<i>proRate</i>: an R package to infer gene transcription rates with a novel least sum of squares method

The dynamics of transcriptional elongation influence many biological activities, such as RNA splicing, polyadenylation, and nuclear export. To quantify the elongation rate, a typical method is to treat cells with drugs that inhibit RNA polymerase II (Pol II) from entering the gene body and then track Pol II using Pro-seq or Gro-seq. However, the downstream data analysis is challenged by the problem of identifying the transition point between the gene regions inhibited by the drug and not, which is necessary to calculate the transcription rate. Although the traditional hidden Markov model (HMM) can be used to solve it, this method is complicated with its hidden variable and many parameters to be estimated. Hence, we developed the R package <i>proRate</i>, which identifies the transition point with a novel least sum of squares (LSS) method and calculates the elongation rate accordingly. In addition, <i>proRate</i> also covers other functions frequently used in transcription dynamic study, including metagene plotting, pause index calculation, gene structure analysis, etc. The effectiveness of this package is proved by its performance on three Pro-seq or Gro-seq datasets, showing higher accuracy than HMM. <i>proRate</i> is freely available at https://github.com/yuabrahamliu/proRate or https://github.com/FADHLyemen/proRate.

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Publication Details

Journal
NAR Genomics and Bioinformatics
Published
2025-07-04
DOI
https://doi.org/10.1093/nargab/lqaf123
Primary Topic
Genomics and Chromatin Dynamics
Type
article
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article

proRate: an R package to infer gene transcription rates with a novel least sum of squares method

Fadhl Alakwaa, Yu Liu
1 links
NAR Genomics and Bioinformatics
Genomics and Chromatin Dynamics
article

proRate: an R package to infer gene transcription rates with a novel least sum of squares method

Fadhl Alakwaa, Yu Liu
article en

Abstract

The dynamics of transcriptional elongation influence many biological activities, such as RNA splicing, polyadenylation, and nuclear export. To quantify the elongation rate, a typical method is to treat cells with drugs that inhibit RNA polymerase II (Pol II) from entering the gene body and then track Pol II using Pro-seq or Gro-seq. However, the downstream data analysis is challenged by the problem of identifying the transition point between the gene regions inhibited by the drug and not, which is necessary to calculate the transcription rate. Although the traditional hidden Markov model (HMM) can be used to solve it, this method is complicated with its hidden variable and many parameters to be estimated. Hence, we developed the R package <i>proRate</i>, which identifies the transition point with a novel least sum of squares (LSS) method and calculates the elongation rate accordingly. In addition, <i>proRate</i> also covers other functions frequently used in transcription dynamic study, including metagene plotting, pause index calculation, gene structure analysis, etc. The effectiveness of this package is proved by its performance on three Pro-seq or Gro-seq datasets, showing higher accuracy than HMM. <i>proRate</i> is freely available at https://github.com/yuabrahamliu/proRate or https://github.com/FADHLyemen/proRate.

NAR Genomics and BioinformaticsVol. 7(3)
University of Michigan (US), Michigan Medicine (US)
Openalex Percentile: Top 79%
Genomics and Chromatin Dynamics
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