Missing coverage evidence... | ||||||||||
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seq id | start | end | size | ←reads | reads→ | gene | description | |||
* | * | ÷ | NC_013198 | 392237–393747 | 474456–472946 | 79200–82220 | 40 [39] | [39] 41 | is11–[is26] | 84 genes is11, LGG_00384, LGG_00385, LGG_00386, slyA, LGG_00388, LGG_00389, aroE, LGG_00391, LGG_00392, manR, LGG_00394, frwA1, frwB1, frwC1, tal, rpe, ulaA, ulaB, pts, is12, ulaC, tktN, tktC, scrK, lacR, frwA2, frwB2, frwC2, is13, fba, gatY, pts, pts, manZ, tal, LGG_00419, yhfZ, LGG_00421, LGG_00422, LGG_00423, php, yhfS, yhfX, YHFW, ilvH, LGG_00429, cbiO, cbiQ, LGG_00432, menC, nagZ, is14, tnpR, LGG_00437, LGG_00438, LGG_00439, LGG_00440, srtC1, spaA, spaB, spaC, is15, LGG_00446, LGG_00447, LGG_00448, LGG_00449, ybjD, is16, is17, is18, is19, LGG_00455, pacL, is20, is21, napA, is22, is23, is24, eriC, is25, LGG_00465, [is26] |