Пример #1
0
void doTracks(char *proteinID, char *mrnaID, char *aa, int *yOffp, char *psOutput)
/* draw various protein tracks */
{
int l;

char aaOrigOffsetStr[20];
int hasResFreq;
char uniProtDbName[50];
char *protDbDate;
char *chrom;
char strand;
char *kgId, *kgPep, *protPep;
char cond_str[255];
char *answer;
//int i, ll;
//char *chp1, *chp2;

g_font = mgSmallFont();
safef(pbScaleStr, sizeof(pbScaleStr), "%d", pbScale);

if (psOutput != NULL)
    {
    pbScale         = atoi(cartOptionalString(cart, "pbt.pbScaleStr"));
    }

if (cgiOptionalString("trackOffset") != NULL)
	{
	trackOrigOffset = atoi(cgiOptionalString("trackOffset")); 
	}

if (cgiOptionalString("pbScaleStr") != NULL)
	{
	pbScale  = atoi(cgiOptionalString("pbScaleStr")); 
	}

if (cgiOptionalString("pbScale") != NULL)
    {
    scaleButtonPushed = TRUE;
    if (strcmp(cgiOptionalString("pbScale"), "1/6")  == 0) pbScale = 1;
    if (strcmp(cgiOptionalString("pbScale"), "1/2")  == 0) pbScale = 3;
    if (strcmp(cgiOptionalString("pbScale"), "FULL") == 0) pbScale = 6;
    if (strcmp(cgiOptionalString("pbScale"), "DNA")  == 0) pbScale =22;
    safef(pbScaleStr, sizeof(pbScaleStr), "%d", pbScale);
    cgiMakeHiddenVar("pbScaleStr", pbScaleStr);
    }
else
    {
    scaleButtonPushed = FALSE;
    }

if (psOutput == NULL)
{
if (cgiVarExists("pbt.left3"))
    {
    relativeScroll(-0.95);
    initialWindow = FALSE;
    }
else if (cgiVarExists("pbt.left2"))
    {
    relativeScroll(-0.475);
    initialWindow = FALSE;
    }
else if (cgiVarExists("pbt.left1"))
    {
    relativeScroll(-0.02);
    initialWindow = FALSE;
    }
else if (cgiVarExists("pbt.right1"))
    {
    relativeScroll(0.02);
    initialWindow = FALSE;
    }
else if (cgiVarExists("pbt.right2"))
    {
    relativeScroll(0.475);
    initialWindow = FALSE;
    }
else if (cgiVarExists("pbt.right3"))
    {
    relativeScroll(0.95);
    initialWindow = FALSE;
    }
}

dnaUtilOpen();

l=strlen(aa);

/* initialize AA properties */
aaPropertyInit(&hasResFreq);
sfCount = getSuperfamilies2(proteinID);
if (sfCount == 0)
    {
    sfCount = getSuperfamilies(proteinID);
    }
if (mrnaID != NULL)
    {
    if (kgVersion == KG_III)
    	{
	doExonTrack = FALSE;
	sqlSafefFrag(cond_str, sizeof(cond_str), "spId='%s'", proteinID);
        kgId = sqlGetField(database, "kgXref", "kgId", cond_str);
	if (kgId != NULL)
	    {
	    sqlSafefFrag(cond_str, sizeof(cond_str), "name='%s'", kgId);
            kgPep = sqlGetField(database, "knownGenePep", "seq", cond_str);
      	    //printf("<pre><br>%s", kgPep);fflush(stdout);
	    if (kgPep != NULL)
	    	{
		if (strstr(protDbName, "proteins") != NULL)
		    {
		    protDbDate = strstr(protDbName, "proteins") + strlen("proteins");
		    safef(uniProtDbName, sizeof(uniProtDbName),"sp%s", protDbDate);
		
