Flowcell QC summary (lanes 1,2,3,4,5,6,7,8)
Date |
Flowcell |
Lane |
Platform Unit |
Readgroup |
Sample |
Library |
Type |
Project |
Genome |
Centre |
|
B04DHABXX |
1 |
110302_SN553_0085_BB04DHABXX_1 |
WTCHG_11891 |
samples |
4618/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
2 |
110302_SN553_0085_BB04DHABXX_2 |
WTCHG_11892 |
samples |
4619/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
3 |
110302_SN553_0085_BB04DHABXX_3 |
WTCHG_11893 |
samples |
4620/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
4 |
110302_SN553_0085_BB04DHABXX_4 |
WTCHG_11894 |
samples |
4623/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
5 |
110302_SN553_0085_BB04DHABXX_5 |
WTCHG_11895 |
samples |
4624/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
6 |
110302_SN553_0085_BB04DHABXX_6 |
WTCHG_11896 |
samples |
4625/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
7 |
110302_SN553_0085_BB04DHABXX_7 |
WTCHG_11897 |
samples |
4626/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
|
B04DHABXX |
8 |
110302_SN553_0085_BB04DHABXX_8 |
WTCHG_11898 |
samples |
4628/10 |
gDNA PE |
P100244 |
Mouse37 |
WTCHG |
Lane |
Length |
Tiles |
Clusters PF |
% PF |
Yield (Mrd) |
Yield (Mb) |
Yield (Mb Q20) |
% Mapped |
% Coverage⊥ |
% Primer |
% Variants |
Mean cov.* |
% high cov.ℵ |
% dups |
% pair dups |
Link |
1.1 |
101 |
32 |
2736687 |
87.2 |
76.35 |
7711.66 |
6621.45 |
98.2 |
83.0 |
0.00 |
1.06 ± 0.17 |
3.35 |
13.87 |
5.45 |
4.51 |
lane |
1.2 |
101 |
32 |
2736687 |
87.2 |
76.35 |
7711.66 |
7151.51 |
98.0 |
83.0 |
0.00 |
1.03 ± 0.24 |
3.34 |
13.88 |
5.44 |
4.53 |
|
2.1 |
101 |
32 |
2691267 |
87.4 |
75.28 |
7602.98 |
6492.73 |
98.2 |
79.1 |
0.00 |
1.07 ± 0.00 |
3.46 |
14.40 |
5.41 |
4.42 |
lane |
2.2 |
101 |
32 |
2691267 |
87.4 |
75.28 |
7602.98 |
7053.94 |
98.1 |
79.1 |
0.00 |
1.00 ± 0.17 |
3.46 |
14.40 |
5.41 |
4.43 |
|
3.1 |
101 |
32 |
2683419 |
87.1 |
74.82 |
7556.40 |
6444.32 |
98.3 |
82.2 |
0.00 |
1.08 ± 0.00 |
3.31 |
14.53 |
6.98 |
6.14 |
lane |
3.2 |
101 |
32 |
2683419 |
87.1 |
74.82 |
7556.40 |
6994.12 |
98.1 |
82.2 |
0.00 |
1.00 ± 0.00 |
3.31 |
14.55 |
6.98 |
6.16 |
|
4.1 |
101 |
32 |
2471085 |
88.0 |
69.59 |
7028.35 |
6041.22 |
98.3 |
80.6 |
0.00 |
1.07 ± 0.00 |
3.15 |
14.73 |
6.74 |
6.02 |
lane |
4.2 |
101 |
32 |
2471085 |
88.0 |
69.59 |
7028.35 |
6546.42 |
98.1 |
80.5 |
0.00 |
0.98 ± 0.00 |
3.14 |
14.73 |
6.75 |
6.04 |
|
5.1 |
101 |
32 |
2479347 |
88.3 |
70.04 |
7073.92 |
6027.52 |
98.2 |
81.1 |
0.00 |
1.04 ± 0.00 |
3.15 |
14.01 |
5.81 |
5.04 |
lane |
5.2 |
101 |
32 |
2479347 |
88.3 |
70.04 |
7073.92 |
6616.72 |
