Entering edit mode
                    9.6 years ago
        Shicheng Guo
        
    
        ★
    
    9.6k
    Here, suppose I have lots of BSP primers, I want to know where these primers were located?
Therefore, I try to assemble them to fa and then transfer to fastq and then align them to human hg19 genome.
However, You can image, only few of them can be aligned since reads too short?
Any suggestion, how to align BSP primers to human hg19 genome?
my alignment command:
step 1:
bismark --non_directional ~/oasis/db/hg19/meth/bismark/ primer.fastq
step 2:
bismark --non_directional ~/oasis/db/hg19/meth/bismark/ primer.fastq -1 primer1.fastq -2 primer2.fastq
only 4 primers were successfully mapped to hg19
MBP3R   0       chr18   74692190        42      24M     *       0       0       TTATGTTTTTATTTAATTGTTGGT        IIIIIIIIIIIIIIIIIIIIIIII        NM:i:5  MD:Z:1C5C1C6C6C0        XM:Z:.h.....h.h......x......x   XR:Z:GA XG:Z:CT
Brain1L 16      chr4    104106668       42      24M     *       0       0       TTATTTTAAAGATTTGGGTAGTTT        IIIIIIIIIIIIIIIIIIIIIIII        NM:i:7  MD:Z:7G2A0G3A0A0A1G4    XM:Z:.......h...h.......hH...   XR:Z:GA XG:Z:GA
REG1AL  0       chr2    79347449        42      25M     *       0       0       AGTTGTGATTATTTTTAGTGTGTGT       IIIIIIIIIIIIIIIIIIIIIIIII       NM:i:7  MD:Z:8C0C1C1C0C0C8C0    XM:Z:........hh.h.hhx........x  XR:Z:CT XG:Z:CT
CUX2R   16      chr2    82200171        42      25M     *       0       0       TTTAATAATAATTAGTTTGTGTGGA       IIIIIIIIIIIIIIIIIIIIIIIII       NM:i:4  MD:Z:3G10A8A0G0 XM:Z:...h..............H.H.H.h  XR:Z:CT XG:Z:GA
The fastq file were as the following:
@INSL TTTTGGGGATTTGATTTAGT + IIIIIIIIIIIIIIIIIIII @INSR ACTCACCCTACAAATCCTCTAC + IIIIIIIIIIIIIIIIIIIIII @MBP3L GTGTATTTGGTTTTTTGAAGATT + IIIIIIIIIIIIIIIIIIIIIII @MBP3R ACCAACAATTAAATAAAAACATAA + IIIIIIIIIIIIIIIIIIIIIIII @WM1L GTTGGATGTGTTTGGTATATTAA + IIIIIIIIIIIIIIIIIIIIIII @WM1R AAAAACCAATAATAACCTTAAAA + IIIIIIIIIIIIIIIIIIIIIII @Brain1L TTATTTTAAAGATTTGGGTAGTTT + IIIIIIIIIIIIIIIIIIIIIIII @Brain1R AAATCCTTTACAACTCCCTAAC + IIIIIIIIIIIIIIIIIIIIII @REG1AL AGTTGTGATTATTTTTAGTGTGTGT + IIIIIIIIIIIIIIIIIIIIIIIII @REG1AR ATATCAAAATCTAAAATAAAAACCA + IIIIIIIIIIIIIIIIIIIIIIIII @CUX2L TTTGTAGAGGAATGGGTTGG + IIIIIIIIIIIIIIIIIIII @CUX2R TCCACACAAACTAATTATTATTAAA + IIIIIIIIIIIIIIIIIIIIIIIII
Hi - did you ever figure out how to get Bismark to recognize all primers? I am getting the same result with the same set of primers from Lehmann-Werman 2016. Thanks
Yes. Ask the authors where the primers located and then apply bismark to align these primer to these small regions.