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 | % 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 |
∋ 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.
∝ HiSeq tiles are grouped in order: swathe 1 top; swathe 1 bottom; swathe 2 top; etc.
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QC version: 2.1