breseq  version 0.35.4  revision f352f80f4bc9
mutation predictions | marginal predictions | summary statistics | genome diff | command line log

Marginal read alignment evidence
  seq id position ref new freq score (cons/poly) reads annotation genes product
*NC_000913_3_bme_pgi526,7920AC33.3% 108.2 / 87.4 99S1178R (AGC→CGC) rhsDRhs protein with DUF4329 family putative toxin domain; putative neighboring cell growth inhibitor
*NC_000913_3_bme_pgi526,8000AG33.3% 125.0 / 77.1 96E1180E (GAA→GAGrhsDRhs protein with DUF4329 family putative toxin domain; putative neighboring cell growth inhibitor
*NC_000913_3_bme_pgi526,7960CG33.0% 140.4 / 103.1 98A1179G (GCG→GGG) rhsDRhs protein with DUF4329 family putative toxin domain; putative neighboring cell growth inhibitor

Marginal new junction evidence (lowest skew 10 of 47 shown)
  seq id position reads (cov) reads (cov) score skew freq annotation gene product
* ? NC_000913_3_bme_pgi = 454269140 (0.640)14 (0.240) 13/262 4.7 22.7% intergenic (+57/‑425) fimE/fimA tyrosine recombinase/inversion of on/off regulator of fimA/major type 1 subunit fimbrin (pilin)
?NC_000913_3_bme_pgi = 4542987 58 (0.990)intergenic (+353/‑129) fimE/fimA tyrosine recombinase/inversion of on/off regulator of fimA/major type 1 subunit fimbrin (pilin)
* ? NC_000913_3_bme_pgi = 417180352 (0.830)17 (0.270) 8/276 6.9 22.5% intergenic (+47/‑254) rrfB/murB 5S ribosomal RNA of rrnB operon/UDP‑N‑acetylenolpyruvoylglucosamine reductase, FAD‑binding
?NC_000913_3_bme_pgi = 4213162 66 (1.070)intergenic (+3/‑72) rrfE/yjaA 5S ribosomal RNA of rrnE operon/stress‑induced protein
* ? NC_000913_3_bme_pgi 4542683 =40 (0.640)7 (0.120) 7/262 7.0 12.7% intergenic (+49/‑433) fimE/fimA tyrosine recombinase/inversion of on/off regulator of fimA/major type 1 subunit fimbrin (pilin)
?NC_000913_3_bme_pgi 4542997 = 59 (1.000)intergenic (+363/‑119) fimE/fimA tyrosine recombinase/inversion of on/off regulator of fimA/major type 1 subunit fimbrin (pilin)
* ? NC_000913_3_bme_pgi 2617968 =NA (NA)6 (0.100) 6/266 7.6 NA noncoding (1/37 nt) REP182 (repetitive extragenic palindromic) element; contains 1 REP sequences REP182 (repetitive extragenic palindromic) element; contains 1 REP sequences
?NC_000913_3_bme_pgi 2618001 = NA (NA)noncoding (34/37 nt) REP182 (repetitive extragenic palindromic) element; contains 1 REP sequences REP182 (repetitive extragenic palindromic) element; contains 1 REP sequences
* ? NC_000913_3_bme_pgi = 417160740 (0.640)8 (0.130) 6/268 7.7 17.3% intergenic (+63/‑30) rrlB/rrfB 23S ribosomal RNA of rrnB operon/5S ribosomal RNA of rrnB operon
?NC_000913_3_bme_pgi = 4213022 NA (NA)intergenic (+76/‑18) rrlE/rrfE 23S ribosomal RNA of rrnE operon/5S ribosomal RNA of rrnE operon
* ? NC_000913_3_bme_pgi = 394668875 (1.190)8 (0.130) 6/268 7.7 10.0% intergenic (+81/‑12) rrlC/rrfC 23S ribosomal RNA of rrnC operon/5S ribosomal RNA of rrnC operon
?NC_000913_3_bme_pgi = 4171601 NA (NA)intergenic (+57/‑36) rrlB/rrfB 23S ribosomal RNA of rrnB operon/5S ribosomal RNA of rrnB operon
* ? NC_000913_3_bme_pgi 2726200 =NA (NA)8 (0.130) 6/268 7.7 NA intergenic (‑12/+81) rrfG/rrlG 5S ribosomal RNA of rrnG operon/23S ribosomal RNA of rrnG operon
?NC_000913_3_bme_pgi 2726224 = NA (NA)intergenic (‑36/+57) rrfG/rrlG 5S ribosomal RNA of rrnG operon/23S ribosomal RNA of rrnG operon
* ? NC_000913_3_bme_pgi = 22874451 (0.810)8 (0.130) 6/268 7.7 14.1% intergenic (+82/‑12) rrlH/rrfH 23S ribosomal RNA of rrnH operon/5S ribosomal RNA of rrnH operon
?NC_000913_3_bme_pgi 2726224 = NA (NA)intergenic (‑36/+57) rrfG/rrlG 5S ribosomal RNA of rrnG operon/23S ribosomal RNA of rrnG operon
* ? NC_000913_3_bme_pgi 225154 =NA (NA)6 (0.100) 6/270 7.7 NA noncoding (1384/1542 nt) rrsH 16S ribosomal RNA of rrnH operon
?NC_000913_3_bme_pgi 225176 = NA (NA)noncoding (1406/1542 nt) rrsH 16S ribosomal RNA of rrnH operon
* ? NC_000913_3_bme_pgi 4409590 =74 (1.180)5 (0.080) 5/266 8.2 6.2% coding (315/732 nt) rlmB 23S rRNA mG2251 2'‑O‑ribose methyltransferase, SAM‑dependent
?NC_000913_3_bme_pgi 4409626 = 82 (1.370)coding (351/732 nt) rlmB 23S rRNA mG2251 2'‑O‑ribose methyltransferase, SAM‑dependent