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De novoAssembly and Comparative Analyses of Mitochondrial Genomes in Piperales
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajb2.1286openalex-snapshot
Sequential horizontal gene transfers from different hosts in a widespread Eurasian parasitic plant, Cynomorium coccineum
inferredcites →https://doi.org/10.1007/978-3-7091-1130-7_9openalex-snapshot
Plant Mitochondrial Genome Diversity: The Genomics Revolution
inferredcites →https://doi.org/10.1007/s00239-004-2606-yopenalex-snapshot
Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron
inferredcites →https://doi.org/10.1007/s00239-004-5951-yopenalex-snapshot
Many Independent Origins of trans Splicing of a Plant Mitochondrial Group II Intron
inferredcites →https://doi.org/10.1007/s00294-010-0290-6openalex-snapshot
Comparison of mitochondrial and chloroplast genome segments from three onion (Allium cepa L.) cytoplasm types and identification of a trans-splicing intron of cox2
inferredcites →https://doi.org/10.1007/s11103-018-0734-9openalex-snapshot
Towards a comprehensive picture of C-to-U RNA editing sites in angiosperm mitochondria
inferredcites →https://doi.org/10.1007/s11103-020-01014-xopenalex-snapshot
Multichromosomal structure and foreign tracts in the Ombrophytum subterraneum (Balanophoraceae) mitochondrial genome
inferredcites →https://doi.org/10.1007/s40415-021-00704-0openalex-snapshot
A living bridge between two enemies: haustorium structure and evolution across parasitic flowering plants
inferredcites →https://doi.org/10.1016/bs.abr.2017.11.013openalex-snapshot
Structural Diversity Among Plastid Genomes of Land Plants
inferredcites →https://doi.org/10.1016/j.mito.2020.03.007openalex-snapshot
Interchangeable parts: The evolutionarily dynamic tRNA population in plant mitochondria
inferredcites →https://doi.org/10.1016/j.mito.2020.06.002openalex-snapshot
Variation in protein gene and intron content among land plant mitogenomes
inferredcites →https://doi.org/10.1016/j.molp.2018.11.002openalex-snapshot
Tension and Resolution: Dynamic, Evolving Populations of Organelle Genomes within Plant Cells
inferredcites →https://doi.org/10.1016/j.pbi.2015.05.008openalex-snapshot
Horizontal gene transfer in parasitic plants
inferredcites →https://doi.org/10.1016/j.xplc.2020.100027openalex-snapshot
Phylogenomic Insights into Deep Phylogeny of Angiosperms Based on Broad Nuclear Gene Sampling
inferredcites →https://doi.org/10.1016/j.ympev.2008.09.009openalex-snapshot
Relative rates of synonymous substitutions in the mitochondrial, chloroplast and nuclear genomes of seed plants
inferredcites →https://doi.org/10.1016/j.ympev.2019.05.012openalex-snapshot
The complete organelle genomes of Physochlaina orientalis: Insights into short sequence repeats across seed plant mitochondrial genomes
inferredcites →https://doi.org/10.1038/nmeth.1923openalex-snapshot
Fast gapped-read alignment with Bowtie 2
inferredcites →https://doi.org/10.1038/nmeth.4285openalex-snapshot
ModelFinder: fast model selection for accurate phylogenetic estimates
inferredcites →https://doi.org/10.1038/s41437-018-0153-3openalex-snapshot
Recombination and intraspecific polymorphism for the presence and absence of entire chromosomes in mitochondrial genomes
inferredcites →https://doi.org/10.1038/s41467-020-20507-3openalex-snapshot
Genome-wide macroevolutionary signatures of key innovations in butterflies colonizing new host plants
inferredcites →https://doi.org/10.1038/s41477-021-00990-2openalex-snapshot
Insights into angiosperm evolution, floral development and chemical biosynthesis from the Aristolochia fimbriata genome
inferredcites →https://doi.org/10.1038/s41586-022-04823-wopenalex-snapshot
Synonymous mutations in representative yeast genes are mostly strongly non-neutral
inferredcites →https://doi.org/10.1073/pnas.1504491112openalex-snapshot
