Author Correction: cuteFC: regenotyping structural variants through an accurate and efficient force-calling method

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Tao Jiang, Shuqi Cao, Yadong Liu, Zhendong Zhang, Bo Liu, Ruibang Luo, Guohua Wang, Yadong Wang
{"title":"Author Correction: cuteFC: regenotyping structural variants through an accurate and efficient force-calling method","authors":"Tao Jiang, Shuqi Cao, Yadong Liu, Zhendong Zhang, Bo Liu, Ruibang Luo, Guohua Wang, Yadong Wang","doi":"10.1186/s13059-025-03726-z","DOIUrl":null,"url":null,"abstract":"<p><b>Author Correction: Genome Biol 26, 166 (2025)</b></p><p><b>https://doi.org/10.1186/s13059-025-03642-2</b></p><br/><p>Following publication of the original article [1], the authors identified three errors in <i>Methods</i> and <i>Funding, and Fig. 2D</i>.</p><p>1. In the original version, the total number of simulated structural variations was incorrectly stated as 3,668 in the <i>Process the benchmarking datasets</i> part of <i>Methods</i> section. The correct sum of the simulated SVs: 2,191 insertions, 1,333 deletions, 450 inversions, 450 duplications, and 250 inter-chromosomal translocations, should be 4,674.</p><p>The original version was: “For the simulation datasets, we first simulated 3668 structural variations on chromosomes 1 and 2, including 2191 insertions, 1333 deletions, 450 inversions, 450 duplications, and 250 inter-chromosomal translocations, and reconstructed the reference genome GRCh38 with these SVs for the donor genome.”</p><p>The corrected version was: “For the simulation datasets, we first simulated <b>4674</b> structural variations on chromosomes 1 and 2, including 2191 insertions, 1333 deletions, 450 inversions, 450 duplications, and 250 inter-chromosomal translocations, and reconstructed the reference genome GRCh38 with these SVs for the donor genome”. The change was marked as bold. This correction does not affect the study’s results or conclusions.</p><p>2. In the <i>Funding</i> section, there contained redundant text, with the same grant details repeated in two separate paragraphs. We removed the duplicated paragraph and preserved the original content in the first paragraph.</p><p>The original version was: “This work has been supported by the National Key R&amp;D Program of China (Grant number 2022YFF1202101, 2024YFC3406303, 2017YFC0907503), the National Natural Science Foundation of China (Grant number 62472120, 62331012), China Postdoctoral Science Foundation (Grant Number 2022M720965), and Heilongjiang Postdoctoral Foundation (Grant Number LBH-Z22174).</p><p><b>National Key Research and Development Program of China, 2024YFC3406303, 2022YFF1202101, 2017YFC0907503, National Natural Science Foundation of China, 62472120, 62331012, China Postdoctoral Science Foundation, 2022M720965, Heilongjiang Postdoctoral Science Foundation, LBH-Z22174”</b>.</p><p>The corrected version was: “This work has been supported by the National Key R&amp;D Program of China (Grant number 2022YFF1202101, 2024YFC3406303, 2017YFC0907503), the National Natural Science Foundation of China (Grant number 62472120, 62331012), China Postdoctoral Science Foundation (Grant Number 2022M720965), and Heilongjiang Postdoctoral Foundation (Grant Number LBH-Z22174)”.</p><p>The deleted paragraph was marked as bold. This correction only removes the duplicated funding, and does not alter the funding sources or their attribution.</p><p>3. In the left portion of Fig. 2D, the proportion of simulated reads for alternative alleles to simulated reads for reference alleles was incorrectly reversed. In the original version, the proportions were listed as “10:0, 9:1, 8:2, …, 2:8, 1:9, 0:10” from top to bottom. However, as described in the figure legend, the top zygosity corresponds to homozygous reference alleles, while the bottom zygosity represents homozygous alternative alleles. Therefore, the proportions should instead be listed in reverse order as “0:10, 1:9, 2:8, …, 8:2, 9:1, 10:0”. This correction ensures consistency in the presentation of allele proportions throughout the manuscript. The reverse of these values does not affect any other data in the figure or its conclusions.