Flowcell QC summary (lanes 1,2,3,4,5,6,7)


Date Flowcell Lane Platform Unit Readgroup Sample Library Type Project Genome Centre
1 110225_SN685_0056_B702MGABXX_1 WTCHG_11728 samples 035/11 P100244 Mouse37 WTCHG
2 110225_SN685_0056_B702MGABXX_2 WTCHG_11729 samples 036/11 P100244 Mouse37 WTCHG
3 110225_SN685_0056_B702MGABXX_3 WTCHG_11730 samples 037/11 P100244 Mouse37 WTCHG
4 110225_SN685_0056_B702MGABXX_4 WTCHG_11731 samples 4617/10 P100244 Mouse37 WTCHG
5 110225_SN685_0056_B702MGABXX_5 WTCHG_11732 samples 4618/10 P100244 Mouse37 WTCHG
6 110225_SN685_0056_B702MGABXX_6 WTCHG_11733 samples 4625/10 P100244 Mouse37 WTCHG
7 110225_SN685_0056_B702MGABXX_7 WTCHG_11734 samples 4626/10 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 2581351 8.8 73.07 7380.41 7061.11 98.2 81.8 0.00 0.88 ± 0.17 3.25 12.91 7.16 6.34 lane
1.2 101 32 2581351 8.8 73.07 7380.41 6822.95 97.9 81.7 0.00 0.94 ± 0.17 3.24 12.90 7.14 6.35
2.1 101 32 2849818 8.8 80.53 8133.83 7756.92 98.3 84.1 0.00 0.92 ± 0.00 3.49 14.43 4.78 3.89 lane
2.2 101 32 2849818 8.8 80.53 8133.83 7525.80 98.0 84.1 0.00 0.98 ± 0.17 3.48 14.42 4.77 3.90
3.1 101 32 2538481 8.9 72.53 7325.43 7011.39 98.3 81.3 0.00 0.95 ± 0.29 3.25 13.91 5.50 4.69 lane
3.2 101 32 2538481 8.9 72.53 7325.43 6810.79 98.1 81.3 0.00 0.98 ± 0.24 3.24 13.90 5.48 4.69
4.1 101 32 2712281 8.9 77.48 7825.32 7507.31 98.1 83.8 0.00 0.92 ± 0.17 3.36 13.67 4.29 3.42 lane
4.2 101 32 2712281 8.9 77.48 7825.32 7313.19 97.9 83.8 0.00 0.97 ± 0.17 3.36 13.66 4.28 3.42
5.1 101 32 3227075 8.8 90.52 9142.04 8736.79 98.3 86.5 0.00 0.94 ± 0.17 3.81 14.47 3.46 2.35 lane
5.2 101 32 3227075 8.8 90.52 9142.04 8482.17 98.1 86.5 0.00 1.00 ± 0.17 3.80 14.46 3.44 2.35
6.1 101 32 2867570 8.9 81.89 8271.27 7928.68 98.1 84.8 0.00 0.90 ± 0.00 3.51 13.51 3.90 2.97 lane
6.2 101 32 2867570 8.9 81.89 8271.27 7727.08 97.9 84.8 0.00 0.94 ± 0.00 3.50 13.49 3.88 2.97
7.1 101 32 3167671 8.8 88.85 8974.02 8572.63 98.3 86.3 0.00 0.90 ± 0.00 3.75 13.79 3.98 3.01 lane
7.2 101 32 3167671 8.8 88.85 8974.02 8299.50 98.1 86.2 0.00 0.96 ± 0.00 3.74 13.78 3.97 3.01

  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 41.6 ± 8.2 41.6 ± 8.1 0.31 457 ± 47 1.4 91.5 0.0 0.1 3.2 14.6 32.2
1.2 40.7 ± 9.9 40.8 ± 9.6 0.38 457 ± 47 1.4 91.6 0.1 0.0 5.8 24.9 30.2
2.1 40.9 ± 8.1 40.9 ± 8.0 0.32 408 ± 43 1.2 91.7 0.0 0.1 3.4 16.9 32.2
2.2 39.9 ± 9.8 40.0 ± 9.5 0.36 408 ± 43 1.2 91.9 0.1 0.0 5.8 25.4 30.3
3.1 41.8 ± 8.1 41.8 ± 8.1 0.33 419 ± 40 1.4 91.4 0.0 0.2 3.1 14.9 32.2
3.2 41.0 ± 9.8 41.6 ± 8.4 0.38 419 ± 40 1.4 91.4 0.1 0.0 5.5 24.1 30.4
4.1 40.9 ± 7.9 40.8 ± 8.0 0.32 388 ± 46 1.1 88.3 0.0 0.2 3.0 13.6 32.4
4.2 39.9 ± 9.5 40.5 ± 8.2 0.29 388 ± 46 1.1 88.1 0.0 0.0 5.1 21.7 30.6
5.1 41.1 ± 8.0 41.1 ± 7.9 0.67 366 ± 50 1.2 92.3 0.0 0.1 3.2 14.4 32.3
5.2 40.1 ± 9.7 40.2 ± 9.4 0.62 366 ± 50 1.2 92.1 0.1 0.0 5.6 23.0 30.4
6.1 41.1 ± 7.9 41.0 ± 7.9 0.36 373 ± 42 1.1 89.4 0.0 0.1 3.0 13.9 32.3
6.2 40.1 ± 9.5 40.7 ± 8.1 0.32 373 ± 42 1.1 89.2 0.1 0.0 5.1 21.7 30.6
7.1 41.0 ± 8.0 41.0 ± 8.0 0.34 402 ± 42 1.2 92.6 0.0 0.1 3.3 14.7 32.2
7.2 39.9 ± 9.8 40.1 ± 9.5 0.31 402 ± 42 1.2 92.5 0.1 0.0 5.8 23.9 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