X-Git-Url: http://source.jalview.org/gitweb/?a=blobdiff_plain;f=src%2Fjalview%2Fanalysis%2FDna.java;h=16cae4945920e174d6bf1f8c4966c915a0c923e9;hb=47168f025aefdaa044802bd5f8f510ffe43a4808;hp=482c54a8bdacf41999ab959535528f592059b994;hpb=8a6fa9ea9900d0f106529c3f6283e7f9d76dd2cb;p=jalview.git
diff --git a/src/jalview/analysis/Dna.java b/src/jalview/analysis/Dna.java
index 482c54a..16cae49 100644
--- a/src/jalview/analysis/Dna.java
+++ b/src/jalview/analysis/Dna.java
@@ -1,716 +1,799 @@
-/*
- * Jalview - A Sequence Alignment Editor and Viewer (Version 2.6)
- * Copyright (C) 2010 J Procter, AM Waterhouse, G Barton, M Clamp, S Searle
- *
- * This file is part of Jalview.
- *
- * Jalview is free software: you can redistribute it and/or
- * modify it under the terms of the GNU General Public License
- * as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version.
- *
- * Jalview is distributed in the hope that it will be useful, but
- * WITHOUT ANY WARRANTY; without even the implied warranty
- * of MERCHANTABILITY or FITNESS FOR A PARTICULAR
- * PURPOSE. See the GNU General Public License for more details.
- *
- * You should have received a copy of the GNU General Public License along with Jalview. If not, see .
- */
-package jalview.analysis;
-
-import java.util.Enumeration;
-import java.util.Hashtable;
-import java.util.Vector;
-
-import jalview.datamodel.AlignedCodonFrame;
-import jalview.datamodel.Alignment;
-import jalview.datamodel.AlignmentAnnotation;
-import jalview.datamodel.AlignmentI;
-import jalview.datamodel.Annotation;
-import jalview.datamodel.ColumnSelection;
-import jalview.datamodel.DBRefEntry;
-import jalview.datamodel.FeatureProperties;
-import jalview.datamodel.Mapping;
-import jalview.datamodel.Sequence;
-import jalview.datamodel.SequenceFeature;
-import jalview.datamodel.SequenceI;
-import jalview.schemes.ResidueProperties;
-import jalview.util.MapList;
-import jalview.util.ShiftList;
-
-public class Dna
-{
- /**
- *
- * @param cdp1
- * @param cdp2
- * @return -1 if cdp1 aligns before cdp2, 0 if in the same column or cdp2 is
- * null, +1 if after cdp2
- */
- private static int compare_codonpos(int[] cdp1, int[] cdp2)
- {
- if (cdp2 == null
- || (cdp1[0] == cdp2[0] && cdp1[1] == cdp2[1] && cdp1[2] == cdp2[2]))
- return 0;
- if (cdp1[0] < cdp2[0] || cdp1[1] < cdp2[1] || cdp1[2] < cdp2[2])
- return -1; // one base in cdp1 precedes the corresponding base in the
- // other codon
- return 1; // one base in cdp1 appears after the corresponding base in the
- // other codon.
- }
-
- /**
- * DNA->mapped protein sequence alignment translation given set of sequences
- * 1. id distinct coding regions within selected region for each sequence 2.
- * generate peptides based on inframe (or given) translation or (optionally
- * and where specified) out of frame translations (annotated appropriately) 3.
- * align peptides based on codon alignment
- */
- /**
- * id potential products from dna 1. search for distinct products within
- * selected region for each selected sequence 2. group by associated DB type.
- * 3. return as form for input into above function
- */
- /**
- *
- */
- /**
- * create a new alignment of protein sequences by an inframe translation of
- * the provided NA sequences
- *
- * @param selection
- * @param seqstring
- * @param viscontigs
- * @param gapCharacter
- * @param annotations
- * @param aWidth
- * @param dataset
- * destination dataset for translated sequences and mappings
- * @return
- */
- public static AlignmentI CdnaTranslate(SequenceI[] selection,
- String[] seqstring, int viscontigs[], char gapCharacter,
- AlignmentAnnotation[] annotations, int aWidth, Alignment dataset)
- {
- return CdnaTranslate(selection, seqstring, null, viscontigs,
- gapCharacter, annotations, aWidth, dataset);
- }
-
- /**
- *
- * @param selection
- * @param seqstring
- * @param product
- * - array of DbRefEntry objects from which exon map in seqstring is
- * derived
- * @param viscontigs
- * @param gapCharacter
- * @param annotations
- * @param aWidth
- * @param dataset
- * @return
- */
- public static AlignmentI CdnaTranslate(SequenceI[] selection,
- String[] seqstring, DBRefEntry[] product, int viscontigs[],
- char gapCharacter, AlignmentAnnotation[] annotations, int aWidth,
- Alignment dataset)
- {
- AlignedCodonFrame codons = new AlignedCodonFrame(aWidth); // stores hash of
- // subsequent
- // positions for
- // each codon
- // start position
- // in alignment
- int s, sSize = selection.length;
- Vector pepseqs = new Vector();
- for (s = 0; s < sSize; s++)
- {
- SequenceI newseq = translateCodingRegion(selection[s], seqstring[s],
- viscontigs, codons, gapCharacter,
- (product != null) ? product[s] : null); // possibly anonymous
- // product
- if (newseq != null)
- {
- pepseqs.addElement(newseq);
- SequenceI ds = newseq;
- while (ds.getDatasetSequence() != null)
- {
- ds = ds.getDatasetSequence();
- }
- dataset.addSequence(ds);
- }
- }
- if (codons.aaWidth == 0)
- return null;
- SequenceI[] newseqs = new SequenceI[pepseqs.size()];
- pepseqs.copyInto(newseqs);
- AlignmentI al = new Alignment(newseqs);
- al.padGaps(); // ensure we look aligned.