</p><p>The original Fig. 2 was:\n</p><figure><picture><source srcset=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13059-025-03726-z/MediaObjects/13059_2025_3726_Figa_HTML.png?as=webp\" type=\"image/webp\"/><img alt=\"figure a\" aria-describedby=\"Figa\" height=\"887\" loading=\"lazy\" src=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13059-025-03726-z/MediaObjects/13059_2025_3726_Figa_HTML.png\" width=\"685\"/></picture></figure><p> The corrected Fig. 2 is:\n</p><figure><picture><source srcset=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13059-025-03726-z/MediaObjects/13059_2025_3726_Figb_HTML.png?as=webp\" type=\"image/webp\"/><img alt=\"figure b\" aria-describedby=\"Figb\" height=\"887\" loading=\"lazy\" src=\"//media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs13059-025-03726-z/MediaObjects/13059_2025_3726_Figb_HTML.png\" width=\"685\"/></picture></figure><p>The original article [1] has been corrected.</p><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Jiang T, Cao S, Liu Y, et al. cuteFC: regenotyping structural variants through an accurate and efficient force-calling method. Genome Biol. 2025;26:166. https://doi.org/10.1186/s13059-025-03642-2.</p><p>Article PubMed PubMed Central Google Scholar </p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><span>Author notes</span><ol><li><p>Tao Jiang and Shuqi Cao are joint first authors and contributed equally to this work.</p></li></ol><h3>Authors and Affiliations</h3><ol><li><p>Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, 150001, China</p><p>Tao Jiang, Shuqi Cao, Yadong Liu, Zhendong Zhang, Bo Liu, Guohua Wang &amp; Yadong Wang</p></li><li><p>Zhengzhou Research Institute, Harbin Institute of Technology, Zhengzhou, Henan, 450000, China</p><p>Tao Jiang, Yadong Liu, Bo Liu, Guohua Wang &amp; Yadong Wang</p></li><li><p>Department of Computer Science, The University of Hong Kong, Hong Kong, 999077, China</p><p>Ruibang Luo</p></li><li><p>School of Medicine and Health, Harbin Institute of Technology, Harbin, Heilongjiang, 150001, China</p><p>Yadong Wang</p></li></ol><span>Authors</span><ol><li><span>Tao Jiang</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Shuqi Cao</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Yadong Liu</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Zhendong Zhang</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Bo Liu</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Ruibang Luo</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Guohua Wang</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Yadong Wang</span>View author publications<p><span>Search author on:</span><span>PubMed<span> </span>Google Scholar</span></p></li></ol><h3>Corresponding authors</h3><p>Correspondence to Guohua Wang or Yadong Wang.</p><p><b>Open Access</b> This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.</p>\n<p>Reprints and permissions</p><img alt=\"Check for updates. 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cuteFC: regenotyping structural variants through an accurate and efficient force-calling method. <i>Genome Biol</i> <b>26</b>, 280 (2025). https://doi.org/10.1186/s13059-025-03726-z</p><p>Download citation<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><ul data-test=\"publication-history\"><li><p>Published<span>: </span><span><time datetime=\"2025-09-15\">15 September 2025</time></span></p></li><li><p>DOI</abbr><span>: </span><span>https://doi.org/10.1186/s13059-025-03726-z</span></p></li></ul><h3>Share this article</h3><p>Anyone you share the following link with will be able to read this content:</p><button data-track=\"click\" data-track-action=\"get shareable link\" data-track-external=\"\" data-track-label=\"button\" type=\"button\">Get shareable link</button><p>Sorry, a shareable link is not currently available for this article.</p><p 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Abstract

