コード例 #1
0
static void loadAndAlignAll(struct bzp *bzp, 
        char *target, char *query, char *output)
/* blatz - Align genomic dna across species. */
{
struct dnaLoad *queryDl = dnaLoadOpen(query);
struct dnaLoad *targetDl = dnaLoadOpen(target);
struct blatzIndex *indexList = blatzIndexDl(targetDl, bzp->weight, bzp->unmask);
bzpTime("loaded and indexed target DNA");

// LX BEG
if (bzp->dynaWordCoverage > 0)
   {
   dynaNumWords = (pow(4,bzp->weight)); // ?? check with Jim if this is correct
   AllocArray(dynaWordCount,dynaNumWords);
   printf("Allocated word count table of size %d\n",dynaNumWords);
   dynaWordLimit = bzp->dynaWordCoverage; // cheating, should be more like:
   //dynaWordLimit = bzp->dynaWordCoverage*dynaSequenceSize/dynaNumWords;
   printf("Set word limit to  %d\n",dynaWordLimit);
   }
// LX END

verbose(2, "Loaded %d in %s, opened %s\n", slCount(indexList), target,
        query);
alignAll(bzp, indexList, queryDl, output);
}
コード例 #2
0
ファイル: server.c プロジェクト: davidhoover/kent
void serverStart(char *files[], int fileCount)
/* Load DNA. Build up indexes, set up listing port, and fall into
 * accept loop. */
{
struct blatzIndex *indexList = NULL;
int i;
int acceptor;
struct bzp *bzp = bzpDefault();

/* Daemonize self. */
bzpSetOptions(bzp);

/* Load up all sequences. */
for (i=0; i<fileCount; ++i)
    {
    struct dnaLoad *dl = dnaLoadOpen(files[i]);
    struct blatzIndex *oneList = blatzIndexDl(dl, bzp->weight, bzp->unmask);
    indexList = slCat(indexList, oneList);
    dnaLoadClose(&dl);
    }
bzpTime("Loaded and indexed %d sequences", slCount(indexList));
verbose(1, "Ready for queries\n");

/* Turn self into proper daemon. */
logDaemonize("blatzServer");

acceptor = netAcceptingSocket(port, 100);
serviceLoop(acceptor, bzp, indexList);
}
コード例 #3
0
static void findMotif(char *input)
/* findMotif - find specified motif in sequence file. */
{
struct dnaLoad *dl = dnaLoadOpen(input);
struct dnaSeq *seq; 

while ((seq = dnaLoadNext(dl)) != NULL)
    {
    verbose(2, "#\tprocessing: %s\n", seq->name);
    scanSeq(seq);
    }
}
コード例 #4
0
static void blatzClient(char *input, char *output)
/* Send query message and dna to server and print result. */
{
struct dnaLoad *dl = dnaLoadOpen(input);
struct dnaSeq *seq;
FILE *f = mustOpen(output, "w");
static struct optionSpec options[] = {
   BZP_CLIENT_OPTIONS
};
int i;
while ((seq = dnaLoadNext(dl)) != NULL)
    {
    /* Connect */
    int sd = netMustConnect(host, port);
    FILE *sf = NULL;

    /* Send query command. */
    netSendString(sd, "query");

    /* Send options. */
    for (i=0; i<ArraySize(options); ++i)
        sendOption(sd, options[i].name);

    /* Send sequence. */
    if (optionExists("rna") || optionExists("unmask"))
        toUpperN(seq->dna, seq->size);
    else
	{
	if (seqIsLower(seq))
	    warn("Sequence %s is all lower case, and thus ignored. Use -unmask "
	         "flag to unmask lower case sequence.", seq->name);
	}
    netSendString(sd, "seq");
    netSendString(sd, seq->name);
    netSendHugeString(sd, seq->dna);
    verbose(1, "%s\n", seq->name);
    dnaSeqFree(&seq);

    /* Get and save response. */
    sf = netFileFromSocket(sd);
    copyOpenFile(sf, f);
    carefulClose(&sf);

