Corrigendum

Corrigendum: Profiling the long noncoding RNA interaction network in the regulatory elements of target genes by chromatin in situ reverse transcription sequencing

Published October 1, 2026. Vol 36 Issue 10, pp. 2187-2187. https://doi.org/10.1101/gr.282733.126
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cover of Genome Research Vol 36 Issue 10
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[Related article:] Genome Research 29: 1521–1532 (2019)

The authors would like to make the following corrections to the above-mentioned article:

  1. Two typos were found in the Figure 1C and Figure 3B legends, in which “mean ± SEM” should be “mean ± SD”.

  2. In the Figure 3A schematic diagram, the representative image contained duplications that may have caused confusion. We have replaced the image and updated the figure into a more precise schematic diagram by incorporating the reprogramming workflow, cellular morphology, and pluripotency marker staining.

The revised Figure 3A legend now reads:

Figure 3. Sox2-interacting lncRNAs are associated with reprogramming. (A) Mouse fibroblasts were reprogrammed into iPS cells by lentiviral transduction of OSKM (Oct4, Sox2, Klf4, c-Myc) factors. After reprogramming, iPSC colonies acquired pluripotency-associated characteristics and were stained positive for pluripotency marker (NANOG). Bottom panels: Images of fibroblasts and iPSCs were collected during reprogramming.

These corrections do not affect the interpretation and conclusions of the study.

This article has been corrected online.

doi: 10.1101/gr.282733.126

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