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    Sequence and assembly

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    • Contigs
      Track showing underlying assembly contigs.
    • Sequence
      Track showing sequence in both directions. Only displayed at 1Kb and below.

    GRC alignments

    • FGENESH prediction
      This track comprises multiple analyses; Covariance models from Rfam (release 12.2), aligned to the genome with 'cmscan' from the Infernal suite of programs. Models are restricted to those observed in species that share a last common ancestor (LCA).; tRNA models predicted with tRNAscan-SE (release 1.3.1).
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    • FGENESH prediction
      This track comprises multiple analyses; misc_feature feature annotated in ENA; intron feature annotated in ENA; mRNA feature annotated in ENA; exon feature annotated in ENA

    Genes and transcripts

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    • Genes (Genes (Ensembl))
      This track comprises multiple analyses; Chloroplast protein-coding genes imported from Genbank.; Genes by The Rice Annotation Project (RAP) dated 2022-09-01.; Mitochondrial gene models imported from Genbank.
    • Rfam RNA Genes (Genes)
      RNA genes produced by filtering alignments of Rfam (release 12.2) covariance models.
    • ncRNA Genes (Genes)
      ncRNA genes annotated in ENA
    • tRNA Genes (Genes)
      RNA genes produced by filtering predictions from tRNAscan-SE v1.23.
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    • FGENESH prediction
      Ab initio prediction of protein coding genes, based on the genomic sequence alone AA Salamov et al., Genome Res. 2000 4:516-22.
    • MSU7 TE-related genes
      TE-related Gene annotation by MSU through a process of automatic and manual curation
    • FGENESH prediction
      This track comprises multiple analyses; TE-related Gene annotation by MSU through a process of automatic and manual curation; Fgenesh is a fast and accurate HMM-based ab-initio gene prediction program Salamov AA, Solovyev VV. Genome Res. 2000

    mRNA and protein alignments

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        Comparative genomics

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          Variation

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          • Sequence variants (all sources) (Variant - All sources)
            Sequence variants from all sources
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              • Smaller structural variants (all sources) (SV - Smaller variants)
                Structural variants from all sources which are less than 1Mb in length. The colours correspond to the structural variant classes.
                For an explanation of the display, see the dbVar documentation.

              Repeat regions

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                Information and decorations

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                • Chromosome bands
                  Cytogenetic bands
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                • Information ()
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