Mercurial > repos > galaxyp > cardinal_spectra_plots
diff spectra_plots.xml @ 2:3642ed221eb2 draft
planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/cardinal commit f127be2141cf22e269c85282d226eb16fe14a9c1
author | galaxyp |
---|---|
date | Fri, 15 Feb 2019 10:23:28 -0500 |
parents | 1d9931768896 |
children | 58c4aef16eb0 |
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--- a/spectra_plots.xml Thu Oct 25 07:30:24 2018 -0400 +++ b/spectra_plots.xml Fri Feb 15 10:23:28 2019 -0500 @@ -1,4 +1,4 @@ -<tool id="cardinal_spectra_plots" name="MSI plot spectra" version="@VERSION@.1"> +<tool id="cardinal_spectra_plots" name="MSI plot spectra" version="@VERSION@.2"> <description> mass spectrometry imaging mass spectra plots </description> @@ -27,6 +27,7 @@ library(ggplot2) library(scales) + @READING_MSIDATA@ @DATA_PROPERTIES@ @@ -52,15 +53,17 @@ ## set NA to 0 otherwise plot function will not work - ##spectra(msidata)[is.na(spectra(msidata)[])] = 0 ## in case of NA values they will be set to zero + #if str($processed_cond.processed_file) == "processed": + ##processed file needs to be converted into matrix to be able to replace NAs + iData(msidata) <- iData(msidata)[] + spectra(msidata)[][is.na(spectra(msidata)[])] = 0 + #else + spectra(msidata)[is.na(spectra(msidata))] = 0 + #end if - spectra_df = spectra(msidata)[] - spectra_df[is.na(spectra_df)] = 0 - print(paste0("Number of NA which were converted into 0:",sum(is.na(spectra_df)))) - spectra(msidata) = spectra_df +## run only if mz and pixels are > 0 - -if (npeaks > 0){ +if (ncol(msidata)>0 & nrow(msidata) >0){ pixeldf = data.frame(matrix(ncol = 2, nrow=0)) @@ -73,13 +76,21 @@ #for $chosenpixel in $pixel_conditional.repeatpixel: pixelname = paste0("x = ", $chosenpixel.inputx,", ", "y = ", $chosenpixel.inputy) - pixelisvalid = as.character(pixelname %in% names(pixels(msidata))) + + + + input_pixels = paste($chosenpixel.inputx, $chosenpixel.inputy, sep="_") + dataset_pixels = paste(coord(msidata)\$x, coord(msidata)\$y, sep="_") + + pixelisvalid = as.character(input_pixels %in% dataset_pixels) + + + pixeldf = rbind(pixeldf, cbind(pixelname, pixelisvalid)) ############################# II) control image #################### if (pixelisvalid == "TRUE"){ - print(pixelisvalid) image(msidata, mz=$chosenpixel.inputmz, ylim = c(maximumy+(0.2*maximumy),minimumy-1), colorkey=FALSE, plusminus = $chosenpixel.plusminusinDalton, @@ -188,16 +199,13 @@ key_legend = TRUE }else{key_legend = FALSE} - spectra(msidata)[is.na(spectra(msidata)[])] = 0 ## in case of NA values they will be set to zero plot(msidata, pixel=1:ncol(msidata), pixel.groups=msidata\$annotation, key=key_legend, col=hue_pal()(length(levels(msidata\$annotation))),superpose=TRUE) }else{ - spectra(msidata)[is.na(spectra(msidata)[])] = 0 ## in case of NA values they will be set to zero plot(msidata, pixel=1:ncol(msidata), key=TRUE)} ##################### II) Sample: plot zoom-in mass spectrum ########## #if $pixel_conditional.zoomed_sample: - iData(msidata) <- iData(msidata)[] ## getting back data on disk #for $token in $pixel_conditional.zoomed_sample: print("zoomed sample pixels") @@ -317,7 +325,7 @@ </conditional> </inputs> <outputs> - <data format="pdf" name="plots" from_work_dir="mzplots.pdf" label="${tool.name} on ${on_string}"/> + <data format="pdf" name="plots" from_work_dir="mzplots.pdf" label="${tool.name} on ${on_string}:results"/> </outputs> <tests> <test>