On the public citation graph

Genome-Wide Identification of Early-Firing Human Replication Origins by Optical Replication Mapping

https://doi.org/10.1101/214841
0 signed · 39 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1097-4644(20000901)78:3<442::aid-jcb9>3.0.co;2-1openalex-snapshot
Major DNA replication initiation sites in thec-myc locus in human cells
inferredcites →https://doi.org/10.1002/jcb.21828openalex-snapshot
A revisionist replicon model for higher eukaryotic genomes
inferredcites →https://doi.org/10.1007/s004120050399openalex-snapshot
Heterogeneity of eukaryotic replicons, replicon clusters, and replication foci
inferredcites →https://doi.org/10.1007/s10577-009-9093-3openalex-snapshot
Reconciling stochastic origin firing with defined replication timing
inferredcites →https://doi.org/10.1016/j.jmb.2007.10.046openalex-snapshot
DNA Combing Reveals Intrinsic Temporal Disorder in the Replication of Yeast Chromosome VI
inferredcites →https://doi.org/10.1038/msb.2010.61openalex-snapshot
Modeling genome‐wide replication kinetics reveals a mechanism for regulation of replication timing
inferredcites →https://doi.org/10.1038/nbt.1754openalex-snapshot
Integrative genomics viewer
inferredcites →https://doi.org/10.1038/nbt.2303openalex-snapshot
Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly
inferredcites →https://doi.org/10.1038/ncomms10208openalex-snapshot
Replication landscape of the human genome
inferredcites →https://doi.org/10.1038/nsmb.2339openalex-snapshot
Unraveling cell type–specific and reprogrammable human replication origin signatures associated with G-quadruplex consensus motifs
inferredcites →https://doi.org/10.1074/jbc.m202165200openalex-snapshot
The Origin Recognition Complex Marks a Replication Origin in the Human TOP1 Gene Promoter
inferredcites →https://doi.org/10.1080/15384101.2016.1203492openalex-snapshot
Spatio-temporal re-organization of replication foci accompanies replication domain consolidation during human pluripotent stem cell lineage specification
inferredcites →https://doi.org/10.1083/jcb.200104099openalex-snapshot
Activation of mammalian Chk1 during DNA replication arrest
inferredcites →https://doi.org/10.1083/jcb.201407004openalex-snapshot
Peaks cloaked in the mist: The landscape of mammalian replication origins
inferredcites →https://doi.org/10.1093/nar/gkq343openalex-snapshot
Mathematical modelling of whole chromosome replication
inferredcites →https://doi.org/10.1093/nar/gkw760openalex-snapshot
Genome-wide identification and characterisation of human DNA replication origins by initiation site sequencing (ini-seq)
inferredcites →https://doi.org/10.1101/gr.121830.111openalex-snapshot
Genome-scale analysis of metazoan replication origins reveals their organization in specific but flexible sites defined by conserved features
inferredcites →https://doi.org/10.1101/gr.142331.112openalex-snapshot
Genome-wide mapping of human DNA-replication origins: Levels of transcription at ORC1 sites regulate origin selection and replication timing
inferredcites →https://doi.org/10.1101/gr.155218.113openalex-snapshot
Bubble-seq analysis of the human genome reveals distinct chromatin-mediated mechanisms for regulating early- and late-firing origins
inferredcites →https://doi.org/10.1101/gr.183848.114openalex-snapshot
Characterizing and controlling intrinsic biases of lambda exonuclease in nascent strand sequencing reveals phasing between nucleosomes and G-quadruplex motifs around a subset of human replication origins
inferredcites →https://doi.org/10.1128/mcb.22.9.3053-3065.2002openalex-snapshot
Initiation Sites Are Distributed at Frequent Intervals in the Chinese Hamster Dihydrofolate Reductase Origin of Replication but Are Used with Very Different Efficiencies
inferredcites →https://doi.org/10.1146/annurev.biochem.052308.103205openalex-snapshot
Eukaryotic Chromosome DNA Replication: Where, When, and How?
inferredcites →https://doi.org/10.1186/1471-2105-9-530openalex-snapshot
ReplicationDomain: a visualization tool and comparative database for genome-wide replication timing data
inferredcites →https://doi.org/10.1371/journal.pgen.1004282openalex-snapshot
The Spatiotemporal Program of DNA Replication Is Associated with Specific Combinations of Chromatin Marks in Human Cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/978-981-13-6037-4_7openalex-snapshot
Bionano Genome Mapping: High-Throughput, Ultra-Long Molecule Genome Analysis System for Precision Genome Assembly and Haploid-Resolved Structural Variation Discovery
inferred← citeshttps://doi.org/10.1007/s10577-019-09624-yopenalex-snapshot
Genomic methods for measuring DNA replication dynamics
inferred← citeshttps://doi.org/10.1007/s42764-020-00021-yopenalex-snapshot
The impact of transcription-mediated replication stress on genome instability and human disease
inferred← citeshttps://doi.org/10.1016/j.dnarep.2020.102943openalex-snapshot
Time for remodeling: SNF2-family DNA translocases in replication fork metabolism and human disease
inferred← citeshttps://doi.org/10.1016/j.gde.2023.102031openalex-snapshot
Replication timing and transcriptional control: beyond cause and effect — part IV
inferred← citeshttps://doi.org/10.1038/s41594-018-0171-0openalex-snapshot
Transcription shapes DNA replication initiation and termination in human cells
inferred← citeshttps://doi.org/10.1101/371518openalex-snapshot
CRISPR-bind: a simple, custom CRISPR/dCas9-mediated labeling of genomic DNA for mapping in nanochannel arrays
inferred← citeshttps://doi.org/10.1101/426858openalex-snapshot
Mapping DNA replication with nanopore sequencing
inferred← citeshttps://doi.org/10.1186/s12864-018-5372-8openalex-snapshot
NanoMod: a computational tool to detect DNA modifications using Nanopore long-read sequencing data
inferred← citeshttps://doi.org/10.1186/s13059-020-01983-8openalex-snapshot
High-resolution Repli-Seq defines the temporal choreography of initiation, elongation and termination of replication in mammalian cells
inferred← citeshttps://doi.org/10.1186/s13059-020-02013-3openalex-snapshot
FORK-seq: replication landscape of the Saccharomyces cerevisiae genome by nanopore sequencing
inferred← citeshttps://doi.org/10.3410/f.734706495.793557648openalex-snapshot
Faculty Opinions recommendation of Transcription shapes DNA replication initiation and termination in human cells.
inferred← citeshttps://doi.org/10.3410/f.738031761.793583813openalex-snapshot
Faculty Opinions recommendation of FORK-seq: replication landscape of the Saccharomyces cerevisiae genome by nanopore sequencing.
inferred← citeshttps://doi.org/10.70675/10fe3c51z99cez45f2z9e85zd13f7797db69openalex-snapshot
Cartographie pangénomique à haut débit et en molécule unique de la réplication de l'ADN
inferred← citeshttps://doi.org/10.7916/d8-8hx3-4x61openalex-snapshot
BRCA1 and 53BP1 Mediate Reprogramming Through DNA Repair Pathway Choice
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.