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 |
3,830,083 |
C→A |
intergenic (+9/+30) |
mutM → / ← coaD |
formamidopyrimidine/5‑formyluracil/ 5‑hydroxymethyluracil DNA glycosylase/pantetheine‑phosphate adenylyltransferase |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | W3110S.gb | 3,830,083 | 0 | C | A | 100.0%
| 47.6
/ NA
| 29 | intergenic (+9/+30) | mutM/coaD | formamidopyrimidine/5‑formyluracil/ 5‑hydroxymethyluracil DNA glycosylase/pantetheine‑phosphate adenylyltransferase |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base A (29/0); total (29/0) |
CGGCAGTGCCAGAAGTAATTCATGCGCGCCGGATGGCATACCATCCGGCATAAACGCTACG > W3110S.gb/3830057‑3830117
|
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:50846/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:9385/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:87673/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:87504/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:74579/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:72264/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:69770/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:67377/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:66195/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:65388/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:64830/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:63485/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:62970/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:55300/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:53926/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:16509/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:50226/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:4930/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:48060/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:47139/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:41537/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:37621/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:36127/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:29156/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:27174/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:2390/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:21668/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:21018/1‑61 (MQ=255)
cGGCAGTGCCAGAAGTAATTGATGCGAGCCGGATGGCATACCATCCGGCATAAacgctacg > 1:17302/1‑61 (MQ=255)
|
CGGCAGTGCCAGAAGTAATTCATGCGCGCCGGATGGCATACCATCCGGCATAAACGCTACG > W3110S.gb/3830057‑3830117
|
| 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