2023
DOI: 10.1038/s41588-023-01308-y
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Author Correction: De novo genome assembly and analyses of 12 founder inbred lines provide insights into maize heterosis

Abstract: In the version of this article initially published, Fig. 2b was from an earlier version of the figure, with the cancer types shown in incorrect order. The figure has been amended in the HTML and PDF versions of the article.

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Cited by 3 publications
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“…The multiple sequence alignments (MSA) were computed using famsa (Deorowicz et al, 2016) from pan-genome relationships derived from the software package Pandagma (Cannon, 2023), which uses an all-vs-all approach to align the canonical transcripts in a given pan-gene group. Pandagma generated the MSA on 51 maize reference genomes including two versions of B73 (Hufford et al, 2021;Jiao et al, 2017), a set of 25 diverse maize lines called the Nested Association Mapping (NAM) panel (Hufford et al, 2021), 12 lines used in Chinese breeding programs (Wang et al, 2023), 4 European lines (Haberer et al, 2020), and an additional set of 8 high-quality maize lines available at MaizeGDB. The maize genome Zm-B73-REFERENCE-NAM-5.0 is used as the reference genome and the B73v5 annotation set contains 39,755 gene models and 75,539 transcripts.…”
Section: Pan-genome Multiple Sequence Alignmentsmentioning
confidence: 99%
“…The multiple sequence alignments (MSA) were computed using famsa (Deorowicz et al, 2016) from pan-genome relationships derived from the software package Pandagma (Cannon, 2023), which uses an all-vs-all approach to align the canonical transcripts in a given pan-gene group. Pandagma generated the MSA on 51 maize reference genomes including two versions of B73 (Hufford et al, 2021;Jiao et al, 2017), a set of 25 diverse maize lines called the Nested Association Mapping (NAM) panel (Hufford et al, 2021), 12 lines used in Chinese breeding programs (Wang et al, 2023), 4 European lines (Haberer et al, 2020), and an additional set of 8 high-quality maize lines available at MaizeGDB. The maize genome Zm-B73-REFERENCE-NAM-5.0 is used as the reference genome and the B73v5 annotation set contains 39,755 gene models and 75,539 transcripts.…”
Section: Pan-genome Multiple Sequence Alignmentsmentioning
confidence: 99%
“…In recent years, advances in sequencing technologies and bioinformatics have made pan-genome analysis feasible and affordable. The availability of multiple high-quality reference genomes and the emergence of powerful computational tools have enabled the construction and comparison of pan-genomes for various plant species (Cai et al, 2021;Li et al, 2023;Liu et al, 2020;Qin et al, 2021;Wang et al, 2023a;Wang et al, 2022b;Zhang et al, 2021). These pangenomic investigations have provided valuable insights into the evolutionary dynamics, genetic diversity, and functional variation within/among species, highlighting the importance of studying the pan-genome for a comprehensive understanding of plant biology.…”
Section: Introductionmentioning
confidence: 99%