		    sqlSafefFrag(cond_str, sizeof(cond_str), "acc='%s'", proteinID);
            	    protPep = sqlGetField(uniProtDbName, "protein", "val", cond_str);
            	    //printf("<br>%s\n", protPep);fflush(stdout);
            	    if (protPep != NULL)
		    	{
			if (sameWord(kgPep, protPep))
			    {
			    //printf("<br>MATCH!\n");fflush(stdout);
		    	    sqlSafefFrag(cond_str, sizeof(cond_str), "qName='%s'", kgId);
            	    	    answer = sqlGetField(database, kgProtMapTableName, 
			    			 "qName", cond_str);
            	    	    if (answer != NULL)
			    	{
    			    	/* NOTE: passing in kgId instead of proteinID because
					 kgProtMap2's qName uses kgId instead of 
					 protein display ID */
    			    	getExonInfo(kgId, &exCount, &chrom, &strand);
			    	assert(exCount > 0);
				doExonTrack = TRUE;
			    	}
			    }
			/*
			else
			    {
			    chp1 = kgPep;
			    printf("<br>");
			    chp2 = protPep;
			    ll = strlen(kgPep);
			    if (strlen(protPep) < ll) ll= strlen(protPep);
			    for (i=0; i<ll; i++)
			    	{
				if (*chp1 != *chp2)
					{
					printf("%c", *chp1);
					}
				else
					{
					printf(".");
					}
				chp1++; chp2++;
				}
			    }
			    //printf("</pre>");fflush(stdout);
			*/
			}
		    }
		}
	    }
	}
    else
    	{
	doExonTrack = TRUE;
    	getExonInfo(proteinID, &exCount, &chrom, &strand);
    	assert(exCount > 0);
	}
    /* do the following only if pbTracks called doTracks() */
    if (initialWindow && IAmPbTracks)
	{
	prevGBOffsetSav = calPrevGB(exCount, chrom, strand, l, yOffp, proteinID, mrnaID);
	trackOrigOffset = prevGBOffsetSav;
    	if (trackOrigOffset > (protSeqLen*pbScale - 600))
	    trackOrigOffset = protSeqLen*pbScale - 600;
	/* prevent negative value */
	if (trackOrigOffset < 0) trackOrigOffset = 0;
	}

    /* if this if for PDF/Postscript, the trackOrigOffset is already calculated previously,
        use the saved value */
    if (psOutput != NULL)
    	{
    	trackOrigOffset = atoi(cartOptionalString(cart, "pbt.trackOffset"));
    	}
    }

/*printf("<br>%d %d<br>%d %d\n", prevGBStartPos, prevGBEndPos, 
	blockGenomeStartPositive[exCount-1], blockGenomeStartPositive[0]); fflush(stdout);
*/
if (strand == '-')
    {
    if ((prevGBStartPos <= blockGenomeStartPositive[exCount-1]) && (prevGBEndPos >= blockGenomeStartPositive[0]))
    	{
    	showPrevGBPos = FALSE;
    	}
    }
else
    {
    if ((prevGBStartPos <= blockGenomeStartPositive[0]) && (prevGBEndPos >= blockGenomeStartPositive[exCount-1]))
    	{
    	showPrevGBPos = FALSE;
    	}
    }

if ((cgiOptionalString("aaOrigOffset") != NULL) && scaleButtonPushed)
     {
     trackOrigOffset = atoi(cgiOptionalString("aaOrigOffset"))*pbScale;
     }

pixWidth = 160+ protSeqLen*pbScale;
if (pixWidth > MAX_PB_PIXWIDTH)
   {
   pixWidth = MAX_PB_PIXWIDTH;
   }

if ((protSeqLen*pbScale - trackOrigOffset) < MAX_PB_PIXWIDTH)
    {
    pixWidth = protSeqLen*pbScale - trackOrigOffset + 160;
    }

if (pixWidth < 550) pixWidth = 550;

insideWidth = pixWidth-gfxBorder;

if (proteinInSupportedGenome)
    {
    pixHeight = 250;
    }
else
    {
    pixHeight = 215;
    }

if (sfCount > 0) pixHeight = pixHeight + 20;

