Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_002947 | 3219006 | 3219106 | 101 | 2 [1] | [1] 2 | nfxB | HTH‑type transcriptional regulator NfxB |
TCAGGAACATTTCGGTGAAGATCGCCGCGCTGATATCGATACGGAAAGCCCCCGCCTGCTGGCCGCGCAGGAAGAAGGCATCCAGGGCGTCGGCATAGGCCCGCCACGGGCGGTTCGTCTCGCTGTCGTCGAACGAGTCCGGGCGGTACTGGAA > NC_002947/3218856‑3219009 | tCAGGAACATTTCGGTGAAGATCGCCGCGCTGATATCGATACGGAAAGCCCCCGCCTGCTGGCCGCGCAGGAAGAAGGCATCCAGGGCGTCGGCATAGGCCCGCCACGGGCGGTTCGTCTCGCTGTCGTCGAACGAGTCCGGGCGGTACt > 1:298958/1‑150 (MQ=255) gAACATTTCGGTGAAGATCGCCGCGCTGATATCGATACGGAAAGCCCCCGCCTGCTGGCCGCGCAGGAAGAAGGCATCCAGGGCGTCGGCATAGGCCCGCCACGGGCGGTTCGTCTCGCTGTCGTCGAACGAGTCCGGGCGGTACTGGaa < 2:306826/150‑1 (MQ=255) | TCAGGAACATTTCGGTGAAGATCGCCGCGCTGATATCGATACGGAAAGCCCCCGCCTGCTGGCCGCGCAGGAAGAAGGCATCCAGGGCGTCGGCATAGGCCCGCCACGGGCGGTTCGTCTCGCTGTCGTCGAACGAGTCCGGGCGGTACTGGAA > NC_002947/3218856‑3219009 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |