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 |
413,316 |
A→G |
100% |
R289R (CGT→CGC) |
lnt ← |
apolipoprotein N‑acyltransferase |
| |
seq id |
position |
ref |
new |
freq |
score (cons/poly) |
reads |
annotation |
genes |
product |
| * | minE | 413,316 | 0 | A | G | 79.3%
| 30.6
/ 2.1
| 24 | R289R (CGT→CGC) | lnt | apolipoprotein N‑acyltransferase |
| Reads supporting (aligned to +/- strand): ref base A (2/3); new base G (1/18); total (3/21) |
| Fisher's exact test for biased strand distribution p-value = 9.88e-02 |
| Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.16e-01 |
| Rejected as polymorphism: Variant not supported by required number of reads on each strand. |
GTATCGTAGCGGTTCTGCTTATTGAGACGCGCGTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTCCAGTGCTTTGAGGAACGGTTGCT > minE/413248‑413353
|
gTATCGTAGCGGTTCTGCTTATTGAGACGCGCGTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCa > 1:692732/1‑69 (MQ=255)
tATCGTAGCGGTTCTGCTTATTGAGACGCGCGTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCa > 1:2505720/1‑68 (MQ=255)
tATCGTAGCGGTTCTGCTTATTGAGACGCGCGTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCa > 1:3129310/1‑68 (MQ=255)
aTCGTAGCGGTTCTGTTTATTGAGACGCGCGTCGACAATCCCGG‑‑ACCAGCGAGCTACCTTTATCGCGCa > 1:748042/1‑69 (MQ=255)
cTGCTTATTGAGACGCGCGTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTc < 1:363713/69‑1 (MQ=255)
gcgcgTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTCCAGTGCTTTGAGGa > 1:2018344/1‑69 (MQ=255)
gcgcgTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTCCAGTGCTTTGAGGa > 1:2294955/1‑69 (MQ=255)
cgTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTCCAGTGCTTTGAGGAACg < 1:1415370/69‑1 (MQ=255)
cgTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTCCAGTGCTTTGAGGAACg < 1:2089790/69‑1 (MQ=255)
aCCTTTATCGCGCAACTCTCCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:2648144/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:919501/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1032285/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:790791/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:344507/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:3430976/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:3419718/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:2682686/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:2006545/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1944563/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1907775/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1771658/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1414616/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1367520/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1121884/47‑1 (MQ=255)
aCCTTTATCGCGCAACTCACAGTCCAGAGCTTTGAGGAACGGTTGCt < 1:1107102/47‑1 (MQ=255)
cTTTATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:525198/45‑1 (MQ=255)
tATCGCGCAACTCACCGTCCAGAGCTTTGAGGAACGGTTGCt < 1:395650/42‑1 (MQ=255)
|
GTATCGTAGCGGTTCTGCTTATTGAGACGCGCGTCGACAATCCCGGTTACCAGCGAGCTACCTTTATCACGCAACTCACCGTCCAGTGCTTTGAGGAACGGTTGCT > minE/413248‑413353
|
| Alignment Legend |
|---|
Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 21 ≤ ATCG/ATCG < 32 ≤ ATCG/ATCG < 36 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |
GATK/CNVnator alignment
N/A