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<channel>
	<title><![CDATA[BOL: All site questions]]></title>
	<link>https://bioinformaticsonline.com/answers/?offset=100</link>
	<atom:link href="https://bioinformaticsonline.com/answers/?offset=100" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/30365/why-megamerge-terminated-with-minimusfasta-1devnull-2devnull-failed-error</guid>
	<pubDate>Fri, 23 Dec 2016 14:11:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/30365/why-megamerge-terminated-with-minimusfasta-1devnull-2devnull-failed-error</link>
	<title><![CDATA[Why MeGAMerge terminated with minimus.fasta 1&gt;/dev/null 2&gt;/dev/null failed: error]]></title>
	<description><![CDATA[<p>I am trying to merge contigs, generated from different assemblies with MeGAMerge, but it failed after running few hour !! Following are the error I got on command prompt. Any suggestions??</p><blockquote><p>perl MeGAMerge-1.1.pl -f MergedDIR allContigs_MIRA_assembled.fa<br />Running Newbler assembly with 308261 sequences<br />runAssembly -force -large -rip -mi 98 -ml 80 -pairt -cpu 4 -a 200 -o MergedDIR/newbler MergedDIR/newblerIn.fasta 1&gt;/dev/null 2&gt;/dev/null<br />Running Minimus2 with 331388 sequences<br />minimus2 -D CONSERR=0.06 -D MINID=98 -D OVERLAP=80 MergedDIR/minimus.fasta 1&gt;/dev/null 2&gt;/dev/null<br />minimus2 -D CONSERR=0.06 -D MINID=98 -D OVERLAP=80 MergedDIR/minimus.fasta 1&gt;/dev/null 2&gt;/dev/null failed:<br />Died at MeGAMerge-1.1.pl line 283.<br /><br /></p></blockquote>]]></description>
	<dc:creator>Neel</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/30353/how-to-resolve-following-amos-installation-error</guid>
	<pubDate>Fri, 23 Dec 2016 08:30:34 -0600</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/30353/how-to-resolve-following-amos-installation-error</link>
	<title><![CDATA[How to resolve following Amos installation error ?]]></title>
	<description><![CDATA[<p>make[3]: Entering directory '/home/dept/Tools/amos-3.1.0/src/Align'<br />g++ -DHAVE_CONFIG_H -I. -I../..&nbsp; -I../../src/CelMsg -I../../src/Slice -I../../src/Common -I../../src/AMOS -I../../src/GNU -I../../src/Foundation&nbsp;&nbsp; -g -O2 -MT find-tandem.o -MD -MP -MF .deps/find-tandem.Tpo -c -o find-tandem.o find-tandem.cc<br />find-tandem.cc: In function &lsquo;int main(int, char**)&rsquo;:<br />find-tandem.cc:243:3: error: &lsquo;optarg&rsquo; was not declared in this scope<br />&nbsp;&nbsp; optarg = NULL;<br />&nbsp;&nbsp; ^<br />find-tandem.cc:245:63: error: &lsquo;getopt&rsquo; was not declared in this scope<br />&nbsp;&nbsp; while (!errflg &amp;&amp; ((ch = getopt (argc, argv, "f:u:l:x:m:k:h")) != EOF))<br />&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; ^<br />find-tandem.cc:258:55: error: &lsquo;optopt&rsquo; was not declared in this scope<br />&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; fprintf (stderr, "Unrecognized option -%c\n", optopt);<br />&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; ^<br />Makefile:918: recipe for target 'find-tandem.o' failed<br />make[3]: *** [find-tandem.o] Error 1<br />make[3]: Leaving directory '/home/urbe/Tools/amos-3.1.0/src/Align'<br />Makefile:325: recipe for target 'all-recursive' failed<br />make[2]: *** [all-recursive] Error 1<br />make[2]: Leaving directory '/home/urbe/Tools/amos-3.1.0/src'<br />Makefile:306: recipe for target 'all-recursive' failed<br />make[1]: *** [all-recursive] Error 1<br />make[1]: Leaving directory '/home/urbe/Tools/amos-3.1.0'<br />Makefile:244: recipe for target 'all' failed<br />make: *** [all] Error 2<br /><br /></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/30107/why-breakdancer-does-not-displays-the-amount-of-reads-supporting-sv</guid>
	<pubDate>Sat, 10 Dec 2016 16:44:38 -0600</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/30107/why-breakdancer-does-not-displays-the-amount-of-reads-supporting-sv</link>
	<title><![CDATA[Why BreakDancer does not displays the amount of reads supporting SV?]]></title>
