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stringtie.cpp
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//#define GFF_DEBUG 1 //debugging guides loading
#include "rlink.h"
#include "tmerge.h"
#ifndef NOTHREADS
#include "GThreads.h"
#endif
//#define GMEMTRACE 1 //debugging mem allocation
#ifdef GMEMTRACE
#include "proc_mem.h"
#endif
#define VERSION "2.1.8"
//#define DEBUGPRINT 1
#ifdef DEBUGPRINT
#define DBGPRINT(x) GMessage(x)
#define DBGPRINT2(a,b) GMessage(a,b)
#define DBGPRINT3(a,b,c) GMessage(a,b,c)
#define DBGPRINT4(a,b,c,d) GMessage(a,b,c,d)
#define DBGPRINT5(a,b,c,d,e) GMessage(a,b,c,d,e)
#else
#define DBGPRINT(x)
#define DBGPRINT2(a,b)
#define DBGPRINT3(a,b,c)
#define DBGPRINT4(a,b,c,d)
#define DBGPRINT5(a,b,c,d,e)
#endif
#define USAGE "StringTie v" VERSION " usage:\n\n\
stringtie <in.bam ..> [-G <guide_gff>] [-l <prefix>] [-o <out.gtf>] [-p <cpus>]\n\
[-v] [-a <min_anchor_len>] [-m <min_len>] [-j <min_anchor_cov>] [-f <min_iso>]\n\
[-c <min_bundle_cov>] [-g <bdist>] [-u] [-L] [-e] [--viral] [-E <err_margin>]\n\
[--ptf <f_tab>] [-x <seqid,..>] [-A <gene_abund.out>] [-h] {-B|-b <dir_path>}\n\
[--mix] [--conservative] [--rf] [--fr]\n\
Assemble RNA-Seq alignments into potential transcripts.\n\
Options:\n\
--version : print just the version at stdout and exit\n\
--conservative : conservative transcript assembly, same as -t -c 1.5 -f 0.05\n\
--mix : both short and long read data alignments are provided\n\
(long read alignments must be the 2nd BAM/CRAM input file)\n\
--rf : assume stranded library fr-firststrand\n\
--fr : assume stranded library fr-secondstrand\n\
-G reference annotation to use for guiding the assembly process (GTF/GFF)\n\
--ptf : load point-features from a given 4 column feature file <f_tab>\n\
-o output path/file name for the assembled transcripts GTF (default: stdout)\n\
-l name prefix for output transcripts (default: STRG)\n\
-f minimum isoform fraction (default: 0.01)\n\
-L long reads processing; also enforces -s 1.5 -g 0 (default:false)\n\
-R if long reads are provided, just clean and collapse the reads but\n\
do not assemble\n\
-m minimum assembled transcript length (default: 200)\n\
-a minimum anchor length for junctions (default: 10)\n\
-j minimum junction coverage (default: 1)\n\
-t disable trimming of predicted transcripts based on coverage\n\
(default: coverage trimming is enabled)\n\
-c minimum reads per bp coverage to consider for multi-exon transcript\n\
(default: 1)\n\
-s minimum reads per bp coverage to consider for single-exon transcript\n\
(default: 4.75)\n\
-v verbose (log bundle processing details)\n\
-g maximum gap allowed between read mappings (default: 50)\n\
-M fraction of bundle allowed to be covered by multi-hit reads (default:1)\n\
-p number of threads (CPUs) to use (default: 1)\n\
-A gene abundance estimation output file\n\
-E define window around possibly erroneous splice sites from long reads to\n\
look out for correct splice sites (default: 25)\n\
-B enable output of Ballgown table files which will be created in the\n\
same directory as the output GTF (requires -G, -o recommended)\n\
-b enable output of Ballgown table files but these files will be \n\
created under the directory path given as <dir_path>\n\
-e only estimate the abundance of given reference transcripts (requires -G)\n\
--viral : only relevant for long reads from viral data where splice sites\n\
do not follow consensus (default:false)\n\
-x do not assemble any transcripts on the given reference sequence(s)\n\
-u no multi-mapping correction (default: correction enabled)\n\
-h print this usage message and exit\n\
--ref/--cram-ref reference genome FASTA file for CRAM input\n\
\n\
Transcript merge usage mode: \n\
stringtie --merge [Options] { gtf_list | strg1.gtf ...}\n\
With this option StringTie will assemble transcripts from multiple\n\
input files generating a unified non-redundant set of isoforms. In this mode\n\
the following options are available:\n\
-G <guide_gff> reference annotation to include in the merging (GTF/GFF3)\n\
-o <out_gtf> output file name for the merged transcripts GTF\n\
(default: stdout)\n\
-m <min_len> minimum input transcript length to include in the merge\n\
(default: 50)\n\
-c <min_cov> minimum input transcript coverage to include in the merge\n\
(default: 0)\n\
-F <min_fpkm> minimum input transcript FPKM to include in the merge\n\
(default: 1.0)\n\
-T <min_tpm> minimum input transcript TPM to include in the merge\n\
(default: 1.0)\n\
