Evidence map›Paper›PMID 38200273›Full record

ArticleNature aging2024

TIME-seq reduces time and cost of DNA methylation measurement for epigenetic clock construction.

Patrick T Griffin, Alice E Kane, Alexandre Trapp, Jien Li, Matthew Arnold, Jesse R Poganik, Ryan J Conway, Maeve S McNamara, Margarita V Meer, Noah Hoffman and 14 more

Open access · greenAbstract read
In one paragraph

Article in Nature aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Multiomic clocks to predict phenotypic age in mice.The journals of gerontology. Series A, Biological sciences and medical sciences · 2025
    Article
  6. Article
  7. Sex differences in DNA methylation in bats.Annals of the New York Academy of Sciences · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Time is encoded by methylation changes at clustered CpG sites.bioRxiv : the preprint server for biology · 2024
    Article
  13. Review
  14. Article
  15. 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

24 authors at 6 institutions in 3 countries.

Patrick T GriffinBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Alice E KaneBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Alexandre TrappBrigham and Women's Hospital, Division of Genetics, Department of Medicine, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-7938-0410
Jien LiBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Matthew ArnoldBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Jesse R PoganikBrigham and Women's Hospital, Division of Genetics, Department of Medicine, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-3098-8550
Ryan J ConwayBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Maeve S McNamaraBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Margarita V MeerBrigham and Women's Hospital, Division of Genetics, Department of Medicine, Harvard Medical School, Boston, MA, USA.
Noah HoffmanBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
João A AmorimBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Xiao TianBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5300-3596
Michael R MacArthurDepartment of Health Sciences and Technology, Eidgenössische Technische Hochschule Zürich, Zurich, Switzerland.
Sarah J MitchellDepartment of Health Sciences and Technology, Eidgenössische Technische Hochschule Zürich, Zurich, Switzerland.
Amber L MuellerBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Colleen CarmodyBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Daniel L VeraBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA.
Csaba KerepesiBrigham and Women's Hospital, Division of Genetics, Department of Medicine, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-9541-246X
Kejun YingBrigham and Women's Hospital, Division of Genetics, Department of Medicine, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-1791-6176
Nicole Noren HootenLaboratory of Epidemiology and Population Science, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-1683-3838
James R MitchellDepartment of Health Sciences and Technology, Eidgenössische Technische Hochschule Zürich, Zurich, Switzerland.
Michele K EvansLaboratory of Epidemiology and Population Science, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
Vadim N GladyshevBrigham and Women's Hospital, Division of Genetics, Department of Medicine, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-0372-7016
David A SinclairBlavatnik Institute, Department of Genetics, Paul F. Glenn Center for Biology of Aging Research at Harvard Medical School, Boston, MA, USA. david_sinclair@hms.harvard.edu.ORCID http://orcid.org/0000-0002-9936-436X
Harvard University · USBrigham and Women's Hospital · USNational Institutes of Health · USPrinceton University · USETH Zurich · CHFleet Science Center · US

Funding

The role of hyaluronan in longevity and cancer resistance of longest-lived rodentP01AG047200 · NIA · UNIVERSITY OF ROCHESTER · PI Zhengdong Zhang · 2014 to 2026
$36.9M
Translational CoreP30AG038070 · NIA · JACKSON LABORATORY · PI Gary A Churchill · 2010 to 2026
$19.3M
Role of the Mitochondrial Peptide Humanin in Regulating Aging and HealthspanP01AG055369 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LONGO, VALTER D. · 2018 to 2023
$12.4M
Role of Sgs1 DNA helicase in telomere maintenanceR01AG019719 · NIA · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SINCLAIR, DAVID A. · 2001 to 2022
$5.3M
QUANTITATIVE ASSESSMENT OF BIOLOGICAL AGE AND ITS APPLICATIONSR01AG065403 · NIA · YALE UNIVERSITY · PI Vadim N. Gladyshev, Albert Tzongyang Higgins-Chen · 2020 to 2026
$4.2M
Development of a Predictive Frailty Clock & Longitudinal Investigation of its Epigenetic DeterminantsR00AG070102 · NIA · INSTITUTE FOR SYSTEMS BIOLOGY · PI KANE, ALICE E · 2023 to 2025
$1.0M
Tagmentation-based Indexing for Methylation Sequencing as a novel method of high-throughput methylation clock measurementR21HG011850 · NHGRI · HARVARD MEDICAL SCHOOL · PI SINCLAIR, DAVID A. · 2021 to 2021
$626k
A novel method to identify regulators of biological aging 
based on high-throughput sequencing of epigenetic clocks.K00AG073499 · NIA · HARVARD UNIVERSITY · PI Patrick Griffin · 2023 to 2026
$304k
Development of a Predictive Frailty Clock & Longitudinal Investigation of its Epigenetic DeterminantsK99AG070102 · NIA · HARVARD MEDICAL SCHOOL · PI KANE, ALICE E · 2021 to 2022
$227k
A novel method to identify regulators of biological aging 
based on high-throughput sequencing of epigenetic clocks.F99AG073499 · NIA · HARVARD MEDICAL SCHOOL · PI GRIFFIN, PATRICK · 2021 to 2022
$76k
ELDERLY US IMMIGRANTSR01AG011850 · NIA · UNIVERSITY OF COLORADO AT BOULDER · PI GREENWOOD, MICHAEL J · 1995 to 1997
–
American Federation for Aging Research (American Federation for Aging Research, Inc.) DIAMOND19036National Science Foundation (NSF) DGE1745303NHGRI NIH HHS R21 HG011850NIA NIH HHS F99 AG073499NIA NIH HHS K00 AG073499NIA NIH HHS K99 AG070102NIA NIH HHS P01 AG047200NIA NIH HHS P01 AG055369NIA NIH HHS P30 AG038070NIA NIH HHS R00 AG070102NIA NIH HHS R01 AG019719NIA NIH HHS R01 AG065403U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) AG047200U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) AG065403U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) AG073499U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) P01AG055369U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG019719U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R21HG011850
6 · The paper itself

Abstract

Epigenetic 'clocks' based on DNA methylation have emerged as the most robust and widely used aging biomarkers, but conventional methods for applying them are expensive and laborious. Here we develop tagmentation-based indexing for methylation sequencing (TIME-seq), a highly multiplexed and scalable method for low-cost epigenetic clocks. Using TIME-seq, we applied multi-tissue and tissue-specific epigenetic clocks in over 1,800 mouse DNA samples from eight tissue and cell types. We show that TIME-seq clocks are accurate and robust, enriched for polycomb repressive complex 2-regulated loci, and benchmark favorably against conventional methods despite being up to 100-fold less expensive. Using dietary treatments and gene therapy, we find that TIME-seq clocks reflect diverse interventions in multiple tissues. Finally, we develop an economical human blood clock (R > 0.96, median error = 3.39 years) in 1,056 demographically representative individuals. These methods will enable more efficient epigenetic clock measurement in larger-scale human and animal studies.

Indexed as

DNA MethylationLabor, ObstetricAgingAnimalsEpigenesis, GeneticEpigenomicsFemaleHumansMicePregnancy

Identifiers

PMID38200273
PMCPMC11332592
OpenAlexW4390696379

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.