Evidence map›Paper›PMID 32456659›Full record

ArticleGenome biology2020

FORK-seq: replication landscape of the Saccharomyces cerevisiae genome by nanopore sequencing.

Magali Hennion, Jean-Michel Arbona, Laurent Lacroix, Corinne Cruaud, Bertrand Theulot, Benoît Le Tallec, Florence Proux, Xia Wu, Elizaveta Novikova, Stefan Engelen and 3 more

Abstract readEvaluation Study
In one paragraph

Article in Genome biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed.

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  13. Compact Origins and Where to Find Them: ORC's Guide to Genome-Wide Licensing.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Magali HennionInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Jean-Michel ArbonaUniversité de Lyon, ENS de Lyon, Université Claude Bernard Lyon 1, CNRS, Laboratoire de Physique, Lyon, 69342, France.
Laurent LacroixInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Corinne CruaudCommissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Institut de biologie François-Jacob, Genoscope, 2 rue Gaston Crémieux, Evry, 91057, France.
Bertrand TheulotInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Benoît Le TallecInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Florence ProuxInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Xia WuInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Elizaveta NovikovaInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France.
Stefan EngelenCommissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Institut de biologie François-Jacob, Genoscope, 2 rue Gaston Crémieux, Evry, 91057, France.
Arnaud LemainqueCommissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Institut de biologie François-Jacob, Genoscope, 2 rue Gaston Crémieux, Evry, 91057, France.
Benjamin AuditUniversité de Lyon, ENS de Lyon, Université Claude Bernard Lyon 1, CNRS, Laboratoire de Physique, Lyon, 69342, France.
Olivier HyrienInstitut de Biologie de l'Ecole Normale Supérieure (IBENS), Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 46 rue d'Ulm, Paris, 75005, France. olivier.hyrien@bio.ens.psl.eu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome replication mapping methods profile cell populations, masking cell-to-cell heterogeneity. Here, we describe FORK-seq, a nanopore sequencing method to map replication of single DNA molecules at 200-nucleotide resolution. By quantifying BrdU incorporation along pulse-chased replication intermediates from Saccharomyces cerevisiae, we orient 58,651 replication tracks reproducing population-based replication directionality profiles and map 4964 and 4485 individual initiation and termination events, respectively. Although most events cluster at known origins and fork merging zones, 9% and 18% of initiation and termination events, respectively, occur at many locations previously missed. Thus, FORK-seq reveals the full extent of cell-to-cell heterogeneity in DNA replication.

Indexed as

DNA ReplicationBromodeoxyuridineGenome, FungalNanopore SequencingSaccharomyces cerevisiaeTranscription Initiation, GeneticTranscription Termination, GeneticBromodeoxyuridineBromodeoxyuridineConvolutional neural networkDNA replicationNanopore sequencingReplication originsS. cerevisiaeSingle-molecule analysis

Identifiers

PMID32456659
PMCPMC7251829

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.