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.ℵ | % 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 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 ± 8.0 | 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 |
∋ 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