/* make room for individual residues display */
if (pbScale >=6)  pixHeight = pixHeight + 20;
if (pbScale >=18) pixHeight = pixHeight + 30;

if (psOutput)
    {
    vg = vgOpenPostScript(pixWidth, pixHeight, psOutput);
    suppressHtml = TRUE;
    hideControls = TRUE;
    }
else
    {
    trashDirFile(&gifTn, "pbt", "pbt", ".png");
    vg = vgOpenPng(pixWidth, pixHeight, gifTn.forCgi, FALSE);
    }

/* Put up horizontal scroll controls. */
hWrites("Move ");
hButton("pbt.left3", "<<<");
hButton("pbt.left2", " <<");
hButton("pbt.left1", " < ");
hButton("pbt.right1", " > ");
hButton("pbt.right2", ">> ");
hButton("pbt.right3", ">>>");

hPrintf(" &nbsp &nbsp ");

/* Put up scaling controls. */
hPrintf("Current scale: ");
if (pbScale == 1)  hPrintf("1/6 ");
if (pbScale == 3)  hPrintf("1/2 ");
if (pbScale == 6)  hPrintf("FULL ");
if (pbScale == 22) hPrintf("DNA ");

hPrintf(" &nbsp&nbsp Rescale to ");
hPrintf("<INPUT TYPE=SUBMIT NAME=\"pbScale\" VALUE=\"1/6\">\n");
hPrintf("<INPUT TYPE=SUBMIT NAME=\"pbScale\" VALUE=\"1/2\">\n");
hPrintf("<INPUT TYPE=SUBMIT NAME=\"pbScale\" VALUE=\"FULL\">\n");
if (kgVersion == KG_III)
    {
    /* for KG III, the protein has to exist in the kgProtMap2 table 
       (which will turn on doExonTrack flag)
       to provide the genomic position data needed for DNA sequence display */
    if ((proteinInSupportedGenome) && (doExonTrack))
    hPrintf("<INPUT TYPE=SUBMIT NAME=\"pbScale\" VALUE=\"DNA\">\n");
    }
else
    {
    if (proteinInSupportedGenome) 
   	hPrintf("<INPUT TYPE=SUBMIT NAME=\"pbScale\" VALUE=\"DNA\">\n");
    }
hPrintf("<FONT SIZE=1><BR><BR></FONT>\n");

g_vg = vg;

pbRed    = vgFindColorIx(g_vg, 0xf9, 0x51, 0x59);
pbBlue   = vgFindColorIx(g_vg, 0x00, 0x00, 0xd0);
bkgColor = vgFindColorIx(vg, 255, 254, 232);

vgBox(vg, 0, 0, insideWidth, pixHeight, bkgColor);

/* Start up client side map. */
hPrintf("<MAP Name=%s>\n", mapName);

vgSetClip(vg, 0, gfxBorder, insideWidth, pixHeight - 2*gfxBorder);

/* start drawing indivisual tracks */

doAAScale(l, yOffp, 1);

if (pbScale >= 6)  doResidues(aa, l, yOffp);

if (pbScale >= 18) doDnaTrack(chrom, strand, exCount, l, yOffp);

if ((mrnaID != NULL) && showPrevGBPos)
    {
    doPrevGB(exCount, chrom, strand, l, yOffp, proteinID, mrnaID);
    }

if (mrnaID != NULL)
    {
    if (doExonTrack) doExon(exCount, chrom, l, yOffp, proteinID, mrnaID);
    }

doCharge(aa, l, yOffp);

doHydrophobicity(aa, l, yOffp);

doCysteines(aa, l, yOffp);

if (sfCount > 0) doSuperfamily(ensPepName, sfCount, yOffp); 

if (hasResFreq) doAnomalies(aa, l, yOffp);

doAAScale(l, yOffp, -1);

vgClose(&vg);

/* Finish map and save out picture and tell html file about it. */
hPrintf("</MAP>\n");

