Flowcell QC summary (lanes 1,2,4,5,6,7)


Date Flowcell Lane Platform Unit Readgroup Sample Library Type Project Genome Centre
B04DPABXX 1 110301_SN228_0123_AB04DPABXX_1 WTCHG_11820 samples 035/11 gDNA PE P100244 Mouse37 WTCHG
B04DPABXX 2 GA-DATA_2 WTCHG_11821 samples 036/11 gDNA PE P100244 Mouse37 WTCHG
B04DPABXX 4 GA-DATA_4 WTCHG_11823 samples 038/11 gDNA PE P100244 Mouse37 WTCHG
B04DPABXX 5 GA-DATA_5 WTCHG_11824 samples 039/11 gDNA PE P100244 Mouse37 WTCHG
B04DPABXX 6 GA-DATA_6 WTCHG_11825 samples 040/11 gDNA PE P100244 Mouse37 WTCHG
B04DPABXX 7 GA-DATA_7 WTCHG_11826 samples 4617/10 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 2978886 87.3 83.22 8405.03 7962.02 98.7 84.3 0.00 0.88 ± 0.00 3.61 13.34 7.51 6.57 lane
1.2 101 32 2978886 87.3 83.22 8405.03 7746.93 98.3 84.2 0.00 0.94 ± 0.00 3.60 13.33 7.49 6.58
2.1 101 32 2877096 88.1 81.08 8189.35 7788.70 98.7 83.9 0.00 0.95 ± 0.17 3.54 14.73 5.94 5.04 lane
2.2 101 32 2877096 88.1 81.08 8189.35 7616.02 98.3 83.8 0.00 0.98 ± 0.17 3.52 14.72 5.92 5.05
4.1 101 32 3057470 87.5 85.63 8648.95 8200.36 98.8 85.3 0.00 0.91 ± 0.00 3.68 13.78 5.92 4.97 lane
4.2 101 32 3057470 87.5 85.63 8648.95 8024.58 98.5 85.2 0.00 0.96 ± 0.17 3.67 13.77 5.91 4.98
5.1 101 32 2615717 89.1 74.55 7529.17 7168.33 98.7 81.5 0.00 0.86 ± 0.00 3.34 12.75 6.60 5.77 lane
5.2 101 32 2615717 89.1 74.55 7529.17 7054.67 98.5 81.5 0.00 0.90 ± 0.00 3.34 12.74 6.59 5.78
6.1 101 32 2817205 88.4 79.66 8045.29 7643.55 98.8 83.7 0.00 0.89 ± 0.00 3.48 13.68 6.31 5.44 lane
6.2 101 32 2817205 88.4 79.66 8045.29 7503.32 98.5 83.7 0.00 0.94 ± 0.00 3.47 13.71 6.30 5.45
7.1 101 32 2849209 88.2 80.43 8123.36 7715.89 98.6 84.3 0.00 0.92 ± 0.00 3.48 13.86 5.54 4.63 lane
7.2 101 32 2849209 88.2 80.43 8123.36 7572.08 98.3 84.3 0.00 0.97 ± 0.00 3.48 13.85 5.52 4.64

  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 41.5 ± 8.2 41.5 ± 8.2 0.32 456 ± 47 1.4 93.6 0.0 0.1 4.0 18.3 31.6
1.2 40.3 ± 10.4 40.5 ± 10.0 0.37 456 ± 47 1.4 93.6 0.1 0.0 6.1 22.8 30.2
2.1 40.9 ± 8.1 40.9 ± 8.1 0.33 408 ± 44 1.2 91.6 0.1 0.1 3.6 16.8 31.9
2.2 39.7 ± 10.2 39.9 ± 9.7 0.34 408 ± 44 1.2 91.7 0.1 0.0 5.4 20.3 30.6
4.1 41.6 ± 8.1 41.6 ± 8.1 0.33 410 ± 43 1.3 93.8 0.0 0.2 3.9 18.1 31.7
4.2 40.5 ± 10.1 40.7 ± 9.8 0.42 410 ± 43 1.3 93.9 0.1 0.0 5.6 21.2 30.5
5.1 42.2 ± 8.1 42.1 ± 8.2 0.31 398 ± 30 1.5 92.7 0.0 0.1 3.7 17.2 31.8
5.2 41.3 ± 9.9 41.3 ± 9.5 0.41 398 ± 30 1.5 92.7 0.1 0.0 4.9 19.3 30.8
6.1 41.5 ± 8.1 41.5 ± 8.1 0.37 403 ± 36 1.3 93.0 0.0 0.1 3.8 17.7 31.8
6.2 40.5 ± 10.0 40.6 ± 9.7 0.44 403 ± 36 1.3 93.1 0.0 0.0 5.2 19.9 30.6
7.1 40.8 ± 8.0 40.8 ± 8.0 0.33 388 ± 46 1.1 88.7 0.0 0.1 3.8 17.8 31.8
7.2 39.6 ± 9.9 39.7 ± 9.6 0.28 388 ± 46 1.1 88.5 0.0 0.0 5.3 19.7 30.6

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