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Subchromosome-Scale Nuclear and Complete Mitochondrial Genome Characteristics of Morchella crassipes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471250953.bi0410s05openalex-snapshot
Using Repeat Masker to Identify Repetitive Elements in Genomic Sequences
inferredcites →https://doi.org/10.1002/0471250953.bi0410s25openalex-snapshot
Using RepeatMasker to Identify Repetitive Elements in Genomic Sequences
inferredcites →https://doi.org/10.1007/978-3-642-21878-1_22openalex-snapshot
ProtTest-HPC: Fast Selection of Best-Fit Models of Protein Evolution
inferredcites →https://doi.org/10.1007/pl00009992openalex-snapshot
Mycorrhiza-like interaction by Morchella with species of the Pinaceae in pure culture synthesis
inferredcites →https://doi.org/10.1007/s00449-012-0720-6openalex-snapshot
Production, characterization and antioxidant activity of exopolysaccharides from submerged culture of Morchella crassipes
inferredcites →https://doi.org/10.1007/s11557-017-1309-xopenalex-snapshot
Characterization of mating-type idiomorphs suggests that Morchella importuna, Mel-20 and M. sextelata are heterothallic
inferredcites →https://doi.org/10.1016/j.fgb.2010.09.006openalex-snapshot
Phylogeny and historical biogeography of true morels (Morchella) reveals an early Cretaceous origin and high continental endemism and provincialism in the Holarctic
inferredcites →https://doi.org/10.1016/j.ijbiomac.2019.12.056openalex-snapshot
The mitochondrial genome of Morchella importuna (272.2 kb) is the largest among fungi and contains numerous introns, mitochondrial non-conserved open reading frames and repetitive sequences
inferredcites →https://doi.org/10.1016/j.micron.2015.07.010openalex-snapshot
Morphological and ultrastructural examination of senescence in Morchella elata
inferredcites →https://doi.org/10.1016/j.micron.2017.06.012openalex-snapshot
Live cell confocal laser imaging studies on the nuclear behavior during meiosis and ascosporogenesis in Morchella importuna under artificial cultivation
inferredcites →https://doi.org/10.1016/j.micron.2018.03.005openalex-snapshot
Involvement of autophagy and apoptosis and lipid accumulation in sclerotial morphogenesis of Morchella importuna
inferredcites →https://doi.org/10.1016/j.tem.2015.12.001openalex-snapshot
Mitochondrial Dynamics and Metabolic Regulation
inferredcites →https://doi.org/10.1016/j.tig.2003.10.012openalex-snapshot
Mitochondrial genomes: anything goes
inferredcites →https://doi.org/10.1016/s0007-1536(87)80162-6openalex-snapshot
Association between living roots and ascocarps of Morchella rotunda
inferredcites →https://doi.org/10.1016/s0176-1617(11)80845-xopenalex-snapshot
Synthesis of two types of association between Morchella esculenta and Picea abies under controlled culture conditions
inferredcites →https://doi.org/10.1038/nature08867openalex-snapshot
Périgord black truffle genome uncovers evolutionary origins and mechanisms of symbiosis
inferredcites →https://doi.org/10.1038/nmeth.3317openalex-snapshot
HISAT: a fast spliced aligner with low memory requirements
inferredcites →https://doi.org/10.1038/s41598-017-01682-8openalex-snapshot
Mixed-reproductive strategies, competitive mating-type distribution and life cycle of fourteen black morel species
inferredcites →https://doi.org/10.1038/srep13892openalex-snapshot
Complete mitochondrial genome of the medicinal fungus Ophiocordyceps sinensis
inferredcites →https://doi.org/10.1038/srep31900openalex-snapshot
DBG2OLC: Efficient Assembly of Large Genomes Using Long Erroneous Reads of the Third Generation Sequencing Technologies
inferredcites →https://doi.org/10.1073/pnas.0403984101openalex-snapshot
The timing of eukaryotic evolution: Does a relaxed molecular clock reconcile proteins and fossils?
