>Mon, 23 May 2016 01:31:29 -0500</pubDate>
  <link></link>
  <title><![CDATA[Project Assistant/Junior Research Fellow Position at  Centre of Biomedical Research, Sanjay Gandhi Postgraduate Institute of Medical Sciences Campus, Lucknow.]]></title>
  <description><![CDATA[
<p>Applications are invited from eligible candidates willing to join in a Department of Science and Technology (DST) project entitled “"Mapping neural regions involved in reading process in skilled adult Deaf reader: From neuroimaging perspective (functional Magnetic Resonance Imaging (fMRI) and Diffuse Tensor Imaging (DTI.)" as a Project Assistant/Junior Research Fellow (JRF) at Centre of Biomedical Research, Sanjay Gandhi Postgraduate Institute of Medical Sciences Campus, Lucknow.</p>

<p>Essential Qualification:</p>

<p>1. Master's degree in Bioinformatics / Computer Applications / Cognitive Science /Neuroscience/ Neuropsychology or equivalent. (Advantage will be given to NET JRF qualified candidate) Additional</p>

<p>Desirable Skills:</p>

<p>1) Programming skills (e.g., C++, Matlab, Python) 2) Experience/competent in working Window and Linux based programme.</p>

<p>Please mail your CV and covering letter to dr.uttam.kumar@gmail.com.</p>

<p>To know more about lab works please visit http://uttambrainlab.co.in/lab/.</p>

<p>Last date: 15/06/16</p>

<p>Advertisement: http://cbmr.res.in/wp-content/uploads/2016/05/Advertisement-19-5-2016.pdf</p>
]]></description>
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<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/27554/jrf-bioinformatics-at-actrec-navi-mumbai</guid>
  <pubDate>Mon, 30 May 2016 03:24:22 -0500</pubDate>
  <link></link>
  <title><![CDATA[JRF Bioinformatics at ACTREC, Navi Mumbai]]></title>
  <description><![CDATA[
<p>No. ACTREC/Advt./23/2016<br />JRF Bioinformatics recruitment in ACTREC (On contract Basis- Primeone Workforce Pvt. Ltd.)<br />Title : “Investigating the molecular basis of CaM/c-FLIP interaction to design specific c-FLIP inhibitor for modulating its anti-apoptotic function”.<br />Qualification : Master’s degree in bioinformatics, biochemistry, biotechnology and biological sciences from a recognized university with not less than 55% aggregate marks. Experience: Prior experience in modelling, protein-protein/ligand docking, Molecular dynamics simulation required. Knowledge in database development will be preferred.   </p>

<p>Pay Scale : Rs. 32,500/- <br />How to apply<br />Candidates fulfilling these requirements should pre-register by sending their application in the prescribed format with recent CV and contact details of 2 referees by e-mail to  ‘program.office@actrec.gov.in’ latest by  17.00 hrs on 23-06-2016. The interviews would be held on 27-06-2016 and only pre-registered candidates will be eligible to appear for interview. Candidates should report between 09.30 to 10.00 a.m. in Steno Pool,  3rd floor, Khanolkar Shodhika, ACTREC, Kharghar, Navi Mumbai.</p>

