else {
//valid paramters for this command
string AlignArray[] = {"fasta", "flip", "oligos", "maxambig", "maxhomop", "minlength", "maxlength", "qfile",
- "qthreshold", "qaverage", "allfiles", "qtrim","diffs", "processors", "outputdir","inputdir"};
+ "qthreshold", "qaverage", "allfiles", "qtrim","tdiffs", "pdiffs", "bdiffs", "processors", "outputdir","inputdir"};
vector<string> myArray (AlignArray, AlignArray+(sizeof(AlignArray)/sizeof(string)));
temp = validParameter.validFile(parameters, "maxlength", false); if (temp == "not found") { temp = "0"; }
convert(temp, maxLength);
- temp = validParameter.validFile(parameters, "diffs", false); if (temp == "not found") { temp = "0"; }
- convert(temp, diffs);
+ temp = validParameter.validFile(parameters, "tdiffs", false); if (temp == "not found") { temp = "0"; }
+ convert(temp, tdiffs);
+
+ temp = validParameter.validFile(parameters, "bdiffs", false); if (temp == "not found") { temp = "0"; }
+ convert(temp, bdiffs);
+
+ temp = validParameter.validFile(parameters, "pdiffs", false); if (temp == "not found") { temp = "0"; }
+ convert(temp, pdiffs);
temp = validParameter.validFile(parameters, "qfile", true);
if (temp == "not found") { qFileName = ""; }
m->mothurOut("The maxhomop parameter .... The default is 0.\n");
m->mothurOut("The minlength parameter .... The default is 0.\n");
m->mothurOut("The maxlength parameter .... The default is 0.\n");
- m->mothurOut("The diffs parameter .... The default is 0.\n");
+ m->mothurOut("The tdiffs parameter is used to specify the total number of differences allowed in the sequence. The default is 0.\n");
+ m->mothurOut("The bdiffs parameter is used to specify the number of differences allowed in the barcode. The default is 0.\n");
+ m->mothurOut("The pdiffs parameter is used to specify the number of differences allowed in the primer. The default is 0.\n");
m->mothurOut("The qfile parameter .....\n");
m->mothurOut("The qthreshold parameter .... The default is 0.\n");
m->mothurOut("The qaverage parameter .... The default is 0.\n");
if (origSeq != "") {
int group;
string trashCode = "";
+ int currentSeqsDiffs = 0;
if(qFileName != ""){
if(qThreshold != 0) { success = stripQualThreshold(currSeq, qFile); }
if(barcodes.size() != 0){
success = stripBarcode(currSeq, group);
if(!success){ trashCode += 'b'; }
+ else{ currentSeqsDiffs += currentSeqsTdiffs; }
}
if(numFPrimers != 0){
success = stripForward(currSeq);
if(!success){ trashCode += 'f'; }
+ else{ currentSeqsDiffs += currentSeqsTdiffs; }
}
-
+
+ if (currentSeqsDiffs > tdiffs) { trashCode += 't'; }
+
if(numRPrimers != 0){
success = stripReverse(currSeq);
if(!success){ trashCode += 'r'; }
}
//if you found the barcode or if you don't want to allow for diffs
- if ((diffs == 0) || (success == 1)) { return success; }
+ if ((bdiffs == 0) || (success == 1)) { return success; }
else { //try aligning and see if you can find it
map<string,int>::iterator it=barcodes.begin();
string temp = it->first;
- alignment = new NeedlemanOverlap(-2.0, 1.0, -1.0, (temp.length()+diffs+1));
+ alignment = new NeedlemanOverlap(-2.0, 1.0, -1.0, (temp.length()+bdiffs+1));
}else{ alignment = NULL; }
}
//use needleman to align first barcode.length()+numdiffs of sequence to each barcode
- alignment->align(oligo, rawSequence.substr(0,length+diffs));
+ alignment->align(oligo, rawSequence.substr(0,length+bdiffs));
oligo = alignment->getSeqAAln();
string temp = alignment->getSeqBAln();
//cout << "barcode = " << oligo << " raw = " << rawSequence.substr(0,oligo.length()) << " raw aligned = " << temp << endl;
int newStart=0;
- if(compareDNASeq(oligo, temp, length, newStart)){
+ if(compareDNASeq(oligo, temp, length, newStart, bdiffs)){
group = it->second;
seq.setUnaligned(rawSequence.substr(newStart));
success = 1;
}
//if you found the primer or if you don't want to allow for diffs
- if ((diffs == 0) || (success == 1)) { return success; }
+ if ((pdiffs == 0) || (success == 1)) { return success; }
else { //try aligning and see if you can find it
-
Alignment* alignment;
- if (numFPrimers > 0) { alignment = new NeedlemanOverlap(-2.0, 1.0, -1.0, (forPrimer[0].length()+diffs+1)); } //assumes primers are all the same length
+ if (numFPrimers > 0) { alignment = new NeedlemanOverlap(-2.0, 1.0, -1.0, (forPrimer[0].length()+pdiffs+1)); }
else{ alignment = NULL; }
-
//can you find the primer
for(int i=0;i<numFPrimers;i++){
string oligo = forPrimer[i];
int length = oligo.length();
-
+
if(rawSequence.length() < oligo.length()){
success = 0;
break;
}
+
+ //resize if neccessary
+ if ((length+pdiffs+1) > alignment->getnRows()) { alignment->resize(length+pdiffs+1); }
//use needleman to align first primer.length()+numdiffs of sequence to each primer
- alignment->align(oligo, rawSequence.substr(0,length+diffs));
+ alignment->align(oligo, rawSequence.substr(0,length+pdiffs));
oligo = alignment->getSeqAAln();
string temp = alignment->getSeqBAln();
-
+
int newStart = 0;
- if(compareDNASeq(oligo, temp, length, newStart)){
+ if(compareDNASeq(oligo, temp, length, newStart, pdiffs)){
seq.setUnaligned(rawSequence.substr(newStart));
success = 1;
break;
}
//***************************************************************************************************************
-bool TrimSeqsCommand::compareDNASeq(string oligo, string seq, int numBases, int& end){
+bool TrimSeqsCommand::compareDNASeq(string oligo, string seq, int numBases, int& end, int diffs){
try {
bool success = 1;
int length = oligo.length();
- end = length;
+ end = numBases;
int countBases = 0;
int countDiffs = 0;
if (length != 0) {
- if ((oligo[0] == '-') || (oligo[0] == '.')) { success = 0; return success; } //no gaps allowed at beginning
+ if ((oligo[0] == '-') || (oligo[0] == '.')) { success = 0; return success; } //no gaps allowed at beginning
}
for(int i=0;i<length;i++){
if ((oligo[i] != '-') && (oligo[i] != '.')) { countBases++; }
-
- //cout << oligo[i] << " " << seq[i] << " diffs = " << countDiffs << " countBases = " << countBases << endl;
-
+
if(oligo[i] != seq[i]){
if(oligo[i] == 'A' || oligo[i] == 'T' || oligo[i] == 'G' || oligo[i] == 'C' || oligo[i] == '-' || oligo[i] == '.') { countDiffs++; }
else if((oligo[i] == 'N' || oligo[i] == 'I') && (seq[i] == 'N')) { countDiffs++; }
success = 1;
}
- if (countBases >= numBases) { end = i; break; } //stop checking after end of barcode or primer
+ if (countBases >= numBases) { end = countBases; break; } //stop checking after end of barcode or primer
}
-
+
+ //if it's a success we want to check for total diffs in driver, so save it.
+ if (success == 1) { currentSeqsTdiffs = countDiffs; }
+
return success;
}
catch(exception& e) {