Miniaturized mitogenome of the parasitic plant Viscum scurruloideum is extremely divergent and dynamic and has lost all nad genes
inferredcites →https://doi.org/10.1073/pnas.1704536114openalex-snapshot
Stem parasitic plant Cuscuta australis (dodder) transfers herbivory-induced signals among plants
inferredcites →https://doi.org/10.1073/pnas.2001998117openalex-snapshot
MSH1 is required for maintenance of the low mutation rates in plant mitochondrial and plastid genomes
inferredcites →https://doi.org/10.1073/pnas.95.24.14244openalex-snapshot
Explosive invasion of plant mitochondria by a group I intron
inferredcites →https://doi.org/10.1093/aob/mcab033openalex-snapshot
Gene expression underlying floral epidermal specialization in Aristolochia fimbriata (Aristolochiaceae)
inferredcites →https://doi.org/10.1093/aob/mcu044openalex-snapshot
Major trends in stem anatomy and growth forms in the perianth-bearing Piperales, with special focus on Aristolochia
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1093/bioinformatics/bty191openalex-snapshot
Minimap2: pairwise alignment for nucleotide sequences
inferredcites →https://doi.org/10.1093/bioinformatics/btz305openalex-snapshot
RAxML-NG: a fast, scalable and user-friendly tool for maximum likelihood phylogenetic inference
inferredcites →https://doi.org/10.1093/gbe/evt069openalex-snapshot
Plant Mitochondrial Genome Evolution Can Be Explained by DNA Repair Mechanisms
inferredcites →https://doi.org/10.1093/gbe/evu253openalex-snapshot
History of Plastid DNA Insertions Reveals Weak Deletion and AT Mutation Biases in Angiosperm Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/gbe/evv256openalex-snapshot
Detecting and Characterizing the Highly Divergent Plastid Genome of the Nonphotosynthetic Parasitic PlantHydnora visseri(Hydnoraceae)
inferredcites →https://doi.org/10.1093/gbe/evz263openalex-snapshot
The Mitogenome of Norway Spruce and a Reappraisal of Mitochondrial Recombination in Plants
inferredcites →https://doi.org/10.1093/genetics/iyab039openalex-snapshot
Detecting de novo mitochondrial mutations in angiosperms with highly divergent evolutionary rates
inferredcites →https://doi.org/10.1093/hr/uhac005openalex-snapshot
Chromosome-level genome assembly of Aristolochia contorta provides insights into the biosynthesis of benzylisoquinoline alkaloids and aristolochic acids
inferredcites →https://doi.org/10.1093/molbev/msaa029openalex-snapshot
Extensive Shifts from Cis- to Trans-splicing of Gymnosperm Mitochondrial Introns
inferredcites →https://doi.org/10.1093/molbev/msm088openalex-snapshot
PAML 4: Phylogenetic Analysis by Maximum Likelihood
inferredcites →https://doi.org/10.1093/molbev/msm241openalex-snapshot
Reevaluation of the cox1 Group I Intron in Araceae and Angiosperms Indicates a History Dominated by Loss rather than Horizontal Transfer
inferredcites →https://doi.org/10.1093/molbev/msn129openalex-snapshot
Frequent, Phylogenetically Local Horizontal Transfer of the cox1 Group I Intron in Flowering Plant Mitochondria
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/molbev/msw024openalex-snapshot
GinkgoandWelwitschiaMitogenomes Reveal Extreme Contrasts in Gymnosperm Mitochondrial Evolution
inferredcites →https://doi.org/10.1093/molbev/msy096openalex-snapshot
MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms
inferredcites →https://doi.org/10.1093/molbev/msy176openalex-snapshot
High and Variable Rates of Repeat-Mediated Mitochondrial Genome Rearrangement in a Genus of Plants
inferredcites →https://doi.org/10.1093/molbev/msz198openalex-snapshot
Ancient Mitochondrial Gene Transfer between Fungi and the Orchids
inferredcites →https://doi.org/10.1093/nar/gkab688openalex-snapshot
tRNAscan-SE 2.0: improved detection and functional classification of transfer RNA genes
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkl315openalex-snapshot
PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040567openalex-snapshot
Statistical tests for detecting gene conversion.
inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot
MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space
inferredcites →https://doi.org/10.1101/gr.215087.116openalex-snapshot
Canu: scalable and accurate long-read assembly via adaptive k -mer weighting and repeat separation
inferredcites →https://doi.org/10.1105/tpc.111.087189openalex-snapshot
Origins and Recombination of the Bacterial-Sized Multichromosomal Mitochondrial Genome of Cucumber
inferredcites →https://doi.org/10.1111/ede.12282openalex-snapshot
Floral MADS‐box protein interactions in the early diverging angiosperm Aristolochia fimbriata Cham. (Aristolochiaceae: Piperales)
inferredcites →https://doi.org/10.1111/jse.12708openalex-snapshot
Mitochondrial genes from 18 angiosperms fill sampling gaps for phylogenomic inferences of the early diversification of flowering plants
inferredcites →https://doi.org/10.1111/nph.12395openalex-snapshot
One ring to rule them all? Genome sequencing provides new insights into the ‘master circle’ model of plant mitochondrial DNA structure
inferredcites →https://doi.org/10.1111/nph.13467openalex-snapshot
Dynamic evolution of Geranium mitochondrial genomes through multiple horizontal and intracellular gene transfers
inferredcites →https://doi.org/10.1111/nph.14361openalex-snapshot
Unparalleled replacement of native mitochondrial genes by foreign homologs in a holoparasitic plant
inferredcites →https://doi.org/10.1111/nph.18334openalex-snapshot
Fragaria mitogenomes evolve rapidly in structure but slowly in sequence and incur frequent multinucleotide mutations mediated by microinversions
inferredcites →https://doi.org/10.1126/scitranslmed.3006200openalex-snapshot
Mutational Signature of Aristolochic Acid Exposure as Revealed by Whole-Exome Sequencing
inferredcites →https://doi.org/10.1186/1471-2105-13-238openalex-snapshot
Mapping single molecule sequencing reads using basic local alignment with successive refinement (BLASR): application and theory
inferredcites →https://doi.org/10.1186/1471-2148-7-248openalex-snapshot
Mitochondrial DNA suggests at least 11 origins of parasitism in angiosperms and reveals genomic chimerism in parasitic plants
inferredcites →https://doi.org/10.1186/1741-7007-11-29openalex-snapshot
The “fossilized” mitochondrial genome of Liriodendron tulipifera: ancestral gene content and order, ancestral editing sites, and extraordinarily low mutation rate
inferredcites →https://doi.org/10.1186/1741-7007-8-150openalex-snapshot
Horizontal acquisition of multiple mitochondrial genes from a parasitic plant followed by gene conversion with host mitochondrial genes
inferredcites →https://doi.org/10.1186/s12864-018-4991-4openalex-snapshot
The complete mitochondrial genome of the early flowering plant Nymphaea colorata is highly repetitive with low recombination
inferredcites →https://doi.org/10.1186/s12870-017-0992-8openalex-snapshot
Comparative mitogenomics indicates respiratory competence in parasitic Viscum despite loss of complex I and extreme sequence divergence, and reveals horizontal gene transfer and remarkable variation in genome size
inferredcites →https://doi.org/10.1186/s12915-022-01250-1openalex-snapshot
Unprecedented organelle genomic variations in morning glories reveal independent evolutionary scenarios of parasitic plants and the diversification of plant mitochondrial complexes
inferredcites →https://doi.org/10.1186/s12915-022-01383-3openalex-snapshot
Rearrangement and domestication as drivers of Rosaceae mitogenome plasticity
inferredcites →https://doi.org/10.1186/s13007-019-0435-7openalex-snapshot
PGA: a software package for rapid, accurate, and flexible batch annotation of plastomes
inferredcites →https://doi.org/10.1186/s13059-020-02154-5openalex-snapshot
