New junction evidence
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913 1015208 =22 (0.850)7 (0.330) 3/110 2.1 24.4% coding (313/564 nt) pqiC DUF330 family putative lipoprotein
?NC_000913 1015844 = 25 (1.160)coding (130/168 nt) rmf ribosome modulation factor

TGGATCAACAGTTGCGCAACACCCTGGTTGCCAACCTGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTCGCT  >  NC_000913/1015143‑1015274
                                                                 |                                                                  
ggaggtttctttttaaagagacagaatcaggccattactaccctgtccgccatggcttctcgccagcc                                                                  >  2:482094‑M1/66‑68 (MQ=255)
      aaCAGTTGCGCAACACCCTGGTTGCCAACCTGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAg                                                            >  1:777293/1‑68 (MQ=255)
          ttttaaagagacagaatcaggccattactaccctgtccgccatggcttctcgccagcctcccagcctc                                                        <  1:801866‑M1/13‑1 (MQ=255)
          ttttaaagagacagaatcaggccattactaccctgtccgccatggcttctcgccagcctcccagcctc                                                        <  1:803093‑M1/13‑1 (MQ=255)
          gTTGCGCAACACCCTGGTTGCCAACCTGAGTACGCAACTGCCCGGCTGGGCGGTTGCCTCCCAGCctc                                                        <  2:211798/68‑1 (MQ=255)
                                  ccTGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCa                                <  1:427664/68‑1 (MQ=255)
                                  ccTGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCa                                <  2:777290/68‑1 (MQ=255)
                                    tGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAAt                              <  1:184362/68‑1 (MQ=255)
                                    tGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAAt                              <  2:136353/68‑1 (MQ=255)
                                    tGAGTACCCAACTGCCCGTCTGTGTGTTCGCCTCCCAGCCTCTGTGAAGCGCCCTGGACACGCTCAAt                              <  2:894899/68‑1 (MQ=255)
                                    ggAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAAt                              <  1:184363/67‑1 (MQ=255)
                                    cgAGTTCGCAACTGCCCGGCTGGGTGTTCGCCTCCCAGCCGCTGGGAAGCGCCCAGGACACGCTCAAt                              <  2:894898/67‑1 (MQ=255)
                                    cgAGTACGCAACTGCCCGGCTGGGTGGCTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAAt                              <  2:733283/67‑1 (MQ=255)
                                       accctgtccgccatggcttctcgccaGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGtt                           <  1:306247‑M1/42‑1 (MQ=255)
                                         aCGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGttgc                         >  2:68860/1‑66 (MQ=255)
                                         aCGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTAc                         >  2:112913/1‑68 (MQ=255)
                                          ctgtccgccatggcttctcgccaGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTAcc                        >  2:803090‑M1/24‑68 (MQ=255)
                                          ctgtccgccatggcttctcgccaGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTAcc                        >  2:801863‑M1/24‑68 (MQ=255)
                                          ctgtccgccatggcttctcgccaGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTAcc                        >  2:306247‑M1/24‑68 (MQ=255)
                                          ctgtccgccatggcttctcgccaGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTAcc                        >  2:397280‑M1/24‑68 (MQ=255)
                                              aCTGCCCGGCTGGGTGGTTGCCTCACAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGATACCGTaa                    >  1:940912/1‑68 (MQ=255)
                                                   ccGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACgg                 >  2:275833/1‑66 (MQ=255)
                                                   ccGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACgg                 <  1:275833/66‑1 (MQ=255)
                                                    cGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGt              <  2:966360/68‑1 (MQ=255)
                                                           gtggtTGCCGCCCAGCCGCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACgg       <  1:452571/68‑1 (MQ=255)
                                                             ggtTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTc     >  2:157382/1‑68 (MQ=255)
                                                             ggtTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTc     >  1:525874/1‑68 (MQ=255)
                                                              gtTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTCg    <  1:718577/68‑1 (MQ=255)
                                                                tGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTCGCt  <  2:168089/68‑1 (MQ=255)
                                                                tGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTCGCt  <  2:103668/68‑1 (MQ=255)
                                                                 |                                                                  
TGGATCAACAGTTGCGCAACACCCTGGTTGCCAACCTGAGTACGCAACTGCCCGGCTGGGTGGTTGCCTCCCAGCCTCTGGGAAGCGCCCAGGACACGCTCAATGTTACCGTAACGGAGTTTAACGGTCGCT  >  NC_000913/1015143‑1015274

Alignment Legend
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 8 ≤ ATCG/ATCG < 13 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG
Unaligned base: atcg    Masked matching base: atcg    Alignment gap:     Deleted base: 
Reads not counted as support for junction
read_name Not counted due to insufficient overlap past the breakpoint.
read_name Not counted due to not crossing MOB target site duplication.