void doConvertCoordinates(struct cart *theCart)
/* tries to convert the coordinates given */
{
/* Seperate zoo conversions from non-zoo conversions... */

cart = theCart;
hgBotDelay();	/* Prevent abuse. */

if(strstr(origGenome, "zoo")){
    convertCoordinatesZoo(stdout, stdout, doGoodReportZoo, doBadReportZoo);
}
else
    convertCoordinates(stdout, stdout, doGoodReport, doBadReport);
}
Пример #2
0
boolean doPcr(struct pcrServer *server, struct targetPcrServer *targetServer,
              char *fPrimer, char *rPrimer,
              int maxSize, int minPerfect, int minGood, boolean flipReverse)
/* Do the PCR, and show results. */
{
    struct errCatch *errCatch = errCatchNew();
    boolean ok = FALSE;

    hgBotDelay();
    if (flipReverse)
        reverseComplement(rPrimer, strlen(rPrimer));
    if (errCatchStart(errCatch))
    {
        struct gfPcrInput *gpi;

        AllocVar(gpi);
        gpi->fPrimer = fPrimer;
        gpi->rPrimer = rPrimer;
        if (server != NULL)
            doQuery(server, gpi, maxSize, minPerfect, minGood);
        if (targetServer != NULL)
            doTargetQuery(targetServer, gpi, maxSize, minPerfect, minGood);
        ok = TRUE;
    }
    errCatchEnd(errCatch);
    if (errCatch->gotError)
        warn("%s", errCatch->message->string);
    errCatchFree(&errCatch);
    if (flipReverse)
        reverseComplement(rPrimer, strlen(rPrimer));
    webNewSection("Primer Melting Temperatures");
    printf("<TT>");
    printf("<B>Forward:</B> %4.1f C %s<BR>\n", oligoTm(fPrimer, 50.0, 50.0), fPrimer);
    printf("<B>Reverse:</B> %4.1f C %s<BR>\n", oligoTm(rPrimer, 50.0, 50.0), rPrimer);
    printf("</TT>");
    printf("The temperature calculations are done assuming 50 mM salt and 50 nM annealing "
           "oligo concentration.  The code to calculate the melting temp comes from "
           "<A HREF=\"http://frodo.wi.mit.edu/primer3/input.htm\" target=_blank>"
           "Primer3</A>.");
    return ok;
}
Пример #3
0
void cartMain(struct cart *theCart)
/* We got the persistent/CGI variable cart.  Now
 * set up the globals and make a web page. */
{
hgBotDelay();
cart = theCart;
getDbAndGenome(cart, &database, &genome, oldVars);
initGenbankTableNames(database);
getGenomeSettings();
if (cartVarExists(cart, hggDoKgMethod))
    doKgMethod();
else if (cartVarExists(cart, hggDoTxInfoDescription))
    doTxInfoDescription();
else
    {
    struct sqlConnection *conn = NULL;
    char *geneName = cartUsualString(cart, hggGene, NULL);
    if (isEmpty(geneName))
	{
	// Silly googlebots.
	hUserAbort("Error: the hgg_gene parameter is missing from the cart and the CGI params.");
	}

    /* if kgProtMap2 table exists, this means we are doing KG III */
    if (hTableExists(database, "kgProtMap2")) kgVersion = KG_III;

    conn = hAllocConn(database);
    curGeneId = findGeneId(conn, geneName);
    getGenePosition(conn);
    curGenePred = getCurGenePred(conn);
    curGeneName = getGeneName(curGeneId, conn);
    spConn = hAllocConn(UNIPROT_DB_NAME);
    swissProtAcc = getSwissProtAcc(conn, spConn, curGeneId);

