ArticleBioinformatics (Oxford, England)2016
De novo identification of replication-timing domains in the human genome by deep learning.
Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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Who cites it
19 citing papers in PubMed.
- ResNet-Powered Multi-Class Identification of Sequence Patterns for Genome Replication Timing Analysis.Interdisciplinary sciences, computational life sciences · 2026Article
- RNAs anchoring replication complex control initiation and firing of DNA replication.Nature communications · 2026Article
- Human genomic DNA is widely interspersed with i-motif structures.The EMBO journal · 2024Article
- Integrative chromatin domain annotation through graph embedding of Hi-C data.Bioinformatics (Oxford, England) · 2023Article
- Functional annotation of noncoding mutations in cancer.Life science alliance · 2021Article
- Fused in sarcoma regulates DNA replication timing and kinetics.The Journal of biological chemistry · 2021Article
- Application of deep learning in genomics.Science China. Life sciences · 2020Review
- Isolation and analysis of rereplicated DNA by Rerep-Seq.Nucleic acids research · 2020Article
- Protein Interaction Network Reconstruction Through Ensemble Deep Learning With Attention Mechanism.Frontiers in bioengineering and biotechnology · 2020Article
- RT States: systematic annotation of the human genome using cell type-specific replication timing programs.Bioinformatics (Oxford, England) · 2019Article
- Cell Identity Codes: Understanding Cell Identity from Gene Expression Profiles using Deep Neural Networks.Scientific reports · 2019Article
- Genome-wide prediction of cis-regulatory regions using supervised deep learning methods.BMC bioinformatics · 2018Article
- In-depth characterization of the cisplatin mutational signature in human cell lines and in esophageal and liver tumors.Genome research · 2018Article
- Deep Learning and Its Applications in Biomedicine.Genomics, proteomics & bioinformatics · 2018Review
- Computational biology: deep learning.Emerging topics in life sciences · 2017Article
- Genome-scale mutational signatures of aflatoxin in cells, mice, and human tumors.Genome research · 2017Article
- Similar Evolutionary Trajectories for Retrotransposon Accumulation in Mammals.Genome biology and evolution · 2017Article
- PEDLA: predicting enhancers with a deep learning-based algorithmic framework.Scientific reports · 2016Article
- Super hotspots and super coldspots in the repair of UV-induced DNA damage in the human genome.The Journal of biological chemistryArticle
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6 authors.
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Abstract
motivationThe de novo identification of the initiation and termination zones-regions that replicate earlier or later than their upstream and downstream neighbours, respectively-remains a key challenge in DNA replication.
resultsBuilding on advances in deep learning, we developed a novel hybrid architecture combining a pre-trained, deep neural network and a hidden Markov model (DNN-HMM) for the de novo identification of replication domains using replication timing profiles. Our results demonstrate that DNN-HMM can significantly outperform strong, discriminatively trained Gaussian mixture model-HMM (GMM-HMM) systems and other six reported methods that can be applied to this challenge. We applied our trained DNN-HMM to identify distinct replication domain types, namely the early replication domain (ERD), the down transition zone (DTZ), the late replication domain (LRD) and the up transition zone (UTZ), using newly replicated DNA sequencing (Repli-Seq) data across 15 human cells. A subsequent integrative analysis revealed that these replication domains harbour unique genomic and epigenetic patterns, transcriptional activity and higher-order chromosomal structure. Our findings support the 'replication-domain' model, which states (1) that ERDs and LRDs, connected by UTZs and DTZs, are spatially compartmentalized structural and functional units of higher-order chromosomal structure, (2) that the adjacent DTZ-UTZ pairs form chromatin loops and (3) that intra-interactions within ERDs and LRDs tend to be short-range and long-range, respectively. Our model reveals an important chromatin organizational principle of the human genome and represents a critical step towards understanding the mechanisms regulating replication timing. AVAILABILITY AND IMPLEMENTATION: Our DNN-HMM method and three additional algorithms can be freely accessed at https://github.com/wenjiegroup/DNN-HMM The replication domain regions identified in this study are available in GEO under the accession ID GSE53984. CONTACT: shuwj@bmi.ac.cn or boxc@bmi.ac.cn SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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