X-Git-Url: http://source.jalview.org/gitweb/?a=blobdiff_plain;f=src%2Fjalview%2Fanalysis%2FCrossRef.java;h=9fd87dfbab9db8e02129966025fae5243cbcd982;hb=36dceb54710feb97a81f4bd69ad051f316141dc3;hp=2e6431cb804901b36e6914a5a262b54c288b6ddb;hpb=4d7f98a6dd54d9863ba449ec79dcd95d25ed863d;p=jalview.git diff --git a/src/jalview/analysis/CrossRef.java b/src/jalview/analysis/CrossRef.java index 2e6431c..9fd87df 100644 --- a/src/jalview/analysis/CrossRef.java +++ b/src/jalview/analysis/CrossRef.java @@ -24,391 +24,689 @@ import jalview.datamodel.AlignedCodonFrame; import jalview.datamodel.Alignment; import jalview.datamodel.AlignmentI; import jalview.datamodel.DBRefEntry; -import jalview.datamodel.DBRefSource; +import jalview.datamodel.Mapping; import jalview.datamodel.Sequence; +import jalview.datamodel.SequenceFeature; import jalview.datamodel.SequenceI; +import jalview.util.Comparison; import jalview.util.DBRefUtils; -import jalview.ws.SequenceFetcher; +import jalview.util.MapList; +import jalview.ws.SequenceFetcherFactory; import jalview.ws.seqfetcher.ASequenceFetcher; import java.util.ArrayList; +import java.util.Iterator; import java.util.List; -import java.util.Vector; /** - * Functions for cross-referencing sequence databases. user must first specify - * if cross-referencing from protein or dna (set dna==true) + * Functions for cross-referencing sequence databases. * * @author JimP * */ public class CrossRef { - /** - * Select just the DNA or protein references for a protein or dna sequence - * - * @param fromDna - * if true, select references from DNA (i.e. Protein databases), else - * DNA database references - * @param refs - * a set of references to select from - * @return + /* + * the dataset of the alignment for which we are searching for + * cross-references; in some cases we may resolve xrefs by + * searching in the dataset */ - public static DBRefEntry[] findXDbRefs(boolean fromDna, DBRefEntry[] refs) - { - return DBRefUtils.selectRefs(refs, fromDna ? DBRefSource.PROTEINDBS - : DBRefSource.DNACODINGDBS); - // could attempt to find other cross - // refs here - ie PDB xrefs - // (not dna, not protein seq) - } + private AlignmentI dataset; + + /* + * true if we are searching for cross-references from nucleotide, + * i.e. for protein sequences, false if the reverse + */ + private boolean fromDna; + + /* + * the sequences for which we are seeking cross-references + */ + private SequenceI[] fromSeqs; /** - * @param dna - * true if seqs are DNA seqs + * Constructor + * * @param seqs - * @return a list of sequence database cross reference source types + * the sequences for which we are seeking cross-references + * @param ds + * the containing alignment dataset (may be searched to resolve + * cross-references) */ - public static String[] findSequenceXrefTypes(boolean dna, SequenceI[] seqs) + public CrossRef(SequenceI[] seqs, AlignmentI ds) { - return findSequenceXrefTypes(dna, seqs, null); + fromSeqs = seqs; + fromDna = ds.isNucleotide(); + dataset = ds.getDataset() == null ? ds : ds.getDataset(); } /** - * Indirect references are references from other sequences from the dataset to - * any of the direct DBRefEntrys on the given sequences. - * - * @param dna - * true if seqs are DNA seqs - * @param seqs - * @return a list of sequence database cross reference source types + * Returns a list of distinct database sources for which sequences have either + * + * @return */ - public static String[] findSequenceXrefTypes(boolean dna, - SequenceI[] seqs, AlignmentI dataset) + public List findXrefSourcesForSequences() { - String[] dbrefs = null; - List refs = new ArrayList(); - for (int s = 0; s < seqs.length; s++) + List sources = new ArrayList(); + for (SequenceI seq : fromSeqs) { - if (seqs[s] != null) + if (seq != null) { - SequenceI dss = seqs[s]; - while (dss.getDatasetSequence() != null) - { - dss = dss.getDatasetSequence(); - } - DBRefEntry[] rfs = findXDbRefs(dna, dss.getDBRef()); - for (int r = 0; rfs != null && r < rfs.length; r++) - { - if (!refs.contains(rfs[r].getSource())) - { - refs.add(rfs[r].getSource()); - } - } - if (dataset != null) - { - // search for references to this sequence's direct references. - DBRefEntry[] lrfs = CrossRef - .findXDbRefs(!dna, seqs[s].getDBRef()); - List rseqs = new ArrayList(); - CrossRef.searchDatasetXrefs(seqs[s], !dna, lrfs, dataset, rseqs, - null); // don't need to specify codon frame for mapping here - for (SequenceI rs : rseqs) - { - DBRefEntry[] xrs = findXDbRefs(dna, rs.getDBRef()); // not used?? - for (int r = 0; rfs != null && r < rfs.length; r++) - { - if (!refs.contains(rfs[r].getSource())) - { - refs.add(rfs[r].getSource()); - } - } - } - } + findXrefSourcesForSequence(seq, sources); } } - if (refs.size() > 0) - { - dbrefs = new String[refs.size()]; - refs.toArray(dbrefs); - } - return dbrefs; + return sources; } - /* - * if (dna) { if (rfs[r].hasMap()) { // most likely this is a protein cross - * reference if (!refs.contains(rfs[r].getSource())) { - * refs.addElement(rfs[r].getSource()); } } } + /** + * Returns a list of distinct database sources for which a sequence has either + *
    + *
  • a (dna-to-protein or protein-to-dna) cross-reference
  • + *
  • an indirect cross-reference - a (dna-to-protein or protein-to-dna) + * reference from another sequence in the dataset which has a cross-reference + * to a direct DBRefEntry on the given sequence
  • + *
+ * + * @param seq + * the sequence whose dbrefs we are searching against + * @param sources + * a list of sources to add matches to */ - public static boolean hasCdnaMap(SequenceI[] seqs) + void findXrefSourcesForSequence(SequenceI seq, List sources) { - String[] reftypes = findSequenceXrefTypes(false, seqs); - for (int s = 0; s < reftypes.length; s++) + /* + * first find seq's xrefs (dna-to-peptide or peptide-to-dna) + */ + DBRefEntry[] rfs = DBRefUtils.selectDbRefs(!fromDna, seq.getDBRefs()); + addXrefsToSources(rfs, sources); + if (dataset != null) { - if (reftypes.equals(DBRefSource.EMBLCDS)) + /* + * find sequence's direct (dna-to-dna, peptide-to-peptide) xrefs + */ + DBRefEntry[] lrfs = DBRefUtils.selectDbRefs(fromDna, seq.getDBRefs()); + List rseqs = new ArrayList(); + + /* + * find sequences in the alignment which xref one of these DBRefs + * i.e. is xref-ed to a common sequence identifier + */ + searchDatasetXrefs(seq, lrfs, rseqs, null); + + /* + * add those sequences' (dna-to-peptide or peptide-to-dna) dbref sources + */ + for (SequenceI rs : rseqs) { - return true; - // no map + DBRefEntry[] xrs = DBRefUtils + .selectDbRefs(!fromDna, rs.getDBRefs()); + addXrefsToSources(xrs, sources); } } - return false; } - public static SequenceI[] getCdnaMap(SequenceI[] seqs) + /** + * Helper method that adds the source identifiers of some cross-references to + * a (non-redundant) list of database sources + * + * @param xrefs + * @param sources + */ + void addXrefsToSources(DBRefEntry[] xrefs, List sources) { - Vector cseqs = new Vector(); - for (int s = 0; s < seqs.length; s++) + if (xrefs != null) { - DBRefEntry[] cdna = findXDbRefs(true, seqs[s].getDBRef()); - for (int c = 0; c < cdna.length; c++) + for (DBRefEntry ref : xrefs) { - if (cdna[c].getSource().equals(DBRefSource.EMBLCDS)) + /* + * avoid duplication e.g. ENSEMBL and Ensembl + */ + String source = DBRefUtils.getCanonicalName(ref.getSource()); + if (!sources.contains(source)) { - System.err - .println("TODO: unimplemented sequence retrieval for coding region sequence."); - // TODO: retrieve CDS dataset sequences - // need global dataset sequence retriever/resolver to reuse refs - // and construct Mapping entry. - // insert gaps in CDS according to peptide gaps. - // add gapped sequence to cseqs + sources.add(source); } } } - if (cseqs.size() > 0) - { - SequenceI[] rsqs = new SequenceI[cseqs.size()]; - cseqs.copyInto(rsqs); - return rsqs; - } - return null; - - } - - /** - * - * @param dna - * @param seqs - * @return - */ - public static Alignment findXrefSequences(SequenceI[] seqs, boolean dna, - String source) - { - return findXrefSequences(seqs, dna, source, null); } /** + * Attempts to find cross-references from the sequences provided in the + * constructor to the given source database. Cross-references may be found + *
