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 |
3,105,716 |
G→A |
M1M (ATG→ATA) † |
nupG → |
nucleoside:H(+) symporter NupG |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | NC_000913 | 3,105,716 | 0 | G | A | 100.0%
| 87.3
/ NA
| 26 | M1M (ATG→ATA) † | nupG | nucleoside:H(+) symporter NupG |
| Reads supporting (aligned to +/- strand): ref base G (0/0); new base A (14/12); total (14/12) |
ATAGAATCCCATCATCTCGCACGGTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATGAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTGACGACCCTC > NC_000913/3105638‑3105788
|
aTAGAATCCCATCATCTCGCACGGTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATaaa < 2:540184/81‑1 (MQ=255)
tcatcTCGCACGGTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGc < 2:540185/81‑1 (MQ=255)
ctcGCACGGTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCt > 2:540207/1‑81 (MQ=255)
gCACGGTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTg < 2:540186/79‑1 (MQ=255)
gTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATcc < 1:540187/81‑1 (MQ=255)
aTGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCctctct < 1:540188/81‑1 (MQ=255)
cTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCt < 2:540189/81‑1 (MQ=255)
ttCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCa < 1:540190/80‑1 (MQ=255)
cAAACACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGtt > 2:540212/1‑81 (MQ=255)
aaCACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTtct > 2:540226/1‑81 (MQ=255)
aaCACTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTtct < 1:540191/81‑1 (MQ=255)
cTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTtctgtct > 1:540220/1‑81 (MQ=255)
cTCATCCGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTtctgtct < 2:540192/81‑1 (MQ=255)
ccGCATCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTggg > 2:540206/1‑81 (MQ=255)
aTCACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAg < 1:540193/81‑1 (MQ=255)
cACGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGtt > 2:540216/1‑81 (MQ=255)
aCGATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTg > 2:540218/1‑81 (MQ=255)
gATGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGc > 2:540217/1‑81 (MQ=255)
aTGTGAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCt > 2:540222/1‑81 (MQ=255)
tgAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAGTCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTga < 2:540194/80‑1 (MQ=255)
gAGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTgac > 1:540232/1‑80 (MQ=255)
aGGAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTgacga > 1:540228/1‑81 (MQ=255)
ggAAATTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTgacgac > 1:714564/1‑81 (MQ=255)
aaTTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTGACGACCCt > 2:540223/1‑81 (MQ=255)
aTTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTGACGACCCTc < 2:540195/81‑1 (MQ=255)
aTTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTGACGACCCTc < 1:540196/81‑1 (MQ=255)
aTTAACATAAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTGACGACCCTc > 2:540231/1‑81 (MQ=255)
|
ATAGAATCCCATCATCTCGCACGGTCAAATGTGCTTTTTCAAACACTCATCCGCATCACGATGTGAGGAAATTAACATGAATCTTAAGCTGCAGCTGAAAATCCTCTCTTTTCTGCAGTTCTGTCTGTGGGGAAGTTGGCTGACGACCCTC > NC_000913/3105638‑3105788
|
| 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