- al.setDataset(dataset);
- translateAlignedAnnotations(annotations, al, codons);
- al.addCodonFrame(codons);
- return al;
- }
-
- /**
- * fake the collection of DbRefs with associated exon mappings to identify if
- * a translation would generate distinct product in the currently selected
- * region.
- *
- * @param selection
- * @param viscontigs
- * @return
- */
- public static boolean canTranslate(SequenceI[] selection,
- int viscontigs[])
- {
- for (int gd = 0; gd < selection.length; gd++)
- {
- SequenceI dna = selection[gd];
- jalview.datamodel.DBRefEntry[] dnarefs = jalview.util.DBRefUtils
- .selectRefs(dna.getDBRef(),
- jalview.datamodel.DBRefSource.DNACODINGDBS);
- if (dnarefs != null)
- {
- // intersect with pep
- // intersect with pep
- Vector mappedrefs = new Vector();
- DBRefEntry[] refs = dna.getDBRef();
- for (int d = 0; d < refs.length; d++)
- {
- if (refs[d].getMap() != null && refs[d].getMap().getMap() != null
- && refs[d].getMap().getMap().getFromRatio() == 3
- && refs[d].getMap().getMap().getToRatio() == 1)
- {
- mappedrefs.addElement(refs[d]); // add translated protein maps
- }
- }
- dnarefs = new DBRefEntry[mappedrefs.size()];
- mappedrefs.copyInto(dnarefs);
- for (int d = 0; d < dnarefs.length; d++)
- {
- Mapping mp = dnarefs[d].getMap();
- if (mp != null)
- {
- for (int vc = 0; vc < viscontigs.length; vc += 2)
- {
- int[] mpr = mp.locateMappedRange(viscontigs[vc],
- viscontigs[vc + 1]);
- if (mpr != null)
- {
- return true;
- }
- }
- }
- }
- }
- }
- return false;
- }
-
- /**
- * generate a set of translated protein products from annotated sequenceI
- *
- * @param selection
- * @param viscontigs
- * @param gapCharacter
- * @param dataset
- * destination dataset for translated sequences
- * @param annotations
- * @param aWidth
- * @return
- */
- public static AlignmentI CdnaTranslate(SequenceI[] selection,
- int viscontigs[], char gapCharacter, Alignment dataset)
- {
- int alwidth = 0;
- Vector cdnasqs = new Vector();
- Vector cdnasqi = new Vector();
- Vector cdnaprod = new Vector();
- for (int gd = 0; gd < selection.length; gd++)
- {
- SequenceI dna = selection[gd];
- jalview.datamodel.DBRefEntry[] dnarefs = jalview.util.DBRefUtils
- .selectRefs(dna.getDBRef(),
- jalview.datamodel.DBRefSource.DNACODINGDBS);
- if (dnarefs != null)
- {
- // intersect with pep
- Vector mappedrefs = new Vector();
- DBRefEntry[] refs = dna.getDBRef();
- for (int d = 0; d < refs.length; d++)
- {
- if (refs[d].getMap() != null && refs[d].getMap().getMap() != null
- && refs[d].getMap().getMap().getFromRatio() == 3
- && refs[d].getMap().getMap().getToRatio() == 1)
- {
- mappedrefs.addElement(refs[d]); // add translated protein maps
- }
- }
- dnarefs = new DBRefEntry[mappedrefs.size()];
- mappedrefs.copyInto(dnarefs);
- for (int d = 0; d < dnarefs.length; d++)
- {
- Mapping mp = dnarefs[d].getMap();
- StringBuffer sqstr = new StringBuffer();
- if (mp != null)
- {
- Mapping intersect = mp.intersectVisContigs(viscontigs);
- // generate seqstring for this sequence based on mapping
-
- if (sqstr.length() > alwidth)
- alwidth = sqstr.length();
- cdnasqs.addElement(sqstr.toString());
- cdnasqi.addElement(dna);
- cdnaprod.addElement(intersect);
- }
- }
- }
- SequenceI[] cdna = new SequenceI[cdnasqs.size()];
- DBRefEntry[] prods = new DBRefEntry[cdnaprod.size()];
- String[] xons = new String[cdnasqs.size()];
- cdnasqs.copyInto(xons);
- cdnaprod.copyInto(prods);
- cdnasqi.copyInto(cdna);
- return CdnaTranslate(cdna, xons, prods, viscontigs, gapCharacter,
- null, alwidth, dataset);
- }
- return null;
- }
-
- /**
- * translate na alignment annotations onto translated amino acid alignment al
- * using codon mapping codons
- *
- * @param annotations
- * @param al
- * @param codons
- */
- public static void translateAlignedAnnotations(
- AlignmentAnnotation[] annotations, AlignmentI al,
- AlignedCodonFrame codons)
- {
- // //////////////////////////////
- // Copy annotations across
- //
- // Can only do this for columns with consecutive codons, or where
- // annotation is sequence associated.
