geom_protein.Rd
Layer for Protein Coverage Plot.
geom_protein( coverage.file, fasta.file, protein.id, XCorr.threshold = 2, confidence = "High", contaminant = NULL, remove.na = TRUE, color = "grey", mark.bare = TRUE, mark.color = "red", mark.alpha = 0.5, show.table = TRUE, table.position = c("right_top", "left_top", "left_bottom", "right_bottom"), table.size = 4, table.color = "black", range.size = 3, range.position = c("in", "out") )
coverage.file | Exported protein coverage file, should be in excel. |
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fasta.file | Input reference protein fasta file. |
protein.id | The protein ID of exported coverage file. This should be unique and in |
XCorr.threshold | The cross-correlation threshold. Default: 2. |
confidence | The confidence level. Default: High. |
contaminant | Whether to remove contaminant peptides. Default: NULL (not remove). |
remove.na | Logical value, whether to remove NA value in Abundance column. Default: TRUE. |
color | The fill color of coverage plot. Default: grey. |
mark.bare | Logical value, whether to mark region where Abundance is zero or NA. Default: TRUE. |
mark.color | The color used for the marked region. Default: red. |
mark.alpha | The transparency used for the marked region. Default: 0.5. |
show.table | Logical value, whether to show coverage summary table. Default: TRUE. |
table.position | The position of the coverage summary table, choose from right_top, left_top, left_bottom, right_bottom. Default: right_top. |
table.size | The font size of coverage summary table. Default: 4. |
table.color | The font color of coverage summary table. Default: black. |
range.size | The label size of range text, used when |
range.position | The position of y axis range, chosen from in (move y axis in the plot) and out (normal y axis). Default: in. |
A ggplot2 object.
# library(ggplot2) # library(ggcoverage) # coverage.file <- system.file("extdata", "Proteomics", "MS_BSA_coverage.xlsx", package = "ggcoverage") # fasta.file <- system.file("extdata", "Proteomics", "MS_BSA_coverage.fasta", package = "ggcoverage") # protein.id = "sp| # ggplot() + # geom_peptide(coverage.file = coverage.file, fasta.file = fasta.file, protein.id = protein.id)