-f <min_iso> minimum isoform fraction (default: 0.01)\n\
-g <gap_len> gap between transcripts to merge together (default: 250)\n\
-i keep merged transcripts with retained introns; by default\n\
these are not kept unless there is strong evidence for them\n\
-l <label> name prefix for output transcripts (default: MSTRG)\n\
"
/*
-C output a file with reference transcripts that are covered by reads\n\
-U unitigs are treated as reads and not as guides \n\ \\ not used now
-d disable adaptive read coverage mode (default: yes)\n\
-n sensitivity level: 0,1, or 2, 3, with 3 the most sensitive level (default 1)\n\ \\ deprecated for now
-O disable the coverage saturation limit and use a slower two-pass approach\n\
to process the input alignments, collapsing redundant reads\n\
-i the reference annotation contains partial transcripts\n\
-w weight the maximum flow algorithm towards the transcript with higher rate (abundance); default: no\n\
-y include EM algorithm in max flow estimation; default: no\n\
-z don't include source in the max flow algorithm\n\
-P output file with all transcripts in reference that are partially covered by reads
-M fraction of bundle allowed to be covered by multi-hit reads (paper uses default: 1)\n\
-c minimum bundle reads per bp coverage to consider for assembly (paper uses default: 3)\n\
-S more sensitive run (default: no) disabled for now \n\
-s coverage saturation threshold; further read alignments will be\n\ // this coverage saturation parameter is deprecated starting at version 1.0.5
ignored in a region where a local coverage depth of <maxcov> \n\
is reached (default: 1,000,000);\n\ \\ deprecated
-e (mergeMode) include estimated coverage information in the preidcted transcript\n\
-E (mergeMode) enable the name of the input transcripts to be included\n\
in the merge output (default: no)\n\
*/
//---- globals
FILE* f_out=NULL;
FILE* c_out=NULL;
//#define B_DEBUG 1
#ifdef B_DEBUG
FILE* dbg_out=NULL;
#endif
GStr outfname;
GStr out_dir;
GStr tmp_path;
GStr cram_ref; //reference genome FASTA for CRAM input
GStr tmpfname;
GStr genefname;
GStr traindir; // training directory for CDS option
bool guided=false;
bool trim=true;
bool viral=false;
bool eonly=false; // parameter -e ; for mergeMode includes estimated coverage sum in the merged transcripts
bool longreads=false;
bool rawreads=false;
bool nomulti=false;
bool enableNames=false;
bool includecov=false;
bool fr_strand=false;
bool rf_strand=false;
//bool complete=true; // set by parameter -i the reference annotation contains partial transcripts
bool retained_intron=false; // set by parameter -i for merge option
bool geneabundance=false;
//bool partialcov=false;
int num_cpus=1;
int mintranscriptlen=200; // minimum length for a transcript to be printed
//int sensitivitylevel=1;
uint junctionsupport=10; // anchor length for junction to be considered well supported <- consider shorter??
uint sserror=25; // window arround splice sites that we use to generate consensus in case of long read data
int junctionthr=1; // number of reads needed to support a particular junction
float readthr=1; // read coverage per bundle bp to accept it; // paper uses 3
float singlethr=4.75;
uint bundledist=50; // reads at what distance should be considered part of separate bundles
uint runoffdist=200;
float mcov=1; // fraction of bundle allowed to be covered by multi-hit reads paper uses 1
int allowed_nodes=1000;
//bool adaptive=true; // adaptive read coverage -> depends on the overall gene coverage
//GPVec<CDSparam> cds;
int no_xs=0; // number of records without the xs tag
float fpkm_thr=1;
float tpm_thr=1;
// different options of implementation reflected with the next three options
bool includesource=true;
//bool EM=false;
//bool weight=false;
float isofrac=0.01;
bool isunitig=true;
GStr label("STRG");
GStr ballgown_dir;
GFastaDb* gfasta=NULL;
GStr guidegff; // -G option
GStr ptff; // --ptf option (point features)
bool debugMode=false;
bool verbose=false;
bool ballgown=false;
//int maxReadCov=1000000; //max local read coverage (changed with -s option)
//no more reads will be considered for a bundle if the local coverage exceeds this value
//(each exon is checked for this)
//bool forceBAM = false; //useful for stdin (piping alignments into StringTie)
bool mergeMode = false; //--merge option
bool keepTempFiles = false; //--keeptmp
bool mixedMode = false; // both short and long read data alignments are provided
int GeneNo=0; //-- global "gene" counter
