Noi/NOTES/2012-8-1: Difference between revisions

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'''Report file of epMotion run:'''<br>
'''Report file of epMotion run:'''<br>
= Bisulfite conversion using EZ-96 DNA Methylation-Lightning™ MagPrep =
= Bisulfite conversion using EZ-96 DNA Methylation-Lightning™ MagPrep =
* will be filled later
* Performed bisulfite conversion manually and followed the product's protocol: [[Media:EZ-96DNAMethylation-LightninMagPrep.pdf| EZ-96DNAMethylation-LightninMagPrep.pdf]]
* Elute with elution buffer 40ul
* Elute with elution buffer 40ul



Revision as of 01:02, 4 August 2012

[Link to calendar]

WGBS sequencing library preparation using KAPA protocol (Eppendorf) and epMotion (Repeat!)

  • Continued from: http://genome-tech.ucsd.edu/LabNotes/index.php/Noi/NOTES/2012-7-27
  • I have sheared gDNA from the previous batch left ~22ul (conc. ~40ng/ul based on conc. from the HAPMAP plate). I added 25ul H2O to each tube -> total volume 47ul, and will prepare end repair reaction mix in 23ul
  • Note: Since I start with sheared 880ng, I reduce the amount of enzymes in each step, but keep total volume the same (except ligation 50ul -> 40ul total)

End repair

Total reaction 70.00 ul
DNA 47.00 ul
End repair reaction mix 23.00 ul


KAPA End repair mix 1x rxn 8x rxn mix
10X End repai buffer 7.00 56.00
KAPA End repair enzyme 3.00 24.00
H2O 13.00 104.00
Total 23.00 184.00
  • Aliquot to column #1: 23ul

A-tailing

A-tailing reaction mix: Total 30ul/reaction

A-tailing reaction mix 1x rxn 8x rxn mix
KAPA 10X A-tailing buffer 3.00 24.00
KAPA A-tailing enzyme 2.00 16.00
H2O 25.00 200.00
Total 30.00 240.00
  • Aliquot to column #2: 30ul

Adapter ligation

Adapter ligation mix: Total 40ul/reaction -> 10ul is methylation adapters

Ligation reaction mix 1x rxn 8x rxn mix
KAPA 5X Ligation buffer 8.00 64.00
KAPA DNA ligase 3.00 24.00
H2O 19.00 152.00
Total 30.00 240.00
  • Aliquot to column #3: 30ul

Methylation adapter preparation

Alan's note:

  1. Use the methylated adapter with paired-end pcr primer pairs(PCR primer PE1.0 and PCR primer PE 2.0) provided in illumina's paired end genomic DNA sample prep kit
  2. Use 10ul of methylated adapter to 5ug gDNA insert, if starting DNA amount is less than 5ug, titrate the volume of adapter reagent accordingly to maintain 10:1 ratio of DNA. Since I used 1ug of DNA, used 2ul of adapters, but dilute to final volume 10ul (This volume is larger than KAPA protocol, but the total amount is the same)

Prepare adapter 2ulx 8rxn --> 16.00ul
H2O 8ulx8rxn --> 64.00ul
Total 80.00ul

Reagent preparation

Reagents 1rxn Min volume in 30mL reservior
AMPure beads 120ul ~1.1mL
20% PEG/2.5M NaCl 90+50 = 140ul ~1.4mL
80% EtOH 140x6times ~10mL
H2O for elution 22ul ~1mL

epMotion run

Report file of epMotion run:

Bisulfite conversion using EZ-96 DNA Methylation-Lightning™ MagPrep

Amplification of bisulfite sequencing llibraries (Test)

  • Test if the adapter ligation reaction worked before amplify the libraries with barcoded primers
Components 1rxn 10 rxn mix
DNA template (1:9 diluted) 2.50 0.00
10uM PCR_F 0.50 5.00
10uM PCR_R.Ind1 0.50 5.00
2x iQ MM 12.50 125.00
H2O 9.00 90.00
Total 25.00 250.00
  • Aliquot 22.5ul, add 2.5ul of bis-cvt DNA template (2.5 out of 40ul)
Program
98C 2min (98C 15sec ->	64C 20sec -> 72C 30sec) x15cycles -> 72C 3min -> 15CHold

qPCR results

  • Will be added later


  • Loaded 2.5 ul of bis-cvt DNA (#1 & #4) and 2.5ul of amplified amplicons

File:ZhangLab 2 2012-08-02 11hr 31min-HAPMAP-bis-test.jpg

Amplification of bisulfite sequencing libraries with N2 barcoded primers

Components 1 rxn 26rxn mix
DNA template 10.00 0.00
10uM PCR_F 2.00 52.00
10uM PCR_R.Indx (1-8) 2.00 0.00
2x iQ Supermix 50.00 1,300.00
H2O 36.00 936.00
  • Aliquot 88ul, add 2ul of 10uM PCR_R Ind (Ind1-8), 10ul of bis-cvt DNA template
Program	
98C 2min (98C 15sec ->	64C 20sec -> 72C 30sec) x10cycles -> 72C 3min -> 15CHold
Sample ID Labeling Indx
WGBS.GM12891 #1 PCR_R.N2Indx1
WGBS.GM12892 #2 PCR_R.N2Indx2
WGBS.GM10861 #3 PCR_R.N2Indx3
WGBS.GM11994 #4 PCR_R.N2Indx4
WGBS.GM11995 #5 PCR_R.N2Indx5
WGBS.GM18506 #6 PCR_R.N2Indx6
WGBS.GM18507 #7 PCR_R.N2Indx7
WGBS.GM18505 #8 PCR_R.N2Indx8

qPCR results

  • Will be added later


  • Purified sequencing libraries with 0.8x vol AMPure bead with epMotion (3 strips), eluted with 25ul EB for each well -> total volume at the end ~70ul

File:ZhangLab 2 2012-08-02 16hr 05min bead-HAPMAP-WGBS.jpg

PAGE quantification of 400-600bp fragments

  • Dr. Zhang suggested to cut the band around 400-600bp because 250bp is too short for PE sequencing.
  • Perform PAGE size-selection of the size range 400-600bp for a small scale sequencing. Then pooled 60ng of each library and performed PAGE size-selection.

File:ZhangLab 2 2012-08-02 16hr 05min bead-HAPMAP-WGBS-400-600bp PQ.jpg

Lab IDs Final conc.

of 400-600bp (ng/ul)

Total yields in 70ul (ng) Volume for 60ng (ul)
#1 13.50 945.28 4.44
#2 9.66 675.94 6.21
#3 11.24 786.94 5.34
#4 13.64 955.09 4.40
#5 13.85 969.55 4.33
#6 8.95 626.85 6.70
#7 12.40 867.78 4.84
#8 11.29 790.44 5.31


PAGE size-selection

File:ZhangLab 2 2012-08-02 18hr 23min-PAGE-SS.jpg

  • Note: From the image, it seemed like I cut the gel a little smaller than 600bp
  • Resuspend with 12ul H2O each tube -> total volume 24ul.
  • Quantify concentration by PAGE quantification (also verify the size of sequencing libraries) and by dsDNA Qubit
  • Library ID: NP_WGBS_HAPMAP1-8_July27