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	<id>http://bmcwiki.mit.edu/index.php?action=history&amp;feed=atom&amp;title=BioMicroCenter%3AGenome_Seq</id>
	<title>BioMicroCenter:Genome Seq - Revision history</title>
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	<updated>2026-04-29T03:19:24Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>http://bmcwiki.mit.edu/index.php?title=BioMicroCenter:Genome_Seq&amp;diff=58&amp;oldid=prev</id>
		<title>imported&gt;Michael Gravina: /* Sample Submission Guidelines */</title>
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		<updated>2011-09-30T16:39:46Z</updated>

		<summary type="html">&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;Sample Submission Guidelines&lt;/span&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{BioMicroCenter}}&lt;br /&gt;
&lt;br /&gt;
[[Image:BioMicroCenter-72_72_errorRate.png | 400px | right]]Both the HiSeq and the Genome Analyzer support &amp;#039;&amp;#039;de novo&amp;#039;&amp;#039; sequencing with extended read lengths, high passed-filter read counts, and the option to run lanes as paired-end for additional read length and long-range sequence information. &amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
== Sample Submission Guidelines ==&lt;br /&gt;
Users may submit unprepared genomic libraries to the BioMicro Center for [[BioMicroCenter:Illumina_Library_Preparation|Sample Prep]] followed by Illumina sequencing, or they may submit already-prepared libraries directly to sequencing.&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
Standard Illumina protocols for sample preparation can be found [[BioMicroCenter:Protocols| here]]. Illumina Paired End sample preparation kits can be purchased directly from Illumina or through the BioMicro Center for $3,600.00 plus shipping costs (10 sample preps per kit). To request an order or for more information please contact [[BioMicroCenter:People|Kevin Thai]]. Ready-for-sequencing samples should be gel-purified according to your protocol and contain least 5uL of solution at a concentration of at least 10 nM in EB/ Tween 0.1%. [[BioMicroCenter:Sequencing_Quality_Control|Quality control]] will be run on all submitted samples.&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
Samples generated using standard kits with Illumina PCR primers can be submitted without sequencing primers. Sample preparations using customized PCR primer sequences should be submitted with a complementary sequencing primer.&lt;br /&gt;
&lt;br /&gt;
[[BioMicroCenter:Forms#Downloads|&amp;#039;&amp;#039;&amp;#039;Sample Submission Forms&amp;#039;&amp;#039;&amp;#039;]]&lt;br /&gt;
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== Data ==&lt;br /&gt;
&lt;br /&gt;
Images acquired from the solexa sequencer are processed through the bundled solexa inage extraction pipeline to get the sequence and quality score for each base. The data is aligned to a reference genome, if requested, using an interative ELAND algorithm. An in-depth QC report is included in the package.&lt;/div&gt;</summary>
		<author><name>imported&gt;Michael Gravina</name></author>
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