4,804 research outputs found
Machine Learning and Integrative Analysis of Biomedical Big Data.
Recent developments in high-throughput technologies have accelerated the accumulation of massive amounts of omics data from multiple sources: genome, epigenome, transcriptome, proteome, metabolome, etc. Traditionally, data from each source (e.g., genome) is analyzed in isolation using statistical and machine learning (ML) methods. Integrative analysis of multi-omics and clinical data is key to new biomedical discoveries and advancements in precision medicine. However, data integration poses new computational challenges as well as exacerbates the ones associated with single-omics studies. Specialized computational approaches are required to effectively and efficiently perform integrative analysis of biomedical data acquired from diverse modalities. In this review, we discuss state-of-the-art ML-based approaches for tackling five specific computational challenges associated with integrative analysis: curse of dimensionality, data heterogeneity, missing data, class imbalance and scalability issues
An AUC-based Permutation Variable Importance Measure for Random Forests
The random forest (RF) method is a commonly used tool for classification with high dimensional data as well as for ranking candidate predictors based on the so-called random forest variable importance measures (VIMs). However the classification performance of RF is known to be suboptimal in case of strongly unbalanced data, i.e. data where response class sizes differ considerably. Suggestions were made to obtain better classification performance based either on sampling procedures or on cost sensitivity analyses. However to our knowledge the performance of the VIMs has not yet been examined in the case of unbalanced response classes. In this paper we explore the performance of the permutation VIM for unbalanced data settings and introduce an alternative permutation VIM based on the area under the curve (AUC) that is expected to be more robust towards class imbalance. We investigated the performance of the standard permutation VIM and of our novel AUC-based permutation VIM for different class imbalance levels using simulated data and real data. The results suggest that the standard permutation VIM loses its ability to discriminate between associated predictors and predictors not associated with the response for increasing class imbalance. It is outperformed by our new AUC-based permutation VIM for unbalanced data settings, while the performance of both VIMs is very similar in the case of balanced classes. The new AUC-based VIM is implemented in the R package party for the unbiased RF variant based on conditional inference trees. The codes implementing our study are available from the companion website: http://www.ibe.med.uni-muenchen.de/organisation/mitarbeiter/070_drittmittel/janitza/index.html
A Comparative Analysis of Ensemble Classifiers: Case Studies in Genomics
The combination of multiple classifiers using ensemble methods is
increasingly important for making progress in a variety of difficult prediction
problems. We present a comparative analysis of several ensemble methods through
two case studies in genomics, namely the prediction of genetic interactions and
protein functions, to demonstrate their efficacy on real-world datasets and
draw useful conclusions about their behavior. These methods include simple
aggregation, meta-learning, cluster-based meta-learning, and ensemble selection
using heterogeneous classifiers trained on resampled data to improve the
diversity of their predictions. We present a detailed analysis of these methods
across 4 genomics datasets and find the best of these methods offer
statistically significant improvements over the state of the art in their
respective domains. In addition, we establish a novel connection between
ensemble selection and meta-learning, demonstrating how both of these disparate
methods establish a balance between ensemble diversity and performance.Comment: 10 pages, 3 figures, 8 tables, to appear in Proceedings of the 2013
International Conference on Data Minin
The Parallelism Motifs of Genomic Data Analysis
Genomic data sets are growing dramatically as the cost of sequencing
continues to decline and small sequencing devices become available. Enormous
community databases store and share this data with the research community, but
some of these genomic data analysis problems require large scale computational
platforms to meet both the memory and computational requirements. These
applications differ from scientific simulations that dominate the workload on
high end parallel systems today and place different requirements on programming
support, software libraries, and parallel architectural design. For example,
they involve irregular communication patterns such as asynchronous updates to
shared data structures. We consider several problems in high performance
genomics analysis, including alignment, profiling, clustering, and assembly for
both single genomes and metagenomes. We identify some of the common
computational patterns or motifs that help inform parallelization strategies
and compare our motifs to some of the established lists, arguing that at least
two key patterns, sorting and hashing, are missing
Oversampling for Imbalanced Learning Based on K-Means and SMOTE
Learning from class-imbalanced data continues to be a common and challenging
problem in supervised learning as standard classification algorithms are
designed to handle balanced class distributions. While different strategies
exist to tackle this problem, methods which generate artificial data to achieve
a balanced class distribution are more versatile than modifications to the
classification algorithm. Such techniques, called oversamplers, modify the
training data, allowing any classifier to be used with class-imbalanced
datasets. Many algorithms have been proposed for this task, but most are
complex and tend to generate unnecessary noise. This work presents a simple and
effective oversampling method based on k-means clustering and SMOTE
oversampling, which avoids the generation of noise and effectively overcomes
imbalances between and within classes. Empirical results of extensive
experiments with 71 datasets show that training data oversampled with the
proposed method improves classification results. Moreover, k-means SMOTE
consistently outperforms other popular oversampling methods. An implementation
is made available in the python programming language.Comment: 19 pages, 8 figure
DanQ: a hybrid convolutional and recurrent deep neural network for quantifying the function of DNA sequences.
Modeling the properties and functions of DNA sequences is an important, but challenging task in the broad field of genomics. This task is particularly difficult for non-coding DNA, the vast majority of which is still poorly understood in terms of function. A powerful predictive model for the function of non-coding DNA can have enormous benefit for both basic science and translational research because over 98% of the human genome is non-coding and 93% of disease-associated variants lie in these regions. To address this need, we propose DanQ, a novel hybrid convolutional and bi-directional long short-term memory recurrent neural network framework for predicting non-coding function de novo from sequence. In the DanQ model, the convolution layer captures regulatory motifs, while the recurrent layer captures long-term dependencies between the motifs in order to learn a regulatory 'grammar' to improve predictions. DanQ improves considerably upon other models across several metrics. For some regulatory markers, DanQ can achieve over a 50% relative improvement in the area under the precision-recall curve metric compared to related models. We have made the source code available at the github repository http://github.com/uci-cbcl/DanQ
PMLB: A Large Benchmark Suite for Machine Learning Evaluation and Comparison
The selection, development, or comparison of machine learning methods in data
mining can be a difficult task based on the target problem and goals of a
particular study. Numerous publicly available real-world and simulated
benchmark datasets have emerged from different sources, but their organization
and adoption as standards have been inconsistent. As such, selecting and
curating specific benchmarks remains an unnecessary burden on machine learning
practitioners and data scientists. The present study introduces an accessible,
curated, and developing public benchmark resource to facilitate identification
of the strengths and weaknesses of different machine learning methodologies. We
compare meta-features among the current set of benchmark datasets in this
resource to characterize the diversity of available data. Finally, we apply a
number of established machine learning methods to the entire benchmark suite
and analyze how datasets and algorithms cluster in terms of performance. This
work is an important first step towards understanding the limitations of
popular benchmarking suites and developing a resource that connects existing
benchmarking standards to more diverse and efficient standards in the future.Comment: 14 pages, 5 figures, submitted for review to JML
- ā¦