4.7 Article

Chromatin loop anchors predict transcript and exon usage

Journal

BRIEFINGS IN BIOINFORMATICS
Volume 22, Issue 6, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbab254

Keywords

gene expression; transcript; exon usage; machine learning; ChIA-PET; chromatin loop anchors; histone modifications; alternative splicing

Funding

  1. National Research Foundation (NRF) Singapore through an NRF Fellowship [NRF-NRFF2012-054]
  2. Nanyang Technological University
  3. RNA Biology Center at the Cancer Science Institute of Singapore, NUS, under the Singapore Ministry of Education Academic Research Fund Tier 3 [MOE2014-T3-1-006]
  4. National Research Foundation Competitive Research Programme [NRF-CRP17-2017-02]
  5. National Research Foundation Singapore
  6. Singapore Ministry of Education under its Research Centres of Excellence initiative
  7. Ministry of Education Tier II grant [T2EP30120-0020]
  8. Advancing Creativity and Excellence (ACE) - Nanyang Technological University [NTU-ACE2019-03]

Ask authors/readers for more resources

The study developed machine learning models using ChIA-PET data, demonstrating the importance of chromatin loop anchors in predicting transcript and exon usage.
Epigenomics and transcriptomics data from high-throughput sequencing techniques such as RNA-seq and ChIP-seq have been successfully applied in predicting gene transcript expression. However, the locations of chromatin loops in the genome identified by techniques such as Chromatin Interaction Analysis with Paired End Tag sequencing (ChIA-PET) have never been used for prediction tasks. Here, we developed machine learning models to investigate if ChIA-PET could contribute to transcript and exon usage prediction. In doing so, we used a large set of transcription factors as well as ChIA-PET data. We developed different Gradient Boosting Trees models according to the different tasks with the integrated datasets from three cell lines, including GM12878, HeLaS3 and K562. We validated the models via 10-fold cross validation, chromosome-split validation and cross-cell validation. Our results show that both transcript and splicing-derived exon usage can be effectively predicted with at least 0.7512 and 0.7459 of accuracy, respectively, on all cell lines from all kinds of validations. Examining the predictive features, we found that RNA Polymerase II ChIA-PET was one of the most important features in both transcript and exon usage prediction, suggesting that chromatin loop anchors are predictive of both transcript and exon usage.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available