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Comparative mitogenomics of kingdom Fungi – evolutionary insights and metagenomic applications

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4939-7804-5_15openalex-snapshot
Fungal Genome Annotation
inferredcites →https://doi.org/10.1007/s002390010220openalex-snapshot
How Mitochondria Redefine the Code
inferredcites →https://doi.org/10.1007/s002940050220openalex-snapshot
The fungal mitochondrial genome project: evolution of fungal mitochondrial genomes and their gene expression
inferredcites →https://doi.org/10.1007/s002940050234openalex-snapshot
Mitochondrial ATP synthase subunit 9 is not required for viability of the petite-negative yeast Kluyveromyces lactis
inferredcites →https://doi.org/10.1016/j.angen.2023.200161openalex-snapshot
Does Atp8 Exist in the Mitochondrial Genome of Proseriata (Metazoa: Platyhelminthes)?
inferredcites →https://doi.org/10.1016/j.cell.2012.02.035openalex-snapshot
Mitochondria: In Sickness and in Health
inferredcites →https://doi.org/10.1016/j.cub.2013.06.057openalex-snapshot
Shared Signatures of Parasitism and Phylogenomics Unite Cryptomycota and Microsporidia
inferredcites →https://doi.org/10.1016/j.cub.2016.03.053openalex-snapshot
A Eukaryote without a Mitochondrial Organelle
inferredcites →https://doi.org/10.1016/j.cub.2017.03.075openalex-snapshot
Marine Protists Are Not Just Big Bacteria
inferredcites →https://doi.org/10.1016/j.cub.2017.09.015openalex-snapshot
The Origin and Diversification of Mitochondria
inferredcites →https://doi.org/10.1016/j.funeco.2023.101274openalex-snapshot
ITS alchemy: On the use of ITS as a DNA marker in fungal ecology
inferredcites →https://doi.org/10.1016/j.funeco.2024.101383openalex-snapshot
Fungal diversity and function in metagenomes sequenced from extreme environments
inferredcites →https://doi.org/10.1016/j.margen.2010.01.001openalex-snapshot
Characterization of a mitochondrial ORF from the gender-associated mtDNAs of Mytilus spp. (Bivalvia: Mytilidae): Identification of the “missing” ATPase 8 gene
inferredcites →https://doi.org/10.1016/j.ympev.2012.08.023openalex-snapshot
MITOS: Improved de novo metazoan mitochondrial genome annotation
inferredcites →https://doi.org/10.1016/j.ympev.2018.04.037openalex-snapshot
Mt-rps3 is an ancient gene which provides insight into the evolution of fungal mitochondrial genomes
inferredcites →https://doi.org/10.1038/nature12985openalex-snapshot
Mitochondrial form and function
inferredcites →https://doi.org/10.1038/nbt.3988openalex-snapshot
MMseqs2 enables sensitive protein sequence searching for the analysis of massive data sets
inferredcites →https://doi.org/10.1038/s41559-021-01638-2openalex-snapshot
Site-and-branch-heterogeneous analyses of an expanded dataset favour mitochondria as sister to known Alphaproteobacteria
inferredcites →https://doi.org/10.1038/s41576-018-0035-9openalex-snapshot
Cytonuclear integration and co-evolution
inferredcites →https://doi.org/10.1038/s41598-018-25759-0openalex-snapshot
The bipartite mitochondrial genome of Ruizia karukerae (Rhigonematomorpha, Nematoda)
inferredcites →https://doi.org/10.1038/s41598-022-09512-2openalex-snapshot
Comparative genomic analysis of vertebrate mitochondrial reveals a differential of rearrangements rate between taxonomic class
inferredcites →https://doi.org/10.1073/pnas.1017351108openalex-snapshot
High-quality draft assemblies of mammalian genomes from massively parallel sequence data
inferredcites →https://doi.org/10.1073/pnas.1410442111openalex-snapshot
Evolution of a morphological novelty occurred before genome compaction in a lineage of extreme parasites
inferredcites →https://doi.org/10.1073/pnas.1604560113openalex-snapshot
Assembly of long error-prone reads using de Bruijn graphs
inferredcites →https://doi.org/10.1093/bioinformatics/bth352openalex-snapshot
Automatic annotation of organellar genomes with DOGMA
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp348openalex-snapshot
trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses
inferredcites →https://doi.org/10.1093/bioinformatics/btt509openalex-snapshot
