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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/31156?offset=1490</link>
	<atom:link href="https://bioinformaticsonline.com/related/31156?offset=1490" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</guid>
	<pubDate>Tue, 14 Jun 2016 10:28:58 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27821/blobsplorer</link>
	<title><![CDATA[Blobsplorer]]></title>
	<description><![CDATA[<p>Blobsplorer is a tool for interactive visualization of assembled DNA sequence data ("contigs") derived from (often unintentionally) mixed-species pools. It allows the simultaneous display of GC content, coverage, and taxonomic annotation for collections of contigs with a view to separating out those belonging to different taxa.</p>
<p>Blobsplorer is unlikely to be of use on its own as it requires contig data to be supplied in a format that involves considerable preprocessing (see below for a description). The easiest way to use Blobsplorer is as part of a workflow using scripts from <a href="https://github.com/blaxterlab/blobology">here</a>.</p><p>Address of the bookmark: <a href="http://nematodes.org/martin/blobsplorer/blobsplorer.html" rel="nofollow">http://nematodes.org/martin/blobsplorer/blobsplorer.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27845/cnidaria-fast-reference-free-phylogenomic-clustering</guid>
	<pubDate>Thu, 16 Jun 2016 17:55:17 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27845/cnidaria-fast-reference-free-phylogenomic-clustering</link>
	<title><![CDATA[CNIDARIA: fast, reference-free phylogenomic clustering]]></title>
	<description><![CDATA[<p>Motivation: Identification of biological specimens is a major requirement for a range of applications. Reference-free methods analyse unprocessed sequencing data without relying on prior knowledge, but these do not scale to arbitrarily large genomes and arbitrarily large phylogenetic distances.</p>
<p>Results: We present Cnidaria, a practical tool for clustering genomic and transcriptomic data with no limitation on ge-nome size or phylogenetic distances. We successfully simultaneously clustered 169 genomic and transcriptomic datasets from 4 kingdoms, achieving 100% accuracy at supra-species level and 78% accuracy for species level.</p>
<p>Availability and Implementation: Cnidaria is written in C++ and Python and is available at http://www.ab.wur.nl/cnidaria.</p>
<p>Contact: Saulo Aflitos - sauloal@gmail.com</p>
<p>Supplementary information: Supplementary data are available at Bioinformatics online.</p><p>Address of the bookmark: <a href="https://github.com/sauloal/cnidaria/wiki" rel="nofollow">https://github.com/sauloal/cnidaria/wiki</a></p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/27959/darkhorse</guid>
	<pubDate>Wed, 22 Jun 2016 05:37:38 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/27959/darkhorse</link>
	<title><![CDATA[DarkHorse]]></title>
	<description><![CDATA[<p><em>DarkHorse</em>&nbsp;is a bioinformatic method for rapid, automated identification and ranking of phylogenetically atypical proteins on a genome-wide basis. It works by selecting potential ortholog matches from a reference database of amino acid sequences, then using these matches to calculate a lineage probability index (LPI) score for each genome protein.</p>
<p>LPI scores are inversely proportional to the phylogenetic distance between database match sequences and the query genome. These scores are useful not only for large-scale<em>de novo</em>&nbsp;predictions of horizontally transferred proteins, but can also serve as an independent quality control test for potential horizontal transfer candidates identified by alternative methods, especially those based on nucleic acid signatures. Candidates having high LPI scores are unlikely to have been horizontally transferred, since they are highly conserved among closely related organisms.</p>
<p>One unique and powerful feature of the DarkHorse HGT Candidate database is the opportunity to explore the phylogenetic background of potential HGT donors as well as recipients. The breadth of the database allows not only query sequences, but also their database match partners to be evaluated for sequence similarity or novelty compared to taxonomically related organisms.</p>
<p><em>DarkHorse</em>&nbsp;is configurable for varying degrees of phylogenetic granularity and protein sequence conservation. Users should consult the&nbsp;<a href="http://darkhorse.ucsd.edu/#references">references</a>&nbsp;cited below for a complete explanation of parameter selection and result interpretation. A brief&nbsp;<a href="http://darkhorse.ucsd.edu/tutorial.html">tutorial</a>&nbsp;page is also available on-line.</p><p>Address of the bookmark: <a href="http://darkhorse.ucsd.edu/download.html" rel="nofollow">http://darkhorse.ucsd.edu/download.html</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/28168/sam-flags</guid>
	<pubDate>Wed, 29 Jun 2016 15:38:15 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28168/sam-flags</link>
	<title><![CDATA[SAM flags]]></title>
	<description><![CDATA[<p>Decoding SAM flags</p>
