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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/27850?offset=290</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/27311/release-notes-for-genome-workbench-2105</guid>
	<pubDate>Thu, 12 May 2016 13:49:41 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/27311/release-notes-for-genome-workbench-2105</link>
	<title><![CDATA[Release Notes for Genome Workbench 2.10.5]]></title>
	<description><![CDATA[<p>New Features in latest release</p><ul>
<li>New ProSplign tool integrated with Genome Workbench (<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial13">Tutorial</a>,&nbsp;<a href="https://www.youtube.com/watch?v=V9UqKJprzAg&amp;feature=youtu.be" target="_blank">Video</a>)</li>
<li>New export function for BAM/cSRA coverage graphs (<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial14">Tutorial</a>)</li>
<li>New export function for alignments GFF3 format ((<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial15">Tutorial</a>))</li>
<li>Tree View: implemented new export mode based on selections (tutorial coming)</li>
<li>Tree View: added support for&nbsp;<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial3/#distance_based_circular_trees">distance based circular trees</a></li>
<li>Tree View: new rooting mode (Midpoint Root) results in more balanced trees (<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial3#reroot_tree">Tutorial</a>)</li>
<li>Tree View: added possibility to right-click on an edge between two nodes and "Place Root at Middle of Branch" &ndash; to re-root at mid-branch (<a href="https://www.ncbi.nlm.nih.gov/tools/gbench/tutorial3#reroot_tree">Tutorial</a>)</li>
</ul>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27323/cutadapt</guid>
	<pubDate>Fri, 13 May 2016 04:54:50 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27323/cutadapt</link>
	<title><![CDATA[cutadapt]]></title>
	<description><![CDATA[<p>Cutadapt finds and removes adapter sequences, primers, poly-A tails and other types of unwanted sequence from your high-throughput sequencing reads.</p>
<p>Cleaning your data in this way is often required: Reads from small-RNA sequencing contain the 3&rsquo; sequencing adapter because the read is longer than the molecule that is sequenced. Amplicon reads start with a primer sequence. Poly-A tails are useful for pulling out RNA from your sample, but often you don&rsquo;t want them to be in your reads.</p>
<p>Cutadapt helps with these trimming tasks by finding the adapter or primer sequences in an error-tolerant way. It can also modify and filter reads in various ways. Adapter sequences can contain IUPAC wildcard characters. Also, paired-end reads and even colorspace data is supported. If you want, you can also just demultiplex your input data, without removing adapter sequences at all.</p>
<p>Cutadapt comes with an extensive suite of automated tests and is available under the terms of the MIT license.</p>
<p>If you use cutadapt, please cite <a href="http://dx.doi.org/10.14806/ej.17.1.200">DOI:10.14806/ej.17.1.200</a> .</p><p>Address of the bookmark: <a href="https://cutadapt.readthedocs.io/en/stable/installation.html#quickstart" rel="nofollow">https://cutadapt.readthedocs.io/en/stable/installation.html#quickstart</a></p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/27344/orffinder-with-smart-blast</guid>
	<pubDate>Tue, 17 May 2016 01:43:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/27344/orffinder-with-smart-blast</link>
	<title><![CDATA[ORFfinder with smart BLAST]]></title>