    + *
  • in dbrefs on the sequence which hold a mapping to a sequence + *
      + *
    • provided with a fetched sequence (e.g. ENA translation), or
    • + *
    • populated previously after getting cross-references
    • + *
    + *
  • as other sequences in the alignment which share a dbref identifier with + * the sequence
  • + *
  • by fetching from the remote database
  • + *
+ * The cross-referenced sequences, and mappings to them, are added to the + * alignment dataset. * - * @param seqs - * @param dna * @param source - * @param dataset - * alignment to search for product sequences. - * @return products (as dataset sequences) + * @return cross-referenced sequences (as dataset sequences) */ - public static Alignment findXrefSequences(SequenceI[] seqs, boolean dna, - String source, AlignmentI dataset) + public Alignment findXrefSequences(String source) { + List rseqs = new ArrayList(); - Alignment ral = null; - AlignedCodonFrame cf = new AlignedCodonFrame(); // nominal width - for (int s = 0; s < seqs.length; s++) + AlignedCodonFrame cf = new AlignedCodonFrame(); + SequenceIdMatcher matcher = new SequenceIdMatcher( + dataset.getSequences()); + + for (SequenceI seq : fromSeqs) { - SequenceI dss = seqs[s]; + SequenceI dss = seq; while (dss.getDatasetSequence() != null) { dss = dss.getDatasetSequence(); } boolean found = false; - DBRefEntry[] xrfs = CrossRef.findXDbRefs(dna, dss.getDBRef()); + DBRefEntry[] xrfs = DBRefUtils + .selectDbRefs(!fromDna, dss.getDBRefs()); if ((xrfs == null || xrfs.length == 0) && dataset != null) { - System.out.println("Attempting to find ds Xrefs refs."); - DBRefEntry[] lrfs = CrossRef.findXDbRefs(!dna, seqs[s].getDBRef()); - // less ambiguous would be a 'find primary dbRefEntry' method. - // filter for desired source xref here - found = CrossRef.searchDatasetXrefs(dss, !dna, lrfs, dataset, - rseqs, cf); + /* + * found no suitable dbrefs on sequence - look for sequences in the + * alignment which share a dbref with this one + */ + DBRefEntry[] lrfs = DBRefUtils.selectDbRefs(fromDna, + seq.getDBRefs()); + + /* + * find sequences (except this one!), of complementary type, + * which have a dbref to an accession id for this sequence, + * and add them to the results + */ + found = searchDatasetXrefs(dss, lrfs, rseqs, cf); } - for (int r = 0; xrfs != null && r < xrfs.length; r++) + if (xrfs == null && !found) { - if (source != null && !source.equals(xrfs[r].getSource())) - { - continue; - } - if (xrfs[r].hasMap()) + /* + * no dbref to source on this sequence or matched + * complementary sequence in the dataset + */ + continue; + } + List sourceRefs = DBRefUtils.searchRefsForSource(xrfs, + source); + Iterator refIterator = sourceRefs.iterator(); + while (refIterator.hasNext()) + { + DBRefEntry xref = refIterator.next(); + found = false; + if (xref.hasMap()) { - if (xrfs[r].getMap().getTo() != null) + SequenceI mappedTo = xref.getMap().getTo(); + if (mappedTo != null) { - SequenceI rsq = new Sequence(xrfs[r].getMap().getTo()); + /* + * dbref contains the sequence it maps to; add it to the + * results unless we have done so already (could happen if + * fetching xrefs for sequences which have xrefs in common) + * for example: UNIPROT {P0CE19, P0CE20} -> EMBL {J03321, X06707} + */ + found = true; + /* + * problem: matcher.findIdMatch() is lenient - returns a sequence + * with a dbref to the search arg e.g. ENST for ENSP - wrong + * but findInDataset() matches ENSP when looking for Uniprot... + */ + SequenceI matchInDataset = findInDataset(xref); + /*matcher.findIdMatch(mappedTo);*/ + if (matchInDataset != null) + { + if (!rseqs.contains(matchInDataset)) + { + rseqs.add(matchInDataset); + } + refIterator.remove(); + continue; + } + SequenceI rsq = new Sequence(mappedTo); rseqs.add(rsq); - if (xrfs[r].getMap().getMap().getFromRatio() != xrfs[r] - .getMap().getMap().getToRatio()) + if (xref.getMap().getMap().getFromRatio() != xref.getMap() + .getMap().getToRatio()) { // get sense of map correct for adding to product alignment. - if (dna) + if (fromDna) { // map is from dna seq to a protein product - cf.addMap(dss, rsq, xrfs[r].getMap().getMap()); + cf.addMap(dss, rsq, xref.getMap().getMap()); } else { // map should be from protein seq to its coding dna - cf.addMap(rsq, dss, xrfs[r].getMap().getMap().getInverse()); + cf.addMap(rsq, dss, xref.getMap().getMap().getInverse()); } } - found = true; } } + if (!found) { - // do a bit more work - search for sequences with references matching - // xrefs on this sequence. - if (dataset != null) + SequenceI matchedSeq = matcher.findIdMatch(xref.getSource() + "|" + + xref.getAccessionId()); + if (matchedSeq != null) { - found |= searchDataset(dss, xrfs[r], dataset, rseqs, cf); // ,false,!dna); - if (found) + if (constructMapping(seq, matchedSeq, xref, cf)) { - xrfs[r] = null; // we've recovered seqs for this one. + found = true; } } } + + if (!found) + { + // do a bit more work - search for sequences with references matching + // xrefs on this sequence. + found = searchDataset(dss, xref, rseqs, cf, false); + } + if (found) + { + refIterator.remove(); + } } - if (!found) + + /* + * fetch from source database any dbrefs we haven't resolved up to here + */ + if (!sourceRefs.isEmpty()) { - if (xrfs != null && xrfs.length > 0) + ASequenceFetcher sftch = SequenceFetcherFactory + .getSequenceFetcher(); + SequenceI[] retrieved = null; + try { - // Try and get the sequence reference... - /* - * Ideal world - we ask for a sequence fetcher implementation here if - * (jalview.io.RunTimeEnvironment.getSequenceFetcher()) ( - */ - ASequenceFetcher sftch = new SequenceFetcher(); - SequenceI[] retrieved = null; - int l = xrfs.length; - for (int r = 0; r < xrfs.length; r++) - { - // filter out any irrelevant or irretrievable references - if (xrfs[r] == null - || ((source != null && !source.equals(xrfs[r] - .getSource())) || !sftch.isFetchable(xrfs[r] - .getSource()))) - { - l--; - xrfs[r] = null; - } - } - if (l > 0) + retrieved = sftch.getSequences(sourceRefs, !fromDna); + } catch (Exception e) + { + System.err + .println("Problem whilst retrieving cross references for Sequence : " + + seq.getName()); + e.printStackTrace(); + } + + if (retrieved != null) + { + updateDbrefMappings(seq, xrfs, retrieved, cf); + for (SequenceI retrievedSequence : retrieved) { - System.out - .println("Attempting to retrieve cross referenced sequences."); - DBRefEntry[] t = new DBRefEntry[l]; - l = 0; - for (int r = 0; r < xrfs.length; r++) + SequenceI retrievedDss = retrievedSequence.getDatasetSequence() == null ? retrievedSequence + : retrievedSequence.getDatasetSequence(); + DBRefEntry[] dbr = retrievedSequence.getDBRefs(); + if (dbr != null) { - if (xrfs[r] != null) + for (DBRefEntry dbref : dbr) { - t[l++] = xrfs[r]; - } - } - xrfs = t; - try - { - retrieved = sftch.getSequences(xrfs); // problem here is we don't - // know which of xrfs - // resulted in which - // retrieved element - } catch (Exception e) - { - System.err - .println("Problem whilst retrieving cross references for Sequence : " - + seqs[s].getName()); - e.printStackTrace(); - } - if (retrieved != null) - { - for (int rs = 0; rs < retrieved.length; rs++) - { - // TODO: examine each sequence for 'redundancy' - jalview.datamodel.DBRefEntry[] dbr = retrieved[rs] - .getDBRef(); - if (dbr != null && dbr.length > 0) + // find any entry where we should put in the sequence being + // cross-referenced into the map + Mapping map = dbref.getMap(); + if (map != null) { - for (int di = 0; di < dbr.length; di++) + if (map.getTo() != null && map.getMap() != null) { - // find any entry where we should put in the sequence being - // cross-referenced into the map - jalview.datamodel.Mapping map = dbr[di].getMap(); - if (map != null) + // TODO findInDataset requires exact sequence match but + // 'congruent' test is only for the mapped part + // maybe not a problem in practice since only ENA provide a + // mapping and it is to the full protein translation of CDS + SequenceI matched = findInDataset(dbref); + // matcher.findIdMatch(map.getTo()); + if (matched != null) + { + /* + * already got an xref to this sequence; update this + * map to point to the same sequence, and add + * any new dbrefs to it + */ + DBRefEntry[] toRefs = map.getTo().getDBRefs(); + if (toRefs != null) + { + for (DBRefEntry ref : toRefs) + { + matched.addDBRef(ref); // add or update mapping + } + } + map.setTo(matched); + } + else + { + matcher.add(map.getTo()); + } + try { - if (map.getTo() != null && map.getMap() != null) + // compare ms with dss and replace with dss in mapping + // if map is congruent + SequenceI ms = map.getTo(); + int sf = map.getMap().getToLowest(); + int st = map.getMap().getToHighest(); + SequenceI mappedrg = ms.getSubSequence(sf, st); + // SequenceI loc = dss.getSubSequence(sf, st); + if (mappedrg.getLength() > 0 + && ms.getSequenceAsString().equals( + dss.getSequenceAsString())) + // && mappedrg.getSequenceAsString().equals( + // loc.getSequenceAsString())) { - // should search the local dataset to find any existing - // candidates for To ! - try + String msg = "Mapping updated from " + ms.getName() + + " to retrieved crossreference " + + dss.getName(); + System.out.println(msg); + map.setTo(dss); + + /* + * give the reverse reference the inverse mapping + * (if it doesn't have one already) + */ + setReverseMapping(dss, dbref, cf); + + /* + * copy sequence features as well, avoiding + * duplication (e.g. same variation from two + * transcripts) + */ + SequenceFeature[] sfs = ms.getSequenceFeatures(); + if (sfs != null) { - // compare ms with dss and replace with dss in mapping - // if map is congruent - SequenceI ms = map.getTo(); - int sf = map.getMap().getToLowest(); - int st = map.getMap().getToHighest(); - SequenceI mappedrg = ms.getSubSequence(sf, st); - SequenceI loc = dss.getSubSequence(sf, st); - if (mappedrg.getLength() > 0 - && mappedrg.getSequenceAsString().equals( - loc.getSequenceAsString())) + for (SequenceFeature feat : sfs) { - System.err - .println("Mapping updated for retrieved crossreference"); - // method to update all refs of existing To on - // retrieved sequence with dss and merge any props - // on To onto dss. - map.setTo(dss); + /* + * make a flyweight feature object which ignores Parent + * attribute in equality test; this avoids creating many + * otherwise duplicate exon features on genomic sequence + */ + SequenceFeature newFeature = new SequenceFeature( + feat) + { + @Override + public boolean equals(Object o) + { + return super.equals(o, true); + } + }; + dss.addSequenceFeature(newFeature); } - } catch (Exception e) - { - System.err - .println("Exception when consolidating Mapped sequence set..."); - e.printStackTrace(System.err); } } + cf.addMap(retrievedDss, map.getTo(), map.getMap()); + } catch (Exception e) + { + System.err + .println("Exception when consolidating Mapped sequence set..."); + e.printStackTrace(System.err); } } } - retrieved[rs].updatePDBIds(); - rseqs.add(retrieved[rs]); } } + retrievedSequence.updatePDBIds(); + rseqs.add(retrievedDss); + dataset.addSequence(retrievedDss); + matcher.add(retrievedDss); } } } } + + Alignment ral = null; if (rseqs.size() > 0) { - SequenceI[] rsqs = new SequenceI[rseqs.size()]; - rseqs.toArray(rsqs); - ral = new Alignment(rsqs); - if (cf != null && cf.getProtMappings() != null) + ral = new Alignment(rseqs.toArray(new SequenceI[rseqs.size()])); + if (!cf.isEmpty()) { - ral.addCodonFrame(cf); + dataset.addCodonFrame(cf); } } return