    if (isRgdGene(conn)) swissProtAcc=getRgdGeneUniProtAcc(curGeneId, conn);
    /* Check command variables, and do the ones that
     * don't want to put up the hot link bar etc. */
    if (cartVarExists(cart, hggDoGetMrnaSeq))
	doGetMrnaSeq(conn, curGeneId, curGeneName);
    else if (cartVarExists(cart, hggDoWikiTrack))
	doWikiTrack(conn);
    else if (cartVarExists(cart, hggDoGetProteinSeq))
	doGetProteinSeq(conn, curGeneId, curGeneName);
    else if (cartVarExists(cart, hggDoRnaFoldDisplay))
	doRnaFoldDisplay(conn, curGeneId, curGeneName);
    else if (cartVarExists(cart, hggDoOtherProteinSeq))
	doOtherProteinSeq(conn, curGeneName);
    else if (cartVarExists(cart, hggDoOtherProteinAli))
	doOtherProteinAli(conn, curGeneId, curGeneName);
    else
	{
	/* Default case - start fancy web page. */
	measureTiming =  isNotEmpty(cartOptionalString(cart, "measureTiming"));
        struct trackDb *tdb = hTrackDbForTrack(database, genomeSetting("knownGene"));
        isGencode = trackDbSettingOn(tdb, "isGencode");
        isGencode2 = trackDbSettingOn(tdb, "isGencode2");
	cartWebStart(cart, database, "%s Gene %s (%s) Description and Page Index",
	    genome, curGeneName, isGencode2 ? curGeneId : curAlignId);
	webMain(conn, tdb);
	cartWebEnd();
	}
    hFreeConn(&spConn);
    hFreeConn(&conn);
    }
cartRemovePrefix(cart, hggDoPrefix);
}
Пример #4
0
void blatSeq(char *userSeq, char *organism)
/* Blat sequence user pasted in. */
{
FILE *f;
struct dnaSeq *seqList = NULL, *seq;
struct tempName pslTn, faTn;
int maxSingleSize, maxTotalSize, maxSeqCount;
int minSingleSize = minMatchShown;
char *genome, *db;
char *type = cgiString("type");
char *seqLetters = cloneString(userSeq);
struct serverTable *serve;
int conn;
int oneSize, totalSize = 0, seqCount = 0;
boolean isTx = FALSE;
boolean isTxTx = FALSE;
boolean txTxBoth = FALSE;
struct gfOutput *gvo;
boolean qIsProt = FALSE;
enum gfType qType, tType;
struct hash *tFileCache = gfFileCacheNew();
boolean feelingLucky = cgiBoolean("Lucky");

getDbAndGenome(cart, &db, &genome, oldVars);
if(!feelingLucky)
    cartWebStart(cart, db, "%s BLAT Results",  trackHubSkipHubName(organism));
/* Load user sequence and figure out if it is DNA or protein. */
if (sameWord(type, "DNA"))
    {
    seqList = faSeqListFromMemText(seqLetters, TRUE);
    uToT(seqList);
    isTx = FALSE;
    }
else if (sameWord(type, "translated RNA") || sameWord(type, "translated DNA"))
    {
    seqList = faSeqListFromMemText(seqLetters, TRUE);
    uToT(seqList);
    isTx = TRUE;
    isTxTx = TRUE;
    txTxBoth = sameWord(type, "translated DNA");
    }
else if (sameWord(type, "protein"))
    {
    seqList = faSeqListFromMemText(seqLetters, FALSE);
    isTx = TRUE;
    qIsProt = TRUE;
    }
else 
    {
    seqList = faSeqListFromMemTextRaw(seqLetters);
    isTx = !seqIsDna(seqList);
    if (!isTx)
	{
	for (seq = seqList; seq != NULL; seq = seq->next)
	    {
	    seq->size = dnaFilteredSize(seq->dna);
	    dnaFilter(seq->dna, seq->dna);
	    toLowerN(seq->dna, seq->size);
	    subChar(seq->dna, 'u', 't');
	    }
	}
    else
	{
	for (seq = seqList; seq != NULL; seq = seq->next)
	    {
	    seq->size = aaFilteredSize(seq->dna);
	    aaFilter(seq->dna, seq->dna);
	    toUpperN(seq->dna, seq->size);
	    }
	qIsProt = TRUE;
	}
    }
if (seqList != NULL && seqList->name[0] == 0)
    {
    freeMem(seqList->name);
    seqList->name = cloneString("YourSeq");
    }
trimUniq(seqList);

/* If feeling lucky only do the first on. */
if(feelingLucky && seqList != NULL)
    {
    seqList->next = NULL;
    }

/* Figure out size allowed. */
maxSingleSize = (isTx ? 10000 : 75000);
maxTotalSize = maxSingleSize * 2.5;
#ifdef LOWELAB
maxSeqCount = 200;
#else
maxSeqCount = 25;
#endif

/* Create temporary file to store sequence. */
trashDirFile(&faTn, "hgSs", "hgSs", ".fa");
faWriteAll(faTn.forCgi, seqList);

/* Create a temporary .psl file with the alignments against genome. */
trashDirFile(&pslTn, "hgSs", "hgSs", ".pslx");
f = mustOpen(pslTn.forCgi, "w");
gvo = gfOutputPsl(0, qIsProt, FALSE, f, FALSE, TRUE);
serve = findServer(db, isTx);
/* Write header for extended (possibly protein) psl file. */
if (isTx)
    {
    if (isTxTx)
        {
	qType = gftDnaX;
	tType = gftDnaX;
	}
    else
        {
	qType = gftProt;
	tType = gftDnaX;
	}
    }
else
    {
    qType = gftDna;
    tType = gftDna;
    }
pslxWriteHead(f, qType, tType);

if (qType == gftProt)
    {
    minSingleSize = 14;
    }
else if (qType == gftDnaX)
    {
    minSingleSize = 36;
    }