	<description><![CDATA[<p><span>ORF Finder</span></p><p><span><a href="http://www.ncbi.nlm.nih.gov/orffinder">ORFfinder</a><span>&nbsp;is a graphical analysis tool for finding open reading frames (ORFs). We&rsquo;ve been working on a few updates, and we&rsquo;d like to find out what you think about them. Read on to find out what you can do with the new ORFfinder.</span></span></p><p>Smart BLAST (https://ncbiinsights.ncbi.nlm.nih.gov/2015/07/29/smartblast/)</p><p>Select one or a group of ORFs and BLAST several databases at once, and use the newly developed&nbsp;<a href="http://blast.ncbi.nlm.nih.gov/smartblast/">SmartBLAST</a>&nbsp;to verify protein names.&nbsp;Looking for the traditional results from&nbsp;<a href="http://blast.ncbi.nlm.nih.gov/Blast.cgi">BLAST</a>? They&rsquo;re there too.</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/27455/blosum50-matrix</guid>
	<pubDate>Sat, 21 May 2016 22:12:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/27455/blosum50-matrix</link>
	<title><![CDATA[BLOSUM50 Matrix]]></title>
	<description><![CDATA[]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/27455" length="2088" type="text/x-fortran" />
</item>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27696/methylkit</guid>
	<pubDate>Fri, 03 Jun 2016 10:09:29 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27696/methylkit</link>
	<title><![CDATA[methylKit]]></title>
	<description><![CDATA[<p><em>methylKit</em> is an <a href="http://en.wikipedia.org/wiki/R_%28programming_language%29">R</a> package for DNA methylation analysis and annotation from high-throughput bisulfite sequencing. The package is designed to deal with sequencing data from <a href="http://www.nature.com/nprot/journal/v6/n4/abs/nprot.2010.190.html">RRBS</a> and its variants, but also target-capture methods such as <a href="http://www.halogenomics.com/sureselect/methyl-seq">Agilent SureSelect methyl-seq</a>. In addition, methylKit can deal with base-pair resolution data for 5hmC obtained from Tab-seq or oxBS-seq. It can also handle whole-genome bisulfite sequencing data if proper input format is provided.</p><p>Address of the bookmark: <a href="https://github.com/al2na/methylKit" rel="nofollow">https://github.com/al2na/methylKit</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28269/4dgenome</guid>
	<pubDate>Mon, 04 Jul 2016 00:44:55 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28269/4dgenome</link>
	<title><![CDATA[4DGenome]]></title>
	<description><![CDATA[<p><span>Records in 4DGenome are compiled through comprehensive literature curation of experimentally-derived and computationally-predicted interactions. The current release contains 4,433,071 experimentally-derived and 3,605,176 computationally-predicted interactions in 5 organisms. Experimental data cover both high throughput datasets and individiual focused studies.&nbsp;</span><br><br><span>All interaction data are freely available in a standardized file format. Records can be queried by genomic regions, gene names, organism, and detection technology.&nbsp;</span></p><p>Address of the bookmark: <a href="http://4dgenome.research.chop.edu/" rel="nofollow">http://4dgenome.research.chop.edu/</a></p>]]></description>
	<dc:creator>Jitendra Narayan</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/27827/guest-faculty-centre-for-bioinformatics-at-pondicherry-university</guid>
  <pubDate>Wed, 15 Jun 2016 03:44:31 -0500</pubDate>
  <link></link>
  <title><![CDATA[Guest Faculty Centre for Bioinformatics at Pondicherry University]]></title>
  <description><![CDATA[
<p>Guest Faculty Centre For Bioinformatics Jobs opportunity in Pondicherry University<br />Qualification : M.Phil. (with NET/SLET)/ M.Tech. / M.E. in Computer Science with a minimum of 55% of marks as per UGC norms.<br />Desirable : Ph.D and Teaching experience in Perl and Java programming.<br />Honorarium : Rs. 1,000/- per lecture (subject to a maximum of Rs. 25,000/- per month)<br />How to apply<br />Walk-in-Interview will be held on 29.06.2016 (Wednesday) at 2:30 P.M at the office of Centre for Bioinformatics, Pondicherry University, Puducherry — 605 014. Interested eligible candidates may attend the Walk-in-Interview along with all original certificates, self attested photocopies and testimonials with a copy of their bio-data. Candidates reporting after 2:30 P.M will not be entertained.</p>

