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 F1 I1 R1
|
315 |
33.5 |
1889570 |
98.7% |
1865005 |
80.6 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
annotation |
gene |
description |
| RA |
NC_000913 |
1,301,472 |
C→T |
V97V (GTC→GTT) |
oppA → |
oligopeptide ABC transporter periplasmic binding protein |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | NC_000913 | 1,301,472 | 0 | C | T | 100.0%
| 97.7
/ NA
| 27 | V97V (GTC→GTT) | oppA | oligopeptide ABC transporter periplasmic binding protein |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (15/12); total (15/12) |
GCTTACTGGTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTCTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGTATAGCT > NC_000913/1301396‑1301548
|
gCTTACTGGTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGa > 2:252357/1‑81 (MQ=255)
cTTACTGGTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGAc < 1:252319/81‑1 (MQ=255)
aCTGGTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCtt > 1:252360/1‑81 (MQ=255)
aCTGGTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCt < 1:252320/80‑1 (MQ=255)
gTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTcc < 1:252321/79‑1 (MQ=255)
gCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGc < 2:252322/81‑1 (MQ=255)
gCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGc > 1:252361/1‑81 (MQ=255)
ttGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTa > 1:252365/1‑78 (MQ=255)
aCGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGAt < 2:252323/80‑1 (MQ=255)
aTCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAAt > 2:252358/1‑81 (MQ=255)
cAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGt > 2:252355/1‑81 (MQ=255)
ggCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATgg > 1:252364/1‑80 (MQ=255)
cGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCAc > 1:252375/1‑81 (MQ=255)
atacTGGGATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTcac < 2:252324/78‑1 (MQ=255)
gggATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGca > 1:252376/1‑80 (MQ=255)
ggATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGcac < 1:252325/80‑1 (MQ=255)
gATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGcac > 1:252362/1‑79 (MQ=255)
gATAATAAAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACaa < 1:252326/81‑1 (MQ=255)
taaAGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACtt < 2:252327/81‑1 (MQ=255)
aaaGACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACttt > 1:252363/1‑81 (MQ=255)
gACGCGAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTtgtg > 1:252367/1‑81 (MQ=255)
gcgAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGta > 2:252373/1‑80 (MQ=255)
gAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGTATAg > 1:252366/1‑81 (MQ=255)
gAAAGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGAAGGCACGCCAGTCACAGCACAAGACTTTGTGTATAg > 1:252377/1‑81 (MQ=255)
aaGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGTATAGCt < 2:252328/81‑1 (MQ=255)
aaGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGTATAGCt < 1:252330/81‑1 (MQ=255)
aaGTTTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGTATAGCt < 1:252329/81‑1 (MQ=255)
|
GCTTACTGGTCAGCGATCTTGACGGTCATCCAGCACCTGGCGTCGCTGAATCCTGGGATAATAAAGACGCGAAAGTCTGGACCTTCCATTTGCGTAAAGATGCGAAATGGTCTGATGGCACGCCAGTCACAGCACAAGACTTTGTGTATAGCT > NC_000913/1301396‑1301548
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 35 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A