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<channel>
	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/33741?offset=640</link>
	<atom:link href="https://bioinformaticsonline.com/related/33741?offset=640" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30090/standardized-velvet-assembly-report</guid>
	<pubDate>Fri, 09 Dec 2016 03:59:59 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30090/standardized-velvet-assembly-report</link>
	<title><![CDATA[Standardized velvet assembly report]]></title>
	<description><![CDATA[<p>Requirements:</p>
<ul>
<li>velvet (velveth velvetg should be in your PATH)</li>
<li>R (with Sweave)</li>
<li>pdflatex (usually part of TeTeX)</li>
<li>ggplot2 (from R prompt type install.packages("ggplot2","proto","xtable"))</li>
<li>Perl</li>
</ul>
<p>Optional:</p>
<ul>
<li>BLAT or BLAST (to generate alignments against a reference genome). If using BLAT, add faToTwoBit,gfClient,gfServer to your PATH. If using BLAST, add blastall and formatdb.</li>
</ul>
<p>Edit permute.sh to your liking, paying particular attention to the kmer, cvCut, expCov, and other flags</p>
<p>To Run:</p>
<ol>
<li><code>perl fastaAllSize mysequences.fa &gt; mysequences.stat or gunzip -c mysequences.fa.gz | fastaAllSize &gt; mysequences.stat</code>&nbsp;Substitute fastqAllSize for fastq files.</li>
<li><code>./permute.sh mysequences</code>&nbsp;(leave out the .fa)</li>
</ol>
<p>https://github.com/leipzig/standardized-velvet-assembly-report</p><p>Address of the bookmark: <a href="https://github.com/leipzig/standardized-velvet-assembly-report" rel="nofollow">https://github.com/leipzig/standardized-velvet-assembly-report</a></p>]]></description>
	<dc:creator>Poonam Mahapatra</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30207/gam-ngs-genomic-assemblies-merger-for-next-generation-sequencing</guid>
	<pubDate>Mon, 19 Dec 2016 06:07:05 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30207/gam-ngs-genomic-assemblies-merger-for-next-generation-sequencing</link>
	<title><![CDATA[GAM-NGS: genomic assemblies merger for next generation sequencing]]></title>
	<description><![CDATA[<p><span>GAM-NGS (Genomic Assemblies Merger for Next Generation Sequencing), whose primary goal is to merge two or more assemblies in order to enhance contiguity and correctness of both. GAM-NGS does not rely on global alignment: regions of the two assemblies representing the same genomic&nbsp;</span><em>locus</em><span>&nbsp;(called&nbsp;</span><em>blocks</em><span>) are identified through reads' alignments and stored in a&nbsp;</span><em>weighted</em><span>graph. The merging phase is carried out with the help of this weighted graph that allows an&nbsp;</span><em>optimal</em><span>&nbsp;resolution of&nbsp;</span><em>local</em><span>&nbsp;problematic regions.</span></p><p>Address of the bookmark: <a href="https://github.com/vice87/gam-ngs" rel="nofollow">https://github.com/vice87/gam-ngs</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30249/genome-assembly-tutorial</guid>
	<pubDate>Tue, 20 Dec 2016 07:56:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30249/genome-assembly-tutorial</link>
	<title><![CDATA[Genome Assembly Tutorial]]></title>
	<description><![CDATA[<p><span>If genomes were completely random sequences in a statistical sense, 'overlap-consensus-layout' method would have been enough to assemble large genomes from Sanger reads. In contrast, real genomes often have long repetitive regions, and they are hard to assemble using overlap-consensus-layout approach. De Bruijn graph-based assembly approach was originally proposed to handle the assembly of repetitive regions better.</span></p>
<p><span>More at&nbsp;http://www.homolog.us/Tutorials/index.php?p=1.4&amp;s=1</span></p><p>Address of the bookmark: <a href="http://www.homolog.us/Tutorials/index.php?p=1.4&amp;s=1" rel="nofollow">http://www.homolog.us/Tutorials/index.php?p=1.4&amp;s=1</a></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30336/finding-patterns-in-biological-sequences</guid>
	<pubDate>Thu, 22 Dec 2016 10:30:49 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30336/finding-patterns-in-biological-sequences</link>
	<title><![CDATA[Finding Patterns in Biological Sequences]]></title>