<p>More at http://www.pondiuni.edu.in/news?quicktabs_2=5#quicktabs-2</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28809/kissplice</guid>
	<pubDate>Tue, 16 Aug 2016 08:34:19 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28809/kissplice</link>
	<title><![CDATA[KisSplice]]></title>
	<description><![CDATA[<p>KisSplice is a software that enables to analyse RNA-seq data with or without a reference genome. It is an exact local transcriptome assembler that allows to identify SNPs, indels and alternative splicing events. It can deal with an arbitrary number of biological conditions, and will quantify each variant in each condition. It has been tested on Illumina datasets of up to 1G reads. Its memory consumption is around 5Gb for 100M reads.</p>
<p>KisSplice is not a full-length transcriptome assembler. This means that it will output the variable regions of the transcripts, not reconstruct them entirely.</p>
<p>KisSplice comes as a workflow, with several possible post-treatments meant to facilitate the analysis of the results. The choice of the post-treatment depends on the availability of a reference genome/transcriptome and on the need to perform a differential analysis, as summarised in the following table.</p><p>Address of the bookmark: <a href="http://kissplice.prabi.fr/" rel="nofollow">http://kissplice.prabi.fr/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/27965/cheatsheet-for-linux</guid>
	<pubDate>Wed, 22 Jun 2016 07:55:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/27965/cheatsheet-for-linux</link>
	<title><![CDATA[Cheatsheet for Linux !!]]></title>
	<description><![CDATA[<p>Linux Commands Cheat Sheet<br /><br />&nbsp;&nbsp;&nbsp; File System<br /><br />&nbsp;&nbsp;&nbsp; ls &mdash; list items in current directory<br /><br />&nbsp;&nbsp;&nbsp; ls -l &mdash; list items in current directory and show in long format to see perimissions, size, an modification date<br /><br />&nbsp;&nbsp;&nbsp; ls -a &mdash; list all items in current directory, including hidden files<br /><br />&nbsp;&nbsp;&nbsp; ls -F &mdash; list all items in current directory and show directories with a slash and executables with a star<br /><br />&nbsp;&nbsp;&nbsp; ls dir &mdash; list all items in directory dir<br /><br />&nbsp;&nbsp;&nbsp; cd dir &mdash; change directory to dir<br /><br />&nbsp;&nbsp;&nbsp; cd .. &mdash; go up one directory<br /><br />&nbsp;&nbsp;&nbsp; cd / &mdash; go to the root directory<br /><br />&nbsp;&nbsp;&nbsp; cd ~ &mdash; go to to your home directory<br /><br />&nbsp;&nbsp;&nbsp; cd - &mdash; go to the last directory you were just in<br /><br />&nbsp;&nbsp;&nbsp; pwd &mdash; show present working directory<br /><br />&nbsp;&nbsp;&nbsp; mkdir dir &mdash; make directory dir<br /><br />&nbsp;&nbsp;&nbsp; rm file &mdash; remove file<br /><br />&nbsp;&nbsp;&nbsp; rm -r dir &mdash; remove directory dir recursively<br /><br />&nbsp;&nbsp;&nbsp; cp file1 file2 &mdash; copy file1 to file2<br /><br />&nbsp;&nbsp;&nbsp; cp -r dir1 dir2 &mdash; copy directory dir1 to dir2 recursively<br /><br />&nbsp;&nbsp;&nbsp; mv file1 file2 &mdash; move (rename) file1 to file2<br /><br />&nbsp;&nbsp;&nbsp; ln -s file link &mdash; create symbolic link to file<br /><br />&nbsp;&nbsp;&nbsp; touch file &mdash; create or update file<br /><br />&nbsp;&nbsp;&nbsp; cat file &mdash; output the contents of file<br /><br />&nbsp;&nbsp;&nbsp; less file &mdash; view file with page navigation<br /><br />&nbsp;&nbsp;&nbsp; head file &mdash; output the first 10 lines of file<br /><br />&nbsp;&nbsp;&nbsp; tail file &mdash; output the last 10 lines of file<br /><br />&nbsp;&nbsp;&nbsp; tail -f file &mdash; output the contents of file as it grows, starting with the last 10 lines<br /><br />&nbsp;&nbsp;&nbsp; vim file &mdash; edit file<br /><br />&nbsp;&nbsp;&nbsp; alias name 'command' &mdash; create an alias for a command<br />&nbsp;&nbsp;&nbsp; System<br /><br />&nbsp;&nbsp;&nbsp; shutdown &mdash; shut down machine<br /><br />&nbsp;&nbsp;&nbsp; reboot &mdash; restart machine<br /><br />&nbsp;&nbsp;&nbsp; date &mdash; show the current date and time<br /><br />&nbsp;&nbsp;&nbsp; whoami &mdash; who you are logged in as<br /><br />&nbsp;&nbsp;&nbsp; finger user &mdash; display information about user<br /><br />&nbsp;&nbsp;&nbsp; man command &mdash; show the manual for command<br /><br />&nbsp;&nbsp;&nbsp; df &mdash; show disk usage<br /><br />&nbsp;&nbsp;&nbsp; du &mdash; show directory space usage<br /><br />&nbsp;&nbsp;&nbsp; free &mdash; show memory and swap usage<br /><br />&nbsp;&nbsp;&nbsp; whereis app &mdash; show possible locations of app<br /><br />&nbsp;&nbsp;&nbsp; which app &mdash; show which app will be run by default<br />&nbsp;&nbsp;&nbsp; Process Management<br /><br />&nbsp;&nbsp;&nbsp; ps &mdash; display your currently active processes<br /><br />&nbsp;&nbsp;&nbsp; top &mdash; display all running processes<br /><br />&nbsp;&nbsp;&nbsp; kill pid &mdash; kill process id pid<br /><br />&nbsp;&nbsp;&nbsp; kill -9 pid &mdash; force kill process id pid<br />&nbsp;&nbsp;&nbsp; Permissions<br /><br />&nbsp;&nbsp;&nbsp; ls -l &mdash; list items in current directory and show permissions<br /><br />&nbsp;&nbsp;&nbsp; chmod ugo file &mdash; change permissions of file to ugo - u is the user's permissions, g is the group's permissions, and o is everyone else's permissions. The values of u, g, and o can be any number between 0 and 7.<br /><br />&nbsp;&nbsp;&nbsp; 7 &mdash; full permissions<br /><br />&nbsp;&nbsp;&nbsp; 6 &mdash; read and write only<br /><br />&nbsp;&nbsp;&nbsp; 5 &mdash; read and execute only<br /><br />&nbsp;&nbsp;&nbsp; 4 &mdash; read only<br /><br />&nbsp;&nbsp;&nbsp; 3 &mdash; write and execute only<br /><br />&nbsp;&nbsp;&nbsp; 2 &mdash; write only<br /><br />&nbsp;&nbsp;&nbsp; 1 &mdash; execute only<br /><br />&nbsp;&nbsp;&nbsp; 0 &mdash; no permissions<br /><br />&nbsp;&nbsp;&nbsp; chmod 600 file &mdash; you can read and write - good for files<br /><br />&nbsp;&nbsp;&nbsp; chmod 700 file &mdash; you can read, write, and execute - good for scripts<br /><br />&nbsp;&nbsp;&nbsp; chmod 644 file &mdash; you can read and write, and everyone else can only read - good for web pages<br /><br />&nbsp;&nbsp;&nbsp; chmod 755 file &mdash; you can read, write, and execute, and everyone else can read and execute - good for programs that you want to share<br />&nbsp;&nbsp;&nbsp; Networking<br /><br />&nbsp;&nbsp;&nbsp; wget file &mdash; download a file<br /><br />&nbsp;&nbsp;&nbsp; curl file &mdash; download a file<br /><br />&nbsp;&nbsp;&nbsp; scp user@host:file dir &mdash; secure copy a file from remote server to the dir directory on your machine<br /><br />&nbsp;&nbsp;&nbsp; scp file user@host:dir &mdash; secure copy a file from your machine to the dir directory on a remote server<br /><br />&nbsp;&nbsp;&nbsp; scp -r user@host:dir dir &mdash; secure copy the directory dir from remote server to the directory dir on your machine<br /><br />&nbsp;&nbsp;&nbsp; ssh user@host &mdash; connect to host as user<br /><br />&nbsp;&nbsp;&nbsp; ssh -p port user@host &mdash; connect to host on port as user<br /><br />&nbsp;&nbsp;&nbsp; ssh-copy-id user@host &mdash; add your key to host for user to enable a keyed or passwordless login<br /><br />&nbsp;&nbsp;&nbsp; ping host &mdash; ping host and output results<br /><br />&nbsp;&nbsp;&nbsp; whois domain &mdash; get information for domain<br /><br />&nbsp;&nbsp;&nbsp; dig domain &mdash; get DNS information for domain<br /><br />&nbsp;&nbsp;&nbsp; dig -x host &mdash; reverse lookup host<br /><br />&nbsp;&nbsp;&nbsp; lsof -i tcp:1337 &mdash; list all processes running on port 1337<br />&nbsp;&nbsp;&nbsp; Searching<br /><br />&nbsp;&nbsp;&nbsp; grep pattern files &mdash; search for pattern in files<br /><br />&nbsp;&nbsp;&nbsp; grep -r pattern dir &mdash; search recursively for pattern in dir<br /><br />&nbsp;&nbsp;&nbsp; grep -rn pattern dir &mdash; search recursively for pattern in dir and show the line number found<br /><br />&nbsp;&nbsp;&nbsp; grep -r pattern dir --include='*.ext &mdash; search recursively for pattern in dir and only search in files with .ext extension<br /><br />&nbsp;&nbsp;&nbsp; command | grep pattern &mdash; search for pattern in the output of command<br /><br />&nbsp;&nbsp;&nbsp; find file &mdash; find all instances of file in real system<br /><br />&nbsp;&nbsp;&nbsp; locate file &mdash; find all instances of file using indexed database built from the updatedb command. Much faster than find<br /><br />&nbsp;&nbsp;&nbsp; sed -i 's/day/night/g' file &mdash; find all occurrences of day in a file and replace them with night - s means substitude and g means global - sed also supports regular expressions<br />&nbsp;&nbsp;&nbsp; Compression<br /><br />&nbsp;&nbsp;&nbsp; tar cf file.tar files &mdash; create a tar named file.tar containing files<br /><br />&nbsp;&nbsp;&nbsp; tar xf file.tar &mdash; extract the files from file.tar<br /><br />&nbsp;&nbsp;&nbsp; tar czf file.tar.gz files &mdash; create a tar with Gzip compression<br /><br />&nbsp;&nbsp;&nbsp; tar xzf file.tar.gz &mdash; extract a tar using Gzip<br /><br />&nbsp;&nbsp;&nbsp; gzip file &mdash; compresses file and renames it to file.gz<br /><br />&nbsp;&nbsp;&nbsp; gzip -d file.gz &mdash; decompresses file.gz back to file<br />&nbsp;&nbsp;&nbsp; Shortcuts<br /><br />&nbsp;&nbsp;&nbsp; ctrl+a &mdash; move cursor to beginning of line<br /><br />&nbsp;&nbsp;&nbsp; ctrl+f &mdash; move cursor to end of line<br /><br />&nbsp;&nbsp;&nbsp; alt+f &mdash; move cursor forward 1 word<br /><br />&nbsp;&nbsp;&nbsp; alt+b &mdash; move cursor backward 1 word</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28835/a5-miseq</guid>
	<pubDate>Thu, 18 Aug 2016 04:05:23 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28835/a5-miseq</link>
	<title><![CDATA[A5-miseq]]></title>
	<description><![CDATA[<p><span><span>_A5-miseq_ is a pipeline for assembling DNA sequence data generated on the Illumina sequencing platform. This README will take you through the steps necessary for running _A5-miseq_. </span></span></p>
<p><span>Point to note:</span></p>
<p><span>There are many situations where A5-miseq is not the right tool for the job. In order to produce accurate results, A5-miseq requires Illumina data with certain characteristics. A5-miseq will likely not work well with Illumina reads shorter than around 80nt, or reads where the base qualities are low in all or most reads before 60nt. A5-miseq assumes it is assembling homozygous haploid genomes. Use a different assembler for metagenomes and heterozygous diploid or polyploid organisms. Use a different assembler if a tool like FastQC reports your data quality is dubious. You have been warned! Datasets consisting solely of unpaired reads are not currently supported.</span></p><p>Address of the bookmark: <a href="https://sourceforge.net/projects/ngopt/" rel="nofollow">https://sourceforge.net/projects/ngopt/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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