-
- int pos, a, aSize;
- if (annotations != null)
- {
- for (int i = 0; i < annotations.length; i++)
- {
- // Skip any autogenerated annotation
- if (annotations[i].autoCalculated)
- {
- continue;
- }
-
- aSize = codons.getaaWidth(); // aa alignment width.
- jalview.datamodel.Annotation[] anots = (annotations[i].annotations == null) ? null
- : new jalview.datamodel.Annotation[aSize];
- if (anots != null)
- {
- for (a = 0; a < aSize; a++)
- {
- // process through codon map.
- if (codons.codons[a] != null
- && codons.codons[a][0] == (codons.codons[a][2] - 2))
- {
- anots[a] = getCodonAnnotation(codons.codons[a],
- annotations[i].annotations);
- }
- }
- }
-
- jalview.datamodel.AlignmentAnnotation aa = new jalview.datamodel.AlignmentAnnotation(
- annotations[i].label, annotations[i].description, anots);
- aa.graph = annotations[i].graph;
- aa.graphGroup = annotations[i].graphGroup;
- aa.graphHeight = annotations[i].graphHeight;
- if (annotations[i].getThreshold() != null)
- {
- aa.setThreshold(new jalview.datamodel.GraphLine(annotations[i]
- .getThreshold()));
- }
- if (annotations[i].hasScore)
- {
- aa.setScore(annotations[i].getScore());
- }
- if (annotations[i].sequenceRef != null)
- {
- SequenceI aaSeq = codons
- .getAaForDnaSeq(annotations[i].sequenceRef);
- if (aaSeq != null)
- {
- // aa.compactAnnotationArray(); // throw away alignment annotation
- // positioning
- aa.setSequenceRef(aaSeq);
- aa.createSequenceMapping(aaSeq, aaSeq.getStart(), true); // rebuild
- // mapping
- aa.adjustForAlignment();
- aaSeq.addAlignmentAnnotation(aa);
- }
-
- }
- al.addAnnotation(aa);
- }
- }
- }
-
- private static Annotation getCodonAnnotation(int[] is,
- Annotation[] annotations)
- {
- // Have a look at all the codon positions for annotation and put the first
- // one found into the translated annotation pos.
- int contrib = 0;
- Annotation annot = null;
- for (int p = 0; p < 3; p++)
- {
- if (annotations[is[p]] != null)
- {
- if (annot == null)
- {
- annot = new Annotation(annotations[is[p]]);
- contrib = 1;
- }
- else
- {
- // merge with last
- Annotation cpy = new Annotation(annotations[is[p]]);
- if (annot.colour == null)
- {
- annot.colour = cpy.colour;
- }
- if (annot.description == null || annot.description.length() == 0)
- {
- annot.description = cpy.description;
- }
- if (annot.displayCharacter == null)
- {
- annot.displayCharacter = cpy.displayCharacter;
- }
- if (annot.secondaryStructure == 0)
- {
- annot.secondaryStructure = cpy.secondaryStructure;
- }
- annot.value += cpy.value;
- contrib++;
- }
- }
- }
- if (contrib > 1)
- {
- annot.value /= (float) contrib;
- }
- return annot;
- }
-
- /**
- * Translate a na sequence
- *
- * @param selection
- * sequence displayed under viscontigs visible columns
- * @param seqstring
- * ORF read in some global alignment reference frame
- * @param viscontigs
- * mapping from global reference frame to visible seqstring ORF read
- * @param codons
- * Definition of global ORF alignment reference frame
- * @param gapCharacter
- * @param newSeq
- * @return sequence ready to be added to alignment.
- */
- public static SequenceI translateCodingRegion(SequenceI selection,
- String seqstring, int[] viscontigs, AlignedCodonFrame codons,
- char gapCharacter, DBRefEntry product)
- {
- Vector skip = new Vector();
- int skipint[] = null;
- ShiftList vismapping = new ShiftList(); // map from viscontigs to seqstring
- // intervals
- int vc, scontigs[] = new int[viscontigs.length];
- int npos = 0;
- for (vc = 0; vc < viscontigs.length; vc += 2)
- {
- if (vc == 0)
- {
- vismapping.addShift(npos, viscontigs[vc]);
- }
- else
- {
- // hidden region
- vismapping.addShift(npos, viscontigs[vc] - viscontigs[vc - 1] + 1);
- }
- scontigs[vc] = viscontigs[vc];
- scontigs[vc + 1] = viscontigs[vc + 1];
- }
-
- StringBuffer protein = new StringBuffer();
- String seq = seqstring.replace('U', 'T');
- char codon[] = new char[3];
- int cdp[] = new int[3], rf = 0, lastnpos = 0, nend;
- int aspos = 0;
- int resSize = 0;
- for (npos = 0, nend = seq.length(); npos < nend; npos++)
- {
- if (!jalview.util.Comparison.isGap(seq.charAt(npos)))
- {
- cdp[rf] = npos; // store position
- codon[rf++] = seq.charAt(npos); // store base
- }
- // filled an RF yet ?