inferredcites →https://doi.org/10.1080/00275514.1978.12020350openalex-snapshot
Cultural Studies of Single Ascospore Isolates of Morchella Esculenta
inferredcites →https://doi.org/10.1080/00275514.1982.12021480openalex-snapshot
Notes on the Development of the Morel Ascocarp:Morchella Esculenta
inferredcites →https://doi.org/10.1080/15572536.2006.11832614openalex-snapshot
Dating divergences in the Fungal Tree of Life: review and new analyses
inferredcites →https://doi.org/10.1080/21553769.2014.901925openalex-snapshot
Comparative evaluation of antimutagenic and antimitotic effects ofMorchella esculentaextracts and protocatechuic acid
inferredcites →https://doi.org/10.1093/bioinformatics/17.9.847openalex-snapshot
InterProScan – an integration platform for the signature-recognition methods in InterPro
inferredcites →https://doi.org/10.1093/bioinformatics/bti610openalex-snapshot
Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research
inferredcites →https://doi.org/10.1093/bioinformatics/btl097openalex-snapshot
CAFE: a computational tool for the study of gene family evolution
inferredcites →https://doi.org/10.1093/bioinformatics/btq683openalex-snapshot
Scaffolding pre-assembled contigs using SSPACE
inferredcites →https://doi.org/10.1093/bioinformatics/btr088openalex-snapshot
ProtTest 3: fast selection of best-fit models of protein evolution
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/bioinformatics/btv351openalex-snapshot
BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs
inferredcites →https://doi.org/10.1093/bioinformatics/btx198openalex-snapshot
MISA-web: a web server for microsatellite prediction
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/30.1.276openalex-snapshot
The Pfam Protein Families Database
inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot
MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform
inferredcites →https://doi.org/10.1093/nar/gkl200openalex-snapshot
AUGUSTUS: ab initio prediction of alternative transcripts
inferredcites →https://doi.org/10.1093/nar/gkr1065openalex-snapshot
The Pfam protein families database
inferredcites →https://doi.org/10.1093/nar/gks479openalex-snapshot
dbCAN: a web resource for automated carbohydrate-active enzyme annotation
inferredcites →https://doi.org/10.1093/nar/gkt289openalex-snapshot
OrganellarGenomeDRAW—a suite of tools for generating physical maps of plastid and mitochondrial genomes and visualizing expression data sets
inferredcites →https://doi.org/10.1093/nar/gkw654openalex-snapshot
Contiguous and accurate de novo assembly of metazoan genomes with modest long read coverage
inferredcites →https://doi.org/10.1101/gr.1224503openalex-snapshot
OrthoMCL: Identification of Ortholog Groups for Eukaryotic Genomes
inferredcites →https://doi.org/10.1101/gr.2289704openalex-snapshot
Mauve: Multiple Alignment of Conserved Genomic Sequence With Rearrangements
inferredcites →https://doi.org/10.1101/gr.7337908openalex-snapshot
ALLPATHS: De novo assembly of whole-genome shotgun microreads
inferredcites →https://doi.org/10.1111/1574-6968.12387openalex-snapshot
Mobile elements and mitochondrial genome expansion in the soil fungus and potato pathogenRhizoctonia solaniAG-3
inferredcites →https://doi.org/10.1111/j.1469-8137.1990.tb00528.xopenalex-snapshot
The association of Morchella rotunda (Pers.) Boudier with roots of Picea abies (L.) Karst
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02614.xopenalex-snapshot
A genetic linkage map for the ectomycorrhizal fungus Laccaria bicolor and its alignment to the whole‐genome sequence assemblies
inferredcites →https://doi.org/10.1128/aem.55.12.3095-3100.1989openalex-snapshot
Physiological and Environmental Studies of Sclerotium Formation and Maturation in Isolates of Morchella crassipes
inferredcites →https://doi.org/10.1139/b88-239openalex-snapshot
Ultrastructural observations on Helvellaceae (Pezizales). II. Ascosporogenesis of Gyromitra esculenta
inferredcites →https://doi.org/10.1186/2047-217x-1-18openalex-snapshot
SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler
inferredcites →https://doi.org/10.1371/journal.pone.0097141openalex-snapshot
Mitochondrial Genome of Phlebia radiata Is the Second Largest (156 kbp) among Fungi and Features Signs of Genome Flexibility and Recent Recombination Events
inferredcites →https://doi.org/10.1371/journal.pone.0107536openalex-snapshot
The 203 kbp Mitochondrial Genome of the Phytopathogenic Fungus Sclerotinia borealis Reveals Multiple Invasions of Introns and Genomic Duplications
inferredcites →https://doi.org/10.1615/intjmedmushrooms.2019032891openalex-snapshot
Effect of Aging on Culture and Cultivation of the Culinary-Medicinal Mushrooms Morchella importuna and M. sextelata (Ascomycetes)
inferredcites →https://doi.org/10.16488/j.cnki.1005-9873.2019.02.018openalex-snapshot
Occurrence and Control of Pests and Diseases in Field Cultivation of Morchella Mushrooms
inferredcites →https://doi.org/10.2737/pnw-gtr-710openalex-snapshot
Ecology and management of morels harvested from the forests of western North America.
