3a11a2cb7b1bc56c0ee32ae18fe900683d9e2120
lrnassar
  Wed Nov 6 16:57:19 2024 -0800
Adding a new RTS for the ENIGMA VCEP. No RM.

diff --git src/hg/htdocs/inc/recTrackSets.hg38.tab src/hg/htdocs/inc/recTrackSets.hg38.tab
index 9589162..ed37fd0 100644
--- src/hg/htdocs/inc/recTrackSets.hg38.tab
+++ src/hg/htdocs/inc/recTrackSets.hg38.tab
@@ -1,14 +1,15 @@
 # List of curated sessions for clinical, etc. users
 #
 # File is tab-separated.  userName and sessionName are fields in hgcentral.namedSessionDb table
 #       sessionName is cgi-decoded to readable text
 # Note that named sessions support description in settings field, however the description in
 #       this file is used in browser (allows non-owner of session, e.g. QA, to edit)
 #       
 # For details on how to update this file, see the wiki: http://genomewiki.ucsc.edu/genecats/index.php/Recommended_Track_Sets
 #       
 # Format: label, userName, sessionName, description
 Clinical SNVs	View	Clinical_SNVs_hg38	Assess potential disease contributions of single nucleotide variants in coding regions
 Clinical CNVs	View	Clinical_CNVs_hg38	Assess potential disease contributions of structural variants in coding regions
 Non-coding SNVs	View	Non_Coding_SNVs_hg38	Investigate functional aspects of non-coding variants
 Problematic Regions	View	Problematic_Regions_hg38	Evaluate if annotations are on potential low confidence regions due to high homology or other reported concerns
+ENIGMA BRCA1/BRCA2 VCEP View    BRCA1_BRCA2_ENIGMA_hg38 Asses potential disease contribution of variants on BRCA1 and BRCA2 according to the ENIGMA VCEP guidelines