- if (rf == 3)
- {
- String aa = ResidueProperties.codonTranslate(new String(codon));
- rf = 0;
- if (aa == null)
- {
- aa = String.valueOf(gapCharacter);
- if (skipint == null)
- {
- skipint = new int[]
- { cdp[0], cdp[2] };
- }
- skipint[1] = cdp[2];
- }
- else
- {
- if (skipint != null)
- {
- // edit scontigs
- skipint[0] = vismapping.shift(skipint[0]);
- skipint[1] = vismapping.shift(skipint[1]);
- for (vc = 0; vc < scontigs.length; vc += 2)
- {
- if (scontigs[vc + 1] < skipint[0])
- {
- continue;
- }
- if (scontigs[vc] <= skipint[0])
- {
- if (skipint[0] == scontigs[vc])
- {
-
- }
- else
- {
- int[] t = new int[scontigs.length + 2];
- System.arraycopy(scontigs, 0, t, 0, vc - 1);
- // scontigs[vc]; //
- }
- }
- }
- skip.addElement(skipint);
- skipint = null;
- }
- if (aa.equals("STOP"))
- {
- aa = "X";
- }
- resSize++;
- }
- // insert/delete gaps prior to this codon - if necessary
- boolean findpos = true;
- while (findpos)
- {
- // first ensure that the codons array is long enough.
- codons.checkCodonFrameWidth(aspos);
- // now check to see if we place the aa at the current aspos in the
- // protein alignment
- switch (Dna.compare_codonpos(cdp, codons.codons[aspos]))
- {
- case -1:
- codons.insertAAGap(aspos, gapCharacter);
- findpos = false;
- break;
- case +1:
- // this aa appears after the aligned codons at aspos, so prefix it
- // with a gap
- aa = "" + gapCharacter + aa;
- aspos++;
- // if (aspos >= codons.aaWidth)
- // codons.aaWidth = aspos + 1;
- break; // check the next position for alignment
- case 0:
- // codon aligns at aspos position.
- findpos = false;
- }
- }
- // codon aligns with all other sequence residues found at aspos
- protein.append(aa);
- lastnpos = npos;
- if (codons.codons[aspos] == null)
- {
- // mark this column as aligning to this aligned reading frame
- codons.codons[aspos] = new int[]
- { cdp[0], cdp[1], cdp[2] };
- }
- if (aspos >= codons.aaWidth)
- {
- // update maximum alignment width
- // (we can do this without calling checkCodonFrameWidth because it was
- // already done above)
- codons.setAaWidth(aspos);
- }
- // ready for next translated reading frame alignment position (if any)
- aspos++;
- }
- }
- if (resSize > 0)
- {
- SequenceI newseq = new Sequence(selection.getName(),
- protein.toString());
- if (rf != 0)
- {
- jalview.bin.Cache.log
- .debug("trimming contigs for incomplete terminal codon.");
- // map and trim contigs to ORF region
- vc = scontigs.length - 1;
- lastnpos = vismapping.shift(lastnpos); // place npos in context of
- // whole dna alignment (rather
- // than visible contigs)
- // incomplete ORF could be broken over one or two visible contig
- // intervals.
- while (vc >= 0 && scontigs[vc] > lastnpos)
- {
- if (vc > 0 && scontigs[vc - 1] > lastnpos)
- {
- vc -= 2;
- }
- else
- {
- // correct last interval in list.
- scontigs[vc] = lastnpos;
- }
- }
-
- if (vc > 0 && (vc + 1) < scontigs.length)
- {
- // truncate map list to just vc elements
- int t[] = new int[vc + 1];
- System.arraycopy(scontigs, 0, t, 0, vc + 1);
- scontigs = t;
- }
- if (vc <= 0)
- scontigs = null;
- }
- if (scontigs != null)
- {
- npos = 0;
- // map scontigs to actual sequence positions on selection
- for (vc = 0; vc < scontigs.length; vc += 2)
- {
- scontigs[vc] = selection.findPosition(scontigs[vc]); // not from 1!
- scontigs[vc + 1] = selection.findPosition(scontigs[vc + 1]); // exclusive
- if (scontigs[vc + 1] == selection.getEnd())
- break;
- }
- // trim trailing empty intervals.
- if ((vc + 2) < scontigs.length)
- {
- int t[] = new int[vc + 2];
- System.arraycopy(scontigs, 0, t, 0, vc + 2);
- scontigs = t;
- }
- /*
- * delete intervals in scontigs which are not translated. 1. map skip
- * into sequence position intervals 2. truncate existing ranges and add
- * new ranges to exclude untranslated regions. if (skip.size()>0) {
- * Vector narange = new Vector(); for (vc=0; vc=skipint[0] &&
- * iv[0]<=skipint[1]) { if (iv[0]==skipint[0]) { // delete beginning of
- * range } else { // truncate range and create new one if necessary iv =
- * (int[]) narange.elementAt(vc+1); if (iv[0]<=skipint[1]) { // truncate
- * range iv[0] = skipint[1]; } else { } } } else if (iv[0].
+ * The Jalview Authors are detailed in the 'AUTHORS' file.
