c613ca6dd305b556af1148511ecd737317b3fe5b max Tue Jun 17 08:48:49 2025 -0700 improving docs page of deleteriousness supertrack, no redmine, email from Heidi Rehm diff --git src/hg/makeDb/trackDb/human/revel.html src/hg/makeDb/trackDb/human/revel.html index b1f5e14851b..7df62e53547 100644 --- src/hg/makeDb/trackDb/human/revel.html +++ src/hg/makeDb/trackDb/human/revel.html @@ -172,27 +172,25 @@ <p> Thanks to the REVEL development team for providing precomputed data and fixing duplicated values in the hg38 files. </p> <h2>References</h2> <p> Ioannidis NM, Rothstein JH, Pejaver V, Middha S, McDonnell SK, Baheti S, Musolf A, Li Q, Holzinger E, Karyadi D, et al. <a href="https://doi.org/10.1016/j.ajhg.2016.08.016" target = _blank"> REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants</a> <em>Am J Hum Genet</em>. 2016 Oct 6;99(4):877-885. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/27666373" target="_blank">27666373</a>; PMC: <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065685/" target="_blank">PMC5065685</a> </p> - - <p> Bergquist T, Stenton SL, Nadeau EAW, Byrne AB, Greenblatt MS, Harrison SM, Tavtigian SV, O'Donnell-Luria A, Biesecker LG, Radivojac P <em>et al</em>. <a href="https://linkinghub.elsevier.com/retrieve/pii/S1098-3600(25)00049-8" target="_blank"> Calibration of additional computational tools expands ClinGen recommendation options for variant classification with PP3/BP4 criteria</a>. <em>Genet Med</em>. 2025 Mar 10;27(6):101402. PMID: <a href="https://www.ncbi.nlm.nih.gov/pubmed/40084623" target="_blank">40084623</a> </p>