	<description><![CDATA[<p><span>Using breakdancer the output consists of DEL, INV, INS, CTX and ITX. Using following commands:</span></p><p><span><span>bam2cfg.pl -g -h dis.bam normal.bam &gt; config_file.cfg</span><br /><span>breakdancer_max -d test config_file.cfg &gt; dis_normal.ctx</span></span></p><p><span>the 11th output column should displays the amount of reads supporting the called SV per bam-file. I have some unusual research in 11th column, can you please helpme to fix it.</span><br /><br /><br /></p>]]></description>
	<dc:creator>Bulbul</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/29164/which-are-the-best-known-web-server-for-protein-structure-prediction</guid>
	<pubDate>Sat, 10 Sep 2016 11:26:42 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/29164/which-are-the-best-known-web-server-for-protein-structure-prediction</link>
	<title><![CDATA[Which are the best known web server for protein structure prediction?]]></title>
	<description><![CDATA[<p>Anyone PhD here ? &nbsp;I need help in protein structure prediction.</p>]]></description>
	<dc:creator>Tayyba Jadoon</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/29118/how-to-validate-the-assembly</guid>
	<pubDate>Wed, 07 Sep 2016 03:27:12 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/29118/how-to-validate-the-assembly</link>
	<title><![CDATA[How to validate the assembly?]]></title>
	<description><![CDATA[<p>I am working on assembly of new genome. I am just wondering how to validate my assembled genome?&nbsp;</p>]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/29022/is-there-a-list-of-human-snps-associated-with-a-disease</guid>
	<pubDate>Mon, 05 Sep 2016 04:28:09 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/29022/is-there-a-list-of-human-snps-associated-with-a-disease</link>
	<title><![CDATA[Is there a list of human SNPs associated with a disease?]]></title>
	<description><![CDATA[<p>Looking for list of human SNPs associated with a disease?&nbsp;We need to evaluate a large number of human SNPs for their possible association with a disease. So far, the closest I've seen is SNPedia, but a database would be more helpful.<em><br /></em></p>]]></description>
	<dc:creator>Abhimanyu Singh</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/28931/how-to-intrepet-the-fastq-files</guid>
	<pubDate>Tue, 30 Aug 2016 05:54:01 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/28931/how-to-intrepet-the-fastq-files</link>
	<title><![CDATA[How to intrepet the FASTQ files?]]></title>
	<description><![CDATA[<p>How to intrepet the FASTQ files? What does Q score mean? Does + have any meanings?&nbsp;</p>]]></description>
	<dc:creator>Hardeep Kaur</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/28899/how-can-i-get-the-allele-frequency-of-my-variant</guid>
	<pubDate>Fri, 26 Aug 2016 03:20:06 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/28899/how-can-i-get-the-allele-frequency-of-my-variant</link>
	<title><![CDATA[How can I get the allele frequency of my variant?]]></title>
	<description><![CDATA[]]></description>
	<dc:creator>Shruti Paniwala</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/28830/how-to-extract-50-of-the-reads</guid>
	<pubDate>Thu, 18 Aug 2016 03:20:27 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/28830/how-to-extract-50-of-the-reads</link>
	<title><![CDATA[How to extract 50% of the reads?]]></title>
	<description><![CDATA[<p>I would like to extract a subset of PE reads (50%) and store them in seperate files. It should be in both way "split by middle" or "random". Is there any way to achieve it?</p>]]></description>
	<dc:creator>Radha Agarkar</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/answers/view/28393/what-does-phasing-mean-in-biologygenetics</guid>
	<pubDate>Mon, 11 Jul 2016 04:29:37 -0500</pubDate>
	<link>https://bioinformaticsonline.com/answers/view/28393/what-does-phasing-mean-in-biologygenetics</link>
	<title><![CDATA[What does phasing mean in biology/genetics?]]></title>
	<description><![CDATA[<p>Hi There,&nbsp;</p><p>I recently came across a new term "phasing". What does it mean? I only know it means "<span>genes separated by chromosome" only, can anyone please explain it for me.</span></p><p><span>Thanks in advance.</span></p>]]></description>
	<dc:creator>Priya Singh</dc:creator>
</item>

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