import jalview.io.FileParse;
import jalview.io.gff.SequenceOntologyFactory;
import jalview.io.gff.SequenceOntologyI;
+import jalview.util.Comparison;
import jalview.util.DBRefUtils;
import jalview.util.MapList;
{
private static final String ALLELES = "alleles";
- protected static final String CONSEQUENCE_TYPE = "consequence_type";
-
protected static final String PARENT = "Parent";
protected static final String ID = "ID";
GENOMIC("genomic"),
/**
- * type=cdna to fetch dna including UTRs
+ * type=cdna to fetch coding dna including UTRs
*/
CDNA("cdna"),
ds.setSourceDBRef(proteinSeq.getSourceDBRef());
Mapping map = new Mapping(ds, mapList);
- DBRefEntry dbr = new DBRefEntry(getDbSource(), getDbVersion(),
- proteinSeq.getName(), map);
+ DBRefEntry dbr = new DBRefEntry(getDbSource(),
+ getEnsemblDataVersion(), proteinSeq.getName(), map);
querySeq.getDatasetSequence().addDBRef(dbr);
/*
/*
* and add a reference to itself
*/
- DBRefEntry self = new DBRefEntry(getDbSource(), "0", seq.getName());
+ DBRefEntry self = new DBRefEntry(getDbSource(),
+ getEnsemblDataVersion(), seq.getName());
seq.addDBRef(self);
}
if (ids.contains(name)
|| ids.contains(name.replace("ENSP", "ENST")))
{
- DBRefUtils.parseToDbRef(sq, DBRefSource.ENSEMBL, "0", name);
+ DBRefUtils.parseToDbRef(sq, getDbSource(),
+ getEnsemblDataVersion(), name);
}
}
if (alignment == null)
{
complement.append(",");
}
- if ("HGMD_MUTATION".equalsIgnoreCase(allele))
+
+ /*
+ * some 'alleles' are actually descriptive terms
+ * e.g. HGMD_MUTATION, PhenCode_variation
+ * - we don't want to 'reverse complement' these
+ */
+ if (!Comparison.isNucleotideSequence(allele, true))
{
complement.append(allele);
}
else
{
- char[] alleles = allele.toCharArray();
- for (int i = alleles.length - 1; i >= 0; i--)
+ for (int i = allele.length() - 1; i >= 0; i--)
{
- complement.append(Dna.getComplement(alleles[i]));
+ complement.append(Dna.getComplement(allele.charAt(i)));
}
}
}