/* Loop through each sequence. */
for (seq = seqList; seq != NULL; seq = seq->next)
    {
    printf(" "); fflush(stdout);  /* prevent apache cgi timeout by outputting something */
    oneSize = realSeqSize(seq, !isTx);
    if ((seqCount&1) == 0)	// Call bot delay every 2nd time starting with first time
	hgBotDelay();
    if (++seqCount > maxSeqCount)
        {
	warn("More than 25 input sequences, stopping at %s.",
	    seq->name);
	break;
	}
    if (oneSize > maxSingleSize)
	{
	warn("Sequence %s is %d letters long (max is %d), skipping",
	    seq->name, oneSize, maxSingleSize);
	continue;
	}
    if (oneSize < minSingleSize)
        {
	warn("Warning: Sequence %s is only %d letters long (%d is the recommended minimum)", 
		seq->name, oneSize, minSingleSize);
	// we could use "continue;" here to actually enforce skipping, 
	// but let's give the short sequence a chance, it might work.
	// minimum possible length = tileSize+stepSize, so mpl=16 for dna stepSize=5, mpl=10 for protein.
	if (qIsProt && oneSize < 1) // protein does not tolerate oneSize==0
	    continue;
	}
    totalSize += oneSize;
    if (totalSize > maxTotalSize)
        {
	warn("Sequence %s would take us over the %d letter limit, stopping here.",
	     seq->name, maxTotalSize);
	break;
	}
    conn = gfConnect(serve->host, serve->port);
    if (isTx)
	{
	gvo->reportTargetStrand = TRUE;
	if (isTxTx)
	    {
	    gfAlignTransTrans(&conn, serve->nibDir, seq, FALSE, 5, 
	    	tFileCache, gvo, !txTxBoth);
	    if (txTxBoth)
		{
		reverseComplement(seq->dna, seq->size);
		conn = gfConnect(serve->host, serve->port);
		gfAlignTransTrans(&conn, serve->nibDir, seq, TRUE, 5, 
			tFileCache, gvo, FALSE);
		}
	    }
	else
	    {
	    gfAlignTrans(&conn, serve->nibDir, seq, 5, tFileCache, gvo);
	    }
	}
    else
	{
	gfAlignStrand(&conn, serve->nibDir, seq, FALSE, minMatchShown, tFileCache, gvo);
	reverseComplement(seq->dna, seq->size);
	conn = gfConnect(serve->host, serve->port);
	gfAlignStrand(&conn, serve->nibDir, seq, TRUE, minMatchShown, tFileCache, gvo);
	}
    gfOutputQuery(gvo, f);
    }
carefulClose(&f);
showAliPlaces(pslTn.forCgi, faTn.forCgi, serve->db, qType, tType, 
	      organism, feelingLucky);
if(!feelingLucky)
    cartWebEnd();
gfFileCacheFree(&tFileCache);
}
Пример #5
0
static void mafOrAxtClick2(struct sqlConnection *conn, struct sqlConnection *conn2, struct trackDb *tdb, char *axtOtherDb, char *fileName)
/* Display details for MAF or AXT tracks. */
{
hgBotDelay();
if (winEnd - winStart > 30000)
    {
    printf("Zoom so that window is 30,000 bases or less to see alignments and conservation statistics\n");
    }
else
    {
    struct mafAli *mafList = NULL, *maf, *subList = NULL;
    int aliIx = 0, realCount = 0;
    char dbChrom[64];
    char option[128];
    char *capTrack;
    struct consWiggle *consWig, *consWiggles;
    struct hash *speciesOffHash = NULL;
    char *speciesOrder = NULL;
    char *speciesTarget = trackDbSetting(tdb, SPECIES_TARGET_VAR);
    char buffer[1024];
    int useTarg = FALSE;
    int useIrowChains = FALSE;

    safef(option, sizeof(option), "%s.%s", tdb->track, MAF_CHAIN_VAR);
    if (cartCgiUsualBoolean(cart, option, FALSE) &&
	trackDbSetting(tdb, "irows") != NULL)
	    useIrowChains = TRUE;