	<description><![CDATA[<p>In this report we provide an overview of known techniques for discovery of patterns of biological sequences (DNA and proteins). We also provide biological motivation, and methods of biological verification of such patterns. Finally we list publicly available tools and databases for pattern discovery. On-line supplement is available through http://genetics.uwaterloo.ca/&sim;tvinar/cs798g/motif.</p><p>Address of the bookmark: <a href="http://engr.case.edu/li_jing/papers/00798gpattern.pdf" rel="nofollow">http://engr.case.edu/li_jing/papers/00798gpattern.pdf</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30550/genomering-alignment-visualization-based-on-supergenome-coordinates</guid>
	<pubDate>Wed, 18 Jan 2017 10:24:10 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30550/genomering-alignment-visualization-based-on-supergenome-coordinates</link>
	<title><![CDATA[GenomeRing: alignment visualization based on SuperGenome coordinates]]></title>
	<description><![CDATA[<p>The number of completely sequenced genomes is continuously rising, allowing for comparative analyses of genomic variation. Such analyses are often based on whole-genome alignments to elucidate structural differences arising from insertions, deletions or from rearrangement events. Computational tools that can visualize genome alignments in a meaningful manner are needed to help researchers gain new insights into the underlying data. Such visualizations typically are either realized in a linear fashion as in genome browsers or by using a circular approach, where relationships between genomic regions are indicated by arcs. Both methods allow for the integration of additional information such as experimental data or annotations. However, providing a visualization that still allows for a quick and comprehensive interpretation of all important genomic variations together with various supplemental data, which may be highly heterogeneous, remains a challenge.</p>
<p>More at https://academic.oup.com/bioinformatics/article/28/12/i7/268598/GenomeRing-alignment-visualization-based-on</p><p>Address of the bookmark: <a href="http://it.informatik.uni-tuebingen.de/?page_id=185" rel="nofollow">http://it.informatik.uni-tuebingen.de/?page_id=185</a></p>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/pages/view/30654/source-code-and-pseudo-code</guid>
	<pubDate>Mon, 23 Jan 2017 10:17:35 -0600</pubDate>
	<link>https://bioinformaticsonline.com/pages/view/30654/source-code-and-pseudo-code</link>
	<title><![CDATA[Source Code and Pseudo Code !!]]></title>
	<description><![CDATA[<p>An <span style="text-decoration: underline;">algorithm</span> is a procedure for solving a problem in terms of the actions to be executed and the order in which those actions are to be executed. An algorithm is merely the sequence of steps taken to solve a problem. The steps are normally "sequence," "selection, " "iteration," and a case-type statement.</p><p>In C, "sequence statements" are imperatives. The "selection" is the "if then else" statement, and the iteration is satisfied by a number of statements, such as the "while," " do," and the "for," while the case-type statement is satisfied by the "switch" statement.</p><hr><p><span style="text-decoration: underline;">Pseudocode</span> is an artificial and informal language that helps programmers develop algorithms. Pseudocode is a "text-based" detail (algorithmic) design tool.</p><p>The rules of Pseudocode are reasonably straightforward. All statements showing "dependency" are to be indented. These include while, do, for, if, switch. Examples below will illustrate this notion.</p><p><strong> GUIDE TO PSEUDOCODE LEVEL OF DETAIL: Given record/file descriptions, pseudocode should be created in sufficient detail so as to directly support the programming effort. It is the purpose of pseudocode to elaborate on the algorithmic detail and not just cite an abstraction. </strong></p><hr><p>Examples:</p><p>1.</p><pre>If student's grade is greater than or equal to 60
    Print "passed"
else
    Print "failed"  
endif
</pre><hr><p>2.</p><pre>  
Set total to zero
Set grade counter to one
While grade counter is less than or equal to ten
    Input the next grade
    Add the grade into the total
endwhile 
Set the class average to the total divided by ten
Print the class average.
</pre><hr><p>3.</p><pre>Initialize total to zero
Initialize counter to zero
Input the first grade
while the user has not as yet entered the sentinel
   add this grade into the running total 
   add one to the grade counter  
   input the next grade (possibly the sentinel)
endwhile

