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 I2 R1
|
524 |
31.4 |
1748232 |
97.8% |
1709770 |
80.6 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
annotation |
gene |
description |
| RA |
NC_000913 |
1,450,418 |
C→T |
G311D (GGT→GAT) |
tynA ← |
copper‑containing amine oxidase |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | NC_000913 | 1,450,418 | 0 | C | T | 100.0%
| 86.9
/ NA
| 26 | G311D (GGT→GAT) | tynA | copper‑containing amine oxidase |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (16/10); total (16/10) |
CATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGCCCAGTAG > NC_000913/1450342‑1450495
|
cATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATcttc > 1:256245/1‑81 (MQ=255)
aTAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGAtcttct > 1:256246/1‑81 (MQ=255)
aaCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCt > 1:256249/1‑80 (MQ=255)
aaCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCt > 1:256259/1‑80 (MQ=255)
aCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCtt > 1:256254/1‑80 (MQ=255)
aCTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCtt < 2:256222/80‑1 (MQ=255)
cTGCCAGAGCGACGCGGTCACGACCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTaa < 1:256223/81‑1 (MQ=255)
gCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAAc > 2:256250/1‑80 (MQ=255)
gCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAAc > 1:256256/1‑80 (MQ=255)
ccGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAAc < 2:256224/79‑1 (MQ=255)
cGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGAt > 2:256243/1‑81 (MQ=255)
cACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCt > 2:256253/1‑80 (MQ=255)
ccATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCa < 2:256225/81‑1 (MQ=255)
aaaTGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGa < 2:256226/80‑1 (MQ=255)
aaaTGGGCGTGCGGTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGAc > 1:256264/1‑81 (MQ=255)
ggTCATTGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGtt < 2:256227/81‑1 (MQ=255)
ttGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGa < 1:256228/81‑1 (MQ=255)
ttGGCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGa < 2:256229/81‑1 (MQ=255)
ggCACCGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATg > 1:256260/1‑81 (MQ=255)
ccGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGAt < 2:256230/81‑1 (MQ=255)
cGGAACTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGAtg > 2:256271/1‑81 (MQ=255)
aaCTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGc < 2:256231/81‑1 (MQ=255)
aaCTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGc > 2:256261/1‑81 (MQ=255)
cTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGcc > 1:256268/1‑80 (MQ=255)
cTACCGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGcc > 2:256257/1‑80 (MQ=255)
cGGATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGCCCag > 1:256284/1‑79 (MQ=255)
ggATCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGCCCagtag > 1:256258/1‑81 (MQ=255)
|
CATAGGCTTAACTGCCGGAGCAACGCGGTCACGGCCATCAAATGGGCGTGCGGTCATTGGCACCGGAACTACCGGACCTTCTTCAATCTTAACGATTTTTTTCTGTTCTAAATCAACGACCGCCACCAGGTTTTCGATGGGATGTGCCCAGTAG > NC_000913/1450342‑1450495
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 31 ≤ ATCG/ATCG < 34 ≤ ATCG/ATCG < 38 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A