+ */
+package jalview.analysis;
+
+import java.util.ArrayList;
+import java.util.Hashtable;
+import java.util.Vector;
+
+import jalview.datamodel.AlignedCodonFrame;
+import jalview.datamodel.Alignment;
+import jalview.datamodel.AlignmentAnnotation;
+import jalview.datamodel.AlignmentI;
+import jalview.datamodel.Annotation;
+import jalview.datamodel.DBRefEntry;
+import jalview.datamodel.FeatureProperties;
+import jalview.datamodel.Mapping;
+import jalview.datamodel.Sequence;
+import jalview.datamodel.SequenceFeature;
+import jalview.datamodel.SequenceI;
+import jalview.schemes.ResidueProperties;
+import jalview.util.MapList;
+import jalview.util.ShiftList;
+
+public class Dna
+{
+ /**
+ *
+ * @param cdp1
+ * @param cdp2
+ * @return -1 if cdp1 aligns before cdp2, 0 if in the same column or cdp2 is
+ * null, +1 if after cdp2
+ */
+ private static int compare_codonpos(int[] cdp1, int[] cdp2)
+ {
+ if (cdp2 == null
+ || (cdp1[0] == cdp2[0] && cdp1[1] == cdp2[1] && cdp1[2] == cdp2[2]))
+ return 0;
+ if (cdp1[0] < cdp2[0] || cdp1[1] < cdp2[1] || cdp1[2] < cdp2[2])
+ return -1; // one base in cdp1 precedes the corresponding base in the
+ // other codon
+ return 1; // one base in cdp1 appears after the corresponding base in the
+ // other codon.
+ }
+
+ /**
+ * DNA->mapped protein sequence alignment translation given set of sequences
+ * 1. id distinct coding regions within selected region for each sequence 2.
+ * generate peptides based on inframe (or given) translation or (optionally
+ * and where specified) out of frame translations (annotated appropriately) 3.
+ * align peptides based on codon alignment
+ */
+ /**
+ * id potential products from dna 1. search for distinct products within
+ * selected region for each selected sequence 2. group by associated DB type.
+ * 3. return as form for input into above function
+ */
+ /**
+ *
+ */
+ /**
+ * create a new alignment of protein sequences by an inframe translation of
+ * the provided NA sequences
+ *
+ * @param selection
+ * @param seqstring
+ * @param viscontigs
+ * @param gapCharacter
+ * @param annotations
+ * @param aWidth
+ * @param dataset
+ * destination dataset for translated sequences and mappings
+ * @return
+ */
+ public static AlignmentI CdnaTranslate(SequenceI[] selection,
+ String[] seqstring, int viscontigs[], char gapCharacter,
+ AlignmentAnnotation[] annotations, int aWidth, Alignment dataset)
+ {
+ return CdnaTranslate(selection, seqstring, null, viscontigs,
+ gapCharacter, annotations, aWidth, dataset);
+ }
+
+ /**
+ *
+ * @param selection
+ * @param seqstring
+ * @param product
+ * - array of DbRefEntry objects from which exon map in seqstring is
+ * derived
+ * @param viscontigs
+ * @param gapCharacter
+ * @param annotations
+ * @param aWidth
+ * @param dataset
+ * @return
+ */
+ public static AlignmentI CdnaTranslate(SequenceI[] selection,
+ String[] seqstring, DBRefEntry[] product, int viscontigs[],
+ char gapCharacter, AlignmentAnnotation[] annotations, int aWidth,
+ Alignment dataset)
+ {
+ AlignedCodonFrame codons = new AlignedCodonFrame(aWidth); // stores hash of
+ // subsequent
+ // positions for
+ // each codon
+ // start position
+ // in alignment
+ int s, sSize = selection.length;
+ Vector pepseqs = new Vector();
+ for (s = 0; s < sSize; s++)
+ {
+ SequenceI newseq = translateCodingRegion(selection[s], seqstring[s],
+ viscontigs, codons, gapCharacter,
+ (product != null) ? product[s] : null, false); // possibly anonymous
+ // product
+ if (newseq != null)
+ {
+ pepseqs.addElement(newseq);
+ SequenceI ds = newseq;
+ if (dataset != null)
+ {
+ while (ds.getDatasetSequence() != null)
+ {
+ ds = ds.getDatasetSequence();
+ }
+ dataset.addSequence(ds);
+ }
+ }
+ }
+ if (codons.aaWidth == 0)
+ return null;
+ SequenceI[] newseqs = new SequenceI[pepseqs.size()];
+ pepseqs.copyInto(newseqs);
+ AlignmentI al = new Alignment(newseqs);
+ al.padGaps(); // ensure we look aligned.
+ al.setDataset(dataset);
+ translateAlignedAnnotations(annotations, al, codons);
+ al.addCodonFrame(codons);
+ return al;
+ }
+
+ /**
+ * fake the collection of DbRefs with associated exon mappings to identify if
+ * a translation would generate distinct product in the currently selected
+ * region.