<p>This utility makes it easy to identify what are the properties of a read based on its SAM flag value, or conversely, to find what the SAM Flag value would be for a given combination of properties.</p>
<p>To decode a given SAM flag value, just enter the number in the field below. The encoded properties will be listed under Summary below, to the right.</p><p>Address of the bookmark: <a href="https://broadinstitute.github.io/picard/explain-flags.html" rel="nofollow">https://broadinstitute.github.io/picard/explain-flags.html</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/28141/csbb-v10</guid>
	<pubDate>Wed, 29 Jun 2016 07:33:05 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/28141/csbb-v10</link>
	<title><![CDATA[CSBB-v1.0]]></title>
	<description><![CDATA[<p>CSBB is a command line based bioinformatics suite to analyze biological data acquired through varied avenues of biological experiments. CSBB is implemented in Perl, while it also leverages the use of R and python in background for specific modules. Major focus of CSBB is to allow users from biology and bioinformatics community, to get benefited by performing down-stream analysis tasks while eliminating the need to write programming code. CSBB is currently available on Linux, UNIX, MAC OS and Windows platforms.</p>
<p>Currently CSBB provides 13 modules focused on analytical tasks like performing upper-quantile normalization on expression data or convert genome wide gene expression to z-scores when comparing expression data from different platforms.</p>
<p>More at&nbsp;https://github.com/skygenomics/CSBB-v1.0</p><p>Address of the bookmark: <a href="https://github.com/skygenomics/CSBB-v1.0" rel="nofollow">https://github.com/skygenomics/CSBB-v1.0</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
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<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/blog/view/28439/binc-exam-preparation-tips</guid>
	<pubDate>Fri, 15 Jul 2016 20:53:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/blog/view/28439/binc-exam-preparation-tips</link>
	<title><![CDATA[BINC exam preparation tips !!]]></title>
	<description><![CDATA[<p>How to prepare for <span>BINC (BioInformatics National Certification)</span>&nbsp;exam? What are the expected questions?</p><p>These are just a scant few of the common questions asked by bioinformatics students as they ready themselves for the next exam sitting. If you read the entire <a href="http://bioinformaticsonline.com/bookmarks/view/2334/binc-bioinformatics-national-certification-website-address">Syllabus</a> (and I know that everyone does), you will see a section devoted to study and exam techniques. The section discusses such broad concepts as motivation, scheduling, and retention. Upon reading this section, however, I find the "hints" to be too general. Much of the advice boils down to read, study, understand, and memorize the material. The techniques mentioned apply to everyone and thus the overall advice ends up as a broad overview of the learning process.</p><p>The idea behind this article is to give students ideas on different approaches and techniques in the preparation for exams. By providing various ways to prepare for the exam process, fascinated readers may gain some additional insight to help complement their studying methodology. There are, of course, many common themes expressed in this small empirical sample of students' study habits. The idea of note cards, memorization, and problem solving are frequently mentioned by all students. No matter what technique a candidate uses, it always takes a significant amount of time and personal resources to successfully complete the examination process.</p><p>1 Explain it in your own word</p><p>Your teacher or lecturer can explain something to you, you can learn it from a text book, your friends can study with you, even your own notes can explain it to you but all these explanations are of little use if, by the end, you can&rsquo;t explain what you have learned to yourself. The BINC exam looking for ability to write and explain the concept in your own word. You, therefore, need to illustrate in an exam to get top exam results, then you won&rsquo;t be happy with your end exam result. So don&rsquo;t just memorise and tick off the list &ndash; make sure you understand your theory.</p><p>2 Be an examiner yourself</p><p>Of course, depending on what you&rsquo;re studying, it may be quite difficult to get into a position to understand a concept, theory or other information you need to learn. Ask &lsquo;stupid&rsquo; question to yourself and train yourself for the worst! Embrace your curiosity, for as William Arthur Ward said: &ldquo;Curiosity is the wick in the candle of learning.&rdquo; Doing so will allow you to fill in the blanks and better prepare you for exams.</p><p>3 Quiz yourself</p><p>Once you feel you understand topic, it is important to test yourself regularly. Try yourself to replicate exam conditions as much as possible: turn your phone off, don&rsquo;t talk, time yourself etc. You can set yourself a study quiz or practice exam questions and, so long as you approach it with the right mindset, you can get a very good idea of how much you know. You gain a greater insight into where you stand in relation to what you&rsquo;ve studied so far.