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  • weird sam flags

    Hi, there,

    I am trying to extract the mapped second read from a bam file (tophat output) using the following command:

    ====
    samtools view -f 80 accepted_hits.bam|head -3

    HWI-ST446:124987429:C0W8FACXX:6:1312:2288:18978 89 A_Cont1 3303 50 65M * 0 0 CACTGCTATATGGAGCGTACTGCCCATTATTCGCAATGCTACGATCAGCACAATCCAACCAATCGIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII AS:i:0 XN:i:0 XM:i:0 XO:i:0 XG:i:0 NM:i:0 MD:Z:65 YT:Z:UU NH:i:1
    HWI-ST446:124987429:C0W8FACXX:6:2204:4776:94752 81 A_Cont1 3312 50 65M A_Cont103 386245 0 ATGGAGCGTACTGCCCATTATTCGCAATGCTACGATCAGCACAATCCAACCAATCGTCACCAAGA IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII AS:i:0 XN:i:0 XM:i:0 XO:i:0 XG:i:0 NM:i:0 MD:Z:65 YT:Z:UU NH:i:1
    HWI-ST446:124987429:C0W8FACXX:6:2108:2853:42840 89 A_Cont1 3542 50 59M1002N6M * 0 0 TCTCTGAGCACAGCCATCAGATCATCGATATCCTGAGAATAGCCATTCTGTCCAGGATTCTGCTC IIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIIII AS:i:0 XM:i:0 XO:i:0 XG:i:0 MD:Z:65 NM:i:0 XS:A:- NH:i:1
    ====

    however all those flags, 89 or 81, indicate that they are actually the first read, according to the following website

    Flag: 81

    Explanation:
    V read paired
    read mapped in proper pair
    read unmapped
    mate unmapped
    V read reverse strand
    mate reverse strand
    V first in pair
    second in pair
    not primary alignment
    read fails platform/vendor quality checks
    read is PCR or optical duplicate
    supplementary alignment

    anybody can help me figure out why?

    Thank you very much!

  • #2
    If you want the second read from a pair, then "-f 129" would make more sense.

    Comment


    • #3
      Thank you for the message. It worked!

      Comment

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