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


Date Flowcell Lane Platform Unit Readgroup Sample Library Type Project Genome Centre
B04CRABXX 1 110307_SN685_0058_BB04CRABXX_1 WTCHG_12341 samples 4629/10 gDNA PE P100244 Mouse37 WTCHG
B04CRABXX 2 110307_SN685_0058_BB04CRABXX_2 WTCHG_12342 samples 4630/10 gDNA PE P100244 Mouse37 WTCHG
B04CRABXX 3 110307_SN685_0058_BB04CRABXX_3 WTCHG_12343 samples 4633/10 gDNA PE P100244 Mouse37 WTCHG
B04CRABXX 4 110307_SN685_0058_BB04CRABXX_4 WTCHG_12344 samples 4634/10 gDNA PE P100244 Mouse37 WTCHG
B04CRABXX 5 110307_SN685_0058_BB04CRABXX_5 WTCHG_12345 samples 4635/10 gDNA PE P100244 Mouse37 WTCHG
B04CRABXX 6 110307_SN685_0058_BB04CRABXX_6 WTCHG_12346 samples 038/11 gDNA PE P100244 Mouse37 WTCHG
B04CRABXX 7 110307_SN685_0058_BB04CRABXX_7 WTCHG_12347 samples 039/11 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 3244874 86.2 89.51 9040.48 8418.09 98.3 85.7 0.00 0.94 ± 0.17 3.80 12.50 9.85 8.87 lane
1.2 101 32 3244874 86.2 89.51 9040.48 8345.12 98.1 85.7 0.00 0.95 ± 0.17 3.79 12.48 9.83 8.88
2.1 101 32 3117225 86.9 86.73 8760.00 8185.41 98.2 84.1 0.00 0.98 ± 0.00 3.75 14.60 10.54 9.62 lane
2.2 101 32 3117225 86.9 86.73 8760.00 8099.50 98.0 84.1 0.00 0.99 ± 0.00 3.74 14.59 10.53 9.64
3.1 101 32 3113709 87.0 86.72 8758.45 8196.95 98.3 84.6 0.00 0.96 ± 0.17 3.74 13.92 10.31 9.43 lane
3.2 101 32 3113709 87.0 86.72 8758.45 8102.81 98.1 84.6 0.00 0.97 ± 0.17 3.73 13.91 10.30 9.45
4.1 101 32 2790939 88.3 78.87 7966.28 7509.88 98.0 83.1 0.00 0.86 ± 0.00 3.45 11.81 8.41 7.54 lane
4.2 101 32 2790939 88.3 78.87 7966.28 7425.53 97.8 83.1 0.00 0.89 ± 0.00 3.44 11.80 8.39 7.55
5.1 101 32 2846642 88.3 80.43 8123.01 7649.51 98.2 83.3 0.00 0.91 ± 0.00 3.51 13.61 8.76 7.86 lane
5.2 101 32 2846642 88.3 80.43 8123.01 7560.74 98.0 83.3 0.00 0.94 ± 0.00 3.50 13.60 8.75 7.87
6.1 101 32 3478166 85.8 95.54 9649.34 8998.68 98.4 86.1 0.00 0.98 ± 0.00 4.04 14.69 11.09 10.12 lane
6.2 101 32 3478166 85.8 95.54 9649.34 8872.29 98.2 86.1 0.00 0.99 ± 0.00 4.04 14.69 11.08 10.14
7.1 101 32 3234845 86.4 89.48 9037.22 8378.19 98.4 84.9 0.00 1.01 ± 0.33 3.84 13.29 8.66 7.72 lane
7.2 101 32 3234845 86.4 89.48 9037.22 8315.37 98.2 84.8 0.00 0.94 ± 0.00 3.84 13.29 8.65 7.74

  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 40.7 ± 8.0 40.7 ± 7.9 0.36 371 ± 45 1.0 88.0 0.0 0.0 5.1 25.8 31.1
1.2 39.5 ± 9.6 39.6 ± 9.4 0.39 371 ± 45 1.0 87.9 0.1 0.1 6.0 24.6 30.0
2.1 41.1 ± 8.1 41.0 ± 8.2 0.38 376 ± 63 1.2 90.7 0.0 0.0 4.9 25.2 31.2
2.2 40.1 ± 9.8 40.2 ± 9.5 0.35 375 ± 63 1.2 91.0 0.0 0.1 5.9 24.7 30.0
3.1 41.0 ± 8.0 40.9 ± 8.0 0.35 377 ± 38 1.2 90.8 0.0 0.0 4.8 24.6 31.3
3.2 39.9 ± 9.7 40.0 ± 9.4 0.35 377 ± 38 1.2 90.8 0.0 0.1 5.9 24.5 30.0
4.1 41.0 ± 7.9 40.9 ± 7.9 0.48 365 ± 36 1.1 85.6 0.0 0.0 4.4 21.6 31.5
4.2 39.9 ± 9.4 40.5 ± 8.0 0.59 366 ± 36 1.0 85.4 0.0 0.2 5.3 22.6 30.3
5.1 41.0 ± 7.9 41.0 ± 8.0 0.38 377 ± 44 1.1 88.4 0.0 0.0 4.4 21.9 31.4
5.2 40.0 ± 9.6 40.1 ± 9.3 0.34 377 ± 45 1.1 88.4 0.1 0.2 5.5 22.8 30.2
6.1 41.3 ± 8.1 41.3 ± 8.0 0.37 411 ± 43 1.2 93.7 0.0 0.0 5.0 25.4 31.1
6.2 40.3 ± 10.0 40.4 ± 9.7 0.46 411 ± 43 1.2 94.0 0.0 0.1 6.4 25.7 29.8
7.1 41.8 ± 8.1 41.7 ± 8.1 0.38 398 ± 30 1.3 94.4 0.0 0.0 5.4 28.5 30.9
7.2 40.9 ± 9.8 40.9 ± 9.5 0.46 398 ± 30 1.4 94.6 0.0 0.1 6.3 27.4 29.9

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