</p><p>4 Online study</p><p>Keeping the fact that, bioinformatics is ever changing subject, you might need to update yourself on timely basis. Don&rsquo;t feel obliged to just sit in front of a book with a highlighter; there are many different ways to improve your bioinformatics knowledge. Login and check almost all web servers and keep yourself updated, like how many genomes sequenced, sizes, techniques used, software names etc.</p><p>5 Study plan</p><p>In order to achieve exam success, you need to know what you want to achieve and focus on. That&rsquo;s why it is extremely important to set your Study Goals now and outline to yourself what you need to do. With your study goals in mind, you properly need to attention all subjects. It should be broad enough to allow you to add and change aspects but concise enough so you know you&rsquo;re covering each subject/topic as best you can at this point.</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34922/camsa-a-tool-for-comparative-analysis-and-merging-of-scaffold-assemblies</guid>
	<pubDate>Thu, 28 Dec 2017 09:10:26 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34922/camsa-a-tool-for-comparative-analysis-and-merging-of-scaffold-assemblies</link>
	<title><![CDATA[CAMSA :: a tool for Comparative Analysis and Merging of Scaffold Assemblies]]></title>
	<description><![CDATA[<p>CAMSA &ndash; is a tool for&nbsp;<span>C</span>omparative&nbsp;<span>A</span>nalysis and&nbsp;<span>M</span>erging of&nbsp;<span>S</span>caffold&nbsp;<span>A</span>ssemblies, distributed both as a standalone software package and as Python library under the MIT license.</p>
<p>Main features:</p>
<ol>
<li>works with any number of scaffold assemblies in de-novo non-progressive fashion</li>
<li>allows to simultaneously work with scaffold assemblies obtained from any&nbsp;<em>in silico</em>&nbsp;and&nbsp;<em>in vitro</em>&nbsp;techniques, supporting multiple existing formats via built-in converters</li>
<li>creates an extensive report with several comparative quality metrics (both on assembly level and on the level of individual assembly points)</li>
<li>constructs a merged combined scaffold assembly</li>
<li>provides an interactive framework for a visual comparative analysis of the given assemblies</li>
</ol><p>Address of the bookmark: <a href="https://cblab.org/camsa/" rel="nofollow">https://cblab.org/camsa/</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/news/view/28563/find-predicted-crispr-sites-using-ensembl</guid>
	<pubDate>Wed, 27 Jul 2016 03:15:59 -0500</pubDate>
	<link>https://bioinformaticsonline.com/news/view/28563/find-predicted-crispr-sites-using-ensembl</link>
	<title><![CDATA[Find predicted CRISPR sites using Ensembl]]></title>
	<description><![CDATA[<p>Did you know that you can now use Ensembl to help design your CRISPR experiments? Just turn on the brand new track that shows you the CRISPR sites that have been predicted by the WGE group (<a href="http://www.sanger.ac.uk/science/tools/wge" target="_blank">http://www.sanger.ac.uk/science/tools/wge</a>)</p><p><img src="http://www.ensembl.info/wp-content/uploads/2016/07/Screen-Shot-2016-07-22-at-13.04.33.png" width="1400" height="544" alt="image" style="border: 0px;"></p><p>Find out more on our blog:<br /><a href="http://www.ensembl.info/blog/2016/07/26/find-predicted-crispr-sites-using-ensembl/" target="_blank">http://www.ensembl.info/&hellip;/find-predicted-crispr-sites-usin&hellip;/</a></p><p>&nbsp;</p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/37233/rna-seq-analysis-workshop-course-materials</guid>
	<pubDate>Tue, 03 Jul 2018 08:14:14 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/37233/rna-seq-analysis-workshop-course-materials</link>
	<title><![CDATA[RNA-seq Analysis Workshop Course Materials]]></title>
	<description><![CDATA[RNAseq can be roughly divided into two "types":

Reference genome-based - an assembled genome exists for a species for which an RNAseq experiment is performed. It allows reads to be aligned against the reference genome and significantly improves our ability to reconstruct transcripts. This category would obviously include humans and most model organisms but excludes the majority of truly biologically intereting species (e.g., Hyacinth macaw);

Reference genome-free - no genome assembly for the species of interest is available. In this case one would need to assemble the reads into transcripts using de novo approaches. This type of RNAseq is as much of an art as well as science because assembly is heavily parameter-dependent and difficult to do well.
In this lesson we will focus on the Reference genome-based type of RNA seq.

http://chagall.med.cornell.edu/RNASEQcourse/<p>Address of the bookmark: <a href="http://chagall.med.cornell.edu/RNASEQcourse/" rel="nofollow">http://chagall.med.cornell.edu/RNASEQcourse/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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