GetOrganelle: a fast and versatile toolkit for accurate de novo assembly of organelle genomes
inferredcites →https://doi.org/10.1371/journal.pbio.1001241openalex-snapshot
Rapid Evolution of Enormous, Multichromosomal Genomes in Flowering Plant Mitochondria with Exceptionally High Mutation Rates
inferredcites →https://doi.org/10.1371/journal.pcbi.1005595openalex-snapshot
Unicycler: Resolving bacterial genome assemblies from short and long sequencing reads
inferredcites →https://doi.org/10.1371/journal.pgen.1003265openalex-snapshot
Massive Mitochondrial Gene Transfer in a Parasitic Flowering Plant Clade
inferredcites →https://doi.org/10.1371/journal.pone.0231020openalex-snapshot
The draft mitochondrial genome of Magnolia biondii and mitochondrial phylogenomics of angiosperms
inferredcites →https://doi.org/10.1534/g3.118.200948openalex-snapshot
Repeats of Unusual Size in Plant Mitochondrial Genomes: Identification, Incidence and Evolution
inferredcites →https://doi.org/10.3389/fonc.2021.828314openalex-snapshot
High Level of Aristolochic Acid Detected With a Unique Genomic Landscape Predicts Early UTUC Onset After Renal Transplantation in Taiwan
inferredcites →https://doi.org/10.3389/fphar.2019.00648openalex-snapshot
Systematic Overview of Aristolochic Acids: Nephrotoxicity, Carcinogenicity, and Underlying Mechanisms
inferredcites →https://doi.org/10.3389/fpls.2021.642598openalex-snapshot
Discordant Phylogenomic Placement of Hydnoraceae and Lactoridaceae Within Piperales Using Data From All Three Genomes
inferredcites →https://doi.org/10.3390/plants9030306openalex-snapshot
The First Plastid Genome of the Holoparasitic Genus Prosopanche (Hydnoraceae)
inferredcites →https://doi.org/10.7717/peerj.12260openalex-snapshot
Shifts from cis-to trans-splicing of five mitochondrial introns in Tolypanthus maclurei
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.141848zenodo-depositor-declared
Comparative mitogenomic analysis reveals variations and evolution of ectomycorrhizal fungal Strobilomyces
inferred← citeshttps://doi.org/10.1002/ajb2.16300openalex-snapshot
A comparative analysis of plastome evolution in autotrophic Piperales
inferred← citeshttps://doi.org/10.1002/ece3.71737openalex-snapshot
Altered Mitochondrial Respiration Is Associated With Loss of Nuclear‐Encoded OXPHOS Genes in Parasitic Broomrapes
inferred← citeshttps://doi.org/10.1007/s00227-024-04424-3openalex-snapshot
A foundation for comparative genomics and evolutionary studies in Nucella lapillus based on complete mitogenome assembly
inferred← citeshttps://doi.org/10.1007/s11033-023-09184-9openalex-snapshot
Mitochondrial genome of Hancornia speciosa gomes: intergenic regions containing retrotransposons and predicted genes
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.121817openalex-snapshot
Structural variations and phylogenetic implications of mitochondrial genomes in oaks
inferred← citeshttps://doi.org/10.1016/j.pld.2023.11.001openalex-snapshot
The first mitogenome of Lauraceae (Cinnamomum chekiangense)
inferred← citeshttps://doi.org/10.1016/j.pld.2025.10.003openalex-snapshot
Dissecting mitogenomic conflict to illuminate angiosperm deep phylogeny: Sequence and architectural evidence
inferred← citeshttps://doi.org/10.1016/j.ygeno.2026.111281openalex-snapshot
The large mitochondrial genome of Syndiclis anlungensis (Lauraceae): Genome structure, comparative analysis, and phylogenetic relationships among Syndiclis species
inferred← citeshttps://doi.org/10.1038/s41598-025-26696-5openalex-snapshot
Complete mitochondrial genome of Persicaria maackiana reveals genome features, phylogenetic relationships, and nucleotide substitution rates
inferred← citeshttps://doi.org/10.1038/s42003-025-08418-9openalex-snapshot
Evolution of mitochondrial RNA editing sites and stop codon-lacking transcripts in angiosperms