double Num_Fragments=0; //global fragment counter (aligned pairs)
double Frag_Len=0;
double Cov_Sum=0;
//bool firstPrint=true; //just for writing the GFF header before the first transcript is printed
GffNames* gseqNames=NULL; //used as a dictionary for reference sequence names and ids
int refseqCount=0; // number of reference sequences found in the guides file
#ifdef GMEMTRACE
double maxMemRS=0;
double maxMemVM=0;
GStr maxMemBundle;
#endif
#ifndef NOTHREADS
//single producer, multiple consumers
//main thread/program is always loading the producer
GMutex dataMutex; //manage availability of data records ready to be loaded by main thread
GVec<int> dataClear; //indexes of data bundles cleared for loading by main thread (clear data pool)
GConditionVar haveBundles; //will notify a thread that a bundle was loaded in the ready queue
//(or that no more bundles are coming)
int bundleWork=1; // bit 0 set if bundles are still being prepared (BAM file not exhausted yet)
// bit 1 set if there are Bundles ready in the queue
//GFastMutex waitMutex;
GMutex waitMutex; // controls threadsWaiting (idle threads counter)
int threadsWaiting; // idle worker threads
GConditionVar haveThreads; //will notify the bundle loader when a thread
//is available to process the currently loaded bundle
GConditionVar haveClear; //will notify when bundle buf space available
GMutex queueMutex; //controls bundleQueue and bundles access
GFastMutex printMutex; //for writing the output to file
GFastMutex logMutex; //only when verbose - to avoid mangling the log output
GFastMutex bamReadingMutex;
GFastMutex countMutex;
#endif
GStrSet<> excludeGseqs; //hash of chromosomes/contigs to exclude (e.g. chrM)
bool NoMoreBundles=false;
bool moreBundles(); //thread-safe retrieves NoMoreBundles
void noMoreBundles(); //sets NoMoreBundles to true
//--
void processOptions(GArgs& args);
int loadPtFeatures(FILE* f, GArray<GRefPtData>& refpts);
char* sprintTime();
void processBundle(BundleData* bundle);
//void processBundle1stPass(BundleData* bundle); //two-pass testing
void writeUnbundledGuides(GVec<GRefData>& refdata, FILE* fout, FILE* gout=NULL);
#ifndef NOTHREADS
bool noThreadsWaiting();
void workerThread(GThreadData& td); // Thread function
//prepare the next free bundle for loading
int waitForData(BundleData* bundles);
#endif
//#define DBG_ALN_DATA 1
#ifdef DBG_ALN_DATA
FILE* fdbgaln=NULL;
void dbg_waln(GSamRecord* b) {
if (fdbgaln==NULL) {
GStr fn=outfname;
if (fn.rindex('.')>0)
fn=fn.cut(fn.rindex('.'));
fn+="_alndbg.tab";
fdbgaln=fopen(fn.chars(), "w");
if (fdbgaln==NULL) GError("Error creating file %s\n", fn.chars());
}
// gseqname, flags, readname, start, end, cigar, nh, hi
char* pcigar=b->cigar();
fprintf(fdbgaln, "%s\t%d\t%s\t%d\t%d\t%s\t%d\t%d\t%d\t%d\t%d\t%d\t%d\n", b->refName(), b->flags(),
b->name(), b->start, b->end, pcigar, (uint)b->tag_int("NM"), (uint)b->tag_int("NH"), (uint)b->tag_int("HI"),
b->mate_refId(), b->mate_start(), b->clipL, b->clipR);
GFREE(pcigar);
}
#endif
TInputFiles bamreader;
int main(int argc, char* argv[]) {
// == Process arguments.
GArgs args(argc, argv,
"debug;help;version;viral;conservative;mix;ref=;cram-ref=cds=;keeptmp;rseq=;ptf=;bam;fr;rf;merge;"
"exclude=zihvteuLRx:n:j:s:D:G:C:S:l:m:o:a:j:c:f:p:g:P:M:Bb:A:E:F:T:");
args.printError(USAGE, true);
processOptions(args);
GVec<GRefData> refguides; // plain vector with transcripts for each chromosome
GArray<GRefPtData> refpts(true, true); // sorted,unique array of refseq point-features data
//table indexes for Ballgown Raw Counts data (-B/-b option)
GPVec<RC_TData> guides_RC_tdata(true); //raw count data or other info for all guide transcripts
GPVec<RC_Feature> guides_RC_exons(true); //raw count data for all guide exons
GPVec<RC_Feature> guides_RC_introns(true);//raw count data for all guide introns
GVec<int> alncounts(30); //keep track of the number of read alignments per chromosome [gseq_id]
int bamcount=bamreader.start(); //setup and open input files
#ifndef GFF_DEBUG
if (bamcount<1) {
GError("%sError: no input files provided!\n",USAGE);
}
#endif
#ifdef DEBUGPRINT
verbose=true;
#endif
const char* ERR_BAM_SORT="\nError: the input alignment file is not sorted!\n";
if(guided) { // read guiding transcripts from input gff file
if (verbose) {
printTime(stderr);
GMessage(" Loading reference annotation (guides)..\n");
}
FILE* f=fopen(guidegff.chars(),"r");
if (f==NULL) GError("Error: could not open reference annotation file (%s)!\n",
guidegff.chars());
// transcripts_only sort by location?
