Kun:LabNotes/CpgSeq
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<calendar> name=Kun:LabNotes/CpgSeq format=%name/%year-%month-%day date=2007/11/01 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: Version 4, same as the eSNP84k set
- Linker sequences: Version 7, same as the exonome probe E55kv1
AP1: GTAGACTGGAAGAGCACTGTT AP2: GATCGGATACGCATGAGGCTA Linker: GTTGGAGGCTCATCGTTCCTATTCAGCTGCAGATGTTATCGAGGTCCGAC ------ ---- ------ Mme I Alu I Mme I
- Conversion of PCR primers to padlock probes: AP1 + revcomp(FP) + linker + RP + AP2.
- Here is the perl code for primer design. The input file is cpgIslandExt.txt downloaded from UCSC GoldenPath database.