ral; } /** + * Sets the inverse sequence mapping in the corresponding dbref of the mapped + * to sequence (if any). This is used after fetching a cross-referenced + * sequence, if the fetched sequence has a mapping to the original sequence, + * to set the mapping in the original sequence's dbref. + * + * @param mapFrom + * the sequence mapped from + * @param dbref + * @param mappings + */ + void setReverseMapping(SequenceI mapFrom, DBRefEntry dbref, + AlignedCodonFrame mappings) + { + SequenceI mapTo = dbref.getMap().getTo(); + if (mapTo == null) + { + return; + } + DBRefEntry[] dbrefs = mapTo.getDBRefs(); + if (dbrefs == null) + { + return; + } + for (DBRefEntry toRef : dbrefs) + { + if (toRef.hasMap() && mapFrom == toRef.getMap().getTo()) + { + /* + * found the reverse dbref; update its mapping if null + */ + if (toRef.getMap().getMap() == null) + { + MapList inverse = dbref.getMap().getMap().getInverse(); + toRef.getMap().setMap(inverse); + mappings.addMap(mapTo, mapFrom, inverse); + } + } + } + } + + /** + * Returns the first identical sequence in the dataset if any, else null + * + * @param xref + * @return + */ + SequenceI findInDataset(DBRefEntry xref) + { + if (xref == null || !xref.hasMap() || xref.getMap().getTo() == null) + { + return null; + } + SequenceI mapsTo = xref.getMap().getTo(); + String name = xref.getAccessionId(); + String name2 = xref.getSource() + "|" + name; + SequenceI dss = mapsTo.getDatasetSequence() == null ? mapsTo : mapsTo + .getDatasetSequence(); + for (SequenceI seq : dataset.getSequences()) + { + /* + * clumsy alternative to using SequenceIdMatcher which currently + * returns sequences with a dbref to the matched accession id + * which we don't want + */ + if (name.equals(seq.getName()) || seq.getName().startsWith(name2)) + { + if (sameSequence(seq, dss)) + { + return seq; + } + } + } + return null; + } + + /** + * Answers true if seq1 and seq2 contain exactly the same characters (ignoring + * case), else false. This method compares the lengths, then each character in + * turn, in order to 'fail fast'. For case-sensitive comparison, it would be + * possible to use Arrays.equals(seq1.getSequence(), seq2.getSequence()). + * + * @param seq1 + * @param seq2 + * @return + */ + // TODO move to Sequence / SequenceI + static boolean sameSequence(SequenceI seq1, SequenceI seq2) + { + if (seq1 == seq2) + { + return true; + } + if (seq1 == null || seq2 == null) + { + return false; + } + char[] c1 = seq1.getSequence(); + char[] c2 = seq2.getSequence(); + if (c1.length != c2.length) + { + return false; + } + for (int i = 0; i < c1.length; i++) + { + int diff = c1[i] - c2[i]; + /* + * same char or differ in case only ('a'-'A' == 32) + */ + if (diff != 0 && diff != 32 && diff != -32) + { + return false; + } + } + return true; + } + + /** + * Updates any empty mappings in the cross-references with one to a compatible + * retrieved sequence if found, and adds any new mappings to the + * AlignedCodonFrame + * + * @param mapFrom + * @param xrefs + * @param retrieved + * @param acf + */ + void updateDbrefMappings(SequenceI mapFrom, + DBRefEntry[] xrefs, SequenceI[] retrieved, AlignedCodonFrame acf) + { + SequenceIdMatcher matcher = new SequenceIdMatcher(retrieved); + for (DBRefEntry xref : xrefs) + { + if (!xref.hasMap()) + { + String targetSeqName = xref.getSource() + "|" + + xref.getAccessionId(); + SequenceI[] matches = matcher.findAllIdMatches(targetSeqName); + if (matches == null) + { + return; + } + for (SequenceI seq : matches) + { + constructMapping(mapFrom, seq, xref, acf); + } + } + } + } + + /** + * Tries to make a mapping between sequences. If successful, adds the mapping + * to the dbref and the mappings collection and answers true, otherwise + * answers false. The following methods of making are mapping are tried in + * turn: + *
    + *
  • if 'mapTo' holds a mapping to 'mapFrom', take the inverse; this is, for + * example, the case after fetching EMBL cross-references for a Uniprot + * sequence