Infernal 1.1: 100-fold faster RNA homology searches
inferredcites →https://doi.org/10.1093/femsyr/fov023openalex-snapshot
Mitochondrial genome evolution in yeasts: an all-encompassing view
inferredcites →https://doi.org/10.1093/g3journal/jkac285openalex-snapshot
Evolution and codon usage bias of mitochondrial and nuclear genomes in Aspergillus section Flavi
inferredcites →https://doi.org/10.1093/gbe/evaa126openalex-snapshot
The Coevolution of Fungal Mitochondrial Introns and Their Homing Endonucleases (GIY-YIG and LAGLIDADG)
inferredcites →https://doi.org/10.1093/gbe/evu028openalex-snapshot
High Variability of Mitochondrial Gene Order among Fungi
inferredcites →https://doi.org/10.1093/icb/icz025openalex-snapshot
Mitochondria and the Origin of Species: Bridging Genetic and Ecological Perspectives on Speciation Processes
inferredcites →https://doi.org/10.1093/molbev/msaa015openalex-snapshot
IQ-TREE 2: New Models and Efficient Methods for Phylogenetic Inference in the Genomic Era
inferredcites →https://doi.org/10.1093/molbev/msp077openalex-snapshot
FastTree: Computing Large Minimum Evolution Trees with Profiles instead of a Distance Matrix
inferredcites →https://doi.org/10.1093/molbev/msr025openalex-snapshot
Two Nuclear Life Cycle-Regulated Genes Encode Interchangeable Subunits c of Mitochondrial ATP Synthase in Podospora anserina
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/msx197openalex-snapshot
Large Variation in the Ratio of Mitochondrial to Nuclear Mutation Rate across Animals: Implications for Genetic Diversity and the Use of Mitochondrial DNA as a Molecular Marker
inferredcites →https://doi.org/10.1093/nar/25.3.626openalex-snapshot
Mitochondrial tRNAs in the lower fungus Spizellomyces punctatus: tRNA editing and UAG 'stop' codons recognized as leucine
inferredcites →https://doi.org/10.1093/nar/25.5.955openalex-snapshot
tRNAscan-SE: A Program for Improved Detection of Transfer RNA Genes in Genomic Sequence
inferredcites →https://doi.org/10.1093/nar/gkaa1047openalex-snapshot
Rfam 14: expanded coverage of metagenomic, viral and microRNA families
inferredcites →https://doi.org/10.1093/nar/gkaa913openalex-snapshot
Pfam: The protein families database in 2021
inferredcites →https://doi.org/10.1093/nar/gkac278openalex-snapshot
DeepLoc 2.0: multi-label subcellular localization prediction using protein language models
inferredcites →https://doi.org/10.1093/nar/gkac976openalex-snapshot
The IMG/M data management and analysis system v.7: content updates and new features
inferredcites →https://doi.org/10.1093/nar/gkg264openalex-snapshot
Evolution of monoblepharidalean fungi based on complete mitochondrial genome sequences
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/gks1160openalex-snapshot
The Protist Ribosomal Reference database (PR2): a catalog of unicellular eukaryote Small Sub-Unit rRNA sequences with curated taxonomy
inferredcites →https://doi.org/10.1093/nar/gks1219openalex-snapshot
The SILVA ribosomal RNA gene database project: improved data processing and web-based tools
inferredcites →https://doi.org/10.1093/nar/gkt1183openalex-snapshot
MycoCosm portal: gearing up for 1000 fungal genomes
inferredcites →https://doi.org/10.1093/nar/gku1063openalex-snapshot
Rfam 12.0: updates to the RNA families database
inferredcites →https://doi.org/10.1093/nar/gkz173openalex-snapshot
MitoZ: a toolkit for animal mitochondrial genome assembly, annotation and visualization
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004084openalex-snapshot
Hyaloraphidium curvatum: A Linear Mitochondrial Genome, tRNA Editing, and an Evolutionary Link to Lower Fungi
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026334openalex-snapshot
Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis
inferredcites →https://doi.org/10.1101/gr.074492.107openalex-snapshot
Velvet: Algorithms for de novo short read assembly using de Bruijn graphs
inferredcites →https://doi.org/10.1101/gr.092759.109openalex-snapshot
Circos: An information aesthetic for comparative genomics
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01492.xopenalex-snapshot