inferredcites →https://doi.org/10.3390/ijms19092525openalex-snapshot
Opposite Polarity Monospore Genome De Novo Sequencing and Comparative Analysis Reveal the Possible Heterothallic Life Cycle of Morchella importuna
inferredcites →https://doi.org/10.3390/molecules23092331openalex-snapshot
Validation of Internal Control Genes for Quantitative Real-Time PCR Gene Expression Analysis in Morchella
inferredcites →https://doi.org/10.3852/09-232openalex-snapshot
Kalapuya brunneagen. & sp. nov. and its relationship to the other sequestrate genera in Morchellaceae
inferredcites →https://doi.org/10.3852/15-281openalex-snapshot
Isotopic evidence indicates saprotrophy in post-fire Morchella in Oregon and Alaska
inferredcites →https://doi.org/10.5598/imafungus.2018.09.01.13openalex-snapshot
Draft genome sequence of Annulohypoxylon stygium, Aspergillus mulundensis, Berkeleyomyces basicola (syn. Thielaviopsis basicola), Ceratocystis smalleyi, two Cercospora beticola strains, Coleophoma cylindrospora, Fusarium fracticaudum, Phialophora cf. hyalina, and Morchella septimelata
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.16.138363zenodo-depositor-declared
Characterisation and comparative analysis of mitochondrial genomes of false, yellow, black and blushing morels provide insights on their structure and evolution
inferred← citeshttps://doi.org/10.3897/imafungus.16.150451zenodo-depositor-declared
Phylogenetic and evolutionary insights from 30 newly-assembled Onygenales Mitochondrial Genomes: co-evolution of introns and HEGs shapes mitogenome size variation
inferred← citeshttps://doi.org/10.3897/imafungus.17.195879zenodo-depositor-declared
Evolutionary insights into Cordyceps militaris from mitogenome dynamics and genome-wide variation
inferred← citeshttps://doi.org/10.1007/978-981-16-0518-5_7openalex-snapshot
Microbial Degradation of Xenobiotic Compounds
inferred← citeshttps://doi.org/10.1007/s12010-022-04133-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.csbj.2021.11.002openalex-snapshot
Mitogenome-wide comparison and phylogeny reveal group I intron dynamics and intraspecific diversification within the phytopathogen Corynespora cassiicola
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.03.016openalex-snapshot
Comparative mitochondrial genome analyses reveal conserved gene arrangement but massive expansion/contraction in two closely related Exserohilum pathogens
inferred← citeshttps://doi.org/10.1016/j.cub.2025.07.037openalex-snapshot
Pangeneric Analyses Reveal the Divergent Genome Evolution and Ecologies between Morels and Truffles in the Morchellaceae
inferred← citeshttps://doi.org/10.1016/j.fgb.2026.104082openalex-snapshot
Broadly applicable mating type primers for morels: a case study on life cycle and genotyping integrity detection
inferred← citeshttps://doi.org/10.1016/j.jafr.2022.100324openalex-snapshot
Genetic polymorphism of Mel-21 Morchella tissue isolates
inferred← citeshttps://doi.org/10.1038/s41597-024-03794-zopenalex-snapshot
Two near-chromosomal-level genomes of globally-distributed Macroascomycete based on single-molecule fluorescence and Hi-C methods
inferred← citeshttps://doi.org/10.1093/gbe/evac037openalex-snapshot
Independent Size Expansions and Intron Proliferation in Red Algal Plastid and Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1093/nar/gkaf1419openalex-snapshot
Comparative mitogenomics of kingdom Fungi – evolutionary insights and metagenomic applications
inferred← citeshttps://doi.org/10.1099/mgen.0.000720openalex-snapshot
Characterization of the mitochondrial genomes of three powdery mildew pathogens reveals remarkable variation in size and nucleotide composition
inferred← citeshttps://doi.org/10.1101/2025.05.08.652889openalex-snapshot
Resources for molecular studies of unculturable obligate biotrophic fungal plant pathogens using their saprotrophic relatives
inferred← citeshttps://doi.org/10.1111/1755-0998.70045openalex-snapshot
Saprotrophic Arachnopeziza Species as New Resources to Study the Obligate Biotrophic Lifestyle of Powdery Mildew Fungi
inferred← citeshttps://doi.org/10.1128/mmbr.00220-20openalex-snapshot
Mating Systems in True Morels ( Morchella )
inferred← citeshttps://doi.org/10.1139/bcb-2024-0046openalex-snapshot
