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ReplicationDomain: a visualization tool and comparative database for genome-wide replication timing data

TLDR
ReplicationDomain is a novel and powerful tool to facilitate the comparative visualization of replication timing in various cell types as well as other genome-wide chromatin features and is considerably faster and more convenient than existing browsers when viewing multi-megabase segments of chromosomes.
Abstract
Eukaryotic DNA replication is regulated at the level of large chromosomal domains (0.5–5 megabases in mammals) within which replicons are activated relatively synchronously. These domains replicate in a specific temporal order during S-phase and our genome-wide analyses of replication timing have demonstrated that this temporal order of domain replication is a stable property of specific cell types. We have developed ReplicationDomain http://www.replicationdomain.org as a web-based database for analysis of genome-wide replication timing maps (replication profiles) from various cell lines and species. This database also provides comparative information of transcriptional expression and is configured to display any genome-wide property (for instance, ChIP-Chip or ChIP-Seq data) via an interactive web interface. Our published microarray data sets are publicly available. Users may graphically display these data sets for a selected genomic region and download the data displayed as text files, or alternatively, download complete genome-wide data sets. Furthermore, we have implemented a user registration system that allows registered users to upload their own data sets. Upon uploading, registered users may choose to: (1) view their data sets privately without sharing; (2) share with other registered users; or (3) make their published or "in press" data sets publicly available, which can fulfill journal and funding agencies' requirements for data sharing. ReplicationDomain is a novel and powerful tool to facilitate the comparative visualization of replication timing in various cell types as well as other genome-wide chromatin features and is considerably faster and more convenient than existing browsers when viewing multi-megabase segments of chromosomes. Furthermore, the data upload function with the option of private viewing or sharing of data sets between registered users should be a valuable resource for the scientific community.

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Journal ArticleDOI

Evolutionarily conserved replication timing profiles predict long-range chromatin interactions and distinguish closely related cell types

TL;DR: The results reveal evolutionarily conserved aspects of developmentally regulated replication programs in mammals, demonstrate the power of replication profiling to distinguish closely related cell types, and strongly support the hypothesis that replication timing domains are spatially compartmentalized structural and functional units of three-dimensional chromosomal architecture.
Journal ArticleDOI

Collisions between Replication and Transcription Complexes Cause Common Fragile Site Instability at the Longest Human Genes

TL;DR: The results show that, on the longest human genes, collisions of the transcription machinery with a replication fork are inevitable, creating R-loops and consequent CFS formation, and functional replication machinery needs to be involved in the resolution of conflicts between transcription and replication machineries to ensure genomic stability.
Journal Article

Genome-wide DNA replication profile for Drosophila melanogaster: a link between transcription and replication timing: a link between transcription and replication timing

TL;DR: A strategy to measure the timing of DNA replication for thousands of genes in a single DNA array hybridization experiment generated a genome-wide map of replication timing for Drosophila melanogaster and found a strong correlation between DNA replication early in S phase and transcriptional activity.
Journal ArticleDOI

Genome-wide dynamics of replication timing revealed by in vitro models of mouse embryogenesis

TL;DR: A model in which a distinct set of replication domains undergoes a form of "autosomal Lyonization" in the epiblast that is difficult to reprogram and coincides with an epigenetic commitment to differentiation prior to germ layer specification is supported.
References
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Journal ArticleDOI

Treatment of Sickle Cell Anemia Mouse Model with iPS Cells Generated from Autologous Skin

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Journal ArticleDOI

Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture.

TL;DR: It is reported that neither multicellular aggregation nor coculture is necessary for ES cells to commit efficiently to a neural fate and this system provides a platform for defining the molecular machinery of neural commitment and optimizing the efficiency of neuronal and glial cell production from pluripotent mammalian stem cells.
Journal ArticleDOI

Global Reorganization of Replication Domains During Embryonic Stem Cell Differentiation

TL;DR: It is concluded that replication profiles are cell-type specific, and changes in these profiles reveal chromosome segments that undergo large changes in organization during differentiation, a novel characteristic of the pluripotent state.
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