if the counter is not equal to zero
   set the average to the total divided by the counter
   print the average  
else
   print 'no grades were entered' 
endif 
</pre><hr><p>4.</p><pre>initialize passes to zero
initialize failures to zero
initialize student to one
while student counter is less than or equal to ten
    input the next exam result  
    if the student passed</pre><p>add one to passes else add one to failures add one to student counter endif endwhile print the number of passes print the number of failures if eight or more students passed print "raise tuition" endif</p><hr><h3><strong>5.</strong></h3><pre>Larger example:  

NOTE:  NEVER ANY DATA DECLARATIONS IN PSEUDOCODE

Print out appropriate heading and make it pretty
While not EOF do:
     Scan over blanks and white space until a char is found 
	(get first character on the line)
     set can't-be-ascending-flag to 0
     set consec cntr to 1
     set ascending cntr to 1
     putchar first char of string to screen
     set read character to hold character
     While next character read != blanks and white space
          putchar out on screen
          if new char = hold char + 1
               add 1 to consec cntr
               set hold char = new char
               continue
          endif
          if new char &gt;= hold char 
               if consec cntr &lt; 3 
                    set consec cntr to 1
               endif
               set hold char = new char
               continue
          endif
          if new char &lt; hold char
               if consec cntr &lt; 3
                    set consec cntr to 1
               endif
               set hold char = new char
               set can't be ascending flag to 1
               continue
           endif
     end while
     if consec cntr &gt;= 3 
          printf (Appropriate message 1 and skip a line)
          add 1 to consec total
     endif
     if  can't be ascending flag = 0
          printf (Appropriate message 2 and skip a line)
          add 1 to ascending total
     else
          printf (Sorry message and skip a line)
          add 1 to sorry total
     endif
end While
Print out totals:  Number of consecs, ascendings, and sorries.
Stop
</pre><p>Some Keywords That Should be Used And Additional Points</p><p>For looping and selection, The keywords that are to be used include Do While...EndDo; Do Until...Enddo; While .... Endwhile is acceptable. Also, Loop .... endloop is also VERY good and is language independent. Case...EndCase; If...Endif; Call ... with (parameters); Call; Return ....; Return; When;</p><p>Always use scope terminators for loops and iteration.</p><p>As verbs, use the words Generate, Compute, Process, etc. Words such as set, reset, increment, compute, calculate, add, sum, multiply, ... print, display, input, output, edit, test , etc. with careful indentation tend to foster desirable pseudocode. Also, using words such as Set and Initialize, when assigning values to variables is also desirable.</p><p>More on Formatting and Conventions in Pseudocoding</p><ul>
<li>INDENTATION in pseudocode should be identical to its implementation in a programming language. Try to indent at least four spaces.</li>
<li>As noted above, the pseudocode entries are to be cryptic, AND SHOULD NOT BE PROSE. NO SENTENCES.</li>
<li>No flower boxes (discussed ahead) in your pseudocode.</li>
<li>Do not include data declarations in your pseudocode.</li>
<li>But do cite variables that are initialized as part of their declarations. E.g. "initialize count to zero" is a good entry.<hr>Function Calls, Function Documentation, and Pseudocode</li>
<li>Calls to Functions should appear as:
<ul>     </ul>
</li>
<li>Returns in functions should appear as:
<ul> </ul>
</li>
<li>Function headers should appear as:
<ul>     </ul>
</li>
<li>Note that in C, arguments and parameters such as "fieldn" could be written: "pointer to fieldn ...."</li>
<li>Functions called with addresses should be written as:
<ul>         </ul>
</li>
<li>Function headers containing pointers should be indicated as:
<ul>        </ul>
</li>
<li>Returns in functions where a pointer is returned:
<ul>   </ul>
</li>
<li>It would not hurt the appearance of your pseudocode to draw a line or make your function header line "bold" in your pseudocode. Try to set off your functions.</li>
<li>Try to use scope terminators in your pseudocode and source code too. It really hels the readability of the text.<hr>Source Code</li>
<li>EVERY function should have a flowerbox PRECEDING IT. This flower box is to include the functions name, the main purpose of the function, parameters it is expecting (number and type), and the type of the data it returns. All of these listed items are to be on separate lines with spaces in between each explanatory item.</li>
<li>FORMAT of flowerbox should be
<p>&nbsp;</p>
<pre>	 ********************************************************
	 Function:   ( cryptic text describing single function
		     ....... (indented like this) 	
		     .......
	 Calls:      Start listing functions "this" function calls
		     Show these functions:  one per line, indented

	 Called by:  List of functions that calls "this" function
		     Show these functions:  one per line, indented.

