Flowcell QC summary (lanes 1,2,3,4,5)


Date Flowcell Lane Platform Unit Readgroup Sample Library Type Project Genome Centre
B04C2ABXX 1 110311_SN553_0087_AB04C2ABXX_1 WTCHG_13229 samples 4629/10 gDNA PE P100244 Mouse37 WTCHG
B04C2ABXX 2 110311_SN553_0087_AB04C2ABXX_2 WTCHG_13230 samples 4630/10 gDNA PE P100244 Mouse37 WTCHG
B04C2ABXX 3 110311_SN553_0087_AB04C2ABXX_3 WTCHG_13231 samples 4633/10 gDNA PE P100244 Mouse37 WTCHG
B04C2ABXX 4 110311_SN553_0087_AB04C2ABXX_4 WTCHG_13232 samples 4634/10 gDNA PE P100244 Mouse37 WTCHG
B04C2ABXX 5 110311_SN553_0087_AB04C2ABXX_5 WTCHG_13233 samples 4635/10 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. % dups % pair dups Link
1.1 101 32 2410707 96.0 74.04 7477.71 7110.20 98.3 83.9 0.00 0.87 ± 0.00 3.21 11.76 1.48 0.58 lane
1.2 101 32 2410707 96.0 74.04 7477.71 6880.48 98.0 83.9 0.00 0.93 ± 0.00 3.20 11.75 1.48 0.58
2.1 101 32 2405461 95.8 73.77 7450.89 7080.19 98.2 83.0 0.00 0.92 ± 0.00 3.24 13.67 1.32 0.44 lane
2.2 101 32 2405461 95.8 73.77 7450.89 6866.15 97.9 82.9 0.00 0.98 ± 0.00 3.23 13.66 1.32 0.44
3.1 101 32 2419374 95.7 74.12 7486.00 7124.80 98.4 83.5 0.00 0.91 ± 0.29 3.23 12.98 1.38 0.53 lane
3.2 101 32 2419374 95.7 74.12 7486.00 6912.56 98.1 83.5 0.00 0.95 ± 0.00 3.23 12.98 1.38 0.53
4.1 101 32 2386916 95.4 72.86 7358.37 7021.28 98.1 83.1 0.00 0.83 ± 0.00 3.19 11.16 1.68 0.81 lane
4.2 101 32 2386916 95.4 72.86 7358.37 6804.12 97.9 83.1 0.00 0.88 ± 0.00 3.18 11.14 1.68 0.81
5.1 101 32 2325154 95.9 71.39 7210.23 6869.80 98.3 82.7 0.00 0.86 ± 0.00 3.14 12.63 1.38 0.50 lane
5.2 101 32 2325154 95.9 71.39 7210.23 6660.20 98.0 82.6 0.00 0.92 ± 0.00 3.14 12.62 1.38 0.50

  Fraction of reference that is covered at least once   *   Mean coverage is computed over regions that are covered at least once      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 ± 8.0 41.0 ± 8.0 0.35 370 ± 45 1.1 87.0 0.0 0.5 3.6 18.0 32.0
1.2 40.7 ± 8.2 40.7 ± 8.1 0.42 370 ± 45 1.1 86.8 0.1 0.0 6.2 29.9 30.1
2.1 41.4 ± 8.2 41.3 ± 8.2 0.36 374 ± 64 1.3 90.4 0.0 0.6 3.6 19.0 32.0
2.2 40.7 ± 9.6 41.2 ± 8.4 0.38 374 ± 64 1.3 90.6 0.1 0.0 6.1 29.2 30.1
3.1 41.3 ± 8.0 41.3 ± 8.0 0.34 377 ± 39 1.2 90.5 0.0 0.6 3.5 18.1 32.0
3.2 41.0 ± 8.4 41.1 ± 8.3 0.36 377 ± 39 1.2 90.4 0.1 0.0 5.9 28.3 30.2
4.1 41.2 ± 7.9 41.2 ± 7.8 0.50 365 ± 37 1.1 86.3 0.0 0.6 3.4 16.9 32.2
4.2 40.8 ± 8.2 40.8 ± 8.1 0.59 365 ± 36 1.1 85.9 0.1 0.1 5.8 28.1 30.2
5.1 41.3 ± 8.0 41.3 ± 8.0 0.38 376 ± 45 1.2 88.5 0.1 0.5 3.5 17.2 32.0
5.2 40.4 ± 9.4 41.0 ± 8.1 0.36 376 ± 45 1.2 88.4 0.2 0.1 5.9 28.1 30.2

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