prime3_PRP8_50 | R Documentation |
Splicing events occurring in 3'UTR of 50 genes were detected in the knockdowned PRP8 cell line.
data("prime3_PRP8_50")
A data frame with 50 observations on the following 24 variables.
chr
a factor with levels
strand
a factor with levels
isoform
a factor with levels
Gene
a factor with levels
exon_const_start
a numeric vector
exon_const_end
a numeric vector
exon_alt1_start
a numeric vector
exon_alt1_end
a numeric vector
exon_alt2_start
a numeric vector
exon_alt2_end
a numeric vector
Siha_Ctl_I_S3
a numeric vector
Siha_Ctl_II_S7
a numeric vector
Siha_Ctl_III_S11
a numeric vector
PRP8_I_S2
a numeric vector
PRP8_II_S6
a numeric vector
PRP8_III_S10
a numeric vector
tvalue
a numeric vector
rho
a numeric vector
pvalue
a numeric vector
adjp
a numeric vector
w
a numeric vector
X
a numeric vector
X.1
a numeric vector
X.2
a numeric vector
This dataset is an example for annotation of genes within which splicing events occurring in 3'UTR were detected by spladder-NBBttest in knockdowned PRP8 cell line. Gene information columns are assigned to "chr","Gene", "isoform", "exon_const_start" and "exon_const_end" that are start and end positions of constituted exons and "exon_alt1_start" and "exon_alt1_end" that are start and end positions of alternative exons. Count data of RNA reads are assigned to three replicate control columns (Siha_Ctl_I_S3,II-S7, III_S11) and three replicate knokdowned PRP8 columns (PRP8_I_S2,II_S6 and III_S10). The tvalue is t-statistic, rho is gene-wise variable, pvalue is p-value for t-statistic, w is ω,a threshold for rho, FDR (X.1)is false discovery rate with α= 0.05, selection (X.2)= 1 if pvalue < FDR, 0, otherwise.
data(prime3_PRP8_50)
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