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		<id>http://amos.sourceforge.net/wiki/index.php?title=AMOScmp-shortReads-alignmentTrimmed&amp;diff=51&amp;oldid=prev</id>
		<title>Mcschatz: New page: == Overview ==  AMOScmp-shortReads-alignmentTrimmed is a modified version of AMOScmp designed for alignment based trimming and assembling of short reads. Differences compared to AMOScmp:  ...</title>
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				<updated>2009-07-07T20:43:06Z</updated>
		
		<summary type="html">&lt;p&gt;New page: == Overview ==  AMOScmp-shortReads-alignmentTrimmed is a modified version of AMOScmp designed for alignment based trimming and assembling of short reads. Differences compared to AMOScmp:  ...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Overview ==&lt;br /&gt;
&lt;br /&gt;
AMOScmp-shortReads-alignmentTrimmed is a modified version of AMOScmp designed for alignment based trimming and assembling of short reads.&lt;br /&gt;
Differences compared to AMOScmp:&lt;br /&gt;
&lt;br /&gt;
* runs a reference based alignment trimming of the reads prior to the assembly&lt;br /&gt;
* uses a smaller nucmer alignment cluster size&lt;br /&gt;
* uses a smaller make-consensus alignment wiggle value&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Algorithm ==&lt;br /&gt;
&lt;br /&gt;
The trimming is performed as a set of several processing steps following the alignment of reads to the reference.&lt;br /&gt;
Steps:&lt;br /&gt;
&lt;br /&gt;
1. identify the zero coverage regions in the reference sequence (delta2cvg)&lt;br /&gt;
2. extract the read clear ranges from the alignment file (delta2clr)&lt;br /&gt;
3. extend the read clear ranges for the ones adjacent to zero coverage regions (delta2clr)&lt;br /&gt;
4. update the bank with the new clear ranges (updateClrRanges)&lt;br /&gt;
5. update the alignment file with the new read lengths and clear ranges (updateDeltaClr)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Three Perl scripts recently added to the AMOS package (release 2.0.8) are called by the AMOScmp-shortReads-alignmentTrimmed pipeline. Their main purpose is to parse and update the nucmer alignment(delta) file.&lt;br /&gt;
Scripts:&lt;br /&gt;
&lt;br /&gt;
* [[delta2cvg]]: computes the alignment coverage of the reference sequence(s)&lt;br /&gt;
* [[delta2clr]]: computes the minimum 5&amp;#039; and maximum 3&amp;#039; alignment coordinates of the aligned reads&lt;br /&gt;
* [[updateDeltaClr]]: shifts the alignment coordinates 5&amp;#039; positions to the left (for reads with the minimum 5&amp;#039;&amp;gt;0)&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== Parameters ==&lt;br /&gt;
&lt;br /&gt;
AMOScmp-shortReads-alignmentTrimmed also allows additional parameters than AMOScmp.&lt;br /&gt;
Defaults:&lt;br /&gt;
&lt;br /&gt;
   MINCLUSTER  = 16&lt;br /&gt;
   MINMATCH    = 16&lt;br /&gt;
   MINLEN      = 24  # delta-filter -l 24&lt;br /&gt;
   MINOVL      = 5&lt;br /&gt;
   MAXTRIM     = 10&lt;br /&gt;
   MAJORITY    = 50&lt;br /&gt;
   CONSERR     = 0.06&lt;br /&gt;
   ALIGNWIGGLE = 2&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== How to Run ==&lt;br /&gt;
&lt;br /&gt;
Input files:&lt;br /&gt;
Assuming that prefix is the name of the organism to assemble, two files are required:&lt;br /&gt;
&lt;br /&gt;
   1. prefix.1con : reference sequence: a related organism sequence in FASTA format (complete or well assembled, usually downloaded from GenBank)&lt;br /&gt;
   2. prefix.afg : AMOS message file that contains read/fragment messages corresponding to each short read; it can be generated using the toAmos script&lt;br /&gt;
&lt;br /&gt;
Example:&lt;br /&gt;
&lt;br /&gt;
   $ toAmos -s prefix.seq -o prefix.afg                           # create an AMOS message file from short read FASTA sequences&lt;br /&gt;
   $ AMOScmp-shortReads-alignmentTrimmed prefix                   # assemble reads (alignment based trimming, default parameters)&lt;/div&gt;</summary>
		<author><name>Mcschatz</name></author>	</entry>

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