Author Correction: Genome Biol 26, 166 (2025)

https://doi.org/10.1186/s13059-025-03642-2


Following publication of the original article [1], the authors identified three errors in Methods and Funding, and Fig. 2D.

1. In the original version, the total number of simulated structural variations was incorrectly stated as 3,668 in the Process the benchmarking datasets part of Methods section. The correct sum of the simulated SVs: 2,191 insertions, 1,333 deletions, 450 inversions, 450 duplications, and 250 inter-chromosomal translocations, should be 4,674.

The original version was: “For the simulation datasets, we first simulated 3668 structural variations on chromosomes 1 and 2, including 2191 insertions, 1333 deletions, 450 inversions, 450 duplications, and 250 inter-chromosomal translocations, and reconstructed the reference genome GRCh38 with these SVs for the donor genome.”

The corrected version was: “For the simulation datasets, we first simulated 4674 structural variations on chromosomes 1 and 2, including 2191 insertions, 1333 deletions, 450 inversions, 450 duplications, and 250 inter-chromosomal translocations, and reconstructed the reference genome GRCh38 with these SVs for the donor genome”. The change was marked as bold. This correction does not affect the study’s results or conclusions.

2. In the Funding section, there contained redundant text, with the same grant details repeated in two separate paragraphs. We removed the duplicated paragraph and preserved the original content in the first paragraph.

The original version was: “This work has been supported by the National Key R&D Program of China (Grant number 2022YFF1202101, 2024YFC3406303, 2017YFC0907503), the National Natural Science Foundation of China (Grant number 62472120, 62331012), China Postdoctoral Science Foundation (Grant Number 2022M720965), and Heilongjiang Postdoctoral Foundation (Grant Number LBH-Z22174).

National Key Research and Development Program of China, 2024YFC3406303, 2022YFF1202101, 2017YFC0907503, National Natural Science Foundation of China, 62472120, 62331012, China Postdoctoral Science Foundation, 2022M720965, Heilongjiang Postdoctoral Science Foundation, LBH-Z22174”.

The corrected version was: “This work has been supported by the National Key R&D Program of China (Grant number 2022YFF1202101, 2024YFC3406303, 2017YFC0907503), the National Natural Science Foundation of China (Grant number 62472120, 62331012), China Postdoctoral Science Foundation (Grant Number 2022M720965), and Heilongjiang Postdoctoral Foundation (Grant Number LBH-Z22174)”.

The deleted paragraph was marked as bold. This correction only removes the duplicated funding, and does not alter the funding sources or their attribution.

3. In the left portion of Fig. 2D, the proportion of simulated reads for alternative alleles to simulated reads for reference alleles was incorrectly reversed. In the original version, the proportions were listed as “10:0, 9:1, 8:2, …, 2:8, 1:9, 0:10” from top to bottom. However, as described in the figure legend, the top zygosity corresponds to homozygous reference alleles, while the bottom zygosity represents homozygous alternative alleles. Therefore, the proportions should instead be listed in reverse order as “0:10, 1:9, 2:8, …, 8:2, 9:1, 10:0”. This correction ensures consistency in the presentation of allele proportions throughout the manuscript. The reverse of these values does not affect any other data in the figure or its conclusions.

The original Fig. 2 was:

Abstract Image

The corrected Fig. 2 is:

Abstract Image

The original article [1] has been corrected.

  1. Jiang T, Cao S, Liu Y, et al. cuteFC: regenotyping structural variants through an accurate and efficient force-calling method. Genome Biol. 2025;26:166. https://doi.org/10.1186/s13059-025-03642-2.

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Author notes
  1. Tao Jiang and Shuqi Cao are joint first authors and contributed equally to this work.

Authors and Affiliations

  1. Faculty of Computing, Harbin Institute of Technology, Harbin, Heilongjiang, 150001, China

    Tao Jiang, Shuqi Cao, Yadong Liu, Zhendong Zhang, Bo Liu, Guohua Wang & Yadong Wang

  2. Zhengzhou Research Institute, Harbin Institute of Technology, Zhengzhou, Henan, 450000, China

    Tao Jiang, Yadong Liu, Bo Liu, Guohua Wang & Yadong Wang

  3. Department of Computer Science, The University of Hong Kong, Hong Kong, 999077, China

    Ruibang Luo

  4. School of Medicine and Health, Harbin Institute of Technology, Harbin, Heilongjiang, 150001, China

    Yadong Wang

Authors
  1. Tao JiangView author publications

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  2. Shuqi CaoView author publications

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  3. Yadong LiuView author publications

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  4. Zhendong ZhangView author publications

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  5. Bo LiuView author publications

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  6. Ruibang LuoView author publications

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  7. Guohua WangView author publications

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  8. Yadong WangView author publications

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Corresponding authors

Correspondence to Guohua Wang or Yadong Wang.

