GPrank: an R package for detecting dynamic elements from genome-wide time series
Abstract Background Genome-wide high-throughput sequencing (HTS) time series experiments are a powerful tool for monitoring various genomic elements over time. They can be used to monitor, for example, gene or transcript expression with RNA sequencing (RNA-seq), DNA methylation levels with bisulfite...
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doaj-a382d5f11c42415f9b79e51a629bd5542020-11-25T02:05:57ZengBMCBMC Bioinformatics1471-21052018-10-011911610.1186/s12859-018-2370-4GPrank: an R package for detecting dynamic elements from genome-wide time seriesHande Topa0Antti Honkela1Institute for Molecular Medicine Finland FIMM, University of HelsinkiHelsinki Institute for Information Technology HIIT, Department of Mathematics and Statistics, University of HelsinkiAbstract Background Genome-wide high-throughput sequencing (HTS) time series experiments are a powerful tool for monitoring various genomic elements over time. They can be used to monitor, for example, gene or transcript expression with RNA sequencing (RNA-seq), DNA methylation levels with bisulfite sequencing (BS-seq), or abundances of genetic variants in populations with pooled sequencing (Pool-seq). However, because of high experimental costs, the time series data sets often consist of a very limited number of time points with very few or no biological replicates, posing challenges in the data analysis. Results Here we present the GPrank R package for modelling genome-wide time series by incorporating variance information obtained during pre-processing of the HTS data using probabilistic quantification methods or from a beta-binomial model using sequencing depth. GPrank is well-suited for analysing both short and irregularly sampled time series. It is based on modelling each time series by two Gaussian process (GP) models, namely, time-dependent and time-independent GP models, and comparing the evidence provided by data under two models by computing their Bayes factor (BF). Genomic elements are then ranked by their BFs, and temporally most dynamic elements can be identified. Conclusions Incorporating the variance information helps GPrank avoid false positives without compromising computational efficiency. Fitted models can be easily further explored in a browser. Detection and visualisation of temporally most active dynamic elements in the genome can provide a good starting point for further downstream analyses for increasing our understanding of the studied processes.http://link.springer.com/article/10.1186/s12859-018-2370-4Gaussian processHigh-throughput sequencingTime seriesRankingBayes factorVisualization |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hande Topa Antti Honkela |
spellingShingle |
Hande Topa Antti Honkela GPrank: an R package for detecting dynamic elements from genome-wide time series BMC Bioinformatics Gaussian process High-throughput sequencing Time series Ranking Bayes factor Visualization |
author_facet |
Hande Topa Antti Honkela |
author_sort |
Hande Topa |
title |
GPrank: an R package for detecting dynamic elements from genome-wide time series |
title_short |
GPrank: an R package for detecting dynamic elements from genome-wide time series |
title_full |
GPrank: an R package for detecting dynamic elements from genome-wide time series |
title_fullStr |
GPrank: an R package for detecting dynamic elements from genome-wide time series |
title_full_unstemmed |
GPrank: an R package for detecting dynamic elements from genome-wide time series |
title_sort |
gprank: an r package for detecting dynamic elements from genome-wide time series |
publisher |
BMC |
series |
BMC Bioinformatics |
issn |
1471-2105 |
publishDate |
2018-10-01 |
description |
Abstract Background Genome-wide high-throughput sequencing (HTS) time series experiments are a powerful tool for monitoring various genomic elements over time. They can be used to monitor, for example, gene or transcript expression with RNA sequencing (RNA-seq), DNA methylation levels with bisulfite sequencing (BS-seq), or abundances of genetic variants in populations with pooled sequencing (Pool-seq). However, because of high experimental costs, the time series data sets often consist of a very limited number of time points with very few or no biological replicates, posing challenges in the data analysis. Results Here we present the GPrank R package for modelling genome-wide time series by incorporating variance information obtained during pre-processing of the HTS data using probabilistic quantification methods or from a beta-binomial model using sequencing depth. GPrank is well-suited for analysing both short and irregularly sampled time series. It is based on modelling each time series by two Gaussian process (GP) models, namely, time-dependent and time-independent GP models, and comparing the evidence provided by data under two models by computing their Bayes factor (BF). Genomic elements are then ranked by their BFs, and temporally most dynamic elements can be identified. Conclusions Incorporating the variance information helps GPrank avoid false positives without compromising computational efficiency. Fitted models can be easily further explored in a browser. Detection and visualisation of temporally most active dynamic elements in the genome can provide a good starting point for further downstream analyses for increasing our understanding of the studied processes. |
topic |
Gaussian process High-throughput sequencing Time series Ranking Bayes factor Visualization |
url |
http://link.springer.com/article/10.1186/s12859-018-2370-4 |
work_keys_str_mv |
AT handetopa gprankanrpackagefordetectingdynamicelementsfromgenomewidetimeseries AT anttihonkela gprankanrpackagefordetectingdynamicelementsfromgenomewidetimeseries |
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