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	<id>http://bmcwiki.mit.edu/index.php?action=history&amp;feed=atom&amp;title=BioMicroCenter%3APEM</id>
	<title>BioMicroCenter:PEM - Revision history</title>
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	<updated>2026-04-19T13:46:24Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>http://bmcwiki.mit.edu/index.php?title=BioMicroCenter:PEM&amp;diff=107&amp;oldid=prev</id>
		<title>imported&gt;Stuart S. Levine: /* Pricing */</title>
		<link rel="alternate" type="text/html" href="http://bmcwiki.mit.edu/index.php?title=BioMicroCenter:PEM&amp;diff=107&amp;oldid=prev"/>
		<updated>2010-04-01T01:36:54Z</updated>

		<summary type="html">&lt;p&gt;&lt;span class=&quot;autocomment&quot;&gt;Pricing&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;
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==Paired End Sequencing==&lt;br /&gt;
&lt;br /&gt;
[[Image:RtColumnProdServPEModule.jpg|right|100px]]&lt;br /&gt;
The paired-end module of the GAII system allows both ends of a DNA fragment to be sequenced. This gives more specificity to alignment algorithms, especially in highly repetitive regions. The paired-end module allows for up to 36 bases of each end to be sequenced during the same sequencing run. Longer runs (up to 72nt) should be available in early 2009.&lt;br /&gt;
http://illumina.com/downloads/ch2-ILMN_ProdGuide_DNAsequencing.pdf&lt;br /&gt;
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== Sample Submission Guidelines ==&lt;br /&gt;
&lt;br /&gt;
&amp;#039;&amp;#039;&amp;#039;Users are required to prepare their own libraries for sequencing&amp;#039;&amp;#039;&amp;#039; by following the corresponding Illumina [[BioMicroCenter:Protocols| Protocols]]. If this is a service that you would like the BMC to perform in the future please visit the [[BioMicroCenter:Ideas|Ideas]] page.  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|Ali Perrotta]]&lt;br /&gt;
&lt;br /&gt;
Samples which are ready for sequencing should be gel-purified according to your protocol, and provided as at least 5uL of solution at a concentration of at least 10 nM in EB/ Tween 0.1%. To calculate your sample’s molar concentration, you must know the average length of your product. &lt;br /&gt;
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When submitting a sample you must supply the BMC with the molar concentration, average length, and species of origin of all samples. &lt;br /&gt;
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We encourage all those submitting samples to allow us to run QC to obtain/confirm concentration information. For more information on our QC methods please see the [[BioMicroCenter:Sequencing_Quality_Control|Sequencing Quality Control]] page.&lt;br /&gt;
&lt;br /&gt;
Samples generated using standard kits with Illumina PCR primers can be submitted without sequencing primers. Custom sample preparations using customized PCR primer sequences should be provided along with a complementary sequencing primer.&lt;br /&gt;
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[[BioMicroCenter:Forms#Downloads|Sample Submission Forms]]&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. Sample QC report is here.&lt;br /&gt;
&lt;br /&gt;
== Turnaround Time ==&lt;br /&gt;
&lt;br /&gt;
Each Genome Analyzer processes 8 samples per run, or 7 samples plus a control. The control is typically used to improve sequence quality. Full flowcells can be run usually within two weeks of submission. Partial submissions of less than eight samples (or 7 with control) are put into a project queue, where they join existing samples or await others before processing. Wait times for partial submissions vary depending on demand from other users. &lt;br /&gt;
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Once the run has begun approximately 10 days are required for clustering, sequencing, and data analysis for a Paired End read (36bp read x 2).&lt;br /&gt;
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== Pricing ==&lt;br /&gt;
&lt;br /&gt;
Illumina sequencing is currently available &amp;#039;&amp;#039;&amp;#039;only&amp;#039;&amp;#039;&amp;#039; for labs associated with the BioMicro Center [[BioMicroCenter:CoreDeps|Core departments]].&lt;br /&gt;
&lt;br /&gt;
{| border=1 align=&amp;quot;right&amp;quot;&lt;br /&gt;
 ! ILLUMINA SEQUENCING&lt;br /&gt;
 !width=100| [[BioMicroCenter:CoreDeps|CORE LAB]]/MIT&lt;br /&gt;
 !width=100| Non-MIT&lt;br /&gt;
 !width=100| unit&lt;br /&gt;
 ! Notes&lt;br /&gt;
 |-&lt;br /&gt;
 | Paired End (36+36nt)&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $1,450&lt;br /&gt;
|align=&amp;quot;right&amp;quot;| $2,175&lt;br /&gt;
 |align=&amp;quot;center&amp;quot;| per lane&lt;br /&gt;
 | Includes quality control (RT-PCR and BioAnalyzer), sequencing, genome alignment and data storage of Firecrest files for 2 yrs.&lt;br /&gt;
 |-&lt;br /&gt;
 | Add&amp;#039;l 36nt&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $300&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $450&lt;br /&gt;
 |align=&amp;quot;center&amp;quot;| per lane&lt;br /&gt;
 |  &lt;br /&gt;
 |-&lt;br /&gt;
 | Sample Multiplexing&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $50&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $75&lt;br /&gt;
 |align=&amp;quot;center&amp;quot;| per 10 samples&lt;br /&gt;
 | Combined over the whole order. Only applies to samples combined by BCM technicians.&lt;br /&gt;
 |-&lt;br /&gt;
 | Add&amp;#039;l Repriming&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $300&lt;br /&gt;
 |align=&amp;quot;right&amp;quot;| $450&lt;br /&gt;
 |align=&amp;quot;center&amp;quot;| per flow cell&lt;br /&gt;
 | Uses 6nt. Cost is divided by number of lanes requiring repriming. Repriming is required for standard Illumina multiplexing.&lt;br /&gt;
 |}&lt;br /&gt;
&amp;lt;BR&amp;gt;&lt;br /&gt;
&lt;br /&gt;
.&lt;/div&gt;</summary>
		<author><name>imported&gt;Stuart S. Levine</name></author>
	</entry>
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