Mercurial > repos > prog > lcmsmatching
diff NcbigeneEntry.R @ 2:20d69a062da3 draft
planemo upload for repository https://github.com/workflow4metabolomics/lcmsmatching.git commit d4048accde6bdfd5b3e14f5394902d38991854f8
author | prog |
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date | Thu, 02 Mar 2017 08:55:00 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/NcbigeneEntry.R Thu Mar 02 08:55:00 2017 -0500 @@ -0,0 +1,110 @@ +##################### +# CLASS DECLARATION # +##################### + +NcbigeneEntry <- methods::setRefClass("NcbigeneEntry", contains = "BiodbEntry") + +########### +# FACTORY # +########### + +createNcbigeneEntryFromXml <- function(contents, drop = TRUE) { + + entries <- list() + + # Define xpath expressions + xpath.expr <- character() + xpath.expr[[BIODB.ACCESSION]] <- "//Gene-track_geneid" + xpath.expr[[BIODB.KEGG.ID]] <- "/Dbtag_db[text()='KEGG']/..//Object-id_str" + xpath.expr[[BIODB.UNIPROT.ID]] <- "//Gene-commentary_heading[text()='UniProtKB']/..//Dbtag_db[text()='UniProtKB/Swiss-Prot']/..//Object-id_str" + xpath.expr[[BIODB.LOCATION]] <- "//Gene-ref_maploc" + xpath.expr[[BIODB.PROTEIN.DESCRIPTION]] <- "//Gene-ref_desc" + xpath.expr[[BIODB.SYMBOL]] <- "//Gene-ref_locus" + xpath.expr[[BIODB.SYNONYMS]] <- "//Gene-ref_syn_E" + + for (content in contents) { + + # Create instance + entry <- NcbigeneEntry$new() + + # Parse HTML + xml <- XML::xmlInternalTreeParse(content, asText = TRUE) + + # An error occured + if (length(XML::getNodeSet(xml, "//Error")) == 0 && length(XML::getNodeSet(xml, "//ERROR")) == 0) { + + # Test generic xpath expressions + for (field in names(xpath.expr)) { + v <- XML::xpathSApply(xml, xpath.expr[[field]], XML::xmlValue) + if (length(v) > 0) { + + # Eliminate duplicates + v <- v[ ! duplicated(v)] + + # Set field + entry$setField(field, v) + } + } + + # CCDS ID + ccdsid <- .find.ccds.id(xml) + if ( ! is.na(ccdsid)) + entry$setField(BIODB.NCBI.CCDS.ID, ccdsid) + } + + entries <- c(entries, entry) + } + + # Replace elements with no accession id by NULL + entries <- lapply(entries, function(x) if (is.na(x$getField(BIODB.ACCESSION))) NULL else x) + + # If the input was a single element, then output a single object + if (drop && length(contents) == 1) + entries <- entries[[1]] + + return(entries) + + # Get data + +} + +################ +# FIND CCDS ID # +################ + +.find.ccds.id <- function(xml) { + + # 1) Get all CCDS tags. + ccds_elements <- XML::getNodeSet(xml, "//Dbtag_db[text()='CCDS']/..//Object-id_str") + + # 2) If all CCDS are the same, go to point 4. + ccds <- NA_character_ + for (e in ccds_elements) { + current_ccds <- XML::xmlValue(e) + if (is.na(ccds)) + ccds <- current_ccds + else { + if (current_ccds != ccds) { + ccds <- NA_character_ + break + } + } + } + + # 3) There are several CCDS values, we need to find the best one (i.e.: the most current one). + if (is.na(ccds)) { + # For each CCDS, look for the parent Gene-commentary tag. Then look for the text content of the Gene-commentary_label which is situed under. Ignore CCDS that have no Gene-commentary_label associated. Choose the CCDS that has the smallest Gene-commentary_label in alphabetical order. + version <- NA_character_ + for (e in ccds_elements) { + versions <- XML::xpathSApply(e, "ancestor::Gene-commentary/Gene-commentary_label", XML::xmlValue) + if (length(versions) < 1) next + current_version <- versions[[length(versions)]] + if (is.na(version) || current_version < version) { + version <- current_version + ccds <- XML::xmlValue(e) + } + } + } + + return(ccds) +}