	 Input Parameters:  list, if appropriate; else None
	 
	 Returns:    List, if appropriate.
	 ****************************************************************
</pre>
</li>
<li>INDENTATION is critically important in Source Code. Follow standard examples given in class. If in doubt, ASK. Always indent statements within IFs, FOR loops, WILLE loops, SWITCH statements, etc. a consistent number of spaces, such as four. Alternatively, use the tab key. One or two spaces is insufficient.</li>
<li>Use scope terminators at the end of if statements, for statements, while statements, and at the end of functions. It will make your program much more readable.
<p><strong> SPELLING ERRORS ARE NOT ACCEPTABLE </strong></p>
</li>
</ul>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/videolist/watch/3925/genome-annotation</guid>
	<pubDate>Sun, 25 Aug 2013 10:53:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/videolist/watch/3925/genome-annotation</link>
	<title><![CDATA[Genome Annotation]]></title>
	<description><![CDATA[<iframe width="" height="" src="https://www.youtube-nocookie.com/embed/on4TMnuYTaU" frameborder="0" allowfullscreen></iframe>Dr. Rob Edwards describes some of the problems, challenges, and approches in genome annotation, with a particular emphasis on how the Fellowship for the Interpretation of Genomes (FIG) developed subsystems using the SEED database available at http://www.theseed.org/]]></description>
	
