Evidence map›Paper›PMID 18404205›Full record

ArticlePLoS computational biology2008

Estimating cell depth from somatic mutations.

Adam Wasserstrom, Dan Frumkin, Rivka Adar, Shalev Itzkovitz, Tomer Stern, Shai Kaplan, Gabi Shefer, Irena Shur, Lior Zangi, Yitzhak Reizel and 8 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Applications of Single-Cell DNA Sequencing.Annual review of genomics and human genetics · 2021
    Review
  7. Article
  8. Article
  9. Inferring average generation via division-linked labeling.Journal of mathematical biology · 2016
    Article
  10. Theory and Practice of Lineage Tracing.Stem cells (Dayton, Ohio) · 2015
    Review
  11. Aging, clonal hematopoiesis and preleukemia: not just bad luck?International journal of hematology · 2015
    Review
  12. Elevated germline mutation rate in teenage fathers.Proceedings. Biological sciences · 2015
    Article
  13. Hypermutable DNA chronicles the evolution of human colon cancer.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. 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

18 authors.

Adam WasserstromDepartment of Biological Chemistry, Weizmann Institute of Science, Rehovot, Israel.
Dan Frumkin
Rivka Adar
Shalev Itzkovitz
Tomer Stern
Shai Kaplan
Gabi Shefer
Irena Shur
Lior Zangi
Yitzhak Reizel
Alon Harmelin
Yuval Dor
Nava Dekel
Yair Reisner
Dafna Benayahu
Eldad Tzahor
Eran Segal
Ehud Shapiro

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The depth of a cell of a multicellular organism is the number of cell divisions it underwent since the zygote, and knowing this basic cell property would help address fundamental problems in several areas of biology. At present, the depths of the vast majority of human and mouse cell types are unknown. Here, we show a method for estimating the depth of a cell by analyzing somatic mutations in its microsatellites, and provide to our knowledge for the first time reliable depth estimates for several cells types in mice. According to our estimates, the average depth of oocytes is 29, consistent with previous estimates. The average depth of B cells ranges from 34 to 79, linearly related to the mouse age, suggesting a rate of one cell division per day. In contrast, various types of adult stem cells underwent on average fewer cell divisions, supporting the notion that adult stem cells are relatively quiescent. Our method for depth estimation opens a window for revealing tissue turnover rates in animals, including humans, which has important implications for our knowledge of the body under physiological and pathological conditions.

Indexed as

AnimalsBase SequenceB-LymphocytesCells, CulturedCellular SenescenceDNA Mutational AnalysisHybrid CellsMiceMicrosatellite RepeatsMolecular Sequence DataSequence Analysis, DNA

Identifiers

PMID18404205
PMCPMC2275312

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.