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archive:lab_protocols:solid_run1 [2010/03/29 22:04]
hyjkim removed
archive:lab_protocols:solid_run1 [2015/09/02 16:57] (current)
ceisenhart ↷ Page moved from lab_protocols:solid_run1 to archive:lab_protocols:solid_run1
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 ===== Solid Sequencing Run 1 ===== ===== Solid Sequencing Run 1 =====
 +==== Meta ====
 +
 +Prepared by: Eveline Hesson
 +
 +Date:
 +
 Overview: Overview:
  
 ==== DNA Extraction ==== ==== DNA Extraction ====
- 
 ==== Library Preparation ==== ==== Library Preparation ====
 +
 +This library was prepared by following ABI's standard 2x25 mate-pair library preparation protocol. {{:​lab_protocols:​solid3_libprep_guide.pdf|}}
 +
 +Detailed notes of the protocol can be found in the following pdf: {{:​lab_protocols:​solid-mate-pair-notes.pdf|}}
 +
 +=== 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.
 +
 +Total recovered DNA after hydroshear was 217 µl or 26 µg.
 +
 +=== Repair the DNA Ends ===
 +
 +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.
 +
 +=== Purify the End-Repaired DNA using the QIAquick Gel Extraction Kit ===
 +
 +
  
 ==== Emulsion PCR ==== ==== Emulsion PCR ====
  
 ==== Sequencing Data ==== ==== Sequencing Data ====
archive/lab_protocols/solid_run1.1269900246.txt.gz · Last modified: 2010/03/29 22:04 by hyjkim