/* put tracks image here */

hPrintf(
"\n<IMG SRC=\"%s\" BORDER=1 WIDTH=%d HEIGHT=%d USEMAP=#%s><BR>",
        gifTn.forCgi, pixWidth, pixHeight, mapName);

if (proteinInSupportedGenome)
    {
    hPrintf("<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbTracksHelp.shtml#tracks\" TARGET=_blank>");
    }
else
    {
    if (hIsGsidServer())
	{
	hPrintf("<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbGsid/pbTracksHelp.shtml#tracks\" TARGET=_blank>");
    	}
    else
	{
	hPrintf("<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbTracksHelp.shtml#tracks\" TARGET=_blank>");
    	}
    }

hPrintf("Explanation of Protein Tracks</A><br>");

safef(trackOffset, sizeof(trackOffset), "%d", trackOrigOffset);
cgiMakeHiddenVar("trackOffset", trackOffset);

/* remember where the AA base origin is so that it can be passed to next PB page */
aaOrigOffset = trackOrigOffset/pbScale;
safef(aaOrigOffsetStr, sizeof(aaOrigOffsetStr), "%d", aaOrigOffset);
cgiMakeHiddenVar("aaOrigOffset", aaOrigOffsetStr);

/* save the following state variables, to be used by PDF/Postcript processing */
cartSetString(cart,"pbt.pbScaleStr", pbScaleStr);
cartSetString(cart,"pbt.trackOffset", trackOffset);
cartSaveSession(cart);
fflush(stdout);
}
Пример #2
0
void makeActiveImagePB(char *psOutput, char *psOutput2)
/* Make image and image map. */
{
char *mapName = "map";
int pixWidth, pixHeight;

char *answer;
char cond_str[255];
struct sqlConnection *conn;
struct sqlConnection *connCentral;
char query[256];
struct sqlResult *sr;
char **row;
int  iypos;
char *blatGbDb;
char *sciName, *commonName;
char *spDisplayId;
char *oldDisplayId;
conn  = sqlConnect(UNIPROT_DB_NAME);
hPrintf("<br><font size=4>Protein ");

hPrintf("<A HREF=\"http://www.uniprot.org/uniprot/%s\" TARGET=_blank><B>%s</B></A>\n",
        proteinID, proteinID);

spDisplayId = spAccToId(conn, spFindAcc(conn, proteinID));
if (strstr(spDisplayId, spFindAcc(conn, proteinID)) == NULL)
    {
    hPrintf(" (aka %s", spDisplayId);
    /* show once if the new and old displayId are the same */
    oldDisplayId = oldSpDisplayId(spDisplayId);
    if (oldDisplayId != NULL)
        {
        if (!sameWord(spDisplayId, oldDisplayId))
            {
            hPrintf(" or %s", oldSpDisplayId(spDisplayId));
            }
        }
    hPrintf(")\n");
    }
hPrintf(" %s\n", description);
hPrintf("</font><br>");

hPrintf("Organism: ");
/* get scientific and Genbank common name of this organism */
sciName    = NULL;
commonName = NULL;
sqlSafefFrag(cond_str, sizeof(cond_str),"accession='%s'", proteinID);
answer = sqlGetField(PROTEOME_DB_NAME, "spXref3", "division", cond_str);
if (answer != NULL)
    {
    sqlSafefFrag(cond_str, sizeof(cond_str), "id=%s and nameType='scientific name'", answer);
    sciName = sqlGetField(PROTEOME_DB_NAME, "taxonNames", "name", cond_str);

    sqlSafefFrag(cond_str, sizeof(cond_str), "id=%s and nameType='genbank common name'", answer);
    commonName = sqlGetField(PROTEOME_DB_NAME, "taxonNames", "name", cond_str);
    }
if (sciName != NULL)
    {
    hPrintf("%s", sciName);
    }
if (commonName != NULL)
    {
    hPrintf(" (%s)", commonName);
    }
hPrintf("<br>");

protSeq = getAA(proteinID);
if (protSeq == NULL)
    {
    hUserAbort("%s is not a current valid entry in UniProtKB\n", proteinID);
    }
protSeqLen = strlen(protSeq);

fflush(stdout);

iypos = 15;
doTracks(proteinID, mrnaID, protSeq, &iypos, psOutput);
if (!hTableExists(database, "pbStamp")) goto histDone;

pbScale = 3;
pixWidth = 765;
insideWidth = pixWidth-gfxBorder;

pixHeight = 350;