Interconnected roles of fungal nuclear- and intron-encoded maturases: at the crossroads of mitochondrial intron splicing
inferred← citeshttps://doi.org/10.1139/cjm-2020-0589openalex-snapshot
The mitochondrial genome of Ophiostoma himal-ulmi and comparison with other fungi causing Dutch elm disease
inferred← citeshttps://doi.org/10.1139/cjm-2022-0012openalex-snapshot
The mitogenome of Urnula craterium
inferred← citeshttps://doi.org/10.1139/cjm-2022-0038openalex-snapshot
The compact mitogenome of Ceratocystiopsis pallidobrunnea
inferred← citeshttps://doi.org/10.1139/cjm-2024-0179openalex-snapshot
Comparative mitogenomics of Leptographium procerum, Leptographium terebrantis, and Leptographium wingfieldii, an invasive fungal species in Canadian forests
inferred← citeshttps://doi.org/10.1186/s12864-024-10418-8openalex-snapshot
RETRACTED ARTICLE: Genome assembly of M. spongiola and comparative genomics of the genus Morchella provide initial insights into taxonomy and adaptive evolution
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
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The Effect Of Mitochondria on Ganoderma Lucidum Growth And Bioactive Components Based On Transcriptomics
inferred← citeshttps://doi.org/10.3389/fgene.2021.829379openalex-snapshot
Integration of Transcriptomics and Metabolomics for Understanding the Different Vegetative Growth in Morchella Sextelata
inferred← citeshttps://doi.org/10.3389/fmicb.2020.628579openalex-snapshot
Editorial: The Significance of Mitogenomics in Mycology
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The Mitogenomes of Ophiostoma minus and Ophiostoma piliferum and Comparisons With Other Members of the Ophiostomatales
inferred← citeshttps://doi.org/10.3389/fmicb.2021.656609openalex-snapshot
Recent and Ongoing Horizontal Transfer of Mitochondrial Introns Between Two Fungal Tree Pathogens
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1034387openalex-snapshot
Comparative structural analysis on the mitochondrial DNAs from various strains of Lentinula edodes
inferred← citeshttps://doi.org/10.3389/fmicb.2022.1051013openalex-snapshot
Construction of nucleus-directed fluorescent reporter systems and its application to verification of heterokaryon formation in Morchella importuna
inferred← citeshttps://doi.org/10.3389/fmicb.2022.897981openalex-snapshot
Editorial: Mitochondrial Genomes and Mitochondrion Related Gene Insights to Fungal Evolution
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1309703openalex-snapshot
Whole-genome sequencing and evolutionary analysis of the wild edible mushroom, Morchella eohespera
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1344877openalex-snapshot
Editorial: The significance of mitogenomics in mycology, volume II
inferred← citeshttps://doi.org/10.3389/fmolb.2021.632341openalex-snapshot
Untargeted Metabolomics Reveals Alterations in the Primary Metabolites and Potential Pathways in the Vegetative Growth of Morchella sextelata
inferred← citeshttps://doi.org/10.3390/horticulturae10121287openalex-snapshot
Whole-Genome Resequencing and Evolutionary Analysis of Wild Morel Mushroom Morchella sp.
inferred← citeshttps://doi.org/10.3390/jof8101107openalex-snapshot
Epidemic Identification of Fungal Diseases in Morchella Cultivation across China
inferred← citeshttps://doi.org/10.3390/jof9030373openalex-snapshot
Transcriptomic and Metabolomic Profiles Provide Insights into the Red-Stipe Symptom of Morel Fruiting Bodies
inferred← citeshttps://doi.org/10.3390/jof9080855openalex-snapshot
Large-Scale Field Cultivation of Morchella and Relevance of Basic Knowledge for Its Steady Production
inferred← citeshttps://doi.org/10.3390/microorganisms11020345openalex-snapshot
Ultrastructure and Physiological Characterization of Morchella Mitospores and Their Relevance in the Understanding of the Morel Life Cycle
inferred← citeshttps://doi.org/10.6084/m9.figshare.25910047openalex-snapshot
Additional file 1 of Genome assembly of M. spongiola and comparative genomics of the genus Morchella provide initial insights into taxonomy and adaptive evolution
inferred← citeshttps://doi.org/10.70675/1d5ed7dezb138z4504za194z566b690fb2dbopenalex-snapshot
The evolution of red algal organellar genomes and the origin of red complex plastids
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