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 |
|
A2 F1 I0 R1
|
4577 |
57.4 |
3436498 |
77.7% |
2670158 |
63.4 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
freq |
annotation |
gene |
description |
| RA |
minE |
413,751 |
G→T |
51.6% |
T144T (ACC→ACA) |
lnt ← |
apolipoprotein N‑acyltransferase |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | minE | 413,751 | 0 | G | T | 51.6%
| ‑4.5
/ 35.8
| 31 | T144T (ACC→ACA) | lnt | apolipoprotein N‑acyltransferase |
| Reads supporting (aligned to +/- strand): ref base G (9/6); new base T (10/6); total (19/12) |
| Fisher's exact test for biased strand distribution p-value = 1.00e+00 |
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.41e-01 |
ATCGGTGCCAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCAGAGGGCAGGGGCGGCAATCGC > minE/413686‑413810
|
aTCGGTGCCAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTc > 1:365569/1‑69 (MQ=255)
aTCGGTGCCAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTc > 1:2000204/1‑69 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:245815/1‑61 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:907219/1‑61 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:3154908/1‑61 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:2627872/1‑61 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:249840/1‑61 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:1876743/1‑61 (MQ=255)
ccAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGt > 1:1704957/1‑61 (MQ=255)
ttAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACcgcg > 1:2211810/1‑67 (MQ=255)
ttAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCgcgc > 1:1315239/1‑68 (MQ=255)
ttAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCgcgc > 1:3377681/1‑68 (MQ=255)
tAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAg < 1:235062/54‑1 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGa < 1:349955/58‑1 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCAc > 1:808474/1‑69 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCAc > 1:2049875/1‑69 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCAc > 1:1126059/1‑69 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCAc > 1:782014/1‑69 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCAc > 1:405499/1‑69 (MQ=255)
aaTCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCAc > 1:3092122/1‑69 (MQ=255)
tCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACtt < 1:2753943/69‑1 (MQ=255)
gCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACt < 1:1629706/64‑1 (MQ=255)
gCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACt < 1:3050283/64‑1 (MQ=255)
tataGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCa < 1:1133920/67‑1 (MQ=255)
tataGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCa < 1:1252460/67‑1 (MQ=255)
tataGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCa < 1:1360923/67‑1 (MQ=255)
tataGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCa < 1:1472601/67‑1 (MQ=255)
tataGCCGAACTGTAACCACGGGAAGCCTGTTAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCa < 1:1582003/67‑1 (MQ=255)
gCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCAGAGGGc > 1:851023/1‑69 (MQ=255)
cGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCAGAGGGCAGGGGCGGCAATCGc < 1:1582643/69‑1 (MQ=255)
gCCTGTTAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCa < 1:2731093/42‑1 (MQ=38)
|
ATCGGTGCCAGCCCTTTTAACGGGCCATCAATCTGGCTATAGCCGAACTGTAACCACGGGAAGCCGGTCAGTACCCAACCGCGCAGAAACTCGGTCACTTGCCAGAGGGCAGGGGCGGCAATCGC > minE/413686‑413810
|
| 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