European Genome-Phenome Archive

File Quality

File InformationEGAF00002485479

File Data

Base Coverage Distribution

This chart represents the base coverage distribution along the reference file. Y-axis represents the number of times a position in the reference file is covered. The x-axis represents the range of the values for the coverage.

Data is represented in a log scale to minimise the variability. A high peak in the beginning (low coverage) and a curve descending is expected.

401 386211 377150 291123 616108 65597 94489 59584 59979 41973 84469 19264 47561 86458 82754 12852 63249 76846 26143 59640 96739 05336 24934 25632 37230 17928 41327 03024 99022 64720 41718 98417 40916 09215 28013 29012 26411 73010 4089 3458 6207 8006 9646 6685 9455 5015 0544 6154 3714 0573 7513 3602 9702 5282 4252 1062 0361 7821 6661 4991 4191 3101 2791 1591 0671 01988788481775471677864863962961058561456455153253448251152446642639438940738937537237433831433230826324030930830429727825525423418119721723323718219620415421316518717113117717116412712313414714013813615315413217115113517214514112011912313015714514012113710613614013112112711113815915213914114414015411512910014113110012411715014015115516515016113915216816315816415313313215113014012512114212713113414012816315712313713116314813613411514314613215214014813412012011912113211611611610110393111978497861021078494978073647588687159715681558360666848667064584357594447584149464333314940505650394940313932363237274331213133294334283030142330282735223336283634243220242333272819222819202320172412142218172526231614191314161111111414111681081216710119157151281071056651089637117841313448215516464474132211632423610753263325312487413331611476471117415314253221321212311121412111211143145223133312223224134242234312444214326573242333222214421432124314221113122213212324211313113121221211121112113111111111423113115541123111113312121111111123211111111211111111211527241312122221224111121241142121211322112211112111212311212211111211112112212211211112311111212111113221211112113112131563100200300400500600700800900>1000Coverage value1210201002001k2k10k20k100k200k# Bases

Base Quality

The base quality distribution shows the Phred quality scores describing the probability that a nucleotide has been incorrectly assigned; e.g. an error in the sequencing. Specifically, Q=-log10(P), where Q is the Phred score and P is the probability the nucleotide is wrong. The larger the score, the more confident we are in the base call. Depending on the sequencing technology, we can expect to see different distributions, but we expect to see a distribution skewed towards larger (more confident) scores; typically around 40.

5 9220000000000000249 080225 1171 228 183000000003201 089 81759 4820529 906740 542175 316248 8151 742 2104 661 4762 056 6781 517 6413 641 00317 232 25638 536 92400510152025303540Phred quality score0M5M10M15M20M25M30M35M# Bases

Mapped Reads

Number of reads successfully mapped (singletons & both mates) to the reference genome in the sample. Genetic variation, in particular structural variants, ensure that every sequenced sample is genetically different from the reference genome it was aligned to. Small differences against the reference are accepted, but, for more significant variation, the read can fail to be placed. Therefore, it is not expected that the mapped reads rate will hit 100%, but it is supposed to be high (usually >90%). Calculations are made taking into account the proportion of mapped reads against the total number of reads (mapped/mapped+unmapped).

50.1 %493 93550.1 %49.9 %

Both Mates Mapped

When working with paired-end sequencing, each DNA fragment is sequenced from both ends, creating two mates for each pair. This chart shows the fraction of reads in pairs where both of the mates successfully map to the reference genome. .

Notice that reads not mapped to the expected distance are also included as occurs with the proper pairs chart.

47.3 %466 79847.3 %52.7 %

Singletons

When working with paired-end sequencing, each DNA fragment is sequenced from both ends, creating two mates for each pair. If one mate in the pair successfully maps to the reference genome, but the other is unmapped, the mapped mate is a singleton. One way in which a singleton could occur would be if the sample has a large insertion compared with the reference genome; one mate can fall in sequence flanking the insertion and will be mapped, but the other falls in the inserted sequence and so cannot map to the reference genome. There are unlikely to many such structural variants in the sample, or sequencing errors that would cause a read not to be able to map. Consequently, the singleton rate is expected to be very low (<1%).