98.1 |
81.1 |
0.00 |
0.95 ± 0.00 |
3.14 |
14.02 |
5.82 |
5.06 |
|
6.1 |
101 |
32 |
2450811 |
88.2 |
69.14 |
6982.69 |
5953.33 |
98.1 |
80.6 |
0.00 |
1.16 ± 0.41 |
3.12 |
12.86 |
6.91 |
6.11 |
lane |
6.2 |
101 |
32 |
2450811 |
88.2 |
69.14 |
6982.69 |
6528.48 |
98.0 |
80.6 |
0.00 |
0.94 ± 0.00 |
3.11 |
12.87 |
6.90 |
6.13 |
|
7.1 |
101 |
32 |
2574731 |
87.2 |
71.83 |
7254.48 |
6145.45 |
98.2 |
81.6 |
0.00 |
1.03 ± 0.00 |
3.20 |
13.04 |
7.27 |
6.50 |
lane |
7.2 |
101 |
32 |
2574731 |
87.2 |
71.83 |
7254.48 |
6720.78 |
98.1 |
81.6 |
0.00 |
0.95 ± 0.00 |
3.20 |
13.04 |
7.28 |
6.52 |
|
8.1 |
101 |
32 |
2689366 |
86.8 |
74.67 |
7541.19 |
6411.44 |
98.3 |
83.2 |
0.00 |
1.00 ± 0.00 |
3.27 |
11.89 |
6.41 |
5.56 |
lane |
8.2 |
101 |
32 |
2689366 |
86.8 |
74.67 |
7541.19 |
6978.09 |
98.1 |
83.1 |
0.00 |
0.93 ± 0.00 |
3.27 |
11.90 |
6.41 |
5.57 |
|
⊥ Fraction of reference that is covered at least once * Mean coverage is computed over regions that are covered at least once ℵ Proportion of reads in regions with coverage in top 0.1 percentile
Lane QC statistics and plots
Lane |
% GC |
% GCmapped |
σpos(%GC) |
insert ± MAD |
% exonic |
% exon cov'ge |
%N |
maxpos %N |
%lowQ |
%lowQend |
avgQ |
1.1 |
41.1 ± 8.3 |
41.1 ± 8.3 |
0.81 |
367 ± 50 |
1.2 |
89.0 |
0.0 |
0.0 |
11.7 |
49.8 |
27.9 |
1.2 |
40.4 ± 9.4 |
40.9 ± 8.1 |
0.65 |
367 ± 50 |
1.2 |
89.1 |
0.1 |
0.0 |
5.4 |
26.2 |
30.5 |
2.1 |
41.9 ± 8.3 |
41.9 ± 8.3 |
0.41 |
362 ± 53 |
1.4 |
89.6 |
0.0 |
0.1 |
12.2 |
51.0 |
27.7 |
2.2 |
41.8 ± 8.2 |
41.8 ± 8.1 |
0.36 |
362 ± 53 |
1.4 |
89.8 |
0.1 |
0.0 |
5.5 |
26.8 |
30.5 |
3.1 |
41.2 ± 8.5 |
41.2 ± 8.4 |
0.54 |
403 ± 53 |
1.2 |
89.7 |
0.0 |
0.1 |
12.2 |
51.8 |
27.6 |
3.2 |
40.6 ± 9.5 |
41.2 ± 8.3 |
0.38 |
403 ± 53 |
1.3 |
90.0 |
0.1 |
0.0 |
5.6 |
27.6 |
30.4 |
4.1 |
40.8 ± 8.3 |
40.8 ± 8.2 |
0.42 |
379 ± 42 |
1.1 |
85.9 |
0.0 |
0.1 |
11.6 |
50.8 |
27.9 |
4.2 |
40.6 ± 8.2 |
40.6 ± 8.1 |
0.36 |
380 ± 42 |
1.1 |
86.1 |
0.1 |
0.0 |
5.2 |
26.0 |
30.6 |
5.1 |
41.1 ± 8.2 |
41.0 ± 8.2 |
0.46 |
357 ± 38 |
1.1 |
86.8 |
0.0 |
0.1 |
12.3 |
54.0 |
27.5 |
5.2 |
40.8 ± 8.1 |
40.8 ± 8.1 |
0.34 |
357 ± 38 |
1.1 |
86.8 |
0.1 |
0.1 |
4.9 |
24.8 |
30.8 |
6.1 |
41.2 ± 8.2 |
41.1 ± 8.2 |
0.56 |
373 ± 41 |
1.1 |
85.5 |
0.1 |
0.1 |
12.0 |
51.1 |
27.6 |
6.2 |
40.8 ± 8.2 |
40.9 ± 8.1 |
0.34 |
373 ± 41 |
1.1 |
85.4 |
0.1 |
0.1 |
4.9 |
24.4 |
30.8 |
7.1 |
41.2 ± 8.4 |
41.2 ± 8.4 |
0.50 |
403 ± 41 |
1.2 |
88.5 |
0.0 |
0.1 |
12.7 |
54.5 |
27.4 |
7.2 |
40.3 ± 9.5 |
40.9 ± 8.2 |
0.35 |
403 ± 41 |
1.2 |
88.7 |
0.1 |
0.1 |
5.6 |
27.3 |
30.4 |
8.1 |
41.0 ± 8.4 |