GffReader gffr(f, true, true); //loading only recognizable transcript features
gffr.setRefAlphaSorted(); //alphabetical sorting of refseq IDs
gffr.showWarnings(verbose);
// keepAttrs mergeCloseExons noExonAttrs
gffr.readAll(false, true, true);
//the list of GffObj is in gffr.gflst, sorted by chromosome and start-end coordinates
//collect them in other data structures, if it's kept for later call gffobj->isUsed(true)
// (otherwise it'll be deallocated when gffr is destroyed due to going out of scope)
refseqCount=gffr.gseqtable.Count();
if (refseqCount==0 || gffr.gflst.Count()==0) {
GError("Error: could not any valid reference transcripts in %s (invalid GTF/GFF file?)\n",
guidegff.chars());
}
refguides.setCount(refseqCount); //maximum gseqid
uint c_tid=0;
uint c_exon_id=0;
uint c_intron_id=0;
GList<RC_Feature> uexons(true, false, true); //sorted, free items, unique
GList<RC_Feature> uintrons(true, false, true);
//assign unique transcript IDs based on the sorted order
int last_refid=-1;
bool skipGseq=false;
for (int i=0;i<gffr.gflst.Count();i++) {
GffObj* m=gffr.gflst[i];
if (last_refid!=m->gseq_id) {
//chromosome switch
if (ballgown) { //prepare memory storage/tables for all guides on this chromosome
uexons.Clear();
uintrons.Clear();
}
last_refid=m->gseq_id;
skipGseq=excludeGseqs.hasKey(m->getGSeqName());
}
//sanity check: make sure there are no exonless "genes" or other
if (skipGseq) continue;
if (m->exons.Count()==0) {
if (verbose)
GMessage("Warning: exonless GFF %s feature with ID %s found, added implicit exon %d-%d.\n",
m->getFeatureName(), m->getID(), m->start, m->end);
m->addExon(m->start, m->end); //should never happen!
}
//DONE: always keep a RC_TData pointer around, with additional info about guides
RC_TData* tdata=new RC_TData(*m, ++c_tid);
m->uptr=tdata;
guides_RC_tdata.Add(tdata);
if (ballgown) { //already gather exon & intron info for all ref transcripts
tdata->rc_addFeatures(c_exon_id, uexons, guides_RC_exons,
c_intron_id, uintrons, guides_RC_introns);
}
GRefData& grefdata = refguides[m->gseq_id];
grefdata.add(&gffr, m); //transcripts already sorted by location
}
if (verbose) {
printTime(stderr);
GMessage(" %d reference transcripts loaded.\n", gffr.gflst.Count());
}
}
gseqNames=GffObj::names; //might have been populated already by gff data
gffnames_ref(gseqNames); //initialize the names collection if not guided
bool havePtFeatures=false;
// -- loading point-feature data
if (!ptff.is_empty()) {
FILE* f=fopen(ptff.chars(),"r");
if (f==NULL) GError("Error: could not open reference annotation file (%s)!\n",
ptff.chars());
// transcripts_only sort by location?
int numptf=loadPtFeatures(f, refpts); //adds to gseqNames->gseqs accordingly, populates refpts
havePtFeatures=(numptf>0);
fclose(f);
}
#ifdef GFF_DEBUG
for (int r=0;r<refguides.Count();++r) {
GRefData& grefdata = refguides[r];
for (int k=0;k<grefdata.rnas.Count();++k) {
GMessage("#transcript #%d : %s (%d exons)\n", k, grefdata.rnas[k]->getID(), grefdata.rnas[k]->exons.Count());
grefdata.rnas[k]->printGff(stderr);
}
}
GMessage("GFF Debug mode, exiting...\n");
exit(0);
#endif
// --- input processing
GHash<int> hashread; //read_name:pos:hit_index => readlist index
GList<GffObj>* guides=NULL; //list of transcripts on a specific reference
GList<GPtFeature>* refptfs=NULL; //list of point-features on a specific reference
int currentstart=0, currentend=0;
int ng_start=0;
int ng_end=-1;
int ptf_idx=0; //point-feature current index in the current (*refptfs)[]
int ng=0;
GStr lastref;
bool no_ref_used=true;
int lastref_id=-1; //last seen gseq_id
// int ncluster=0; used it for debug purposes only
//Ballgown files
FILE* f_tdata=NULL;
FILE* f_edata=NULL;
FILE* f_idata=NULL;
FILE* f_e2t=NULL;
FILE* f_i2t=NULL;
if (ballgown)
Ballgown_setupFiles(f_tdata, f_edata, f_idata, f_e2t, f_i2t);
#ifndef NOTHREADS
//model: one producer, multiple consumers
#define DEF_TSTACK_SIZE 8388608
size_t defStackSize=DEF_TSTACK_SIZE;
#ifdef _GTHREADS_POSIX_
int tstackSize=GThread::defaultStackSize();
if (tstackSize<DEF_TSTACK_SIZE) defStackSize=DEF_TSTACK_SIZE;
if (verbose) {
if (defStackSize>0){
int ssize=defStackSize;
GMessage("Default stack size for threads: %d (increased to %d)\n", tstackSize, ssize);
}