Inheritance and recombination of mitochondrial genomes in plants, fungi and animals
inferredcites →https://doi.org/10.1111/mec.13195openalex-snapshot
Phylogenetic community ecology of soil biodiversity using mitochondrial metagenomics
inferredcites →https://doi.org/10.1111/nyas.13222openalex-snapshot
Dissecting genome reduction and trait loss in insect endosymbionts
inferredcites →https://doi.org/10.1126/sciadv.abd0079openalex-snapshot
Genome-scale phylogeny and contrasting modes of genome evolution in the fungal phylum Ascomycota
inferredcites →https://doi.org/10.1128/mbio.01676-23openalex-snapshot
Eukaryotic genomes from a global metagenomic data set illuminate trophic modes and biogeography of ocean plankton
inferredcites →https://doi.org/10.1137/040608635openalex-snapshot
Graph Clustering Via a Discrete Uncoupling Process
inferredcites →https://doi.org/10.1146/annurev-biochem-060109-092838openalex-snapshot
Mitochondrial tRNA Import and Its Consequences for Mitochondrial Translation
inferredcites →https://doi.org/10.1371/journal.pgen.1002876openalex-snapshot
Experimental Relocation of the Mitochondrial ATP9 Gene to the Nucleus Reveals Forces Underlying Mitochondrial Genome Evolution
inferredcites →https://doi.org/10.1371/journal.pgen.1008304openalex-snapshot
Variation and selection on codon usage bias across an entire subphylum
inferredcites →https://doi.org/10.1371/journal.pone.0009490openalex-snapshot
FastTree 2 – Approximately Maximum-Likelihood Trees for Large Alignments
inferredcites →https://doi.org/10.1371/journal.pone.0120081openalex-snapshot
Evolutionary Analysis of Mitogenomes from Parasitic and Free-Living Flatworms
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/fmicb.2014.00278openalex-snapshot
Parasites in algae mass culture
inferredcites →https://doi.org/10.3389/fmicb.2020.00765openalex-snapshot
Exploring the Relationship Among Divergence Time and Coding and Non-coding Elements in the Shaping of Fungal Mitochondrial Genomes
inferredcites →https://doi.org/10.3389/fmicb.2021.647989openalex-snapshot
Pan-Mitogenomics Approach Discovers Diversity and Dynamism in the Prominent Brown Rot Fungal Pathogens
inferredcites →https://doi.org/10.3389/fmicb.2021.787283openalex-snapshot
Global Characterization of Fungal Mitogenomes: New Insights on Genomic Diversity and Dynamism of Coding Genes and Accessory Elements
inferredcites →https://doi.org/10.3389/fpls.2023.1222186openalex-snapshot
Mitochondrial genome annotation with MFannot: a critical analysis of gene identification and gene model prediction
inferredcites →https://doi.org/10.3390/ijms21020483openalex-snapshot
Subchromosome-Scale Nuclear and Complete Mitochondrial Genome Characteristics of Morchella crassipes
inferredcites →https://doi.org/10.7717/peerj.2584openalex-snapshot
VSEARCH: a versatile open source tool for metagenomics
inferredcites →https://doi.org/10.7717/peerj.7359openalex-snapshot
MetaBAT 2: an adaptive binning algorithm for robust and efficient genome reconstruction from metagenome assemblies

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/mycokeys.140.205520zenodo-depositor-declared
Assembly and comparative analysis of the complete mitochondrial genomes of five Thaxterogaster species (Cortinariaceae, Basidiomycota): Insights into mitochondrial genome evolution and intrageneric phylogenetic relationships
inferred← citeshttps://doi.org/10.1016/j.fgb.2026.104104openalex-snapshot
An exceptionally large, intron-rich mitochondrial genome and complex RNA processing in the desert-dwelling fungus Helvella bachu
inferred← citeshttps://doi.org/10.1093/g3journal/jkag237openalex-snapshot
Genomic characterization of the endangered medicinal polypore agarikon ( Laricifomes officinalis syn. Fomitopsis officinalis )
inferred← citeshttps://doi.org/10.3390/jof12090648openalex-snapshot
The Complete Mitogenome of Alternaria brassicae Causing Black Spot Disease on Rapeseed-Mustard
inferred← citeshttps://doi.org/10.3390/jof12100729openalex-snapshot
Intron-Associated Mitogenome Size Variation and Gene-Specific Stop Codon Absence in the Lichen-Forming Genus Ramalina
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