+ *
+ * @param selection
+ * @param viscontigs
+ * @return
+ */
+ public static boolean canTranslate(SequenceI[] selection,
+ int viscontigs[])
+ {
+ for (int gd = 0; gd < selection.length; gd++)
+ {
+ SequenceI dna = selection[gd];
+ jalview.datamodel.DBRefEntry[] dnarefs = jalview.util.DBRefUtils
+ .selectRefs(dna.getDBRef(),
+ jalview.datamodel.DBRefSource.DNACODINGDBS);
+ if (dnarefs != null)
+ {
+ // intersect with pep
+ // intersect with pep
+ Vector mappedrefs = new Vector();
+ DBRefEntry[] refs = dna.getDBRef();
+ for (int d = 0; d < refs.length; d++)
+ {
+ if (refs[d].getMap() != null && refs[d].getMap().getMap() != null
+ && refs[d].getMap().getMap().getFromRatio() == 3
+ && refs[d].getMap().getMap().getToRatio() == 1)
+ {
+ mappedrefs.addElement(refs[d]); // add translated protein maps
+ }
+ }
+ dnarefs = new DBRefEntry[mappedrefs.size()];
+ mappedrefs.copyInto(dnarefs);
+ for (int d = 0; d < dnarefs.length; d++)
+ {
+ Mapping mp = dnarefs[d].getMap();
+ if (mp != null)
+ {
+ for (int vc = 0; vc < viscontigs.length; vc += 2)
+ {
+ int[] mpr = mp.locateMappedRange(viscontigs[vc],
+ viscontigs[vc + 1]);
+ if (mpr != null)
+ {
+ return true;
+ }
+ }
+ }
+ }
+ }
+ }
+ return false;
+ }
+
+ /**
+ * generate a set of translated protein products from annotated sequenceI
+ *
+ * @param selection
+ * @param viscontigs
+ * @param gapCharacter
+ * @param dataset
+ * destination dataset for translated sequences
+ * @param annotations
+ * @param aWidth
+ * @return
+ */
+ public static AlignmentI CdnaTranslate(SequenceI[] selection,
+ int viscontigs[], char gapCharacter, Alignment dataset)
+ {
+ int alwidth = 0;
+ Vector cdnasqs = new Vector();
+ Vector cdnasqi = new Vector();
+ Vector cdnaprod = new Vector();
+ for (int gd = 0; gd < selection.length; gd++)
+ {
+ SequenceI dna = selection[gd];
+ jalview.datamodel.DBRefEntry[] dnarefs = jalview.util.DBRefUtils
+ .selectRefs(dna.getDBRef(),
+ jalview.datamodel.DBRefSource.DNACODINGDBS);
+ if (dnarefs != null)
+ {
+ // intersect with pep
+ Vector mappedrefs = new Vector();
+ DBRefEntry[] refs = dna.getDBRef();
+ for (int d = 0; d < refs.length; d++)
+ {
+ if (refs[d].getMap() != null && refs[d].getMap().getMap() != null
+ && refs[d].getMap().getMap().getFromRatio() == 3
+ && refs[d].getMap().getMap().getToRatio() == 1)
+ {
+ mappedrefs.addElement(refs[d]); // add translated protein maps
+ }
+ }
+ dnarefs = new DBRefEntry[mappedrefs.size()];
+ mappedrefs.copyInto(dnarefs);
+ for (int d = 0; d < dnarefs.length; d++)
+ {
+ Mapping mp = dnarefs[d].getMap();
+ StringBuffer sqstr = new StringBuffer();
+ if (mp != null)
+ {
+ Mapping intersect = mp.intersectVisContigs(viscontigs);
+ // generate seqstring for this sequence based on mapping
+
+ if (sqstr.length() > alwidth)
+ alwidth = sqstr.length();
+ cdnasqs.addElement(sqstr.toString());
+ cdnasqi.addElement(dna);
+ cdnaprod.addElement(intersect);
+ }
+ }
+ }
+ SequenceI[] cdna = new SequenceI[cdnasqs.size()];
+ DBRefEntry[] prods = new DBRefEntry[cdnaprod.size()];
+ String[] xons = new String[cdnasqs.size()];
+ cdnasqs.copyInto(xons);
+ cdnaprod.copyInto(prods);
+ cdnasqi.copyInto(cdna);
+ return CdnaTranslate(cdna, xons, prods, viscontigs, gapCharacter,
+ null, alwidth, dataset);
+ }
+ return null;
+ }
+
+ /**
+ * translate na alignment annotations onto translated amino acid alignment al
+ * using codon mapping codons
+ *
+ * @param annotations
+ * @param al
+ * @param codons
+ */
+ public static void translateAlignedAnnotations(
+ AlignmentAnnotation[] annotations, AlignmentI al,
+ AlignedCodonFrame codons)
+ {
+ // //////////////////////////////
+ // Copy annotations across
+ //
+ // Can only do this for columns with consecutive codons, or where
+ // annotation is sequence associated.
+
+ int pos, a, aSize;
+ if (annotations != null)
+ {
+ for (int i = 0; i < annotations.length; i++)
+ {
+ // Skip any autogenerated annotation
+ if (annotations[i].autoCalculated)
+ {
+ continue;
+ }
+
+ aSize = codons.getaaWidth(); // aa alignment width.
+ jalview.datamodel.Annotation[] anots = (annotations[i].annotations == null) ? null
+ : new jalview.datamodel.Annotation[aSize];
+ if (anots != null)
+ {
+ for (a = 0; a < aSize; a++)
+ {
+ // process through codon map.
+ if (codons.codons[a] != null
+ && codons.codons[a][0] == (codons.codons[a][2] - 2))
+ {
+ anots[a] = getCodonAnnotation(codons.codons[a],
+ annotations[i].annotations);
+ }
+ }
+ }
+
+ jalview.datamodel.AlignmentAnnotation aa = new jalview.datamodel.AlignmentAnnotation(
+ annotations[i].label, annotations[i].description, anots);
+ aa.graph = annotations[i].graph;
+ aa.graphGroup = annotations[i].graphGroup;
+ aa.graphHeight = annotations[i].graphHeight;
+ if (annotations[i].getThreshold() != null)
+ {
+ aa.setThreshold(new jalview.datamodel.GraphLine(annotations[i]
+ .getThreshold()));
+ }
+ if (annotations[i].hasScore)
+ {
+ aa.setScore(annotations[i].getScore());
+ }
+ if (annotations[i].sequenceRef != null)
+ {
+ SequenceI aaSeq = codons
+ .getAaForDnaSeq(annotations[i].sequenceRef);
+ if (aaSeq != null)
+ {
+ // aa.compactAnnotationArray(); // throw away alignment annotation
+ // positioning
+ aa.setSequenceRef(aaSeq);
+ aa.createSequenceMapping(aaSeq, aaSeq.getStart(), true); // rebuild
+ // mapping
+ aa.adjustForAlignment();
+ aaSeq.addAlignmentAnnotation(aa);
+ }
+
+ }
+ al.addAnnotation(aa);
+ }
+ }
+ }
+
+ private static Annotation getCodonAnnotation(int[] is,
+ Annotation[] annotations)
+ {
+ // Have a look at all the codon positions for annotation and put the first
+ // one found into the translated annotation pos.