41.0 ± 8.3 |
0.50 |
375 ± 39 |
1.1 |
87.6 |
0.0 |
0.1 |
12.4 |
52.7 |
27.6 |
8.2 |
40.7 ± 8.3 |
40.8 ± 8.2 |
0.46 |
375 ± 39 |
1.1 |
87.8 |
0.1 |
0.1 |
5.6 |
27.9 |
30.4 |
G+C histogram∋
 |
Insert size histogram∞
 |
Mapped coverage by G+C℘
 |
|
Coverage histogram
 |
Exon/genome coverage distribution
 |
Genomic coverage by G+C∅
 |
|
(Predicted) variants by cycle∇ (read 1)
 |
Fraction N/lowQ∋, read 1
 |
G+C by cycle (PF)∋, read 1
 |
|
Mean Q by cycle∇, read 1
 |
Q score histogram, read 1
 |
Variants by Q, read 1
 |
|
(Predicted) variants by cycle∇ (read 2)
 |
Fraction N/lowQ∋, read 2
 |
G+C by cycle (PF)∋, read 2
 |
|
Mean Q by cycle∇, read 2
 |
Q score histogram, read 2
 |
Variants by Q, read 2
 |
|
Variants by GC
 |
Log coverage histogram
 |
Legend
 |
∋ The Fraction N/Low Q plots, and dotted lines on the GC histogram plots, refer to all reads that have
passed chastity filters. If a reference genome was available, all others refer to mapped reads, otherwise
they too refer to chastity-filtered reads. The dotted lines in the fraction N/lowQ plot correspond to the
fraction of bases with quality score 4 or less. ∇ "Predicted variants" (dashed line) is the expected error frequency expressed as a Phred score,
and may be compared with the "Variants by cycle" graph (solid line). "Mean Q" (solid) is the numerical
mean Q score and is a measure of the average information content per read. These graphs use mapped reads only;
the dashed line in the Mean Q plot uses all (PF) reads. All four graphs are calculated on called bases with
Q Phred score above 4 only. ℘ Mapped coverage by G+C. The coverage was averaged over those genomic regions that were covered at least once.
Regions with coverage in the top 0.1 percentile were excluded; the dotted line shows results for all reads.
The G+C fraction was computed from read bases, excluding Ns and bases with quality below 4. ∅ Genomic coverage by G+C. The G+C fraction was computed from the reference genome, over the approximate fragment
Regions with coverage in the top 0.1 percentile were excluded.
The G+C histogram is shown as a dotted line (arbitrary Y scale). ∞ The insert size distribution is summarized by the median and median absolute deviation.
Tile QC statistics and plots
Variant rate by tile∝ (read 1)
 |
Raw/mapped yield by tile (read 1)
 |
Fraction N/lowQ by tile (read 1)
 |
|
Variant rate by tile∝ (read 2)
 |
Raw/mapped yield by tile (read 2)
 |
Fraction N/lowQ by tile (read 2)
 |
∝ HiSeq tiles are grouped in order: swathe 1 top; swathe 1 bottom; swathe 2 top; etc.
QC version: 2.1