if (psOutput2)
    {
    vg2 = vgOpenPostScript(pixWidth, pixHeight, psOutput2);
    }
else
    {
    trashDirFile(&gifTn2, "pbt", "pbt", ".png");
    vg2 = vgOpenPng(pixWidth, pixHeight, gifTn2.forCgi, FALSE);
    }

g_vg = vg2;

pbRed    = vgFindColorIx(vg2, 0xf9, 0x51, 0x59);
pbBlue   = vgFindColorIx(g_vg, 0x00, 0x00, 0xd0);

normalColor   = pbBlue;
abnormalColor = pbRed;

bkgColor = vgFindColorIx(vg2, 255, 254, 232);
vgBox(vg2, 0, 0, insideWidth, pixHeight, bkgColor);

/* Start up client side map. */
mapName=cloneString("pbStamps");
hPrintf("\n<MAP Name=%s>\n", mapName);

vgSetClip(vg2, 0, gfxBorder, insideWidth, pixHeight - 2*gfxBorder);
iypos = 15;

/* Draw stamps. */

doStamps(proteinID, mrnaID, protSeq, vg2, &iypos);

/* Finish map. */
hPrintf("</MAP>\n");

/* Save out picture and tell html file about it. */
vgClose(&vg2);
hPrintf("<P>");

hPrintf("\n<IMG SRC=\"%s\" BORDER=1 WIDTH=%d HEIGHT=%d USEMAP=#%s><BR>",
            gifTn2.forCgi, pixWidth, pixHeight, mapName);
if (proteinInSupportedGenome)
    {
    hPrintf("\n<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbTracksHelp.shtml#histograms\" TARGET=_blank>");
    }
else
    {
    hPrintf("\n<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbTracksHelp.shtml#histograms\" TARGET=_blank>");
    }

hPrintf("Explanation of Protein Property Histograms</A><BR>");

hPrintf("<P>");

histDone:

hPrintf("<P>");
fflush(stdout);

/* See if a UCSC Genome Browser exist for this organism.  If so, display BLAT link. */
connCentral = hConnectCentral();
sqlSafef(query, sizeof(query),
      "select defaultDb.name from dbDb, defaultDb where dbDb.scientificName='%s' and dbDb.name=defaultDb.name",
      sciName);
sr = sqlGetResult(connCentral, query);
row = sqlNextRow(sr);
if (row != NULL)
    {
    blatGbDb = strdup(row[0]);
    }
else
    {
    blatGbDb = NULL;
    }
sqlFreeResult(&sr);
hDisconnectCentral(&connCentral);

if (proteinInSupportedGenome || (blatGbDb != NULL))
    {
    hPrintf("\n<B>UCSC Links:</B><BR>\n ");
    hPrintf("<UL>\n");

    /* Show GB links only if the protein belongs to a supported genome */
    if (proteinInSupportedGenome)
        {
        doGenomeBrowserLink(proteinID, mrnaID, hgsidStr);
        doGeneDetailsLink(proteinID, mrnaID, hgsidStr);
        }

    /* Show Gene Sorter link only if it is valid for this genome */
    if (hgNearOk(database))
        {
        doGeneSorterLink(protDisplayID, mrnaID, hgsidStr);
        }

    /* Show BLAT link if we have UCSC Genome Browser for it */
    if (blatGbDb != NULL)
        {
        doBlatLink(blatGbDb, sciName, commonName, protSeq);
        }

    hPrintf("</UL><P>");
    }

/* This section shows various types of  domains */
conn = sqlConnect(UNIPROT_DB_NAME);
domainsPrint(conn, proteinID);

hPrintf("<P>");

/* Do Pathway section only if the protein belongs to a supported genome */
if (proteinInSupportedGenome);
    {
    doPathwayLinks(proteinID, mrnaID);
    }

printFASTA(proteinID, protSeq);
}
void makeActiveImagePB(char *psOutput, char *psOutput2)
/* Make image and image map. */
{
char *mapName = "map";
int pixWidth, pixHeight;

struct sqlConnection *conn;
char query[256];
struct sqlResult *sr;
char **row;

int  iypos;
char *spDisplayId;
char *oldDisplayId;
conn  = sqlConnect(UNIPROT_DB_NAME);
printf("<BR>");
hPrintf("<BR><font size=4><B>Protein: ");
hPrintf("%s</B>", proteinID);