+ int contrib = 0;
+ Annotation annot = null;
+ for (int p = 0; p < 3; p++)
+ {
+ if (annotations[is[p]] != null)
+ {
+ if (annot == null)
+ {
+ annot = new Annotation(annotations[is[p]]);
+ contrib = 1;
+ }
+ else
+ {
+ // merge with last
+ Annotation cpy = new Annotation(annotations[is[p]]);
+ if (annot.colour == null)
+ {
+ annot.colour = cpy.colour;
+ }
+ if (annot.description == null || annot.description.length() == 0)
+ {
+ annot.description = cpy.description;
+ }
+ if (annot.displayCharacter == null)
+ {
+ annot.displayCharacter = cpy.displayCharacter;
+ }
+ if (annot.secondaryStructure == 0)
+ {
+ annot.secondaryStructure = cpy.secondaryStructure;
+ }
+ annot.value += cpy.value;
+ contrib++;
+ }
+ }
+ }
+ if (contrib > 1)
+ {
+ annot.value /= (float) contrib;
+ }
+ return annot;
+ }
+
+ /**
+ * Translate a na sequence
+ *
+ * @param selection
+ * sequence displayed under viscontigs visible columns
+ * @param seqstring
+ * ORF read in some global alignment reference frame
+ * @param viscontigs
+ * mapping from global reference frame to visible seqstring ORF read
+ * @param codons
+ * Definition of global ORF alignment reference frame
+ * @param gapCharacter
+ * @return sequence ready to be added to alignment.
+ * @deprecated Use {@link #translateCodingRegion(SequenceI,String,int[],AlignedCodonFrame,char,DBRefEntry,boolean)} instead
+ */
+ public static SequenceI translateCodingRegion(SequenceI selection,
+ String seqstring, int[] viscontigs, AlignedCodonFrame codons,
+ char gapCharacter, DBRefEntry product)
+ {
+ return translateCodingRegion(selection, seqstring, viscontigs, codons,
+ gapCharacter, product, false);
+ }
+
+ /**
+ * Translate a na sequence
+ *
+ * @param selection
+ * sequence displayed under viscontigs visible columns
+ * @param seqstring
+ * ORF read in some global alignment reference frame
+ * @param viscontigs
+ * mapping from global reference frame to visible seqstring ORF read
+ * @param codons
+ * Definition of global ORF alignment reference frame
+ * @param gapCharacter
+ * @param starForStop when true stop codons will translate as '*', otherwise as 'X'
+ * @return sequence ready to be added to alignment.
+ */
+ public static SequenceI translateCodingRegion(SequenceI selection,
+ String seqstring, int[] viscontigs, AlignedCodonFrame codons,
+ char gapCharacter, DBRefEntry product, final boolean starForStop)
+ {
+ java.util.List skip = new ArrayList();
+ int skipint[] = null;
+ ShiftList vismapping = new ShiftList(); // map from viscontigs to seqstring
+ // intervals
+ int vc, scontigs[] = new int[viscontigs.length];
+ int npos = 0;
+ for (vc = 0; vc < viscontigs.length; vc += 2)
+ {
+ if (vc == 0)
+ {
+ vismapping.addShift(npos, viscontigs[vc]);
+ }
+ else
+ {
+ // hidden region
+ vismapping.addShift(npos, viscontigs[vc] - viscontigs[vc - 1] + 1);
+ }
+ scontigs[vc] = viscontigs[vc];
+ scontigs[vc + 1] = viscontigs[vc + 1];
+ }
+
+ StringBuffer protein = new StringBuffer();
+ String seq = seqstring.replace('U', 'T');
+ char codon[] = new char[3];
+ int cdp[] = new int[3], rf = 0, lastnpos = 0, nend;
+ int aspos = 0;
+ int resSize = 0;
+ for (npos = 0, nend = seq.length(); npos < nend; npos++)
+ {
+ if (!jalview.util.Comparison.isGap(seq.charAt(npos)))
+ {
+ cdp[rf] = npos; // store position
+ codon[rf++] = seq.charAt(npos); // store base
+ }
+ // filled an RF yet ?
