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. 2016 Dec 19;17:263. doi: 10.1186/s13059-016-1123-9

Erratum to: Statistically based splicing detection reveals neural enrichment and tissue-specific induction of circular RNA during human fetal development

Linda Szabo 1, Robert Morey 2, Nathan J Palpant 3, Peter L Wang 1, Nastaran Afari 2, Chuan Jiang 2, Mana M Parast 4, Charles E Murry 3, Louise C Laurent 2,, Julia Salzman 1,
PMCID: PMC5165717  PMID: 27993159

Erratum

In this version of this article that was originally published [1] the authors had analysed two HeLa samples, SRR1637089 and SRR1637090, in Fig. 3 of the original publication. The authors had respectively analysed the samples as RNaseR+ and Ribominus, due to their incorrect annotations in a public database, but they were both Ribominus samples. The authors have now analysed appropriate positive and negative controls using their method, KNIFE, and find_circ. The results are presented in an amended version of Fig. 3c, please see updated version below. Furthermore, the authors have now provided a list of accession codes for the ENCODE data they analysed, please see the Table 1 below. Please note this was not part of the original article.

Fig. 3.

Fig. 3

Statistical algorithm improves the sensitivity of circular RNA detection. a, b Circular RNA detected by both algorithms are divided into false positives (FP; flagged as false positives due to low posterior probability) or true positives (TP; our posterior probability ≥ 0.9). a Number of circular RNAs detected by our GLM or CIRI in ENCODE BJ poly(A)+/− data and HeLa RNase-R+/− data generated by Gao et al. [23]. CIRI results are based on all default parameters except the -E flag set to exclude false positives resulting from identical colinear exons. b Number of circular RNAs detected by our GLM or find_circ in ENCODE BJ poly(A)+/− data and HeLa RNase-R- data generated by Gao et al. [23]. c Circular RNAs detected in HeLa RNase-R+ and Ribo- data generated by Gao et al. [23] and poly(A)+, and poly(A)- data generated by ENCODE. Number of circular RNAs detected by our GLM method (one or more reads, posterior probability ≥ 0.9) compared with CIRI (default parameters except -E). For GLM results, the first number is the total number of circles and the number of those which were detected by the de novo portion of the algorithm are listed in parentheses. d Venn diagram comparing the number of putative circular RNAs identified by our annotation-dependent algorithm in Rnase-R-treated H9 cells and the results published by Zhang et al. [22]. Green circles and red circles show circular RNA identified by our algorithm with high and low confidence, respectively; the blue circle shows those identified by Zhang et al. e Total junctional reads for circles comprised of a single exon (posterior probability ≥ 0.9, read count > 1) shown by size for same data as in panel (d). Median exon length is shown in red. The x-axis is truncated at 2000 excluding 31 long exons, all but one with total read counts < 50]

Table 1.

ENCODE accession codes

Source Type ACCESSION
A549 cell line, polyA+ GSM758564
AGO4450 cell line, polyA+ GSM758561
BJ cell line, polyA+ GSM758562
GM12878 cell line, polyA+ GSM758559
H1 cell line, polyA+ GSM758566
HMEC cell line, polyA+ GSM758571
HeLa cell line, polyA+ GSM765402
HepG2 cell line, polyA+ GSM758575
HSSM cell line, polyA+ GSM758578
HUVEC cell line, polyA+ GSM758563
IMR90 cell line, polyA+ GSM981249
K562 cell line, polyA+ GSM765405
MCF7 cell line, polyA+ GSM765388
NHEK cell line, polyA+ GSM765401
NHLF cell line, polyA+ GSM765394
SKNSHRA cell line, polyA+ GSM765395
A549 cell line, polyA- GSM767854
AGO4450 cell line, polyA- GSM765396
BJ cell line, polyA- GSM767855
GM12878 cell line, polyA- GSM758572
H1 cell line, polyA- GSM758573
HMEC cell line, polyA- GSM765397
HeLa cell line, polyA- GSM767847
HepG2 cell line, polyA- GSM758567
HSSM cell line, polyA- GSM765391
HUVEC cell line, polyA- GSM767856
K562 cell line, polyA- GSM758577
MCF7 cell line, polyA- GSM767851
NHEK cell line, polyA- GSM765398
NHLF cell line, polyA- GSM765389
SKNSHRA cell line, polyA- GSM767845
camera-type eye tissue ENCSR000AFO
cerebellum tissue ENCSR000AEW
diencephalon tissue ENCSR000AEX
frontal cortex tissue ENCSR000AEY
heart tissue ENCSR000AEZ
heart tissue ENCSR000AHH
liver tissue ENCSR000AEU
liver tissue ENCSR000AFB
lung tissue ENCSR000AFC
metanephros tissue ENCSR000AFA
mononuclear cell tissue ENCSR000CUT
occipital lobe tissue ENCSR000AFD
parietal lobe tissue ENCSR000AFE
skeletal muscle tissue ENCSR000AFF
skin of body tissue ENCSR000AFG
spinal cord tissue ENCSR000AFH
stomach tissue ENCSR000AFI
temporal lobe tissue ENCSR000AFJ
thyroid gland tissue ENCSR000AFK
tongue tissue ENCSR000AFL
umbilical cord tissue ENCSR000AFM
urinary bladder tissue ENCSR000AEV
uterus tissue ENCSR000AFN

Source (cell line name or tissue type), Type of sample (tissue, polyA+ cell line, or polyA- cell line), and Accession code for all ENCODE data analyzed.]

Footnotes

The online version of the original article can be found under doi:10.1186/s13059-015-0690-5.

Contributor Information

Louise C. Laurent, Email: llaurent@ucsd.edu

Julia Salzman, Email: julia.salzman@stanford.edu.

Reference

  • 1.Szabo L, Morey R, Palpant NJ, Wang PL, Afari N, Jiang C, et al. Statistically based splicing detection reveals neural enrichment and tissue-specific induction of circular RNA during human fetal development. Genome Biol. 2016;16:126. doi: 10.1186/s13059-015-0690-5. [DOI] [PMC free article] [PubMed] [Google Scholar]

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