else GMessage("Default stack size for threads: %d\n", tstackSize);
}
#endif
GThread* threads=new GThread[num_cpus]; //bundle processing threads
GPVec<BundleData> bundleQueue(false); //queue of loaded bundles
//the consumers take (pop) bundles out of this queue for processing
//the producer populates this queue with bundles built from reading the BAM input
BundleData* bundles=new BundleData[num_cpus+1];
//bundles[0..num_cpus-1] are processed by threads, loading bundles[num_cpus] first
dataClear.setCapacity(num_cpus+1);
for (int b=0;b<num_cpus;b++) {
threads[b].kickStart(workerThread, (void*) &bundleQueue, defStackSize);
bundles[b+1].idx=b+1;
dataClear.Push(b);
}
BundleData* bundle = &(bundles[num_cpus]);
#else
BundleData bundles[1];
BundleData* bundle = &(bundles[0]);
#endif
GSamRecord* brec=NULL;
bool more_alns=true;
TAlnInfo* tinfo=NULL; // for --merge
int prev_pos=0;
bool skipGseq=false;
while (more_alns) {
bool chr_changed=false;
int pos=0;
const char* refseqName=NULL;
char xstrand=0;
int nh=1;
int hi=0;
int gseq_id=lastref_id; //current chr id
bool new_bundle=false;
//delete brec;
if ((brec=bamreader.next())!=NULL) {
if (brec->isUnmapped()) continue;
if (brec->start<1 || brec->mapped_len<10) {
if (verbose) GMessage("Warning: invalid mapping found for read %s (position=%d, mapped length=%d)\n",
brec->name(), brec->start, brec->mapped_len);
continue;
}
#ifdef DBG_ALN_DATA
dbg_waln(brec);
#endif
refseqName=brec->refName();
xstrand=brec->spliceStrand(); // tagged strand gets priority
if(xstrand=='.' && (fr_strand || rf_strand)) { // set strand if stranded library
if(brec->isPaired()) { // read is paired
if(brec->pairOrder()==1) { // first read in pair
if((rf_strand && brec->revStrand())||(fr_strand && !brec->revStrand())) xstrand='+';
else xstrand='-';
}
else {
if((rf_strand && brec->revStrand())||(fr_strand && !brec->revStrand())) xstrand='-';
else xstrand='+';
}
}
else {
if((rf_strand && brec->revStrand())||(fr_strand && !brec->revStrand())) xstrand='+';
else xstrand='-';
}
}
/*
if (xstrand=='.' && brec->exons.Count()>1) {
no_xs++;
continue; //skip spliced alignments lacking XS tag (e.g. HISAT alignments)
}
// I might still infer strand later */
if (refseqName==NULL) GError("Error: cannot retrieve target seq name from BAM record!\n");
pos=brec->start; //BAM is 0 based, but GBamRecord makes it 1-based
chr_changed=(lastref.is_empty() || lastref!=refseqName);
if (chr_changed) {
skipGseq=excludeGseqs.hasKey(refseqName);
gseq_id=gseqNames->gseqs.addName(refseqName);
if (guided) {
if (gseq_id>=refseqCount) {
if (verbose)
GMessage("WARNING: no reference transcripts found for genomic sequence \"%s\"! (mismatched reference names?)\n",
refseqName);
}
else no_ref_used=false;
}
if (alncounts.Count()<=gseq_id) {
alncounts.Resize(gseq_id+1);
}
else if (alncounts[gseq_id]>0)
GError("%s\nAlignments (%d) already found for %s !\n",
ERR_BAM_SORT, alncounts[gseq_id], refseqName);
prev_pos=0;
}
if (pos<prev_pos) GError("%s\nread %s (start %d) found at position %d on %s when prev_pos=%d\n",
ERR_BAM_SORT, brec->name(), brec->start, pos, refseqName, prev_pos);
prev_pos=pos;
if (skipGseq) continue;
alncounts[gseq_id]++;
nh=brec->tag_int("NH");
if (nh==0) nh=1;
hi=brec->tag_int("HI");
if (mergeMode) {
//tinfo=new TAlnInfo(brec->name(), brec->tag_int("ZF"));
tinfo=new TAlnInfo(brec->name(), brec->uval);
GStr score(brec->tag_str("ZS"));
if (!score.is_empty()) {
GStr srest=score.split('|');
if (!score.is_empty())
tinfo->cov=score.asDouble();
score=srest.split('|');
if (!srest.is_empty())
tinfo->fpkm=srest.asDouble();
srest=score.split('|');
if (!score.is_empty())
tinfo->tpm=score.asDouble();
}
}
if (!chr_changed && currentend>0 && pos>currentend+(int)runoffdist) {
new_bundle=true;
}
}
else { //no more alignments
more_alns=false;
new_bundle=true; //fake a new start (end of last bundle)
}
if (new_bundle || chr_changed) {
hashread.Clear();
if (bundle->readlist.Count()>0) { // process reads in previous bundle
// (readthr, junctionthr, mintranscriptlen are globals)
if (refptfs) { //point-features defined for this reference
while (ptf_idx<refptfs->Count() && (int)(refptfs->Get(ptf_idx)->coord)<currentstart)
ptf_idx++;
//TODO: what if a PtFeature is nearby, just outside the bundle?
