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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/40140?offset=500</link>
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	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36861/eagler-a-scaffolding-tool-for-long-reads</guid>
	<pubDate>Mon, 04 Jun 2018 05:26:03 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36861/eagler-a-scaffolding-tool-for-long-reads</link>
	<title><![CDATA[EAGLER: a scaffolding tool for long reads.]]></title>
	<description><![CDATA[<p>EAGLER is a scaffolding tool for long reads. The scaffolder takes as input a draft genome created by any NGS assembler and a set of long reads. The long reads are used to extend the contigs present in the NGS draft and possibly join overlapping contigs. EAGLER supports both PacBio and Oxford Nanopore reads.</p>
<p>The tool should be compatible with most UNIX flavors and has been successfully tested on the following operating systems:</p>
<ul>
<li>Mac OS X 10.11.1</li>
<li>Mac OS X 10.10.3</li>
<li>Ubuntu 14.04 LTS</li>
</ul>

https://bib.irb.hr/datoteka/844447.Diplomski_2015_Luka_terbi.pdf<p>Address of the bookmark: <a href="https://github.com/mculinovic/EAGLER" rel="nofollow">https://github.com/mculinovic/EAGLER</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/file/view/36945/download-blasr-13-version</guid>
	<pubDate>Fri, 15 Jun 2018 03:01:20 -0500</pubDate>
	<link>https://bioinformaticsonline.com/file/view/36945/download-blasr-13-version</link>
	<title><![CDATA[Download blasr 1.3 version]]></title>
	<description><![CDATA[<p>DOWNLOAD LINK: https://github.com/BioInf-Wuerzburg/proovread/raw/master/util/blasr-1.3.1/blasr</p><p>I'm running "OPERA-LG_v2.0.5/bin/preprocess_reads.pl" and have the following error:</p><p>fail to open file './temporarySam'</p><p><br />[bwa_aln_core] write to the disk... 0.09 sec<br />[bwa_aln_core] 70778880 sequences have been processed.<br />[bwa_aln_core] calculate SA coordinate... 161.35 sec<br />[bwa_aln_core] write to the disk... 0.06 sec<br />[bwa_aln_core] 70989574 sequences have been processed.<br />[main] Version: 0.7.15-r1140<br />[main] CMD: bwa aln -t 30 all_p_ctg.fa -<br />[main] Real time: 2402.523 sec; CPU: 53429.488 sec<br />[E::hts_open_format] Failed to open file temporarySam<br />samtools sort: can't open "temporarySam": No such file or directory<br />[bwa_aln_core] convert to sequence coordinate... 1.00 sec<br />[bwa_aln_core] refine gapped alignments... 6.07 sec<br />[bwa_aln_core] print alignments... PREPROCESS:<br />Fastq format is recognized<br />[Thu Jun 14 18:16:47 2018] Building bwa index...<br />bwa index -p all_p_ctg.fa /home/urbe/Tools/OPERA-LG_v2.0.6/all_p_ctg.fa<br />[Thu Jun 14 18:18:35 2018] Finding the SA coordinates of the reads using BWA aln...<br />[Thu Jun 14 18:58:37 2018] Generate alignments of reads using bwa sampe...<br />bwa samse -n 1 all_p_ctg.fa read.sai - | grep '\(^@\|XT:A:U\)' | /usr/local/bin/samtools view -S -h -b -F 0x4 - | /usr/local/bin/samtools sort -@ 20 -no - temporarySam &gt; FALCON-Unzip-Scaff.bam<br />Mapping long-reads using blasr...<br />/home/urbe/Tools/SSpace/SSPACE-LongRead_v1-1/blasr -nproc 40 -m 1 -minMatch 5 -bestn 10 -noSplitSubreads -advanceExactMatches 1 -nCandidates 1 -maxAnchorsPerPosition 1 -sdpTupleSize 7 /media/urbe/MyDDrive/ONTdata/allONT/allONT.fasta /home/urbe/Tools/OPERA-LG_v2.0.6/all_p_ctg.fa | cut -d ' ' -f1-5,7-12 | sed 's/ /\t/g' &gt; FALCON-Unzip-Scaff.map<br />sh: 1: /home/urbe/Tools/SSpace/SSPACE-LongRead_v1-1/blasr: Permission denied<br />Sorting mapping results...<br />sort -k1,1 -k9,9g FALCON-Unzip-Scaff.map &gt; FALCON-Unzip-Scaff.map.sort<br />Analyzing sorted results...<br />Extracting linking information...<br />i3 2000 5000<br />i2 1000 2000<br />i4 5000 15000<br />i0 -200 300<br />i5 15000 40000<br />i1 300 1000<br />Repeat detection...<br />/home/urbe/Tools/OPERA-LG_v2.0.6/bin//filter_conflicting_edge.pl pairedEdges_i0 contig_length.dat 100 2<br />Illegal division by zero at /home/urbe/Tools/OPERA-LG_v2.0.6/bin//filter_conflicting_edge.pl line 93.<br />readline() on closed filehandle FILE at bin/OPERA-long-read.pl line 250.<br />rm anchor_contig_info.dat contig_length.dat filtered_edges.dat filtered_edges_cov.dat *.sai<br />rm: cannot remove 'anchor_contig_info.dat': No such file or directory<br />mv FALCON-Unzip-Scaff.bam FALCON-Unzip-Scaff-with-repeat.bam<br />/home/urbe/Tools/OPERA-LG_v2.0.6/bin//filter_repeat.pl FALCON-Unzip-Scaff-with-repeat.bam repeat.dat | /usr/local/bin/samtools view - -h -S -b &gt; FALCON-Unzip-Scaff.bam<br />rm FALCON-Unzip-Scaff-with-repeat.bam<br />/home/urbe/Tools/OPERA-LG_v2.0.6/bin/OPERA-LG config &gt; log<br />Analyzing 1 library: FALCON-Unzip-Scaff.bam<br />min library mean : 0<br />minimum contig length is 500<br />Current library: 1 out of 7<br />Analyzing file: pairedEdges_no_repeat_i0<br />Analyzing file: pairedEdges_no_repeat_i1<br />Analyzing file: pairedEdges_no_repeat_i2<br />Analyzing file: pairedEdges_no_repeat_i3<br />Analyzing file: pairedEdges_no_repeat_i4<br />Analyzing file: pairedEdges_no_repeat_i5<br />ln -s results/scaffoldSeq.fasta scaffoldSeq.fasta</p><p>To resolve this, try downloading blasr version 1.3 above and re-run :)</p>]]></description>
	<dc:creator>Jit</dc:creator>
	<enclosure url="https://bioinformaticsonline.com/file/download/36945" length="0" type="inode/x-empty" />
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