Description Usage Arguments Details Value Author(s)
Summary of regions with abnormal coverage as detected by 'call.abnomal.cov'. It's a static version of 'sv.summary.interactive'. It produces graphs to to get an idea of the quality of the calls. For normal samples we would expect: the amount of called genome in each sample to be somewhat similar; the copy number estimates to locate near integer values; No systematic calls (i.e. called in all samples). The output graphs represent the amount of affected genome across samples, the copy number estimates distribution, the frequency distribution.
1 2 | sv.summary(res.df, out.pdf = NULL, print = TRUE, FDR.th = 0.05,
min.cn2Dev = 0, min.cov = 0, max.sing.kb = Inf)
|
res.df |
the data.frame with the results. |
out.pdf |
the name for the output PDF file to create. If NULL (default), the graphs are either displayed directly or returned as a list. |
print |
Should the graphs be displayed ? If 'out.pdf' though, this parameter is not used as no graph will be displayed. |
FDR.th |
the FDR threshold to use. Default is 0.05. |
min.cn2Dev |
the minimum deviation from CN2. Default is 0. Using '0.5' would remove CNVs with CN estimates in [1.5,2.5]. |
min.cov |
the minimum coverage in the reference samples. Default is 0. |
max.sing.kb |
the maximum amount of single-bin calls. Default is Inf. Use and tweak when batches or outliers are visible in the calls. |
A list is returned. Its first element is a list of ggplot object with the different graphs. The second is a data.frame with summary information used to create the graphs.
A list with :
graphs.l |
a list of ggplot graphs |
cnv.df |
a data.frame with the selected CNVs |
info.df |
a data.frame with different summary statistics |
Jean Monlong
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