while (ptf_idx<refptfs->Count() && (int)(refptfs->Get(ptf_idx)->coord)<=currentend) {
bundle->ptfs.Add(refptfs->Get(ptf_idx)); //keep this PtFeature
ptf_idx++;
}
}
bundle->getReady(currentstart, currentend);
if (gfasta!=NULL) { //genomic sequence data requested
GFaSeqGet* faseq=gfasta->fetch(bundle->refseq.chars());
if (faseq==NULL) {
GError("Error: could not retrieve sequence data for %s!\n", bundle->refseq.chars());
}
bundle->gseq=faseq->copyRange(bundle->start, bundle->end, false, true);
}
#ifndef NOTHREADS
//push this in the bundle queue where it'll be picked up by the threads
DBGPRINT2("##> Locking queueMutex to push loaded bundle into the queue (bundle.start=%d)\n", bundle->start);
int qCount=0;
queueMutex.lock();
bundleQueue.Push(bundle);
bundleWork |= 0x02; //set bit 1
qCount=bundleQueue.Count();
queueMutex.unlock();
DBGPRINT2("##> bundleQueue.Count()=%d)\n", qCount);
//wait for a thread to pop this bundle from the queue
waitMutex.lock();
DBGPRINT("##> waiting for a thread to become available..\n");
while (threadsWaiting==0) {
haveThreads.wait(waitMutex);
}
waitMutex.unlock();
haveBundles.notify_one();
DBGPRINT("##> waitMutex unlocked, haveBundles notified, current thread yielding\n");
current_thread::yield();
queueMutex.lock();
DBGPRINT("##> queueMutex locked until bundleQueue.Count()==qCount\n");
while (bundleQueue.Count()==qCount) {
queueMutex.unlock();
DBGPRINT2("##> queueMutex unlocked as bundleQueue.Count()==%d\n", qCount);
haveBundles.notify_one();
current_thread::yield();
queueMutex.lock();
DBGPRINT("##> queueMutex locked again within while loop\n");
}
queueMutex.unlock();
#else //no threads
//Num_Fragments+=bundle->num_fragments;
//Frag_Len+=bundle->frag_len;
processBundle(bundle);
#endif
// ncluster++; used it for debug purposes only
} //have alignments to process
else { //no read alignments in this bundle?
#ifndef NOTHREADS
dataMutex.lock();
DBGPRINT2("##> dataMutex locked for bundle #%d clearing..\n", bundle->idx);
#endif
bundle->Clear();
#ifndef NOTHREADS
dataClear.Push(bundle->idx);
DBGPRINT2("##> dataMutex unlocking as dataClear got pushed idx #%d\n", bundle->idx);
dataMutex.unlock();
#endif
} //nothing to do with this bundle
if (chr_changed) {
if (guided) {
ng=0;
guides=NULL;
ng_start=0;
ng_end=-1;
if (refguides.Count()>gseq_id && refguides[gseq_id].rnas.Count()>0) {
guides=&(refguides[gseq_id].rnas);
ng=guides->Count();
}
}
if (havePtFeatures) {
ptf_idx=-1;
//setup refptf
refptfs=NULL;
GRefPtData rd(gseq_id);
int ridx=refpts.IndexOf(rd);
if (ridx>=0) {
refptfs=&(refpts[ridx].pfs);
ptf_idx=0;
}
}
lastref=refseqName;
lastref_id=gseq_id;
currentend=0;
}
if (!more_alns) {
if (verbose) {
#ifndef NOTHREADS
GLockGuard<GFastMutex> lock(logMutex);
#endif
if (Num_Fragments) {
printTime(stderr);
GMessage(" %g aligned fragments found.\n", Num_Fragments);
}
//GMessage(" Done reading alignments.\n");
}
noMoreBundles();
break;
}
#ifndef NOTHREADS
int new_bidx=waitForData(bundles);
if (new_bidx<0) {
//should never happen!
