Evidence map›Paper›PMID 25662462›Full record

ArticleMethods in enzymology2015

ChIP-seq and RNA-seq methods to study circadian control of transcription in mammals.

Joseph S Takahashi, Vivek Kumar, Prachi Nakashe, Nobuya Koike, Hung-Chung Huang, Carla B Green, Tae-Kyung Kim

Abstract read
In one paragraph

Article in Methods in enzymology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Single-Cell Multiomic Analysis of Circadian Rhythmicity in Mouse Liver.bioRxiv : the preprint server for biology · 2025
    Article
  5. Review
  6. Loss ofZoological research · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. The malaria parasite has an intrinsic clock.Science (New York, N.Y.) · 2020
    Article
  14. Article
  15. Accelerated evolution of oligodendrocytes in the human brain.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  16. Article
  17. Foxp1 in Forebrain Pyramidal Neurons Controls Gene Expression Required for Spatial Learning and Synaptic Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  18. HCFC2 is needed for IRF1- and IRF2-dependentThe Journal of experimental medicine · 2017
    Article
  19. Article
  20. Article
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

7 authors.

Joseph S TakahashiDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA. Electronic address: joseph.takahashi@utsouthwestern.edu.
Vivek KumarDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Prachi NakasheDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Nobuya KoikeDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Hung-Chung HuangDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Carla B GreenDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Tae-Kyung KimDepartment of Neuroscience, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

Funding

Transcriptional Architecture and Chromatin Landscape of Circadian Clocks in AgingR01AG045795 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI GREEN, CARLA B., TAKAHASHI, JOSEPH S · 2013 to 2017
$1.5M
Howard Hughes Medical InstituteNIA NIH HHS R01 AG045795
6 · The paper itself

Abstract

Genome-wide analyses have revolutionized our ability to study the transcriptional regulation of circadian rhythms. The advent of next-generation sequencing methods has facilitated the use of two such technologies, ChIP-seq and RNA-seq. In this chapter, we describe detailed methods and protocols for these two techniques, with emphasis on their usage in circadian rhythm experiments in the mouse liver, a major target organ of the circadian clock system. Critical factors for these methods are highlighted and issues arising with time series samples for ChIP-seq and RNA-seq are discussed. Finally, detailed protocols for library preparation suitable for Illumina sequencing platforms are presented.

Indexed as

Circadian ClocksGene Expression RegulationAcetylationAnimalsCell LineChromatin ImmunoprecipitationCLOCK ProteinsHistonesHumansMethylationProtein Processing, Post-TranslationalSequence Analysis, RNATranscription, GeneticCLOCK ProteinsHistonesAcetylationChIP-seqChromatinCircadianHistoneMethylationRNA polymerase IIRNA-seqSequencingTranscription

Identifiers

PMID25662462
PMCPMC4402199

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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.