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Publisher Correction: Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker

Clinical Epigenetics volume 15, Article number: 3 (2023) Cite this article

The Original Article was published on 14 November 2022

Correction to: Clinical Epigenetics (2022) 14:148 https://doi.org/10.1186/s13148-022-01362-z


Following publication of the original article [1], the author noticed an error in the figure. In the published version, the image of Fig. 5 has been repeated twice. The author has informed to remove the duplicated image during correction process. The typesetter has inadvertently missed to correct the figure. However, the text citation and caption of the figure seem to be correct. The corrected Fig. 5 has been published with this erratum.

Fig. 5
figure 5

Interaction of the gene BCL11B with other genes in CD8+ cells. BCL11B long-range interactions from Promoter Capture Hi-C for total CD8-positive T cells (red: BCL11B–C14orf64 (LINC01550) interactions). Genomic regions are depicted in blue circles (promoter region) or blue square (enhancer region)

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The original has been corrected.

Reference

  1. Bigouret V, Hoffmann T, Arlettaz L, Villard J, Colonna M, Ticheli A, et al. Monoclonal T-cell expansions in asymptomatic individuals and in patients with large granular leukemia consist of cytotoxic effector T cells expressing the activating CD94:NKG2C/E and NKD2D killer cell receptors. Blood. 2003;101:3198–204.

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Author notes

  1. Reiner Siebert

    Present address: Institute of Human Genetics, University of Ulm and University Medical Center Ulm, Ulm, Germany

Authors and Affiliations

  1. Faculty of Medicine, Institute of Cell Biology (Cancer Research), University of Duisburg-Essen, Virchowstr. 177, 45122, Essen, Germany

    Patricia Johansson, Martina Brauser & Ralf Küppers

  2. Computational Biology Group, Precision Nutrition and Cancer Research Program, IMDEA Food Institute, 28049, Madrid, Spain

    Teresa Laguna & Enrique Carrillo-de Santa Pau

  3. Institute for Human Genetics, Christian-Albrechts-University Kiel and University Hospital Schleswig Holstein, Campus Kiel, Kiel, Germany

    Julio Ossowski, Lara Keuneke, Reiner Siebert & Eva M. Murga Penas

  4. Institute of Human Genetics, Medical School Hannover (MHH), Hannover, Germany

    Julio Ossowski, Brigitte Schlegelberger & Anke K. Bergmann

  5. Centre de Recherches en Cancérologie de Toulouse (CRCT), Université de Toulouse, CNRS, Université Toulouse III-Paul Sabatier, Centre de Recherches en Cancérologie de Toulouse, INSERM U1037, 31037, Toulouse, France

    Vera Pancaldi

  6. Barcelona Supercomputing Center, 08034, Barcelona, Spain

    Vera Pancaldi

  7. Department of Hematology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany

    Ulrich Dührsen

  8. Institute for Pathology, Christian-Albrechts-University Kiel and University Hospital Schleswig Holstein, Campus Kiel, Kiel, Germany

    Julia Richter

  9. Institut d’Investigacions Biomediques August Pi I Sunyer (IDIBAPS), University of Barcelona, 08036, Barcelona, Spain

    Ana Queiros & José I. Martín-Subero

  10. Institució Catalana de Recerca i Estudis Avançats (ICREA), 08010, Barcelona, Spain

    José I. Martín-Subero

  11. Department of Internal Medicine, University Hospital Essen, St. Josef-Krankenhaus, University Medicine Essen, Essen, Germany

    Jan Dürig

Authors
  1. Patricia Johansson
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  2. Teresa Laguna
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  3. Julio Ossowski
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  4. Vera Pancaldi
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  5. Martina Brauser
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  7. Lara Keuneke
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  8. Ana Queiros
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  10. José I. Martín-Subero
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  11. Reiner Siebert
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  14. Jan Dürig
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  15. Eva M. Murga Penas
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  16. Enrique Carrillo-de Santa Pau
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  17. Anke K. Bergmann
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Corresponding authors

Correspondence to Patricia Johansson or Teresa Laguna.

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Johansson, P., Laguna, T., Ossowski, J. et al. Publisher Correction: Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker. Clin Epigenet 15, 3 (2023). https://doi.org/10.1186/s13148-022-01405-5

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  • DOI: https://doi.org/10.1186/s13148-022-01405-5

Clinical Epigenetics

ISSN: 1868-7083

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