Ecosyste.ms: Papers
An open API service providing mapping between scientific papers and software projects that are mentioned in them.
All mentions data is based on the CZI Software Mentions dataset.
Projects: cran: hyperSMURF
https://packages.ecosyste.ms/registries/cran.r-project.org/packages/hyperSMURF
Hyper-Ensemble Smote Undersampled Random Forests
5 versions
Latest release: over 6 years ago
0 downloads
Papers Mentioning hyperSMURF 6
10.1186/s12859-019-2877-3
GenePy - a score for estimating gene pathogenicity in individuals using next-generation sequencing dataCited by: 19
Author(s): Enrico Mossotto, James J. Ashton, Luke O’Gorman, Reuben J. Pengelly, R Mark Beattie, Ben D. MacArthur, Sarah Ennis
Software Mentions: 2
Published: over 5 years ago
10.3389/fgene.2020.00350
Reaching the End-Game for GWAS: Machine Learning Approaches for the Prioritization of Complex Disease LociCited by: 91
Author(s): Hannah Nicholls, Christopher R. John, David S. Watson, Patricia B. Munroe, Michael R. Barnes, Claudia Cabrera
Software Mentions: 2
Published: over 4 years ago
10.1186/s13059-018-1546-6
PINES: phenotype-informed tissue weighting improves prediction of pathogenic noncoding variantsCited by: 17
Author(s): Corneliu Bodea, Adele A. Mitchell, Alex Bloemendal, Aaron G. Day‐Williams, Heiko Runz, Shamil Sunyaev
Software Mentions: 2
Published: about 6 years ago
10.3389/fpubh.2020.00178
Over- and Under-sampling Approach for Extremely Imbalanced and Small Minority Data Problem in Health Record AnalysisCited by: 30
Author(s): Koichi Fujiwara, Yukun Huang, Kazuko Hori, Kenichi Nishioji, Masao Kobayashi, Mai Kamaguchi, Manabu Kano
Software Mentions: 1
Published: over 4 years ago
10.1093/gigascience/giaa052
parSMURF, a high-performance computing tool for the genome-wide detection of pathogenic variantsCited by: 8
Author(s): Alessandro Petrini, Marco Mesiti, Max Schubach, Daniel Daniš, Matteo Ré, Giuliano Grossi, Luca Cappelletti, Tiziana Castrignanò, Peter N. Robinson, Giorgio Valentini
Software Mentions: 1
Published: over 4 years ago
10.1038/s41598-017-03011-5
Imbalance-Aware Machine Learning for Predicting Rare and Common Disease-Associated Non-Coding VariantsCited by: 61
Author(s): Max Schubach, Matteo Ré, Peter N. Robinson, Giorgio Valentini
Software Mentions: 1
Published: over 7 years ago