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	<title><![CDATA[BOL: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data]]></title>
	<link>https://bioinformaticsonline.com/bookmarks/view/34292/automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data?</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/34292/automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data</guid>
	<pubDate>Mon, 13 Nov 2017 05:10:23 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/34292/automatic-filtering-trimming-error-removing-and-quality-control-for-fastq-data</link>
	<title><![CDATA[Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data]]></title>
	<description><![CDATA[<p><span>Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data</span><br><code>AfterQC</code><span>&nbsp;can simply go through all fastq files in a folder and then output three folders:&nbsp;</span><span>good</span><span>,&nbsp;</span><span>bad</span><span>&nbsp;and&nbsp;</span><span>QC</span><span>&nbsp;folders, which contains good reads, bad reads and the QC results of each fastq file/pair.</span><br><span>Currently it supports processing data from HiSeq 2000/2500/3000/4000, Nextseq 500/550, MiniSeq...and other&nbsp;</span><a href="http://support.illumina.com/help/SequencingAnalysisWorkflow/Content/Vault/Informatics/Sequencing_Analysis/CASAVA/swSEQ_mCA_FASTQFiles.htm">Illumina 1.8 or newer formats</a></p><p>Address of the bookmark: <a href="https://github.com/OpenGene/AfterQC" rel="nofollow">https://github.com/OpenGene/AfterQC</a></p>]]></description>
	<dc:creator>Rahul Nayak</dc:creator>
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