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30696/many-core-engine-mce-for-perl-example</guid>
	<pubDate>Tue, 31 Jan 2017 05:37:50 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30696/many-core-engine-mce-for-perl-example</link>
	<title><![CDATA[Many-Core Engine (MCE) for Perl example]]></title>
	<description><![CDATA[<p><span>MCE spawns a pool of workers and therefore does not fork a new process per each element of data. Instead, MCE follows a bank queuing model. Imagine the line being the data and bank-tellers the parallel workers. MCE enhances that model by adding the ability to chunk the next n elements from the input stream to the next available worker.</span></p>
<p>CORE MODULES</p>
<p>Three modules make up the core engine for MCE.</p>
<dl><dt id="MCE::Core"><a href="https://metacpan.org/pod/MCE#MCE::Core"><span></span></a><a></a><a href="https://metacpan.org/pod/distribution/MCE/lib/MCE/Core.pod">MCE::Core</a></dt><dd>
<p>Provides the Core API for Many-Core Engine. The various MCE options are described here.</p>
</dd><dt id="MCE::Signal"><a href="https://metacpan.org/pod/MCE#MCE::Signal"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Signal">MCE::Signal</a></dt><dd>
<p>Temporary directory creation, cleanup, and signal handling.</p>
</dd><dt id="MCE::Util"><a href="https://metacpan.org/pod/MCE#MCE::Util"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Util">MCE::Util</a></dt><dd>
<p>Utility functions for Many-Core Engine.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#MCE-EXTRAS"><span></span></a><a></a>MCE EXTRAS</p>
<p>There are 4 add-on modules for use with MCE.</p>
<dl><dt id="MCE::Candy"><a href="https://metacpan.org/pod/MCE#MCE::Candy"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Candy">MCE::Candy</a></dt><dd>
<p>Provides a collection of sugar methods and output iterators for preserving output order.</p>
</dd><dt id="MCE::Mutex"><a href="https://metacpan.org/pod/MCE#MCE::Mutex"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Mutex">MCE::Mutex</a></dt><dd>
<p>Provides a simple semaphore implementation supporting threads and processes.</p>
</dd><dt id="MCE::Queue"><a href="https://metacpan.org/pod/MCE#MCE::Queue"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Queue">MCE::Queue</a></dt><dd>
<p>Provides a hybrid queuing implementation for MCE supporting normal queues and priority queues from a single module. MCE::Queue exchanges data via the core engine to enable queuing to work for both children (spawned from fork) and threads.</p>
</dd><dt id="MCE::Relay"><a href="https://metacpan.org/pod/MCE#MCE::Relay"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Relay">MCE::Relay</a></dt><dd>
<p>Enables workers to receive and pass on information orderly with zero involvement by the manager process while running.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#MCE-MODELS"><span></span></a><a></a>MCE MODELS</p>
<p>The models take Many-Core Engine to a new level for ease of use. Two options (chunk_size and max_workers) are configured automatically as well as spawning and shutdown.</p>
<dl><dt id="MCE::Loop"><a href="https://metacpan.org/pod/MCE#MCE::Loop"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Loop">MCE::Loop</a></dt><dd>
<p>Provides a parallel loop utilizing MCE for building creative loops.</p>
</dd><dt id="MCE::Flow"><a href="https://metacpan.org/pod/MCE#MCE::Flow"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Flow">MCE::Flow</a></dt><dd>
<p>A parallel flow model for building creative applications. This makes use of user_tasks in MCE. The author has full control when utilizing this model. MCE::Flow is similar to MCE::Loop, but allows for multiple code blocks to run in parallel with a slight change to syntax.</p>
</dd><dt id="MCE::Grep"><a href="https://metacpan.org/pod/MCE#MCE::Grep"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Grep">MCE::Grep</a></dt><dd>
<p>Provides a parallel grep implementation similar to the native grep function.</p>
</dd><dt id="MCE::Map"><a href="https://metacpan.org/pod/MCE#MCE::Map"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Map">MCE::Map</a></dt><dd>
<p>Provides a parallel map model similar to the native map function.</p>
</dd><dt id="MCE::Step"><a href="https://metacpan.org/pod/MCE#MCE::Step"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Step">MCE::Step</a></dt><dd>
<p>Provides a parallel step implementation utilizing MCE::Queue between user tasks. MCE::Step is a spin off from MCE::Flow with a touch of MCE::Stream. This model, introduced in 1.506, allows one to pass data from one sub-task into the next transparently.</p>
</dd><dt id="MCE::Stream"><a href="https://metacpan.org/pod/MCE#MCE::Stream"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Stream">MCE::Stream</a></dt><dd>
<p>Provides an efficient parallel implementation for chaining multiple maps and greps together through user_tasks and MCE::Queue. Like with MCE::Flow, MCE::Stream can run multiple code blocks in parallel with a slight change to syntax from MCE::Map and MCE::Grep.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#MISCELLANEOUS"><span></span></a>MISCELLANEOUS</p>
<p>Miscellaneous additions included with the distribution.</p>
<dl><dt id="MCE::Examples"><a href="https://metacpan.org/pod/MCE#MCE::Examples"><span></span></a><a></a><a href="https://metacpan.org/pod/distribution/MCE/lib/MCE/Examples.pod">MCE::Examples</a></dt><dd>
<p>Describes various demonstrations for MCE including a Monte Carlo simulation.</p>
</dd><dt id="MCE::Subs"><a href="https://metacpan.org/pod/MCE#MCE::Subs"><span></span></a><a></a><a href="https://metacpan.org/pod/MCE::Subs">MCE::Subs</a></dt><dd>
<p>Exports functions mapped directly to MCE methods; e.g. mce_wid. The module allows 3 options; :manager, :worker, and :getter.</p>
</dd></dl>
<p><a href="https://metacpan.org/pod/MCE#REQUIREMENTS"><span></span></a>REQUIREMENTS</p>
<p>Perl 5.8.0 or later. PDL::IO::Storable is required in scripts running PDL.</p>
<p><a href="https://metacpan.org/pod/MCE#SOURCE-AND-FURTHER-READING"><span></span></a><a></a>SOURCE AND FURTHER READING</p>
<p>The source, cookbook, and examples are hosted at GitHub.</p>
<ul>
<li>
<p><a href="https://github.com/marioroy/mce-perl">https://github.com/marioroy/mce-perl</a></p>
</li>
<li>
<p><a href="https://github.com/marioroy/mce-cookbook">https://github.com/marioroy/mce-cookbook</a></p>
</li>
<li>
<p><a href="https://github.com/marioroy/mce-examples">https://github.com/marioroy/mce-examples</a></p>
</li>
</ul>
<p><a href="https://metacpan.org/pod/MCE#SEE-ALSO"><span></span></a><a></a>SEE ALSO</p>
<p><code>MCE::Shared</code>&nbsp;provides data sharing capabilities for&nbsp;<code>MCE</code>. It includes&nbsp;<code>MCE::Hobo</code>&nbsp;for running code asynchronously.</p>
<ul>
<li>
<p><a href="https://metacpan.org/pod/MCE::Shared">MCE::Shared</a></p>
</li>
<li>
<p><a href="https://metacpan.org/pod/MCE::Hobo">MCE::Hobo</a></p>
</li>
</ul><p>Address of the bookmark: <a href="https://github.com/marioroy/mce-examples" rel="nofollow">https://github.com/marioroy/mce-examples</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