    safef(buffer, sizeof(buffer), "%s.vis",tdb->track);
    if (useIrowChains)
	{
	if (!cartVarExists(cart, buffer) && (speciesTarget != NULL))
	    useTarg = TRUE;
	else
	    {
	    char *val;

	    val = cartUsualString(cart, buffer, "useCheck");
            useTarg = sameString("useTarg",val);
            }
        }

    if (sameString(tdb->type, "bigMaf"))
        {
        char *fileName = trackDbSetting(tdb, "bigDataUrl");
        struct bbiFile *bbi = bigBedFileOpen(fileName);
        mafList = bigMafLoadInRegion(bbi, seqName, winStart, winEnd);
        }
    else
        mafList = mafOrAxtLoadInRegion2(conn,conn2, tdb, seqName, winStart, winEnd,
                                        axtOtherDb, fileName);
    safef(dbChrom, sizeof(dbChrom), "%s.%s", hubConnectSkipHubPrefix(database), seqName);

    safef(option, sizeof(option), "%s.speciesOrder", tdb->track);
    speciesOrder = cartUsualString(cart, option, NULL);
    if (speciesOrder == NULL)
	speciesOrder = trackDbSetting(tdb, "speciesOrder");

    for (maf = mafList; maf != NULL; maf = maf->next)
        {
        int mcCount = 0;
        struct mafComp *mc;
        struct mafAli *subset;
        struct mafComp *nextMc;

        /* remove empty components and configured off components
         * from MAF, and ignore
         * the entire MAF if all components are empty
         * (solely for gap annotation) */

        if (!useTarg)
            {
            for (mc = maf->components->next; mc != NULL; mc = nextMc)
		{
		char buf[64];
                char *organism;
		mafSrcDb(mc->src, buf, sizeof buf);
                organism = hOrganism(buf);
                if (!organism)
                    organism = buf;
		nextMc = mc->next;
		safef(option, sizeof(option), "%s.%s", tdb->track, buf);
		if (!cartUsualBoolean(cart, option, TRUE))
		    {
		    if (speciesOffHash == NULL)
			speciesOffHash = newHash(4);
		    hashStoreName(speciesOffHash, organism);
		    }
		if (!cartUsualBoolean(cart, option, TRUE))
		    slRemoveEl(&maf->components, mc);
		else
		    mcCount++;
		}
	    }
        if (mcCount == 0)
            continue;

	if (speciesOrder)
	    {
	    int speciesCt;
	    char *species[2048];
	    struct mafComp **newOrder, *mcThis;
	    int i;

	    mcCount = 0;
	    speciesCt = chopLine(cloneString(speciesOrder), species);
	    newOrder = needMem((speciesCt + 1) * sizeof (struct mafComp *));
	    newOrder[mcCount++] = maf->components;

	    for (i = 0; i < speciesCt; i++)
		{
		if ((mcThis = mafMayFindCompSpecies(maf, species[i], '.')) == NULL)
		    continue;
		newOrder[mcCount++] = mcThis;
		}

	    maf->components = NULL;
	    for (i = 0; i < mcCount; i++)
		{
		newOrder[i]->next = 0;
		slAddHead(&maf->components, newOrder[i]);
		}

	    slReverse(&maf->components);
	    }
	subset = mafSubsetE(maf, dbChrom, winStart, winEnd, TRUE);
	if (subset != NULL)
	    {
	    /* Reformat MAF if needed so that sequence from current
	     * database is the first component and on the
	     * plus strand. */
	    mafMoveComponentToTop(subset, dbChrom);
	    if (subset->components->strand == '-')
		mafFlipStrand(subset);
	    subset->score = mafScoreMultiz(subset);
	    slAddHead(&subList, subset);
	    ++realCount;
	    }
	}
    slReverse(&subList);
    mafAliFreeList(&mafList);
    if (subList != NULL)
	{
	char *showVarName = "hgc.showMultiBase";
	char *showVarVal = cartUsualString(cart, showVarName, "all");
	boolean onlyDiff = sameWord(showVarVal, "diff");
#ifdef ADDEXONCAPITAL
	char *codeVarName = "hgc.multiCapCoding";
	char *codeVarVal = cartUsualString(cart, codeVarName, "coding");
	boolean onlyCds = sameWord(codeVarVal, "coding");
#endif
        /* add links for conservation score statistics */
        consWiggles = wigMafWiggles(database, tdb);
        int wigCount = slCount(consWiggles);
        if (wigCount == 1)
            {
            conservationStatsLink(tdb, "Conservation score statistics", consWiggles->table);
            }
        else if (wigCount > 1)
            {
            /* multiple wiggles. List all that have been turned on with
             * checkboxes */