5.5 %27 1375.5 %94.5 %

Forward Strand

Fraction of reads mapped to the forward DNA strand. The general expectation is that the DNA library preparation step will generate DNA from the forward and reverse strands in equal amounts so after mapping the reads to the reference genome, approximately 50% of them will consequently map to the forward strand. Deviations from the 50%, may be due to problems with the library preparation step.

50 %492 93650 %50 %

Proper Pairs

A fragment consisting of two mates is called a proper pair if both mates map to the reference genome at the expected distance according to the reference genome. In particular, if the DNA library consists of fragments ~500 base pairs in length, and 100 base pair reads are sequenced from either end, the expectation would be that the two reads map to the reference genome separated by ~300 base pairs. If the sequenced sample contains large structural variants, e.g. a large insertion, where we expect the reads mapping with a large separation would be a signal for this variant, and the reads would not be considered as proper pairs. Based on the sequencing technology, there is also an expectation of the orientation of each read in the fragment.

The rate of proper pairs is expected to be well over 90%; even if the mapping rate itself is low as a result of bacterial contamination, for example.

42.7 %421 00042.7 %57.3 %

Duplicates

PCR duplicates are two (or more) reads that originate from the same DNA fragment. When sequencing data is analyzed, it is assumed that each observation (i.e. each read) is independent; an assumption that fails in the presence of duplicate reads. Typically, algorithms look for reads that map to the same genomic coordinate, and whose mates also map to identical genomic coordinates. It is important to note that as the sequencing depth increases, more reads are sampled from the DNA library, and consequently it is increasingly likely that duplicate reads will be sampled. As a result, the true duplicate rate is not independent of the depth, and they should both be considered when looking at the duplicate rate. Additionally, as the sequencing depth in increases, it is also increasingly likely that reads will map to the same location and be marked as duplicates, even when they are not. As such, as the sequencing depth approaches and surpasses the read length, the duplicate rate starts to become less indicative of problems.

3.2 %31 9073.2 %96.8 %

Mapping Quality Distribution

The mapping quality distribution shows the Phred quality scores describing the probability that a read does not map to the location that it has been assigned to (specifically, Q=-log10(P), where Q is the Phred score and P is the probability the read is in the wrong location). So the larger the score, the higher the quality of the mapping. Some scores have a specific meaning, e.g. a score of 0 means that the read could map equally to multiple places in the reference genome. The majority of reads should be well mapped, and so we expect to see this distribution heavily skewed to a significant value (typically around 60). It is not unusual to see some scores around zero. Reads originating from repetitive elements in the genome will plausibly map to multiple locations.

549 0281 13048137264914271751 8553352 091918792393 0242281 5051 0851881 768427955 695221 62219124347 01113862226262 19265 001106302181321643632561 836901361242301162662122705641 508292 738051015202530354045505560Phred quality score50k100k150k200k250k300k350k400k450k500k# Reads

Mapped vs Unmapped

Stacked column chart for both mapped and unmapped reads along all chromosomes in the reference file. It is a similar representation as shown in the Mapped reads chart but for each chromosome. Although sequenced sample may be a female, it is possible to get reads in the Y chromosome as there are common regions in both chromosomes called pseudoautosomal regions (PAR1, PAR2).

Unmapped reads belonging to each chromosome are determined when the one mate/pair is aligned and the other is not. The unmapped read should have chromosome and POS identical to its mate. It could also be due when aligning is performed with bwa as it concatenates all the reference sequences together, so if a read hangs off of one reference onto another, it will be given the right chromosome and position, but it also be classified as unmapped.

94.01%94.84%94.68%92.34%96.12%94.92%96.33%95.1%93.21%96.11%95.75%94.52%96.35%95.13%92.42%91.49%95.55%95.53%93.41%95.2%93.9%94.98%96.66%98.17%5.99%5.16%5.32%7.66%3.88%5.08%3.67%4.9%6.79%3.89%4.25%5.48%3.65%4.87%7.58%8.51%4.45%4.47%6.59%4.8%6.1%5.02%3.34%1.83%123456789101112131415161718192021XYM0%10%20%30%40%50%60%70%80%90%100%mappedunmapped