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Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq

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Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq

Hendrik Marks, Hindrik H. D. Kerstens, Tahsin Stefan Barakat, Erik Splinter, René A. M. Dirks, Guido van Mierlo, Onkar Joshi, Shuang-Yin Wang, Tomas

Babak, Cornelis A. Albers, et al.

To cite this version:

Hendrik Marks, Hindrik H. D. Kerstens, Tahsin Stefan Barakat, Erik Splinter, René A. M. Dirks, et al.. Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.

Genome Biology, BioMed Central, 2016, 17, �10.1186/s13059-016-0885-4�. �hal-02630193�

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ERRA T U M Open Access

Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq

Hendrik Marks

1*

, Hindrik H. D. Kerstens

1

, Tahsin Stefan Barakat

3

, Erik Splinter

4

, René A. M. Dirks

1

, Guido van Mierlo

1

, Onkar Joshi

1

, Shuang-Yin Wang

1

, Tomas Babak

5

, Cornelis A. Albers

2

, Tüzer Kalkan

6

, Austin Smith

6

, Alice Jouneau

7

, Wouter de Laat

4

, Joost Gribnau

3

and Hendrik G. Stunnenberg

1*

After the publication of this work [1], we noticed there was an error in Fig. 5 where −1,0 and 1 are incorrectly displayed in the y-axis in panel b. Please see the corrected Fig. 5 below. We apologize for this error.

Author details

1Radboud University, Faculty of Science, Department of Molecular Biology, Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen 6500HB, The Netherlands.2Radboud University, Faculty of Science, Department of Molecular Developmental Biology, Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen 6500HB, The Netherlands.3Department of Reproduction and Development, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.4Hubrecht Institute, University Medical Center Utrecht, Uppsalalaan 8, Utrecht 3584CT, The Netherlands.5Biology Department, Queen’s University, Kingston, ON, Canada.6Wellcome Trust-Medical Research Council Stem Cell Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QR, UK.7INRA, UMR1198 Biologie du Développement et Reproduction, Jouy-en-Josas F-78350, France.

Received: 25 January 2016 Accepted: 25 January 2016

References

1. Marks H, Kerstens HH, Barakat TS, Splinter E, Dirks RAM, van Mierlo G, et al.

Dynamics of gene silencing during X inactivation using allele-specific RNA-seq.

Genome Biol. 2015;16:149.

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* Correspondence:H.Marks@ncmls.ru.nl;H.Stunnenberg@ncmls.ru.nl

1Radboud University, Faculty of Science, Department of Molecular Biology, Radboud Institute for Molecular Life Sciences (RIMLS), Nijmegen 6500HB, The Netherlands

© 2016 Marks et al.Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Markset al. Genome Biology (2016) 17:22 DOI 10.1186/s13059-016-0885-4

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a

c

d

e

b

Fig. 5llele-specific RNA-seq on three NPC lines identifies three distal regions of genes that escape XCI.aRatio of Xi/Xa (y-axis; for each of the three NPC lines sorted from highest to lowest) for genes showing a log2 ratio of at least−5. We set the cutoff for escape on 10 % relative expression from the Xi versus the Xa (log 2 ratio of >−3.32; similar to Yang et al. [37]).bXi/Xa ratio of genes that escape XCI in all three NPC lines.cDistribution of the escape genes identified in *NPC_129-Xi over the four clusters as characterized in Fig. 4a.dLocalization of the escape genes within each NPC line over the linear X chromosome (see also Table 1). Theblack dotson thefourth rowrepresent all X-linked genes for which high-confidence allele-specific ratios were obtained in NPCs.eValidation of the escape genes within the three escape regions by Sanger sequencing of cDNA. See Additional file 1:

Figure S13 for the full panel of 13 genes that we validated, and for further details

Markset al. Genome Biology (2016) 17:22 Page 2 of 2

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