GError("Error: waitForData() returned invalid bundle index(%d)!\n",new_bidx);
break;
}
bundle=&(bundles[new_bidx]);
#endif
currentstart=pos;
currentend=brec->end;
if (guides) { //guided and guides!=NULL
ng_start=ng_end+1;
while (ng_start<ng && (int)(*guides)[ng_start]->end < pos) {
// for now, skip guides which have no overlap with current read
ng_start++;
}
int ng_ovl=ng_start;
//add all guides overlapping the current read and other guides that overlap them
while (ng_ovl<ng && (int)(*guides)[ng_ovl]->start<=currentend) { //while guide overlap
if (currentstart>(int)(*guides)[ng_ovl]->start)
currentstart=(*guides)[ng_ovl]->start;
if (currentend<(int)(*guides)[ng_ovl]->end)
currentend=(*guides)[ng_ovl]->end;
if (ng_ovl==ng_start && ng_ovl>0) { //first time only, we have to check back all possible transitive guide overlaps
//char* geneid=(*guides)[ng_ovlstart]->getGeneID();
//if (geneid==NULL) geneid=(*guides)[ng_ovlstart]->getGeneName();
//if (geneid && !bgeneids.hasKey(geneid))
// bgeneids.shkAdd(geneid, &ng); //whatever pointer to int
int g_back=ng_ovl; //start from the overlapping guide, going backwards
int g_ovl_start=ng_ovl;
while (g_back>ng_end+1) {
--g_back;
//if overlap, set g_back_start=g_back and update currentstart
if (currentstart<=(int)(*guides)[g_back]->end) {
g_ovl_start=g_back;
if (currentstart>(int)(*guides)[g_back]->start)
currentstart=(int)(*guides)[g_back]->start;
}
} //while checking previous guides that could be pulled in this bundle
for (int gb=g_ovl_start;gb<=ng_ovl;++gb) {
bundle->keepGuide((*guides)[gb],
&guides_RC_tdata, &guides_RC_exons, &guides_RC_introns);
}
} //needed to check previous guides for overlaps
else
bundle->keepGuide((*guides)[ng_ovl],
&guides_RC_tdata, &guides_RC_exons, &guides_RC_introns);
ng_ovl++;
} //while guide overlap
ng_end=ng_ovl-1; //MUST update ng_end here, even if no overlaps were found
} //guides present on the current chromosome
bundle->refseq=lastref;
bundle->start=currentstart;
bundle->end=currentend;
} //<---- new bundle started
if (currentend<(int)brec->end) {
//current read extends the bundle
//this might not happen if a longer guide had already been added to the bundle
currentend=brec->end;
if (guides) { //add any newly overlapping guides to bundle
bool cend_changed;
do {
cend_changed=false;
while (ng_end+1<ng && (int)(*guides)[ng_end+1]->start<=currentend) {
++ng_end;
//more transcripts overlapping this bundle?
if ((int)(*guides)[ng_end]->end>=currentstart) {
//it should really overlap the bundle
bundle->keepGuide((*guides)[ng_end],
&guides_RC_tdata, &guides_RC_exons, &guides_RC_introns);
if(currentend<(int)(*guides)[ng_end]->end) {
currentend=(*guides)[ng_end]->end;
cend_changed=true;
}
}
}
} while (cend_changed);
}
} //adjusted currentend and checked for overlapping reference transcripts
GReadAlnData alndata(brec, 0, nh, hi, tinfo);
bool ovlpguide=bundle->evalReadAln(alndata, xstrand);
if(!eonly || ovlpguide) { // in eonly case consider read only if it overlaps guide
//check for overlaps with ref transcripts which may set xstrand
if (xstrand=='+') alndata.strand=1;
else if (xstrand=='-') alndata.strand=-1;
//GMessage("%s\t%c\t%d\thi=%d\n",brec->name(), xstrand, alndata.strand,hi);
//countFragment(*bundle, *brec, hi,nh); // we count this in build_graphs to only include mapped fragments that we consider correctly mapped
//fprintf(stderr,"fragno=%d fraglen=%lu\n",bundle->num_fragments,bundle->frag_len);if(bundle->num_fragments==100) exit(0);
processRead(currentstart, currentend, *bundle, hashread, alndata);
}
} //for each read alignment
//cleaning up
delete brec;
bamreader.stop(); //close all BAM files
if (guided && no_ref_used) {
GMessage("WARNING: no reference transcripts were found for the genomic sequences where reads were mapped!\n"
"Please make sure the -G annotation file uses the same naming convention for the genome sequences.\n");
}
delete gfasta;
#ifndef NOTHREADS
for (int t=0;t<num_cpus;t++)
