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Andrew P. Morris
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2020 – today
- 2023
- [j8]R. Onur Öztornaci, Hamzah Syed, Andrew P. Morris, Bahar Tasdelen:
The use of class imbalanced learning methods on ULSAM data to predict the case-control status in genome-wide association studies. J. Big Data 10(1): 174 (2023)
2010 – 2019
- 2017
- [j7]Reedik Mägi, Yury V. Suleimanov, Geraldine M. Clarke, Marika Kaakinen, Krista Fischer, Inga Prokopenko, Andrew P. Morris:
SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes. BMC Bioinform. 18(1): 25:1-25:8 (2017) - [j6]Marika Kaakinen, Reedik Mägi, Krista Fischer, Jani Heikkinen, Marjo-Riitta Järvelin, Andrew P. Morris, Inga Prokopenko:
MARV: a tool for genome-wide multi-phenotype analysis of rare variants. BMC Bioinform. 18(1): 110:1-110:8 (2017) - [j5]Hamzah Syed, Andrea L. Jorgensen, Andrew P. Morris:
SurvivalGWAS_SV: software for the analysis of genome-wide association studies of imputed genotypes with "time-to-event" outcomes. BMC Bioinform. 18(1): 265:1-265:6 (2017) - 2016
- [j4]Hamzah Syed, Andrea L. Jorgensen, Andrew P. Morris:
SurvivalGWAS_Power: a user friendly tool for power calculations in pharmacogenetic studies with "time to event" outcomes. BMC Bioinform. 17: 523:1-523:8 (2016) - 2010
- [j3]Reedik Mägi, Andrew P. Morris:
GWAMA: software for genome-wide association meta-analysis. BMC Bioinform. 11: 288 (2010) - [j2]Robert Lawrence, Aaron G. Day-Williams, Katherine S. Elliott, Andrew P. Morris, Eleftheria Zeggini:
CCRaVAT and QuTie - enabling analysis of rare variants in large-scale case control and quantitative trait association studies. BMC Bioinform. 11: 527 (2010)
2000 – 2009
- 2008
- [j1]Fredrik Pettersson, Andrew P. Morris, Michael R. Barnes, Lon R. Cardon:
Goldsurfer2 (Gs2): A comprehensive tool for the analysis and visualization of genome wide association studies. BMC Bioinform. 9 (2008)
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