Literature DB >> 27993159

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

Linda Szabo1, Robert Morey2, Nathan J Palpant3, Peter L Wang1, Nastaran Afari2, Chuan Jiang2, Mana M Parast4, Charles E Murry3, Louise C Laurent5, Julia Salzman6.   

Abstract

Entities:  

Year:  2016        PMID: 27993159      PMCID: PMC5165717          DOI: 10.1186/s13059-016-1123-9

Source DB:  PubMed          Journal:  Genome Biol        ISSN: 1474-7596            Impact factor:   13.583


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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

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

SourceTypeACCESSION
A549cell line, polyA+GSM758564
AGO4450cell line, polyA+GSM758561
BJcell line, polyA+GSM758562
GM12878cell line, polyA+GSM758559
H1cell line, polyA+GSM758566
HMECcell line, polyA+GSM758571
HeLacell line, polyA+GSM765402
HepG2cell line, polyA+GSM758575
HSSMcell line, polyA+GSM758578
HUVECcell line, polyA+GSM758563
IMR90cell line, polyA+GSM981249
K562cell line, polyA+GSM765405
MCF7cell line, polyA+GSM765388
NHEKcell line, polyA+GSM765401
NHLFcell line, polyA+GSM765394
SKNSHRAcell line, polyA+GSM765395
A549cell line, polyA-GSM767854
AGO4450cell line, polyA-GSM765396
BJcell line, polyA-GSM767855
GM12878cell line, polyA-GSM758572
H1cell line, polyA-GSM758573
HMECcell line, polyA-GSM765397
HeLacell line, polyA-GSM767847
HepG2cell line, polyA-GSM758567
HSSMcell line, polyA-GSM765391
HUVECcell line, polyA-GSM767856
K562cell line, polyA-GSM758577
MCF7cell line, polyA-GSM767851
NHEKcell line, polyA-GSM765398
NHLFcell line, polyA-GSM765389
SKNSHRAcell line, polyA-GSM767845
camera-type eyetissueENCSR000AFO
cerebellumtissueENCSR000AEW
diencephalontissueENCSR000AEX
frontal cortextissueENCSR000AEY
hearttissueENCSR000AEZ
hearttissueENCSR000AHH
livertissueENCSR000AEU
livertissueENCSR000AFB
lungtissueENCSR000AFC
metanephrostissueENCSR000AFA
mononuclear celltissueENCSR000CUT
occipital lobetissueENCSR000AFD
parietal lobetissueENCSR000AFE
skeletal muscletissueENCSR000AFF
skin of bodytissueENCSR000AFG
spinal cordtissueENCSR000AFH
stomachtissueENCSR000AFI
temporal lobetissueENCSR000AFJ
thyroid glandtissueENCSR000AFK
tonguetissueENCSR000AFL
umbilical cordtissueENCSR000AFM
urinary bladdertissueENCSR000AEV
uterustissueENCSR000AFN
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] ENCODE accession codes 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.]
  1 in total

1.  Statistically based splicing detection reveals neural enrichment and tissue-specific induction of circular RNA during human fetal development.

Authors:  Linda Szabo; Robert Morey; Nathan J Palpant; Peter L Wang; Nastaran Afari; Chuan Jiang; Mana M Parast; Charles E Murry; Louise C Laurent; Julia Salzman
Journal:  Genome Biol       Date:  2015-06-16       Impact factor: 13.583

  1 in total
  6 in total

1.  Identification and Characterization of Circular RNAs in Brassica rapa in Response to Plasmodiophora brassicae.

Authors:  Huishan Liu; Chinedu Charles Nwafor; Yinglan Piao; Xiaonan Li; Zongxiang Zhan; Zhongyun Piao
Journal:  Int J Mol Sci       Date:  2022-05-11       Impact factor: 6.208

Review 2.  Pathophysiology and Clinical Utility of Non-coding RNAs in Epilepsy.

Authors:  Yiye Shao; Yinghui Chen
Journal:  Front Mol Neurosci       Date:  2017-08-10       Impact factor: 5.639

3.  [Circular RNA CircHIPK3 Promotes NCI-H1299 and NCI-H2170 Cell Proliferation through miR-379 and its Target IGF1].

Authors:  Fang Tian; Yun Wang; Zhe Xiao; Xuejun Zhu
Journal:  Zhongguo Fei Ai Za Zhi       Date:  2017-07-20

4.  Screening differential circular RNA expression profiles reveal that hsa_circ_0128298 is a biomarker in the diagnosis and prognosis of hepatocellular carcinoma.

Authors:  Dawei Chen; Chenyue Zhang; Jiamao Lin; Xinyu Song; Haiyong Wang
Journal:  Cancer Manag Res       Date:  2018-05-18       Impact factor: 3.989

Review 5.  Functional Role of circRNAs in the Regulation of Fetal Development, Muscle Development, and Lactation in Livestock.

Authors:  Tianle He; Qingyun Chen; Ke Tian; Yinzhao Xia; Guozhong Dong; Zhenguo Yang
Journal:  Biomed Res Int       Date:  2021-02-19       Impact factor: 3.411

6.  Analysis of circRNA expression in chicken HD11 cells in response to avian pathogenic E.coli.

Authors:  Hongyan Sun; Yexin Yang; Yuyi Ma; Nayin Li; Jishuang Tan; Changhua Sun; Huan Li
Journal:  Front Vet Sci       Date:  2022-09-15
  6 in total

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