<p>More at http://www.actrec.gov.in/</p>
]]></description>
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  <guid isPermaLink='true'>https://bioinformaticsonline.com/researchlabs/view/27695/the-kingsley-lab</guid>
  <pubDate>Fri, 03 Jun 2016 09:55:10 -0500</pubDate>
  <link></link>
  <title><![CDATA[The Kingsley Lab]]></title>
  <description><![CDATA[
<p>The Molecular Basis of Vertebrate Evolution. Naturally occurring species show spectacular differences in morphology, physiology, behavior, disease susceptibility, and life span. Although the genomes of many organisms have now been completely sequenced, Kingsley lab still know relatively little about the specific DNA sequence changes that underlie interesting species-specific traits. Kingsley lab laboratory is using a combination of genetic and genomic approaches to identify the detailed molecular mechanisms that control evolutionary change in vertebrates.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/27799/bbmapbbtools-package-multipurpose-tool-designed-for-converting-reads-or-other-nucleotide-data-between-different-formats</guid>
	<pubDate>Mon, 13 Jun 2016 05:47:21 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/27799/bbmapbbtools-package-multipurpose-tool-designed-for-converting-reads-or-other-nucleotide-data-between-different-formats</link>
	<title><![CDATA[BBMap/BBTools package: Multipurpose tool designed for converting reads or other nucleotide data between different formats.]]></title>
	<description><![CDATA[<div id="post_message_148585"><a href="https://sourceforge.net/projects/bbmap/" target="_blank">Reformat</a>is a member of the <a href="https://sourceforge.net/projects/bbmap/" target="_blank">BBMap/BBTools package</a>. It is a multipurpose tool designed for converting reads or other nucleotide data between different formats. It supports, and can inter-convert:<br /> <br /> fastq<br /> fasta<br /> fasta+qual<br /> sam<br /> scarf (an old Illumina format)<br /> bam (if samtools is installed)<br /> gzip<br /> zip<br /> ascii-33 (sanger)<br /> ascii-64 (old Illumina)<br /> paired files<br /> interleaved files<br /> <br /> It is multithreaded and can process data at over 500 megabytes per second, and can accept streams from standard in and write to standard out, allowing it to be easily dropped into the middle of a pipeline for format conversion. Reformat autodetects formats based on file extensions and content, making it very easy to use; and the autodetection can be overridden, allowing flexibility for people who don't like to follow naming conventions, or out-of-spec fastq files with qualities values like -17 or 120.<br /> <br /> The program has been gradually expanded, and can now perform various other functions. None of these will break pairing, if the input is paired.<br /> <br /> Quality trimming (either or both ends)<br /> Quality filtering<br /> Fixed-length trimming<br /> Generation of histograms (base composition, quality, etc)<br /> Subsampling (to a fraction of input reads, or an exact number of reads or bases)<br /> Changing fasta line-wrapping length<br /> Reverse-complementing (all reads or only read 2)<br /> Adding /1 and /2 suffix to read names<br /> GC-content filtering<br /> Length-filtering<br /> Testing for corrupted interleaved files<br /> <br /> Reformat is compatible with any platform that supports Java 1.7 or higher. It also has a bash shellscript for simpler invocation. Typical usage examples:<br /> <br /> Reformat fastq into fasta:<br /> <strong>reformat.sh in=x.fq out=y.fa</strong><br /> <br /> Interleave paired reads:<br /> <strong>reformat.sh in1=x1.fq in2=x2.fq out=y.fq</strong><br /> <br /> Note - you can actually use a shortcut if paired read files have the same name with a 1 and a 2. This is equivalent to the above command:<br /> <strong>reformat.sh in=x#.fq out=y.fq</strong><br /> <br /> De-interleave reads:<br /> <strong>reformat.sh in=x.fq out1=y1.fq out2=y2.fq</strong><br /> <br /> Verify that interleaving appears correct, assuming Illumina namimg conventions:<br /> <strong>reformat.sh in=x.fq vint</strong><br /> <br /> Convert ASCII-33 to ASCII-64:<br /> <strong>reformat.sh in=x.fq out=y.fq qin=33 qout=64</strong><br /> <br /> Quality-trim paired reads to Q10 on the left and right ends and discard reads shorter than 50bp after trimming:<br /> <strong>reformat.sh in1=x1.fq in2=x2.fq out1=y1.fq out2=y2.fq outsingle=singletons.fq qtrim=rl trimq=10 minlength=50</strong><br /> <br /> Subsample 10% of the first 20000 pairs in an interleaved