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 |
|
A5 F28 I1 R1
|
826 |
0.0 |
88706 |
74.7% |
66263 |
57.1 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
annotation |
gene |
description |
| RA |
W3110S.gb |
1,361,733 |
G→A |
S297F (TCT→TTT) |
puuA ← |
gamma‑Glu‑putrescine synthase |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | W3110S.gb | 1,361,733 | 0 | G | A | 100.0%
| 52.4
/ NA
| 31 | S297F (TCT→TTT) | puuA | gamma‑Glu‑putrescine synthase |
| Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (31/0); total (31/0) |
TCATCCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAGAAAGCACG > W3110S.gb/1361680‑1361741
|
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGccca > 1:55072/1‑59 (MQ=38)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:62412/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:9483/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:83796/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:81738/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:81235/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:79137/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:77717/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:77227/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:75359/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:75220/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:7194/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:70863/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:66022/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:6386/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:63582/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:13672/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:60178/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:59983/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:58640/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:49914/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:46366/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:39262/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:36757/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:36641/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:303/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:2906/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:26007/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:16372/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAca > 1:13915/1‑61 (MQ=39)
tcatcCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAAAGAGCAc > 1:7266/1‑61 (MQ=255)
|
TCATCCCGGCGAGCATCTTTTTCAGCAGCGGCGAATCTTCGCCTTCCGCGTCAGAAAGCACG > W3110S.gb/1361680‑1361741
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 27 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A