+ if (rf == 3)
+ {
+ String aa = ResidueProperties.codonTranslate(new String(codon));
+ rf = 0;
+ if (aa == null)
+ {
+ aa = String.valueOf(gapCharacter);
+ if (skipint == null)
+ {
+ skipint = new int[]
+ { cdp[0], cdp[2] };
+ }
+ skipint[1] = cdp[2];
+ }
+ else
+ {
+ if (skipint != null)
+ {
+ // edit scontigs
+ skipint[0] = vismapping.shift(skipint[0]);
+ skipint[1] = vismapping.shift(skipint[1]);
+ for (vc = 0; vc < scontigs.length; )
+ {
+ if (scontigs[vc + 1] < skipint[0])
+ {
+ // before skipint starts
+ vc += 2;
+ continue;
+ }
+ if (scontigs[vc]>skipint[1])
+ {
+ // finished editing so
+ break;
+ }
+ // Edit the contig list to include the skipped region which did not translate
+ int[] t;
+ // from : s1 e1 s2 e2 s3 e3
+ // to s: s1 e1 s2 k0 k1 e2 s3 e3
+ // list increases by one unless one boundary (s2==k0 or e2==k1) matches, and decreases by one if skipint intersects whole visible contig
+ if (scontigs[vc] <= skipint[0])
+ {
+ if (skipint[0] == scontigs[vc])
+ {
+ // skipint at start of contig
+ // shift the start of this contig
+ if (scontigs[vc + 1] > skipint[1])
+ {
+ scontigs[vc] = skipint[1];
+ vc+=2;
+ }
+ else
+ {
+ if (scontigs[vc+1]==skipint[1])
+ {
+ // remove the contig
+ t = new int[scontigs.length - 2];
+ if (vc > 0)
+ {
+ System.arraycopy(scontigs, 0, t, 0, vc - 1);
+ }
+ if (vc + 2 < t.length)
+ {
+ System.arraycopy(scontigs, vc + 2, t, vc, t.length
+ - vc + 2);
+ }
+ scontigs=t;
+ } else {
+ // truncate contig to before the skipint region
+ scontigs[vc+1] = skipint[0]-1;
+ vc+=2;
+ }
+ }
+ }
+ else
+ {
+ // scontig starts before start of skipint
+ if (scontigs[vc+1]= codons.aaWidth)
+ // codons.aaWidth = aspos + 1;
+ break; // check the next position for alignment
+ case 0:
+ // codon aligns at aspos position.
+ findpos = false;
+ }
+ }
+ // codon aligns with all other sequence residues found at aspos
+ protein.append(aa);
+ lastnpos = npos;
+ if (codons.codons[aspos] == null)
+ {
+ // mark this column as aligning to this aligned reading frame
+ codons.codons[aspos] = new int[]
+ { cdp[0], cdp[1], cdp[2] };
+ }
+ if (aspos >= codons.aaWidth)
+ {
+ // update maximum alignment width
+ // (we can do this without calling checkCodonFrameWidth because it was
+ // already done above)
+ codons.setAaWidth(aspos);
+ }
+ // ready for next translated reading frame alignment position (if any)
+ aspos++;
+ }
+ }
+ if (resSize > 0)
+ {
+ SequenceI newseq = new Sequence(selection.getName(),
+ protein.toString());
+ if (rf != 0)
+ {
+ if (jalview.bin.Cache.log!=null) {
+ jalview.bin.Cache.log.debug("trimming contigs for incomplete terminal codon.");
+ } else {
+ System.err.println("trimming contigs for incomplete terminal codon.");
+ }
+ // map and trim contigs to ORF region
+ vc = scontigs.length - 1;
+ lastnpos = vismapping.shift(lastnpos); // place npos in context of
+ // whole dna alignment (rather
+ // than visible contigs)
+ // incomplete ORF could be broken over one or two visible contig
+ // intervals.
+ while (vc >= 0 && scontigs[vc] > lastnpos)
+ {
+ if (vc > 0 && scontigs[vc - 1] > lastnpos)
+ {
+ vc -= 2;
+ }
+ else
+ {
+ // correct last interval in list.
+ scontigs[vc] = lastnpos;
+ }
+ }
+
+ if (vc > 0 && (vc + 1) < scontigs.length)
+ {
+ // truncate map list to just vc elements
+ int t[] = new int[vc + 1];
+ System.arraycopy(scontigs, 0, t, 0, vc + 1);
+ scontigs = t;
+ }
+ if (vc <= 0)
+ scontigs = null;
+ }
+ if (scontigs != null)
+ {
+ npos = 0;
+ // map scontigs to actual sequence positions on selection
+ for (vc = 0; vc < scontigs.length; vc += 2)
+ {
+ scontigs[vc] = selection.findPosition(scontigs[vc]); // not from 1!
+ scontigs[vc + 1] = selection.findPosition(scontigs[vc + 1]); // exclusive
+ if (scontigs[vc + 1] == selection.getEnd())
+ break;
+ }
+ // trim trailing empty intervals.
+ if ((vc + 2) < scontigs.length)
+ {
+ int t[] = new int[vc + 2];
+ System.arraycopy(scontigs, 0, t, 0, vc + 2);
+ scontigs = t;
+ }
+ /*
+ * delete intervals in scontigs which are not translated. 1. map skip
+ * into sequence position intervals 2. truncate existing ranges and add
+ * new ranges to exclude untranslated regions. if (skip.size()>0) {
+ * Vector narange = new Vector(); for (vc=0; vc=skipint[0] &&
+ * iv[0]<=skipint[1]) { if (iv[0]==skipint[0]) { // delete beginning of
+ * range } else { // truncate range and create new one if necessary iv =
+ * (int[]) narange.elementAt(vc+1); if (iv[0]<=skipint[1]) { // truncate
+ * range iv[0] = skipint[1]; } else { } } } else if (iv[0]