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 F21 I0 R1
|
148 |
22.8 |
1772010 |
97.0% |
1718849 |
61.3 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
freq |
annotation |
gene |
description |
| RA |
W3110S.gb |
3,224,816 |
C→T |
43.3% |
H147Y (CAT→TAT) |
ebgC → |
cryptic beta‑D‑galactosidase, beta subunit |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | W3110S.gb | 3,224,816 | 0 | C | T | 43.3%
| 10.5
/ 34.6
| 30 | H147Y (CAT→TAT) | ebgC | cryptic beta‑D‑galactosidase, beta subunit |
| Reads supporting (aligned to +/- strand): ref base C (9/8); new base T (8/5); total (17/13) |
| Fisher's exact test for biased strand distribution p-value = 7.21e-01 |
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.76e-01 |
TCGGTTTATCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGCTACCCTACTCATTTTCGGAGAT > W3110S.gb/3224749‑3224884
|
tCGGTTTATCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTat < 1:22117/70‑1 (MQ=255)
ttATCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTataacaaa > 1:717292/1‑71 (MQ=255)
ttATCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCataacaa > 1:643945/1‑70 (MQ=255)
aTCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCataacaaat < 1:1363507/70‑1 (MQ=255)
tCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTataacaaat < 1:1025480/69‑1 (MQ=255)
gCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCataa > 1:928642/1‑61 (MQ=255)
gCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCataa > 1:1216516/1‑61 (MQ=255)
aCGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTATAACAAATAACAACTAcgg > 1:55054/1‑71 (MQ=255)
tCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCataacaaataac < 1:1274419/57‑1 (MQ=255)
aaaaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTATAACAAATAACAACTa > 1:1755521/1‑58 (MQ=255)
aaaaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTATAACAAATAACAACTACGGCGGCAAAAgg < 1:602569/71‑1 (MQ=255)
aaaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTATAACAAATAACAACTACGGCGGCaaaa > 1:1635200/1‑68 (MQ=255)
aaaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTATAACAAATAACAACTACGGCGGCAAAAg > 1:838618/1‑69 (MQ=255)
aaaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGa < 1:1594071/71‑1 (MQ=255)
aaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCTataacaaa > 1:1485118/1‑47 (MQ=255)
aaGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCataacaaataacaa > 1:1724762/1‑53 (MQ=255)
aGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGt < 1:1026254/71‑1 (MQ=255)
aGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGt < 1:740488/71‑1 (MQ=255)
gTTCTCAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTg < 1:1189683/70‑1 (MQ=255)
tctcAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTg > 1:68211/1‑68 (MQ=255)
ctcAAAGTCACCATCGAAGATGGTTATTTCTATAACAAATAACAACTAcgg < 1:1602598/51‑1 (MQ=255)
gTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGc > 1:1065863/1‑71 (MQ=255)
ccATCGAAGATGGTTATTTCTATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCa > 1:330783/1‑63 (MQ=255)
tCGAAGATGGTTATTTCTATAACAAATAACAACTACGGCGGCAAAAGGAGTTTgc < 1:418750/55‑1 (MQ=255)
cGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGCTACCCTAc > 1:216061/1‑71 (MQ=255)
aTTTCTATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGCTACCCTACTCATTTTCg > 1:11821/1‑69 (MQ=255)
aTTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGttt < 1:368158/41‑1 (MQ=255)
tCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTgcc < 1:1009267/41‑1 (MQ=255)
tCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGCTACCCTACTCATTTTCGGAGAt > 1:1286358/1‑71 (MQ=255)
tCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGCTACCCTACTCATTTTCGGAGAt > 1:965388/1‑71 (MQ=255)
|
TCGGTTTATCTGCAATAACGCGGTCAAAAAAGTGGTTCTCAAAGTCACCATCGAAGATGGTTATTTCCATAACAAATAACAACTACGGCGGCAAAAGGAGTTTGCCGCCACCGCTACCCTACTCATTTTCGGAGAT > W3110S.gb/3224749‑3224884
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 14 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A