Coverage Summary
If a panel is selected, the app calculates the coverage information based on the on-target genes.
Statistic |
Definition |
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Median CV |
The median coefficient of variation of coverage of the 1000 most highly expressed transcripts, as reported by the CollectRnaSeqMetrics utility from Picard tools. Ideal value = 0. |
Median 3′ |
The median uniformity of coverage of the 1000 most highly expressed transcripts at the 3′ end, as reported by the CollectRnaSeqMetrics utility from Picard tools. 3′ bias is calculated per transcript as the mean coverage of the 3′ most 100 bases divided by the mean coverage of the whole transcript. |
Median 5′ |
The median uniformity of coverage of the 1000 most highly expressed transcripts at the 5′ end, as reported by the CollectRnaSeqMetrics utility from Picard tools. 5′ bias is calculated per transcript as the mean coverage of the 5′ most 100 bases divided by the mean coverage of the whole transcript. |
Reads aligned to correct strand |
Percentage of reads that align to the expected strand of annotated transcripts, as reported by the CollectRnaSeqMetrics utility from Picard tools. |
If a panel is selected, the app calculates the alignment information based on the on-target genes.
Statistic |
Description |
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Coding |
Metrics based on coding bases. |
UTR |
Metrics based on bases in untranslated regions (UTR). |
Intron |
Metrics based on bases in introns. |
Non-targeted |
Metrics based on bases in intergenic or non-targeted regions. The app reports "non-targeted" if a panel is selected. |
Fold Coverage |
The total number of bases in the category divided by the size of the entire category. |
% Bases |
The total number of bases aligned to this region relative to the total number of aligned bases. |
If a panel is selected, the app calculates the gene-level coverage information based on the on-target genes.
Coverage |
Number of Genes |
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1X |
Number of genes covered at the mean base coverage level or deeper. |
10X |
|
30X |
|
100X |