inferred← citeshttps://doi.org/10.1093/aob/mcad108openalex-snapshot
Invited Review Beyond parasitic convergence: unravelling the evolution of the organellar genomes in holoparasites
inferred← citeshttps://doi.org/10.1093/gbe/evag025openalex-snapshot
Recombination and Retroprocessing in Broomrapes Reveal RNA-Mediated Gene Transfer Mechanism and a Generalizable Model for Mitochondrial Evolution in Heterotrophic Plants
inferred← citeshttps://doi.org/10.1093/jxb/erae034openalex-snapshot
Methods for assembling complex mitochondrial genomes in land plants
inferred← citeshttps://doi.org/10.1093/molbev/msaf082openalex-snapshot
Unequally Abundant Chromosomes and Unusual Collections of Transferred Sequences Characterize Mitochondrial Genomes of Gastrodia (Orchidaceae), One of the Largest Mycoheterotrophic Plant Genera
inferred← citeshttps://doi.org/10.1093/pcp/pcae120openalex-snapshot
Mitochondrial Splicing Efficiency Is Lower in Holoparasites Than in Free-Living Plants
inferred← citeshttps://doi.org/10.1093/pcp/pcag009openalex-snapshot
Progress and prospects of parasitic plant biodiversity genomics
inferred← citeshttps://doi.org/10.1101/2024.12.09.626742openalex-snapshot
Diverging repeatomes in holoparasitic Hydnoraceae uncover a playground of genome evolution
inferred← citeshttps://doi.org/10.1101/2025.02.14.637881openalex-snapshot
Recombination and retroprocessing in broomrapes reveal a universal roadmap for mitochondrial evolution in heterotrophic plants
inferred← citeshttps://doi.org/10.1101/2025.06.25.661533openalex-snapshot
Circle-Mediated HGT shapes the multichromosomal mitochondrial genome of the endoparasite Mitrastemon yamamotoi
inferred← citeshttps://doi.org/10.1101/2025.11.14.688545openalex-snapshot
A structural solution to functional HGT: Gene chimerism bypasses mitochondrial expression barriers in parasitic plants
inferred← citeshttps://doi.org/10.1111/nph.70280openalex-snapshot
Diverging repeatomes in holoparasitic Hydnoraceae uncover a playground of genome evolution
inferred← citeshttps://doi.org/10.1111/pbi.70249openalex-snapshot
Advance in the assembly of the plant mitochondrial genomes using high‐throughput DNA sequencing data of total cellular DNAs
inferred← citeshttps://doi.org/10.1111/tpj.70889openalex-snapshot
Circle‐mediated HGT shapes the multichromosomal mitochondrial genome of the endoparasitic plant Mitrastemon yamamotoi
inferred← citeshttps://doi.org/10.1186/s12859-023-05445-3openalex-snapshot
A systematic comparison of human mitochondrial genome assembly tools
inferred← citeshttps://doi.org/10.1186/s12864-024-10818-wopenalex-snapshot
Complete mitochondrial genome assembly of Juglans regia unveiled its molecular characteristics, genome evolution, and phylogenetic implications
inferred← citeshttps://doi.org/10.1186/s12864-024-11184-3openalex-snapshot
Comprehensive analysis of the multi-rings mitochondrial genome of Populus tomentosa
inferred← citeshttps://doi.org/10.1186/s12864-026-13153-4openalex-snapshot
Assembly of the complete mitochondrial genome of Ligusticum chuanxiong and its evolutionary implications
inferred← citeshttps://doi.org/10.1186/s12870-023-04377-7openalex-snapshot
Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution
inferred← citeshttps://doi.org/10.1186/s12870-024-05050-3openalex-snapshot
Phylogenetic incongruence in an Asiatic species complex of the genus Caryodaphnopsis (Lauraceae)
inferred← citeshttps://doi.org/10.1186/s12870-024-05765-3openalex-snapshot
Assembly and comparative analysis of the multichromosomal mitochondrial genome of globally endangered seagrass Halophila beccarii
inferred← citeshttps://doi.org/10.1186/s12870-025-06801-6openalex-snapshot