            /* Scan for cart variables -- do any exist, are any turned on ? */
            boolean wigSet = FALSE;
            boolean wigOn = FALSE;
            for (consWig = consWiggles; consWig != NULL;
                        consWig = consWig->next)
                {
                char *wigVarSuffix = NULL;
                (void)wigMafWiggleVar(tdb->track, consWig, &wigVarSuffix);
                if (cartVarExistsAnyLevel(cart, tdb, FALSE, wigVarSuffix))
                    {
                    wigSet = TRUE;
                    if (cartBooleanClosestToHome(cart, tdb, FALSE, wigVarSuffix))
                        wigOn = TRUE;
                    }
                }
            /* If there are no cart vars, turn on the first (default) wig */
            if (!wigSet)
                {
                char *prefix = tdb->track; // use when setting things to the cart
                if (tdbIsContainerChild(tdb))
                    prefix = tdbGetContainer(tdb)->track;

                cartSetBoolean(cart, wigMafWiggleVar(prefix, consWiggles, NULL), TRUE);
                wigOn = TRUE;
                }
            if (wigOn)
                {
                boolean first = TRUE;
                for (consWig = consWiggles; consWig != NULL;
                            consWig = consWig->next)
                    {
                    if (first)
                        {
                        printf("Conservation score statistics:");
                        first = FALSE;
                        }
                    char *wigVarSuffix = NULL;
                    (void)wigMafWiggleVar(tdb->track, consWig, &wigVarSuffix);
                    if (cartUsualBooleanClosestToHome(cart, tdb, FALSE, wigVarSuffix,FALSE))
                        {
                        printf("&nbsp;&nbsp;");
                        subChar(consWig->uiLabel, '_', ' ');
                        conservationStatsLink(tdb,
                            consWig->uiLabel, consWig->table);
                        }
                    }
                }
            }
        puts("</P>\n");

        /* no alignment to display when in visibilities where only wiggle is shown */
        char *vis = cartOptionalString(cart, tdb->track);
        if (vis)
            {
            enum trackVisibility tv = hTvFromStringNoAbort(vis);
            if (tv == tvSquish || tv == tvDense)
                return;
            }

#ifdef ADDEXONCAPITAL
	puts("<FORM ACTION=\"../cgi-bin/hgc\" NAME=\"gpForm\" METHOD=\"GET\">");
	cartSaveSession(cart);
	cgiContinueHiddenVar("g");
	cgiContinueHiddenVar("c");
	cgiContinueHiddenVar("i");
	printf("Capitalize ");
        cgiMakeDropListFull(codeVarName, codeAll, codeAll,
	    ArraySize(codeAll), codeVarVal, autoSubmit);
	printf("exons based on ");
        capTrack = genePredDropDown(cart, trackHash,
                                       "gpForm", "hgc.multiCapTrack");
#endif
	printf("show ");
        cgiMakeDropListFull(showVarName, showAll, showAll,
	    ArraySize(showAll), showVarVal, autoSubmit);
	printf("bases");
	printf("<BR>\n");
	printf("</FORM>\n");

#ifdef REVERSESTRAND
        /* notify if bases are complemented (hgTracks is on reverse strand) */
        if (cartCgiUsualBoolean(cart, COMPLEMENT_BASES_VAR, FALSE))
            puts("<EM>Alignment displayed on reverse strand</EM><BR>");
#endif
	puts("Place cursor over species for alignment detail. Click on 'B' to link to browser ");
	puts("for aligned species, click on 'D' to get DNA for aligned species.<BR>");

	printf("<TT><PRE>");

        /* notify if species removed from alignment */
        if (speciesOffHash) 
            {
            char *species;
            struct hashCookie hc = hashFirst(speciesOffHash);
            puts("<B>Components not displayed:</B> ");
            while ((species = hashNextName(&hc)) != NULL)
                printf("%s ", species);
            puts("<BR>");
            }


	for (maf = subList; maf != NULL; maf = maf->next)
	    {
	    mafLowerCase(maf);
#ifdef ADDEXONCAPITAL
	    if (capTrack != NULL)
                capMafOnTrack(maf, capTrack, onlyCds);
#endif
            printf("<B>Alignment block %d of %d in window, %d - %d, %d bps </B>\n",
                   ++aliIx,realCount,maf->components->start + 1,
                   maf->components->start + maf->components->size, maf->components->size);
            mafPrettyOut(stdout, maf, 70,onlyDiff, aliIx);
            }
	mafAliFreeList(&subList);
	}
    else
	{
        printf("No multiple alignment in browser window");
	}
    printf("</PRE></TT>");
    }
}