Evidence map›Paper›PMID 26780608›Full record

ArticleNature genetics2016

A predictive computational framework for direct reprogramming between human cell types.

Owen J L Rackham, Jaber Firas, Hai Fang, Matt E Oates, Melissa L Holmes, Anja S Knaupp, FANTOM Consortium, Harukazu Suzuki, Christian M Nefzger, Carsten O Daub and 6 more

Abstract read
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In one paragraph

Article in Nature genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 149 papers.

0numbers the graph read from it
0cells of the map it votes in
149citing 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

149 citing papers in PubMed.

  1. Review
  2. Article
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  5. Review
  6. Computational modelling of cell identity.The Biochemical journal · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
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  15. Review
  16. Article
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  18. Article
  19. Direct Cardiac Reprogramming in the Age of Computational Biology.Journal of cardiovascular development and disease · 2024
    Review
  20. Review

89 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Owen J L RackhamDepartment of Computer Science, University of Bristol, Bristol, UK.
Jaber FirasDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
Hai FangDepartment of Computer Science, University of Bristol, Bristol, UK.
Matt E OatesDepartment of Computer Science, University of Bristol, Bristol, UK.ORCID http://orcid.org/0000-0002-0001-3675
Melissa L HolmesDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
Anja S KnauppDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
FANTOM Consortium
Harukazu SuzukiRIKEN Omics Science Center, Yokohama, Japan (ceased to exist as of 1 April 2013 owing to reorganization).
Christian M NefzgerDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
Carsten O DaubRIKEN Omics Science Center, Yokohama, Japan (ceased to exist as of 1 April 2013 owing to reorganization).
Jay W ShinRIKEN Omics Science Center, Yokohama, Japan (ceased to exist as of 1 April 2013 owing to reorganization).
Enrico PetrettoProgram in Cardiovascular and Metabolic Disorders, Duke-National University of Singapore Medical School, Singapore.
Alistair R R ForrestRIKEN Omics Science Center, Yokohama, Japan (ceased to exist as of 1 April 2013 owing to reorganization).
Yoshihide HayashizakiDivision of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama, Japan.
Jose M PoloDepartment of Anatomy and Developmental Biology, Monash University, Clayton, Victoria, Australia.
Julian GoughDepartment of Computer Science, University of Bristol, Bristol, UK.

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MC_U120097112
6 · The paper itself

Abstract

Transdifferentiation, the process of converting from one cell type to another without going through a pluripotent state, has great promise for regenerative medicine. The identification of key transcription factors for reprogramming is currently limited by the cost of exhaustive experimental testing of plausible sets of factors, an approach that is inefficient and unscalable. Here we present a predictive system (Mogrify) that combines gene expression data with regulatory network information to predict the reprogramming factors necessary to induce cell conversion. We have applied Mogrify to 173 human cell types and 134 tissues, defining an atlas of cellular reprogramming. Mogrify correctly predicts the transcription factors used in known transdifferentiations. Furthermore, we validated two new transdifferentiations predicted by Mogrify. We provide a practical and efficient mechanism for systematically implementing novel cell conversions, facilitating the generalization of reprogramming of human cells. Predictions are made available to help rapidly further the field of cell conversion.

Indexed as

Gene Regulatory NetworksCell DifferentiationCell TransdifferentiationCellular ReprogrammingFibroblastsHumansInduced Pluripotent Stem CellsRegenerative MedicineTranscription FactorsTranscription Factors

Identifiers

PMID26780608

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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.