RESUMO
High-performance data analytics (HPDA) is a current trend in e-science research that aims to integrate traditional HPC with recent data analytic frameworks. Most of the work done in this field has focused on improving data analytic frameworks by implementing their engines on top of HPC technologies such as Message Passing Interface. However, there is a lack of integration from an application development perspective. HPC workflows have their own parallel programming models, while data analytic (DA) algorithms are mainly implemented using data transformations and executed with frameworks like Spark. Task-based programming models (TBPMs) are a very efficient approach for implementing HPC workflows. Data analytic transformations can also be decomposed as a set of tasks and implemented with a task-based programming model. In this paper, we present a methodology to develop HPDA applications on top of TBPMs that allow developers to combine HPC workflows and data analytic transformations seamlessly. A prototype of this approach has been implemented on top of the PyCOMPSs task-based programming model to validate two aspects: HPDA applications can be seamlessly developed and have better performance than Spark. We compare our results using different programs. Finally, we conclude with the idea of integrating DA into HPC applications and evaluation of our method against Spark.
RESUMO
Genome-wide association studies (GWAS) are not fully comprehensive, as current strategies typically test only the additive model, exclude the X chromosome, and use only one reference panel for genotype imputation. We implement an extensive GWAS strategy, GUIDANCE, which improves genotype imputation by using multiple reference panels and includes the analysis of the X chromosome and non-additive models to test for association. We apply this methodology to 62,281 subjects across 22 age-related diseases and identify 94 genome-wide associated loci, including 26 previously unreported. Moreover, we observe that 27.7% of the 94 loci are missed if we use standard imputation strategies with a single reference panel, such as HRC, and only test the additive model. Among the new findings, we identify three novel low-frequency recessive variants with odds ratios larger than 4, which need at least a three-fold larger sample size to be detected under the additive model. This study highlights the benefits of applying innovative strategies to better uncover the genetic architecture of complex diseases.