Complete mitochondrial genome of Houttuynia cordata sheds light on the evolution of complex structural features in early angiosperms
inferred← citeshttps://doi.org/10.1186/s12870-025-06839-6openalex-snapshot
Assembly and comparative analysis of the complete mitochondrial genome of the spice plant Cinnamomum longepaniculatum
inferred← citeshttps://doi.org/10.1186/s12915-024-02040-7openalex-snapshot
New insights into the phylogenetic relationships within the Lauraceae from mitogenomes
inferred← citeshttps://doi.org/10.1186/s12915-025-02449-8openalex-snapshot
A record-setting mitogenome in the holoparasitic plant Balanophora yakushimensis accompanied by exceptional loss of organellar DNA repair and recombination genes
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2023-0301openalex-snapshot
The mitogenomic landscape of Banisteriopsis caapi (Malpighiaceae), the sacred liana used for ayahuasca preparation
inferred← citeshttps://doi.org/10.3389/fpls.2024.1509669openalex-snapshot
Features and evolutionary adaptations of the mitochondrial genome of Garuga forrestii W. W. Sm
inferred← citeshttps://doi.org/10.3390/agronomy13082103openalex-snapshot
Complete Mitochondrial Genome Sequence, Characteristics, and Phylogenetic Analysis of Oenanthe javanica
inferred← citeshttps://doi.org/10.3390/biology14080975openalex-snapshot
Organelle Genome Characteristics and Phylogenetic Analysis of a Warm-Season Turfgrass Eremochloa ophiuroides (Poaceae)
inferred← citeshttps://doi.org/10.3390/biology14091219openalex-snapshot
Organelle Genomes of Nardostachys jatamansi Offer New Perspectives into the Evolutionary Dynamics of Caprifoliaceae
inferred← citeshttps://doi.org/10.3390/biom15030343openalex-snapshot
The Complete Mitochondrial Genome of Thymus mongolicus and Its Phylogenetic Relationship with Lamiaceae Species
inferred← citeshttps://doi.org/10.3390/f15071117openalex-snapshot
Assembly and Comparative Analysis of the Complete Mitochondrial Genome of Ilex rotunda Thunb.
inferred← citeshttps://doi.org/10.3390/life14020182openalex-snapshot
Characterization of the Complete Mitochondrial Genome of Wintersweet (Chimonanthus praecox) and Comparative Analysis within Magnoliids
inferred← citeshttps://doi.org/10.3390/plants15071121openalex-snapshot
Genomic Footprints of Multiple Host Lineages in the Mitochondrial and Nuclear Genomes of the Holoparasite Prosopanche americana
inferred← citeshttps://doi.org/10.48130/gcomm-0026-0003openalex-snapshot
Rapid turnover of mitogenomic repeats and congruent phylogenomic signal among Digitalideae genomes
inferred← citeshttps://doi.org/10.6084/m9.figshare.23949750openalex-snapshot
Additional file 1 of Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution
inferred← citeshttps://doi.org/10.6084/m9.figshare.23949753openalex-snapshot
Additional file 2 of Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution
inferred← citeshttps://doi.org/10.6084/m9.figshare.23949756openalex-snapshot
Additional file 3 of Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution
inferred← citeshttps://doi.org/10.6084/m9.figshare.23949759openalex-snapshot
Additional file 4 of Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution
inferred← citeshttps://doi.org/10.6084/m9.figshare.23949762openalex-snapshot
Additional file 5 of Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617168openalex-snapshot
Additional file 1 of A systematic comparison of human mitochondrial genome assembly tools
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617171openalex-snapshot
Additional file 2 of A systematic comparison of human mitochondrial genome assembly tools
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617174openalex-snapshot
Additional file 3 of A systematic comparison of human mitochondrial genome assembly tools
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