file:<br /> <strong>reformat.sh in=x.fq out=y.fq reads=20000 samplerate=0.1 int=t</strong><br /> (in this case "int=t" overrides interleaving autodetection, to ensure reads are treated as pairs)<br /> <br /> Pipe in a gzipped sam file and pipe out fasta:<br /> <strong>reformat.sh in=stdin.sam.gz out=stdout.fa</strong><br /> <br /> Reverse-complement reads:<br /> <strong>reformat.sh in=x.fq out=y.fq rcomp</strong><br /> <br /> For reformatting a file with very long sequences, Reformat will need more memory; just add the additional flag "-Xmx2g". For example, to change the line-wrapping length on the human genome (which has individual sequences over 200Mbp long) to 70 characters:<br /> <strong>reformat.sh -Xmx2g in=HG19.fa.gz out=HG19_wrapped.fa.gz fastawrap=70</strong><br /> <br /> For additional functions, please run the shellscript with no arguments, or just read it with a text editor. If you have any questions, please post them in this thread.<br /> <br /> For people using a non-bash terminal, you may need to type "bash reformat.sh" instead of just "reformat.sh".<br /> For users of Windows or other platforms that do not support bash shellscripts, replace "reformat.sh" with "java -ea -Xmx200m /path/to/bbmap/current/ jgi.ReformatReads"<br /> for example,<br /> <strong>java -ea -Xmx200m C:\bbmap\current\ jgi.ReformatReads in=x.fq out=y.fa</strong><br /> <br /> Reformat can be downloaded with BBTools here:<br /> <a href="https://sourceforge.net/projects/bbmap/" target="_blank">https://sourceforge.net/projects/bbmap/</a></div>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27839/lorma-a-tool-for-correcting-sequencing-errors-in-long-reads-such-those-produced-by-pacific-biosciences-sequencing-machines</guid>
	<pubDate>Wed, 15 Jun 2016 17:18:36 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27839/lorma-a-tool-for-correcting-sequencing-errors-in-long-reads-such-those-produced-by-pacific-biosciences-sequencing-machines</link>
	<title><![CDATA[LoRMA: a tool for correcting sequencing errors in long reads such those produced by Pacific Biosciences sequencing machines]]></title>
	<description><![CDATA[<p>LoRMA is a tool for correcting sequencing errors in long reads such those produced by Pacific Biosciences sequencing machines.</p>
<p>Publication:</p>
<ul>
<li>L. Salmela, R. Walve, E. Rivals, and E. Ukkonen: Accurate selfcorrection of errors in long reads using de Bruijn graphs. Accepted to RECOMB-Seq 2016.</li>
</ul>
<p>Download:</p>
<ul>
<li><a href="https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/LoRMA-0.3.tar.gz">LoRMA 0.3 source files</a></li>
<li><a href="https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/README.txt">README</a></li>
</ul><p>Address of the bookmark: <a href="https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/" rel="nofollow">https://www.cs.helsinki.fi/u/lmsalmel/LoRMA/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27850/clusterprofiler</guid>
	<pubDate>Thu, 16 Jun 2016 18:57:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27850/clusterprofiler</link>
	<title><![CDATA[clusterProfiler]]></title>
	<description><![CDATA[<p>statistical analysis and visulization of functional profiles for genes and gene clusters<br><br>Bioconductor version: Release (3.3)<br><br>This package implements methods to analyze and visualize functional profiles (GO and KEGG) of gene and gene clusters.<br><br>Author: Guangchuang Yu &lt;guangchuangyu at gmail.com&gt; with contributions from Li-Gen Wang and Giovanni Dall'Olio.<br><br>Maintainer: Guangchuang Yu &lt;guangchuangyu at gmail.com&gt;<br><br>Citation (from within R, enter citation("clusterProfiler")):<br><br>Yu G, Wang L, Han Y and He Q (2012). &ldquo;clusterProfiler: an R package for comparing biological themes among gene clusters.&rdquo; OMICS: A Journal of Integrative Biology, 16(5), pp. 284-287.<br>Installation<br><br>To install this package, start R and enter:<br><br>## try http:// if https:// URLs are not supported<br>source("https://bioconductor.org/biocLite.R")<br>biocLite("clusterProfiler")</p>
<p>https://www.bioconductor.org/packages/devel/bioc/vignettes/clusterProfiler/inst/doc/clusterProfiler.html</p><p>Address of the bookmark: <a href="https://www.bioconductor.org/packages/devel/bioc/vignettes/clusterProfiler/inst/doc/clusterProfiler.html" rel="nofollow">https://www.bioconductor.org/packages/devel/bioc/vignettes/clusterProfiler/inst/doc/clusterProfiler.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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