  • + *
  • else check if the dna translates exactly to the protein (give or take + * start and stop codons>
  • + *
  • else try to map based on CDS features on the dna sequence
  • + *
+ * + * @param mapFrom + * @param mapTo + * @param xref + * @param mappings + * @return + */ + boolean constructMapping(SequenceI mapFrom, SequenceI mapTo, + DBRefEntry xref, AlignedCodonFrame mappings) + { + MapList mapping = null; + + /* + * look for a reverse mapping, if found make its inverse + */ + if (mapTo.getDBRefs() != null) + { + for (DBRefEntry dbref : mapTo.getDBRefs()) + { + String name = dbref.getSource() + "|" + dbref.getAccessionId(); + if (dbref.hasMap() && mapFrom.getName().startsWith(name)) + { + /* + * looks like we've found a map from 'mapTo' to 'mapFrom' + * - invert it to make the mapping the other way + */ + MapList reverse = dbref.getMap().getMap().getInverse(); + xref.setMap(new Mapping(mapTo, reverse)); + mappings.addMap(mapFrom, mapTo, reverse); + return true; + } + } + } + + if (fromDna) + { + mapping = AlignmentUtils.mapCdnaToProtein(mapTo, mapFrom); + } + else + { + mapping = AlignmentUtils.mapCdnaToProtein(mapFrom, mapTo); + if (mapping != null) + { + mapping = mapping.getInverse(); + } + } + if (mapping == null) + { + return false; + } + xref.setMap(new Mapping(mapTo, mapping)); + if (fromDna) + { + AlignmentUtils.computeProteinFeatures(mapFrom, mapTo, mapping); + mappings.addMap(mapFrom, mapTo, mapping); + } + else + { + mappings.addMap(mapTo, mapFrom, mapping.getInverse()); + } + + return true; + } + + /** * find references to lrfs in the cross-reference set of each sequence in * dataset (that is not equal to sequenceI) Identifies matching DBRefEntry * based on source and accession string only - Map and Version are nulled. * * @param sequenceI * @param lrfs - * @param dataset * @param rseqs * @return true if matches were found. */ - private static boolean searchDatasetXrefs(SequenceI sequenceI, - boolean dna, DBRefEntry[] lrfs, AlignmentI dataset, - List rseqs, AlignedCodonFrame cf) + private boolean searchDatasetXrefs(SequenceI sequenceI, + DBRefEntry[] lrfs, List rseqs, AlignedCodonFrame cf) { boolean found = false; if (lrfs == null) @@ -421,50 +719,31 @@ public class CrossRef // add in wildcards xref.setVersion(null); xref.setMap(null); - found = searchDataset(sequenceI, xref, dataset, rseqs, cf, false, dna); + found |= searchDataset(sequenceI, xref, rseqs, cf, false); } return found; } /** - * search a given sequence dataset for references matching cross-references to - * the given sequence + * Searches dataset for DBRefEntrys matching the given one (xrf) and adds the + * associated sequence to rseqs * * @param sequenceI + * a sequence to ignore (start point of search) * @param xrf - * @param dataset + * a cross-reference to try to match * @param rseqs - * set of unique sequences + * result list to add to * @param cf - * @return true if one or more unique sequences were found and added - */ - public static boolean searchDataset(SequenceI sequenceI, DBRefEntry xrf, - AlignmentI dataset, List rseqs, AlignedCodonFrame cf) - { - return searchDataset(sequenceI, xrf, dataset, rseqs, cf, true, false); - } - - /** - * TODO: generalise to different protein classifications Search dataset for - * DBRefEntrys matching the given one (xrf) and add the associated sequence to - * rseq. - * - * @param sequenceI - * @param xrf - * @param dataset - * @param rseqs + * a set of sequence mappings to add to * @param direct * - search all references or only subset - * @param dna - * search dna or protein xrefs (if direct=false) * @return true if relationship found and sequence added. */ - public static boolean searchDataset(SequenceI sequenceI, DBRefEntry xrf, - AlignmentI dataset, List rseqs, AlignedCodonFrame cf, - boolean direct, boolean dna) + boolean searchDataset(SequenceI sequenceI, DBRefEntry