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	<title><![CDATA[BOL: How to get better alignment results of PAcBio data?]]></title>
	<link>https://bioinformaticsonline.com/answers/view/39385/how-to-get-better-alignment-results-of-pacbio-data?</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/39385/how-to-get-better-alignment-results-of-pacbio-data</guid>
	<pubDate>Wed, 22 May 2019 02:01:07 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/39385/how-to-get-better-alignment-results-of-pacbio-data</link>
	<title><![CDATA[How to get better alignment results of PAcBio data?]]></title>
	<description><![CDATA[<p>HI! I am Nadia.</p><p>I am trying to align PAcBio data (data from third generation sequencer) using bwa mem. I am getting very less number of aligned reads in SAM file having coverage of less than 10X. I tried to use minimap2 as well for alignment but again the quality of sam file isn,t good. I am getting only few unique reads and they are aligning on reference with soft clipping. Moreover, my SAM file contains many cases of multimapping. The read length of spots is &gt;2kb.</p><p>What other options are available to get better alignment results? I am working with this data for the very first time.</p>]]></description>
	<dc:creator>Nadia Baig</dc:creator>
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