/* Please note the hiv database name is hard wired here.*/
safef(query, sizeof(query), 
"select subjId from hivVax003Vax004.gsIdXref where aaSeqId = '%s'", proteinID);
sr = sqlMustGetResult(conn, query);
row = sqlNextRow(sr);
if (row != NULL)
    {
    printf("<BR>");
    hPrintf("<font size=4><B>Subject: ");
    hPrintf("<A HREF=\"../cgi-bin/gsidSubj?hgs_subj=%s&submit=Go!\">", row[0]);
    hPrintf("%s</A></B><BR>", row[0]);
    }
sqlFreeResult(&sr);

spDisplayId = spAccToId(conn, spFindAcc(conn, proteinID));
if (strstr(spDisplayId, spFindAcc(conn, proteinID)) == NULL)
	{
	hPrintf(" (aka %s", spDisplayId);
	/* show once if the new and old displayId are the same */
 	oldDisplayId = oldSpDisplayId(spDisplayId);
	if (oldDisplayId != NULL)
 	    {
            if (!sameWord(spDisplayId, oldDisplayId))
	    	{
	    	hPrintf(" or %s", oldSpDisplayId(spDisplayId));
	    	}
	    }
	hPrintf(")\n");
	}
hPrintf("</font><br>");

protSeq = getAA(proteinID);
if (protSeq == NULL)
    {
    errAbort("%s is not a current valid entry in UniProt(SWISS-PROT/TrEMBL)\n", proteinID);
    }
protSeqLen = strlen(protSeq);

fflush(stdout);

iypos = 15; 
doTracks(proteinID, mrnaID, protSeq, &iypos, psOutput);
if (!hTableExists(database, "pbStamp")) goto histDone; 

pbScale = 3;
pixWidth = 520;
insideWidth = pixWidth-gfxBorder;

pixHeight = 350;

if (psOutput2)
    {
    vg2 = vgOpenPostScript(pixWidth, pixHeight, psOutput2);
    }
else
    {
    trashDirFile(&gifTn2, "pbt", "pbt", ".gif");
    vg2 = vgOpenGif(pixWidth, pixHeight, gifTn2.forCgi, FALSE);
    }

g_vg = vg2;

pbRed    = vgFindColorIx(vg2, 0xf9, 0x51, 0x59);
pbBlue   = vgFindColorIx(g_vg, 0x00, 0x00, 0xd0);

normalColor   = pbBlue;
abnormalColor = pbRed;

bkgColor = vgFindColorIx(vg2, 255, 254, 232);
vgBox(vg2, 0, 0, insideWidth, pixHeight, bkgColor);

/* Start up client side map. */
mapName=cloneString("pbStamps");
hPrintf("\n<MAP Name=%s>\n", mapName);

vgSetClip(vg2, 0, gfxBorder, insideWidth, pixHeight - 2*gfxBorder);
iypos = 15;

/* Draw stamps. */

doStamps(proteinID, mrnaID, protSeq, vg2, &iypos);

/* Finish map. */
hPrintf("</MAP>\n");

/* Save out picture and tell html file about it. */
vgClose(&vg2);
hPrintf("<P>");

hPrintf("\n<IMG SRC=\"%s\" BORDER=1 WIDTH=%d HEIGHT=%d USEMAP=#%s><BR>",
            gifTn2.forCgi, pixWidth, pixHeight, mapName);
if (proteinInSupportedGenome)
    {
    hPrintf("\n<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbTracksHelp.shtml#histograms\" TARGET=_blank>");
    }
else
    {
    hPrintf("\n<A HREF=\"../goldenPath/help/pbTracksHelpFiles/pbGsid/pbTracksHelp.shtml#histograms\" TARGET=_blank>");
    }

hPrintf("Explanation of Protein Property Histograms</A><BR>");

hPrintf("<P>");

histDone:

hPrintf("<P>");
fflush(stdout);

printFASTA(proteinID, protSeq);
}