dfa33e7edb8273417ed94e429bc259e9514715c5 lrnassar Thu Jan 7 14:02:15 2021 -0800 Squashing stale pennantIcons refs #26753 diff --git src/hg/makeDb/trackDb/human/trackDb.ra src/hg/makeDb/trackDb/human/trackDb.ra index 5456fb5..677325c 100644 --- src/hg/makeDb/trackDb/human/trackDb.ra +++ src/hg/makeDb/trackDb/human/trackDb.ra @@ -119,31 +119,30 @@ visibility hide type bigBed 9 + itemRgb on tableBrowser off bigDataUrl /gbdb/$D/decipher/decipherCnv.bb url https://decipher.sanger.ac.uk/patient/$$ urlLabel Decipher Patient View: filter.size 0 filterByRange.size on filterLimits.size 2:170487333 filterValues.variant_class Amplification,Copy-Number Gain,Deletion,Duplication,Duplication/Trip filterValues.pathogenicity Benign,Likely Benign,Likely Pathogenic,Pathogenic,Uncertain,Unknown mergeSpannedItems on searchIndex name mouseOverField _mouseOver -pennantIcon Updated red ../goldenPath/newsarch.html#101320 "Updated Oct. 13, 2020" searchTable decipher searchMethod exact searchType bigBed release alpha,beta track decipherSnvs shortLabel DECIPHER SNVs longLabel DECIPHER: Chromosomal Imbalance and Phenotype in Humans (SNVs) group phenDis visibility hide color 0,0,0 type bed 4 tableBrowser off decipherSnvsRaw prevExonText Left edge @@ -3690,31 +3689,30 @@ type bigBed 12 + release alpha bigDataUrl /gbdb/$D/bbi/cancerMutations/BRCA.bb urls case_id=https://portal.gdc.cancer.gov/cases/$$ parent cancerMutations track lovdComp shortLabel LOVD Variants longLabel Leiden Open Variation Database Public Variants group phenDis visibility hide compositeTrack on type bigBed 4 + tableBrowser off lovdComp html lovdComp -pennantIcon Updated red ../goldenPath/newsarch.html#101320 "Updated Oct. 13, 2020" track lovdShort shortLabel LOVD Variants < 50 bp longLabel Leiden Open Variation Database, short < 50 bp variants group phenDis visibility hide urls id="http://varcache.lovd.nl/redirect/$$" noScoreFilter on bigDataUrl /gbdb/$D/lovd/lovd.$D.short.bb parent lovdComp track lovdLong type bigBed 9 + shortLabel LOVD Variants >= 50 bp longLabel Leiden Open Variation Database Public Variants, long >= 50 bp variants @@ -5084,31 +5082,30 @@ include decode.rmap.ra #geneReviews track track geneReviews shortLabel GeneReviews longLabel GeneReviews group phenDis visibility hide color 0, 80, 0 type bigBed 9 + bigDataUrl /gbdb/$D/geneReviews/geneReviews.bb mouseOver $name disease(s): $diseases html geneReviews url https://www.ncbi.nlm.nih.gov/books/NBK1116/?term=$$ noScoreFilter on -pennantIcon Updated red ../goldenPath/newsarch.html#101320 "Updated Oct. 13, 2020" searchName geneReviews searchTable geneReviews searchType bed searchPriority 50 xrefTable geneReviewsDetail xrefQuery select geneSymbol,grTitle from %s where grTitle like '%%%s%%' searchBoth on searchTable dgv searchType bed searchPriority 50 termRegex (dgv_|[en]ss?v)[0-9]+ searchTable coriellDelDup