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 |
|
A1 F21 I0 R1
|
476 |
35.3 |
2812105 |
96.7% |
2719305 |
61.2 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
freq |
annotation |
gene |
description |
| RA |
W3110S.gb |
884,617 |
G→A |
79.0% |
V175I (GTT→ATT) |
cmr → |
multidrug efflux system protein |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | W3110S.gb | 884,617 | 0 | G | A | 79.0%
| 34.0
/ 6.0
| 19 | V175I (GTT→ATT) | cmr | multidrug efflux system protein |
| Reads supporting (aligned to +/- strand): ref base G (2/2); new base A (5/10); total (7/12) |
| Fisher's exact test for biased strand distribution p-value = 6.03e-01 |
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 1.00e+00 |
GCTCCGCTACTTGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTGTTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGCCATGCCTGAAACCGCCAC > W3110S.gb/884551‑884684
|
gCTCCGCTACTTGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATgtttattt < 1:1223645/70‑1 (MQ=255)
gCTCCGCTACTTGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATgtttattt < 1:1879714/70‑1 (MQ=255)
cTCCGCTACTTGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGtttgttttg < 1:1533107/71‑1 (MQ=255)
cTCCGCTACTTGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGtttgttttg < 1:1644763/71‑1 (MQ=255)
tGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCAt > 1:2409647/1‑71 (MQ=255)
cTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGc < 1:1918370/71‑1 (MQ=255)
tggGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGc < 1:329766/58‑1 (MQ=255)
cgcgGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGTATTGGCAGCGATCTCCt < 1:2375316/71‑1 (MQ=255)
cggcgTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCttt < 1:1176932/71‑1 (MQ=255)
gTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTGTTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCg < 1:289903/71‑1 (MQ=255)
aTCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCttttt < 1:1084540/65‑1 (MQ=255)
aTCCATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCttttt < 1:2001339/65‑1 (MQ=255)
tCCATGTGCTGCCCTGGGAGGGGATGTttattttgtt > 1:1873199/1‑37 (MQ=255)
ccATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTg > 1:520416/1‑70 (MQ=255)
cATGTGCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGc < 1:805747/70‑1 (MQ=255)
tgtgCTGCCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCg < 1:943989/49‑1 (MQ=255)
tgctgcCCTGGGAGGGGATGTTTGTTTTGTTTGCCGCATTGGCAGCGAtct < 1:1916343/51‑1 (MQ=255)
tgctgcCCTGGGAGGGGATGTTTGTTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAAc > 1:2730834/1‑69 (MQ=255)
tgctgcCCTGGGAGGGGATGTTTGTTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACgt > 1:151582/1‑70 (MQ=255)
tgctgcCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAAc > 1:2774711/1‑69 (MQ=255)
tgctgcCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAAc > 1:2800758/1‑69 (MQ=255)
ctgcCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGc < 1:2109996/71‑1 (MQ=255)
ctgcCCTGGGAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGc < 1:134378/71‑1 (MQ=255)
gggAGGGGATGTTTATTTTGTTTGCCGCATTGGCAGCGATCTCCttttt > 1:2111083/1‑49 (MQ=255)
tgtttattTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGc < 1:2511457/48‑1 (MQ=255)
tgtttattTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGc < 1:1442847/48‑1 (MQ=255)
tgtttattTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGCCATGCCTGAAACCGc < 1:1410462/70‑1 (MQ=255)
tttgttttgtTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGCCATGcc > 1:2197579/1‑59 (MQ=255)
tttattttgtTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGCCATGCCTGAAACCGCCAc > 1:2769825/1‑71 (MQ=255)
tgttttgtttGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCaa > 1:128119/1‑46 (MQ=255)
|
GCTCCGCTACTTGGTCCGCTGGTGGGCGCGGCGTGGATCCATGTGCTGCCCTGGGAGGGGATGTTTGTTTTGTTTGCCGCATTGGCAGCGATCTCCTTTTTCGGTCTGCAACGAGCCATGCCTGAAACCGCCAC > W3110S.gb/884551‑884684
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A