threads[t].join();
if (verbose) {
printTime(stderr);
GMessage(" All threads finished.\n");
}
delete[] threads;
delete[] bundles;
#else
if (verbose) {
printTime(stderr);
GMessage(" Done.\n");
}
#endif
#ifdef DBG_ALN_DATA
fclose(fdbgaln);
#endif
#ifdef B_DEBUG
fclose(dbg_out);
#endif
if (mergeMode && guided )
writeUnbundledGuides(refguides, f_out);
// clear refpts data, if loaded
if (refpts.Count()>0)
for (int i=0;i<refpts.Count();i++) {
refpts[i].pfs.setFreeItem(true);
}
fclose(f_out);
if (c_out && c_out!=stdout) fclose(c_out);
if(verbose && no_xs>0)
GMessage("Number spliced alignments missing the XS tag (skipped): %d\n",no_xs);
if(!mergeMode) {
if(verbose) {
GMessage("Total count of aligned fragments: %g\n", Num_Fragments);
if (Num_Fragments)
GMessage("Fragment coverage length: %g\n", Frag_Len/Num_Fragments);
}
f_out=stdout;
if(outfname!="stdout") {
f_out=fopen(outfname.chars(), "w");
if (f_out==NULL) GError("Error creating output file %s\n", outfname.chars());
}
fprintf(f_out,"# ");
args.printCmdLine(f_out);
fprintf(f_out,"# StringTie version %s\n",VERSION);
//fprintf(stderr,"cov_sum=%g frag_len=%g num_frag=%g\n",Cov_Sum,Frag_Len,Num_Fragments);
FILE *g_out=NULL;
if(geneabundance) {
g_out=fopen(genefname.chars(),"w");
if (g_out==NULL)
GError("Error creating gene abundance output file %s\n", genefname.chars());
fprintf(g_out,"Gene ID\tGene Name\tReference\tStrand\tStart\tEnd\tCoverage\tFPKM\tTPM\n");
}
FILE* ftmp_in=fopen(tmpfname.chars(),"rt");
if (ftmp_in!=NULL) {
char* linebuf=NULL;
int linebuflen=5000;
GMALLOC(linebuf, linebuflen);
int nl;
int istr;
int tlen;
float tcov; //do we need to increase precision here ? (double)
float calc_fpkm;
float calc_tpm;
int t_id;
while(fgetline(linebuf,linebuflen,ftmp_in)) {
sscanf(linebuf,"%d %d %d %d %g", &istr, &nl, &tlen, &t_id, &tcov);
if (tcov<0) tcov=0;
if (Frag_Len>0.001) calc_fpkm=tcov*1000000000/Frag_Len;
else calc_fpkm=0.0;
if (Cov_Sum>0.00001) calc_tpm=tcov*1000000/Cov_Sum;
else calc_tpm=0.0;
if(istr) { // this is a transcript
if (ballgown && t_id>0) {
guides_RC_tdata[t_id-1]->fpkm=calc_fpkm;
guides_RC_tdata[t_id-1]->cov=tcov;
}
for(int i=0;i<nl;i++) {
fgetline(linebuf,linebuflen,ftmp_in);
if(!i) {
//linebuf[strlen(line)-1]='\0';
fprintf(f_out,"%s",linebuf);
fprintf(f_out," FPKM \"%.6f\";",calc_fpkm);
fprintf(f_out," TPM \"%.6f\";",calc_tpm);
fprintf(f_out,"\n");
}
else fprintf(f_out,"%s\n",linebuf);
}
}
else { // this is a gene -> different file pointer
fgetline(linebuf, linebuflen, ftmp_in);
fprintf(g_out, "%s\t%.6f\t%.6f\n", linebuf, calc_fpkm, calc_tpm);
}
}
if (guided) {
writeUnbundledGuides(refguides, f_out, g_out);
}
fclose(f_out);
fclose(ftmp_in);
if(geneabundance) fclose(g_out);
GFREE(linebuf);
if (!keepTempFiles) {
remove(tmpfname.chars());
}
}
else {
fclose(f_out);
GError("No temporary file %s present!\n",tmpfname.chars());
}
//lastly, for ballgown, rewrite the tdata file with updated cov and fpkm
if (ballgown) {
rc_writeRC(guides_RC_tdata, guides_RC_exons, guides_RC_introns,
f_tdata, f_edata, f_idata, f_e2t, f_i2t);
}
}
if (!keepTempFiles) {
tmp_path.chomp('/');
remove(tmp_path);
}
gffnames_unref(gseqNames); //deallocate names collection
#ifdef GMEMTRACE
if(verbose) GMessage(" Max bundle memory: %6.1fMB for bundle %s\n", maxMemRS/1024, maxMemBundle.chars());
#endif
} // -- END main
//----------------------------------------
char* sprintTime() {
static char sbuf[32];
time_t ltime; /* calendar time */
ltime=time(NULL);
struct tm *t=localtime(<ime);
sprintf(sbuf, "%02d_%02d_%02d:%02d:%02d",t->tm_mon+1, t->tm_mday,
t->tm_hour, t->tm_min, t->tm_sec);
return(sbuf);
}
void processOptions(GArgs& args) {
if (args.getOpt('h') || args.getOpt("help")) {
fprintf(stdout,"%s",USAGE);
exit(0);
}
if (args.getOpt("version")) {
fprintf(stdout,"%s\n",VERSION);
exit(0);
}
if (args.getOpt("viral")) {
viral=true;
}
longreads=(args.getOpt('L')!=NULL);
if(longreads) {
bundledist=0;
singlethr=1.5;
}