<item>
  <guid isPermaLink='true'>https://bioinformaticsonline.com/opportunity/view/30747/11th-international-joint-conference-on-biomedical-engineering-systems-and-technologies</guid>
  <pubDate>Wed, 01 Feb 2017 17:39:27 -0600</pubDate>
  <link></link>
  <title><![CDATA[11th International Joint Conference on Biomedical Engineering Systems and Technologies]]></title>
  <description><![CDATA[
<p>BIOSTEC, the 11th International Joint Conference on Biomedical Engineering Systems and Technologies.<br /> Registration to BIOINFORMATICS allows free access to all other BIOSTEC conferences. </p>

<p>Upcoming Deadlines<br />Regular Paper Submission: July 31, 2017 <br />Regular Paper Authors Notification: October 16, 2017 <br />Regular Paper Camera Ready and Registration: October 30, 2017 </p>

<p>The purpose of the International Conference on Bioinformatics Models, Methods and Algorithms is to bring together researchers and practitioners interested in the application of computational systems, algorithmic concepts and information technologies to address challenging problems in Biomedical research with a particular focus on the emerging problems in Bioinformatics and computational biology. There is a tremendous need to explore how mathematical, statistical and computational models can be used to better understand biological processes and systems, while developing new methodologies and tools to analysis the massive currently-available biological data. Areas of interest to this community include systems biology, sequence analysis, biostatistics, image analysis, network and graph models, scientific data management and data mining, machine learning, pattern recognition, computational evolutionary biology, computational genomics and proteomics, and related areas.</p>
]]></description>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/30831/fsa-fast-statistical-alignment</guid>
	<pubDate>Mon, 06 Feb 2017 04:26:01 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/30831/fsa-fast-statistical-alignment</link>
	<title><![CDATA[FSA: Fast Statistical Alignment]]></title>
	<description><![CDATA[<p><span>FSA is a probabilistic multiple sequence alignment algorithm which uses a "distance-based" approach to aligning homologous protein, RNA or DNA sequences. Much as distance-based phylogenetic reconstruction methods like Neighbor-Joining build a phylogeny using only pairwise divergence estimates, FSA builds a multiple alignment using only pairwise estimations of homology. This is made possible by the sequence annealing technique for constructing a multiple alignment from pairwise comparisons, developed by Ariel Schwartz in&nbsp;</span><a href="http://www.eecs.berkeley.edu/Pubs/TechRpts/2007/EECS-2007-39.html">"Posterior Decoding Methods for Optimization and Control of Multiple Alignments</a><span>."</span></p>
<p>FSA brings the high accuracies previously available only for small-scale analyses of proteins or RNAs to large-scale problems such as aligning thousands of sequences or megabase-long sequences. FSA introduces several novel methods for constructing better alignments:</p>
<ul>
<li>FSA uses machine-learning techniques to estimate gap and substitution parameters on the fly for each set of input sequences. This "query-specific learning" alignment method makes FSA very robust: it can produce superior alignments of sets of homologous sequences which are subject to very different evolutionary constraints.</li>
<li>FSA is capable of aligning hundreds or even thousands of sequences using a randomized inference algorithm to reduce the computational cost of multiple alignment. This randomized inference can be over ten times faster than a direct approach with little loss of accuracy.</li>
<li>FSA can quickly align very long sequences using the "anchor annealing" technique for resolving anchors and projecting them with transitive anchoring. It then stitches together the alignment between the anchors using the methods described above.</li>
<li>The included GUI, MAD (Multiple Alignment Display), can display the intermediate alignments produced by FSA, where each character is colored according to the probability that it is correctly aligned (see the picture and&nbsp;<a href="http://fsa.sourceforge.net/images/Suchard_SIV.fsa.mov">movie</a>&nbsp;at the top of the page).</li>
</ul>
<p><span>You can see more information on the&nbsp;</span><a href="http://fsa.sourceforge.net/FAQ.html">FAQ</a><span>.&nbsp;</span></p>
<p>&nbsp;</p><p>Address of the bookmark: <a href="http://fsa.sourceforge.net/" rel="nofollow">http://fsa.sourceforge.net/</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

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