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 |
|
A6 F1 I1 R1
|
750 |
51.0 |
2595496 |
93.6% |
2429384 |
106.4 |
Breseq alignment
BRESEQ :: Evidence
|
| evidence |
seq id |
position |
mutation |
annotation |
gene |
description |
| RA |
NC_000913 |
1,814,212 |
C→T |
H116Y (CAC→TAC) |
katE → |
catalase HPII, heme d‑containing |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | NC_000913 | 1,814,212 | 0 | C | T | 100.0%
| 54.4
/ NA
| 18 | H116Y (CAC→TAC) | katE | catalase HPII, heme d‑containing |
| Reads supporting (aligned to +/- strand): ref base C (0/0); new base T (8/10); total (8/10) |
CAGTGAAAATTATGCGCTGACCACTAATCAGGGCGTGCGCATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCCACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGTTATTTCCAGCCATATAAAAGCTTAAGCGATATTACCAAAGCGGATTT > NC_000913/1814088‑1814321
|
cAGTGAAAATTATGCGCTGACCACTAATCAGGGCGTGTGCATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAg > 2:1225487/1‑139 (MQ=255)
gTGAAAATTATGCGCTGACCACTAATCAGGGCGTGCGCATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAgcg < 1:1221075/139‑1 (MQ=255)
gTGAAAATTATGCGCTGACCACTAATCAGGGCGTGCGCATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAgcg < 1:724331/139‑1 (MQ=255)
aGGGCGTGCGCATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCAcg > 2:1021025/1‑139 (MQ=255)
aGGGCGTGCACATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAGATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCAcg > 2:373816/1‑139 (MQ=255)
gcgcATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTa > 2:59831/1‑119 (MQ=255)
gcgcATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTa < 1:59831/119‑1 (MQ=255)
gcgcATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCa > 2:663606/1‑139 (MQ=255)
acgaTCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACgg < 1:431535/139‑1 (MQ=255)
tCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGTTATTTCCAGc < 1:1021025/139‑1 (MQ=255)
cTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGt < 2:1132490/126‑1 (MQ=255)
cTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGt > 1:1132490/1‑126 (MQ=255)
ccGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCt < 2:117423/113‑1 (MQ=255)
ccGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCt > 1:117423/1‑113 (MQ=255)
gTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCa > 1:529060/1‑89 (MQ=255)
gTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCa < 2:529060/89‑1 (MQ=255)
ggAAGATTTTATTCTGCGCGAGAAGATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGTTATTTCCAGCCATATAAAAGCTTAAGCGATATTACCAAAGCGGAt < 1:373816/139‑1 (MQ=255)
aaGATTTTATTCTGCGCGAGAAAATCACCTACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGTTATTTCCAGCCATATAAAAGCTTAAGCGATATTACCAAAGCGGAttt < 1:663606/139‑1 (MQ=255)
|
CAGTGAAAATTATGCGCTGACCACTAATCAGGGCGTGCGCATCGCCGACGATCAAAACTCACTGCGTGCCGGTAGCCGTGGTCCAACGCTGCTGGAAGATTTTATTCTGCGCGAGAAAATCACCCACTTTGACCATGAGCGCATTCCGGAACGTATTGTTCATGCACGCGGATCAGCCGCTCACGGTTATTTCCAGCCATATAAAAGCTTAAGCGATATTACCAAAGCGGATTT > NC_000913/1814088‑1814321
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG < 39 ≤ ATCG/ATCG < 40 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A