    /* Close connection */
    close(sd);
    }
dnaLoadClose(&dl);
carefulClose(&f);
}
コード例 #5
0
ファイル: dnaLoad.c プロジェクト: Bioinformaticsnl/SimSeq
struct dnaSeq *dnaLoadAll(char *fileName)
/* Return list of all DNA referenced in file.  File
 * can be either a single fasta file, a single .2bit
 * file, a .nib file, or a text file containing
 * a list of the above files. DNA is mixed case. */
{
struct dnaLoad *dl = dnaLoadOpen(fileName);
struct dnaSeq *seqList = NULL, *seq;
while ((seq = dnaLoadNext(dl)) != NULL)
    {
    slAddHead(&seqList, seq);
    }
dnaLoadClose(&dl);
slReverse(&seqList);
return seqList;
}
コード例 #6
0
void itsaMake(int inCount, char *inputs[], char *output)
/* itsaMake - Make a suffix array file out of input DNA sequences.. */
{
verboseTimeInit();
bits64 maxGenomeSize = 1024LL*1024*1024*4;

itsaBaseToValInit();

/* Load all DNA, make sure names are unique, and alphabetize by name. */
struct dnaSeq *seqList = NULL, *seq;
struct hash *uniqSeqHash = hashNew(0);
bits64 totalDnaSize = 1;	/* FOr space between. */
int inputIx;
for (inputIx=0; inputIx<inCount; ++inputIx)
    {
    char * input = inputs[inputIx];
    struct dnaLoad *dl = dnaLoadOpen(input);
    while ((seq = dnaLoadNext(dl)) != NULL)
	{
	verbose(1, "read %s with %d bases\n", seq->name, seq->size);
	if (hashLookup(uniqSeqHash, seq->name))
	    errAbort("Input sequence name %s repeated, all must be unique.", seq->name);
	totalDnaSize +=  seq->size + 1;
	if (totalDnaSize > maxGenomeSize)
	    errAbort("Too much DNA. Can only handle up to %lld bases", maxGenomeSize);
	slAddHead(&seqList, seq);
	}
    dnaLoadClose(&dl);
    }
slSort(&seqList, dnaSeqCmpName);
verboseTime(1, "Loaded %lld bases in %d sequences", totalDnaSize, slCount(seqList));

/* Allocate big buffer for all DNA. */
DNA *allDna = globalAllDna = needHugeMem(totalDnaSize);
allDna[0] = 0;
bits64 chromOffset = 1;	/* Have zeroes between each chrom, and before and after. */

/* Copy DNA to a single big buffer, and create chromInfo on each sequence. */
struct chromInfo *chrom, *chromList = NULL;
for (seq = seqList; seq != NULL; seq = seq->next)
    {
    AllocVar(chrom);
    chrom->name = cloneString(seq->name);
    chrom->size = seq->size;
    chrom->offset = chromOffset;
    slAddHead(&chromList, chrom);
    toUpperN(seq->dna, seq->size);
    memcpy(allDna + chromOffset, seq->dna, seq->size + 1);
    chromOffset += seq->size + 1;
    }
slReverse(&chromList);

/* Free up separate dna sequences because we're going to need a lot of RAM soon. */


/* Allocate index array, and offset and list arrays. */
dnaSeqFreeList(&seqList);
bits32 *index13;
AllocArray(index13, itsaSlotCount);
bits32 *offsetArray = needHugeMem(totalDnaSize * sizeof(bits32));
bits32 *listArray = needHugeZeroedMem(totalDnaSize * sizeof(bits32));
verboseTime(1, "Allocated buffers %lld bytes total", 
	(long long)(9LL*totalDnaSize + itsaSlotCount*sizeof(bits32)));

/* Where normally we'd keep some sort of structure with a next element to form a list
 * of matching positions in each slot of our index,  to conserve memory we'll do this
 * with two parallel arrays.  Because we're such cheapskates in terms of memory we'll
 * (and still using 9*genomeSize bytes of RAM) we'll use these arrays for two different
 * purposes.   
 *     In the first phase they will together be used to form linked lists of
 * offsets, and the 13mer index will point to the first item in each list.  In this
 * phase the offsetArray contains offsets into the allDna structure, and the listArray
 * contains the next pointers for the list.  After the first phase we write out the
 * suffix array to disk.
 *     In the second phase we read the suffix array back into the offsetArray, and
 * use the listArray for the traverseArray.  We write out the traverse array to finish
 * things up. */


/* Load up all DNA buffer. */
for (chrom = chromList; chrom != NULL; chrom = chrom->next)
    {
    verbose(2, "  About to do first pass index\n");
    indexChromPass1(chrom, allDna, offsetArray, listArray, index13);
    verbose(2, "  Done first pass index\n");
    }
verboseTime(1, "Done big bucket sort");
slReverse(&chromList);
itsaWriteMerged(chromList, allDna, offsetArray, listArray, index13, output);
}