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archive:lab_protocols:solid_run1 [2010/03/29 22:04] hyjkim removed |
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| ===== Solid Sequencing Run 1 ===== | ===== Solid Sequencing Run 1 ===== | ||
| + | ==== Meta ==== | ||
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| + | Prepared by: Eveline Hesson | ||
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| + | Date: | ||
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| Overview: | Overview: | ||
| ==== DNA Extraction ==== | ==== DNA Extraction ==== | ||
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| ==== Library Preparation ==== | ==== Library Preparation ==== | ||
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| + | This library was prepared by following ABI's standard 2x25 mate-pair library preparation protocol. {{:lab_protocols:solid3_libprep_guide.pdf|}} | ||
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| + | Detailed notes of the protocol can be found in the following pdf: {{:lab_protocols:solid-mate-pair-notes.pdf|}} | ||
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| + | === Shearing DNA === | ||
| + | Extracted genomic DNA was sheared using a [[https://products.appliedbiosystems.com/ab/en/US/adirect/ab?cmd=catNavigate2&catID=604432|Hydroshear]] to an approximate size of 4-5kb. The shearing was done using Standard_Assembly, sc 15, 5 cycles for 150 µl total volume. | ||
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| + | Total recovered DNA after hydroshear was 217 µl or 26 µg. | ||
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| + | === Repair the DNA Ends === | ||
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| + | The DNA ends of sheared gDNA were blunt ended and phosphorylated using Epicentre's End-It DNA repair Kit. 217 µl of sheared gDNA was reacted in a total volume of 400 µl according to manufacturer's standards. The reaction was incubated for 30 minutes at room temperature. | ||
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| + | === Purify the End-Repaired DNA using the QIAquick Gel Extraction Kit === | ||
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| ==== Emulsion PCR ==== | ==== Emulsion PCR ==== | ||
| ==== Sequencing Data ==== | ==== Sequencing Data ==== | ||