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Jiang, T., Cao, S., Liu, Y. et al. Author Correction: cuteFC: regenotyping structural variants through an accurate and efficient force-calling method. Genome Biol 26, 280 (2025). https://doi.org/10.1186/s13059-025-03726-z

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作者更正:cuteFC:通过一种准确有效的力调用方法对结构变异进行基因分型
作者更正:Genome Biol 26, 166 (2025)https://doi.org/10.1186/s13059-025-03642-2Following原文章b[1]的发表,作者在Methods and Funding,以及Fig. 2D.1中发现了三个错误。在原始版本中,在方法部分的基准测试数据集部分中,模拟结构变化的总数被错误地表述为3,668。模拟sv的正确总和:2191个插入,1333个缺失,450个反转,450个重复和250个染色体间易位,应该是4674个。最初的版本是:“对于模拟数据集,我们首先模拟了1号和2号染色体上的3668个结构变异,包括2191个插入,1333个缺失,450个反转,450个重复和250个染色体间易位,并利用这些SVs重建了供体基因组的参考基因组GRCh38。”正确的版本是:“对于模拟数据集,我们首先模拟了1号和2号染色体上的4674个结构变异,包括2191个插入,1333个缺失,450个反转,450个重复和250个染色体间易位,并利用这些SVs重建了供体基因组的参考基因组GRCh38”。这一变化被标为粗体。此更正不影响研究的结果或结论。在经费资助一节中,有重复的文字,在两个单独的段落中重复了同样的赠款细节。我们删除了重复的段落,保留了第一段的原始内容。本文得到国家重点研发计划项目(资助号:2022YFF1202101、2024YFC3406303、2017YFC0907503)、国家自然科学基金项目(资助号:62472120、62331012)、中国博士后科学基金项目(资助号:2022M720965)、黑龙江省博士后基金项目(资助号:lhb - z22174)的资助。国家重点研发计划,2024YFC3406303, 2022YFF1202101, 2017YFC0907503,国家自然科学基金,62472120,62331012,中国博士后科学基金,2022M720965,黑龙江省博士后科学基金,LBH-Z22174”。更正后为:“国家重点研发计划项目(资助号:2022YFF1202101、2024YFC3406303、2017YFC0907503)、国家自然科学基金项目(资助号:62472120、62331012)、中国博士后科学基金项目(资助号:2022M720965)、黑龙江省博士后基金项目(资助号:lbhz22174)资助。”已删除的段落用粗体标出。此更正仅删除重复的资金,而不改变资金来源或其归属。在图2D的左侧部分,替代等位基因的模拟reads与参考等位基因的模拟reads的比例被错误地颠倒了。在最初的版本中,比例从上到下排列为“10:0,9:1,8:2,…,2:8,1:9,0:10”。但是,如图图例所示,顶部的合子对应纯合子的参考等位基因,而底部的合子代表纯合子的替代等位基因。因此,比例应该以相反的顺序列出:“0:10,1:9,2:8,…,8:2,9:1,10:0”。这一更正确保了整个手稿中等位基因比例呈现的一致性。这些值的反转不会影响图中的任何其他数据或其结论。原图2为:修改后的图2为:原文章[1]已修改。蒋涛,曹生,刘勇,等。基于准确高效的力调用方法的结构变异基因分型研究。基因工程学报。2025;26:166。https://doi.org/10.1186/s13059-025-03642-2.Article PubMed PubMed Central谷歌学者下载参考文献作者说明姜涛和曹淑琪为共同第一作者,对本文贡献相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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