Inferring time series chromatin states for promoter-enhancer pairs based on Hi-C data

نویسندگان

چکیده

Abstract Background Co-localized combinations of histone modifications (“chromatin states”) have been shown to correlate with promoter and enhancer activity. Changes in chromatin states over multiple time points state trajectories”) previously analyzed at enhancers separately. With the advent series Hi-C data it is now possible connect promoters analyze trajectories promoter-enhancer pairs. Results We present TimelessFlex, a framework for investigating pairs based on information. TimelessFlex extends our previous approach Timeless, Bayesian network clustering modification sets feature regions. utilize ATAC-seq measuring open define candidates. developed an expectation-maximization algorithm assign each other interactions jointly cluster their regions into paired trajectories. find clustered showing same activation patterns both sides but stronger trend side. While side remains accessible across series, becomes dynamically more towards gene point. Promoter show strong correlations expression signals, whereas signals get only slightly activation. The code available https://github.com/henriettemiko/TimelessFlex . Conclusions clusters can identify distinct changes time.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

JCell - a Java-based framework for inferring regulatory networks from time series data

MOTIVATION JCell is a Java-based application for reconstructing gene regulatory networks from experimental data. The framework provides several algorithms to identify genetic and metabolic dependencies based on experimental data conjoint with mathematical models to describe and simulate regulatory systems. Owing to the modular structure, researchers can easily implement new methods. JCell is a ...

متن کامل

An integrated model for detecting significant chromatin interactions from high-resolution Hi-C data

Here we present HiC-DC, a principled method to estimate the statistical significance (P values) of chromatin interactions from Hi-C experiments. HiC-DC uses hurdle negative binomial regression account for systematic sources of variation in Hi-C read counts-for example, distance-dependent random polymer ligation and GC content and mappability bias-and model zero inflation and overdispersion. App...

متن کامل

Statistical confidence estimation for Hi-C data reveals regulatory chromatin contacts.

Our current understanding of how DNA is packed in the nucleus is most accurate at the fine scale of individual nucleosomes and at the large scale of chromosome territories. However, accurate modeling of DNA architecture at the intermediate scale of ∼50 kb-10 Mb is crucial for identifying functional interactions among regulatory elements and their target promoters. We describe a method, Fit-Hi-C...

متن کامل

The sequencing bias relaxed characteristics of Hi-C derived data and implications for chromatin 3D modeling

The 3D chromatin structure modeling by chromatin interactions derived from Hi-C experiments is significantly challenged by the intrinsic sequencing biases in these experiments. Conventional modeling methods only focus on the bias among different chromatin regions within the same experiment but neglect the bias arising from different experimental sequencing depth. We now show that the regional i...

متن کامل

Inferring phage–bacteria infection networks from time-series data

In communities with bacterial viruses (phage) and bacteria, the phage-bacteria infection network establishes which virus types infect which host types. The structure of the infection network is a key element in understanding community dynamics. Yet, this infection network is often difficult to ascertain. Introduced over 60 years ago, the plaque assay remains the gold standard for establishing w...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: BMC Genomics

سال: 2021

ISSN: ['1471-2164']

DOI: https://doi.org/10.1186/s12864-021-07373-z