Sample Resequencing Stats
Note: The mutation counts shown below represent unfiltered mutation sets.
| ALE, Flask, Isolate |
Predicted Mutations |
Mean Coverage |
Total Reads |
Percent Mapped |
Mapped Reads |
Average Read Length |
|
A2 F17 I0 R2
|
278 |
43.2 |
2215644 |
94.6% |
2095999 |
61.4 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
freq |
annotation |
gene |
description |
| RA |
minE |
1,249,224 |
C→T |
27.8% |
D17N (GAT→AAT) |
ruvB ← |
ATP‑dependent DNA helicase, component of RuvABC resolvasome |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | minE | 1,249,224 | 0 | C | T | 27.8%
| 56.3
/ 24.3
| 36 | D17N (GAT→AAT) | ruvB | ATP‑dependent DNA helicase, component of RuvABC resolvasome |
| Reads supporting (aligned to +/- strand): ref base C (15/11); new base T (7/3); total (22/14) |
| Fisher's exact test for biased strand distribution p-value = 7.06e-01 |
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.79e-01 |
TGAACGAACCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAATCATCCTTTACCTCATAACGCGG > minE/1249156‑1249291
|
tgAACGAACCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATc < 1:90374/69‑1 (MQ=255)
aacgaacCTGCGGCTGCCCAACATACTCTTCCAGTAATTTGTGGCGAATGGCGCGATCTGCTACATCTTcc > 1:460973/1‑71 (MQ=255)
aacgaacCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATTTTcc > 1:2087623/1‑71 (MQ=255)
cgaacCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCgg > 1:237573/1‑71 (MQ=255)
aacCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATTTTCCgg > 1:1505757/1‑69 (MQ=255)
aacCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATTTTCCGGCa < 1:140990/71‑1 (MQ=255)
ccTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCtt < 1:416720/63‑1 (MQ=255)
gCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATTTTCCGGCAAAGTg > 1:1926654/1‑71 (MQ=255)
gCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTg > 1:43541/1‑71 (MQ=255)
gCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTg > 1:1623097/1‑71 (MQ=255)
cTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGt < 1:1059898/66‑1 (MQ=255)
cTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGt < 1:1006042/66‑1 (MQ=255)
gACCAACATACTCTTCCAGTAATTTGGGGCGAATGGAGCGATCTGCTACATTTTCCGGCaaa > 1:1576348/1‑62 (MQ=255)
aTACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGaa < 1:936/70‑1 (MQ=255)
tACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATTTTCCGGCAAAGTGGTACCGGCAGAAAt > 1:934661/1‑71 (MQ=255)
tctTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGaaaa > 1:2155275/1‑51 (MQ=255)
ttCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATTTTCCGGCAAAGTGGTACCGGCAGAAATCAGAc > 1:1606519/1‑71 (MQ=255)
tAATTTGGGGCGAATGGCGCGATCTGCTACATTTTCCGGCAAAGTgg > 1:620700/1‑47 (MQ=255)
aaTTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGt > 1:1242667/1‑67 (MQ=255)
aTTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCt < 1:215733/71‑1 (MQ=255)
aTTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCt > 1:1300252/1‑71 (MQ=255)
tttGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCt < 1:159766/70‑1 (MQ=255)
tGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTAc > 1:1609622/1‑45 (MQ=255)
tGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTAc > 1:593810/1‑45 (MQ=255)
tGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCa > 1:1091011/1‑57 (MQ=255)
tGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTc < 1:514025/70‑1 (MQ=255)
tGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTc > 1:1948664/1‑70 (MQ=255)
gggCGAATGGCGCGATCTGCTACATTTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCaa < 1:1296643/70‑1 (MQ=255)
gggCGAATGGCGCGATCTGCTACATTTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAat < 1:387883/71‑1 (MQ=255)
tGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCa < 1:11100/48‑1 (MQ=255)
tGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCa < 1:1892053/48‑1 (MQ=255)
ggCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCtt > 1:1573669/1‑59 (MQ=255)
aTCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAatca > 1:809172/1‑59 (MQ=255)
aCATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACgg > 1:419323/1‑39 (MQ=255)
cATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAATCATCCTTTACCTCATAAcgc < 1:1143311/69‑1 (MQ=255)
cATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAATCATCCTTTACCTCATAAcgc < 1:244801/69‑1 (MQ=255)
cATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAATCATCCTTTACCTCATAACgcgg > 1:751968/1‑71 (MQ=255)
|
TGAACGAACCTGCGGCTGACCAACATACTCTTCCAGTAATTTGGGGCGAATGGCGCGATCTGCTACATCTTCCGGCAAAGTGGTACCGGCAGAAATCAGACGGTCTGCTTCAATCATCCTTTACCTCATAACGCGG > minE/1249156‑1249291
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A