dfe4ce8ecd6ca71b2bc90b98b4f4ac73fad0c9eb
max
  Wed Jun 3 06:47:31 2026 -0700
EVE track QA fixes: longLabel sentence case, dataVersion, relatedTracks cross-links

Co-Authored-By: Claude Sonnet 4.6 <noreply@anthropic.com>

diff --git src/hg/makeDb/trackDb/relatedTracks.ra src/hg/makeDb/trackDb/relatedTracks.ra
index ec59d8759e6..f0ebaa52f3f 100644
--- src/hg/makeDb/trackDb/relatedTracks.ra
+++ src/hg/makeDb/trackDb/relatedTracks.ra
@@ -96,30 +96,40 @@
 
 # hg38 long-read SV supertrack cross-links to other SV resources:
 hg38 lrSv gnomadStructuralVariants Short-read structural variants from gnomAD v4.1
 hg38 gnomadStructuralVariants lrSv Long-read structural variants across multiple cohorts
 hg38 lrSv dbVarSv NCBI dbVar structural variants (short-read and long-read, germline and clinical)
 hg38 dbVarSv lrSv Long-read structural variants across multiple cohorts
 hg38 lrSv dgvPlus Database of Genomic Variants (DGV) structural variation catalog
 hg38 dgvPlus lrSv Long-read structural variants across multiple cohorts
 hg38 lrSv giabSv Genome in a Bottle high-confidence SV benchmark callsets
 hg38 giabSv lrSv Long-read structural variants across multiple cohorts
 hg38 lrSv mei Polymorphic Mobile Element Insertions (Alu, L1, SVA, HERVK, snRNA) from HGSVC3 long-read assemblies
 hg38 mei lrSv Long-read structural variants across multiple cohorts (parent SV callsets for the HGSVC3 MEI track)
 hs1 lrSv mei Polymorphic Mobile Element Insertions (Alu, L1, SVA, HERVK, snRNA) from HGSVC3 long-read assemblies
 hs1 mei lrSv Long-read structural variants across multiple cohorts (parent SV callsets for the HGSVC3 MEI track)
 
+# EVE cross-links:
+hg38 eve alphaMissense AlphaMissense, a similar deep-learning missense pathogenicity predictor
+hg38 alphaMissense eve EVE, a missense pathogenicity predictor trained on evolutionary sequence variation
+hg38 eve primateAi PrimateAI-3D, a similar deep-learning missense pathogenicity predictor using primate variation
+hg38 primateAi eve EVE, a missense pathogenicity predictor trained on evolutionary sequence variation
+hg38 eve revel REVEL, an ensemble missense pathogenicity score built from multiple predictors
+hg38 revel eve EVE, a missense pathogenicity predictor trained on evolutionary sequence variation
+hg38 eve clinPred ClinPred, an ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
+hg38 clinPred eve EVE, a missense pathogenicity predictor trained on evolutionary sequence variation
+
 # PrimateAI-3D cross-links:
 hg38 primateAi alphaMissense AlphaMissense, a similar deep-learning missense pathogenicity predictor
 hg38 alphaMissense primateAi PrimateAI-3D, a similar deep-learning missense pathogenicity predictor using primate variation
 hg38 primateAi revel REVEL, an ensemble missense pathogenicity score built from multiple predictors
 hg38 revel primateAi PrimateAI-3D, a missense pathogenicity predictor using primate variation and 3D protein structure
 
 hg19 primateAi revel REVEL, an ensemble missense pathogenicity score built from multiple predictors
 hg19 revel primateAi PrimateAI-3D, a missense pathogenicity predictor using primate variation and 3D protein structure
 
 # ClinPred cross-links:
 hg38 clinPred revel REVEL, an ensemble missense pathogenicity score using a similar machine-learning approach
 hg38 revel clinPred ClinPred, an ensemble missense pathogenicity predictor that incorporates gnomAD allele frequency
 hg38 clinPred caddSuper CADD, a similar deleteriousness score
 hg38 caddSuper clinPred ClinPred, a missense-only pathogenicity predictor
 hg38 clinPred primateAi PrimateAI-3D, a missense pathogenicity predictor using primate variation