Published May 3, 2021
| Version 1.3
Dataset
Open
REVEL (Rare Exome Variant Ensemble Learner) Scores
Description
REVEL is an ensemble method for predicting the pathogenicity of missense variants in the human genome. For more information, see https://sites.google.com/site/revelgenomics/ and https://dx.doi.org/10.1016/j.ajhg.2016.08.016.
Files
revel-v1.3_all_chromosomes.zip
Files
(1.3 GB)
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Additional details
Related works
- Is described by
- Journal article: 10.1016/j.ajhg.2016.08.016 (DOI)
References
- Ioannidis NM, Rothstein JH, Pejaver V, Middha S, McDonnell SK, Baheti S, Musolf A, Li Q, Holzinger E, Karyadi D, Cannon-Albright LA, Teerlink CC, Stanford JL, Isaacs WB, Xu J, Cooney KA, Lange EM, Schleutker J, Carpten JD, Powell IJ, Cussenot O, Cancel-Tassin G, Giles GG, MacInnis RJ, Maier C, Hsieh CL, Wiklund F, Catalona WJ, Foulkes WD, Mandal D, Eeles RA, Kote-Jarai Z, Bustamante CD, Schaid DJ, Hastie T, Ostrander EA, Bailey-Wilson JE, Radivojac P, Thibodeau SN, Whittemore AS, and Sieh W. "REVEL: An ensemble method for predicting the pathogenicity of rare missense variants." American Journal of Human Genetics 2016; 99(4):877-885