xrf, + List rseqs, AlignedCodonFrame cf, boolean direct) { boolean found = false; - SequenceI[] typer = new SequenceI[1]; if (dataset == null) { return false; @@ -486,105 +765,82 @@ public class CrossRef System.err .println("Implementation warning: getProducts passed a dataset alignment without dataset sequences in it!"); } - if (nxt != sequenceI && nxt != sequenceI.getDatasetSequence()) + if (nxt == sequenceI || nxt == sequenceI.getDatasetSequence()) { - // check if this is the correct sequence type + continue; + } + /* + * only look at same molecule type if 'direct', or + * complementary type if !direct + */ + { + boolean isDna = Comparison + .isNucleotide(new SequenceI[] { nxt }); + if (direct ? (isDna != fromDna) : (isDna == fromDna)) { - typer[0] = nxt; - boolean isDna = jalview.util.Comparison.isNucleotide(typer); - if ((direct && isDna == dna) || (!direct && isDna != dna)) - { - // skip this sequence because it is same molecule type - continue; - } + // skip this sequence because it is wrong molecule type + continue; } + } - // look for direct or indirect references in common - DBRefEntry[] poss = nxt.getDBRef(), cands = null; - if (direct) - { - cands = jalview.util.DBRefUtils.searchRefs(poss, xrf); - } - else - { - poss = CrossRef.findXDbRefs(dna, poss); // - cands = jalview.util.DBRefUtils.searchRefs(poss, xrf); - } - if (cands != null) + // look for direct or indirect references in common + DBRefEntry[] poss = nxt.getDBRefs(); + List cands = null; + /* + * TODO does this make any sense? + * if 'direct', search the dbrefs for xrf + * else, filter the dbrefs by type and then search for xrf + * - the result is the same isn't it? + */ + if (direct) + { + cands = DBRefUtils.searchRefs(poss, xrf); + } + else + { + poss = DBRefUtils.selectDbRefs(!fromDna, poss); + cands = DBRefUtils.searchRefs(poss, xrf); + } + if (!cands.isEmpty()) + { + if (!rseqs.contains(nxt)) { - if (!rseqs.contains(nxt)) + found = true; + rseqs.add(nxt); + if (cf != null) { - rseqs.add(nxt); - boolean foundmap = cf != null; // don't search if we aren't given a codon map object - for (int r = 0; foundmap && r < cands.length; r++) + for (DBRefEntry candidate : cands) { - if (cands[r].hasMap()) + Mapping mapping = candidate.getMap(); + if (mapping != null) { - if (cands[r].getMap().getTo() != null - && cands[r].getMap().getMap().getFromRatio() != cands[r] - .getMap().getMap().getToRatio()) + MapList map = mapping.getMap(); + if (mapping.getTo() != null + && map.getFromRatio() != map.getToRatio()) { - foundmap = true; // get sense of map correct for adding to product // alignment. - if (dna) + if (fromDna) { // map is from dna seq to a protein product - cf.addMap(sequenceI, nxt, cands[r].getMap() - .getMap()); + cf.addMap(sequenceI, nxt, map); } else { // map should be from protein seq to its coding dna - cf.addMap(nxt, sequenceI, cands[r].getMap() - .getMap().getInverse()); + cf.addMap(nxt, sequenceI, map.getInverse()); } } } } - // TODO: add mapping between sequences if necessary - found = true; } + // TODO: add mapping between sequences if necessary } - } } } } return found; } - - /** - * precalculate different products that can be found for seqs in dataset and - * return them. - * - * @param dna - * @param seqs - * @param dataset - * @param fake - * - don't actually build lists - just get types - * @return public static Object[] buildXProductsList(boolean dna, SequenceI[] - * seqs, AlignmentI dataset, boolean fake) { String types[] = - * jalview.analysis.CrossRef.findSequenceXrefTypes( dna, seqs, - * dataset); if (types != null) { System.out.println("Xref Types for: - * "+(dna ? "dna" : "prot")); for (int t = 0; t < types.length; t++) { - * System.out.println("Type: " + types[t]); SequenceI[] prod = - * jalview.analysis.CrossRef.findXrefSequences(seqs, dna, types[t]); - * System.out.println("Found " + ((prod == null) ? "no" : "" + - * prod.length) + " products"); if (prod!=null) { for (int p=0; - * p