Kun:LabNotes/CpgSeq
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2007 <calendar> name=Kun:LabNotes/CpgSeq format=%name/%year-%month-%day date=2007/11/01 view=threemonths </calendar> 2008 <calendar> name=Kun:LabNotes/CpgSeq format=%name/%year-%month-%day date=2008/02/01 view=threemonths </calendar>
Probe design
Column synthesized probes (36)
- Kun:LabNotes/CpgSeq/2007-10-12: probe = revcomp(RP) + linker + FP
- Just realized that there was a mistake in probe design (11-20-2007). I assumed that after bisulfite treatment, the two strands are still complementary, which is not true. The probes have to be designed based on one strand only. If the forward PCR primers contain no "C" and the reverse primers contain no "G", that means the target strand is the forward strand. In that case, the padlock probes should be: revcomp(FP) + linker + RP. Here are the revised perl scripts: first 24 primers; second 12 primers. Here is the new probe file.
Agilent probes, V1
- Several considerations in this design include:
- Degenerate bases: I allowed at most two degenerate bases per primer. To convert PCR primers to padlock probes, multiple probes will be designed for one primer pair in order to cover all combinations.
- Gap size: The range of amplicon size is 225-275bp, so the gap size is approximately 185-225bp.
- Amplification adaptors and linker sequences: Version 7, same as the exonome probe E55kv1
AP1: GTAGACTGGAAGAGCACTGTT V4 AP2: GATCGGATACGCATGAGGCTA V4 Linker: GTTGGAGGCTCATCGTTCCTATTCAGCTGCAGATGTTATCGAGGTCCGAC ------ ---- ------ Mme I Alu I Mme I
- Here is the perl code for primer design. The input file is cpgIslandExt.txt downloaded from UCSC GoldenPath database.
- Conversion of PCR primers to padlock probes: AP1 + revcomp(FP) + linker + RP + AP2. codes.
Some statistics Total probes: 210,498 Total CpG islands: 23,496 Total non-overlapping regions: 12,037,010 bps Total captured sequences: 13,291,608 bps
- First oligo library (Cpg28k) includes chr6(9,875), chr20(6197), chr22(5358) and part of chrX(6558 of 8139).