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Defeatingnumts: Semi-pure mitochondrial DNA from eggs and simple purification methods for field-collected wildlife tissues
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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/(sici)1096-8628(19990827)85:5<498::aid-ajmg13>3.0.co;2-8openalex-snapshot
Nonrandom tissue distribution of mutant mtDNA
inferredcites →https://doi.org/10.1006/mpev.1998.0602openalex-snapshot
Primers for a PCR-Based Approach to Mitochondrial Genome Sequencing in Birds and Other Vertebrates
inferredcites →https://doi.org/10.1007/bf00163806openalex-snapshot
Numt, a recent transfer and tandem amplification of mitochondrial DNA to the nuclear genome of the domestic cat
inferredcites →https://doi.org/10.1007/bf00554547openalex-snapshot
Rapid isolation of animal mitochondrial DNA in a small fixed-angle rotor at ultrahigh speed
inferredcites →https://doi.org/10.1007/bf01732759openalex-snapshot
The use of restriction endonucleases to measure mitochondrial DNA sequence relatedness in natural populations
inferredcites →https://doi.org/10.1007/bf02395525openalex-snapshot
Rapid isolation method of animal mitochondrial DNA by the alkaline lysis procedure
inferredcites →https://doi.org/10.1007/s00239-002-2390-5openalex-snapshot
Evolutionary Dynamics of Large Numts in the Human Genome: Rarity of Independent Insertions and Abundance of Post-Insertion Duplications
inferredcites →https://doi.org/10.1007/s10592-005-5387-yopenalex-snapshot
Single Fish Egg DNA Extraction for PCR Amplification
inferredcites →https://doi.org/10.1016/b978-012498315-1/50002-9openalex-snapshot
Molecular Evolution of the Mitochondrial Genome
inferredcites →https://doi.org/10.1016/s0169-5347(01)02151-6openalex-snapshot
Mitochondrial pseudogenes: evolution's misplaced witnesses
inferredcites →https://doi.org/10.1016/s0169-5347(01)02182-6openalex-snapshot
Intramitochondrial recombination – is it why some mitochondrial genes sleep around?
inferredcites →https://doi.org/10.1016/s0169-5347(03)00125-3openalex-snapshot
Animal mitochondrial DNA recombination revisited
inferredcites →https://doi.org/10.1016/s0378-1119(01)00765-xopenalex-snapshot
The complete DNA sequence of the mitochondrial genome of the self-fertilizing fish Rivulus marmoratus (Cyprinodontiformes, Rivulidae) and the first description of duplication of a control region in fish
inferredcites →https://doi.org/10.1023/a:1019935726807openalex-snapshot
Population differentiation in the red-legged kittiwake (Rissa brevirostris) as revealed by mitochondrial DNA
inferredcites →https://doi.org/10.1046/j.1365-294x.1997.00277.xopenalex-snapshot
Intron variation in marbled murrelets detected using analyses of single‐stranded conformational polymorphisms
inferredcites →https://doi.org/10.1046/j.1365-294x.1997.00284.xopenalex-snapshot
Genetic structure of populations of the threatened eastern massasauga rattlesnake, Sistrurus c. catenatus: evidence from microsatellite DNA markers
inferredcites →https://doi.org/10.1046/j.1365-294x.1998.00389.xopenalex-snapshot
A DNA test to sex most birds
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00802-4.xopenalex-snapshot
Polymerase chain reaction (PCR) primers for the amplification of five nuclear introns in vertebrates
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.00882-5.xopenalex-snapshot
Microsatellite loci from common and thick‐billed murres, Uria aalge and U. lomvia
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.02070.xopenalex-snapshot
Unreliable mtDNA data due to nuclear insertions: a cautionary tale from analysis of humans and other great apes
inferredcites →https://doi.org/10.1056/nejmoa020350openalex-snapshot
Paternal Inheritance of Mitochondrial DNA
inferredcites →https://doi.org/10.1073/pnas.86.16.6196openalex-snapshot
Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers.
inferredcites →https://doi.org/10.1073/pnas.93.26.15239openalex-snapshot
Multiple independent transpositions of mitochondrial DNA control region sequences to the nucleus
inferredcites →https://doi.org/10.1086/302844openalex-snapshot
The Frequency of Heteroplasmy in the HVII Region of mtDNA Differs across Tissue Types and Increases with Age
inferredcites →https://doi.org/10.1093/auk/120.4.982openalex-snapshot
MICROSATELLITE AMPLIFICATION FROM MUSEUM FEATHER SAMPLES: EFFECTS OF FRAGMENT SIZE AND TEMPLATE CONCENTRATION ON GENOTYPING ERRORS
inferredcites →https://doi.org/10.1093/condor/104.1.84openalex-snapshot
MITOCHONDRIAL DNA SUGGESTS HIGH GENE FLOW IN ANCIENT MURRELETS
inferredcites →https://doi.org/10.1093/jhered/esh029openalex-snapshot
Male-biased Mutation Rates and the Overestimation of Extrapair Paternity: Problem, Solution, and Illustration Using Thick-Billed Murres (Uria lomvia, Alcidae)
inferredcites →https://doi.org/10.1093/molbev/msg025openalex-snapshot
Paternal Leakage of Mitochondrial DNA in the Great Tit (Parus major)
inferredcites →https://doi.org/10.1093/molbev/msh110openalex-snapshot
NUMTs in Sequenced Eukaryotic Genomes
inferredcites →https://doi.org/10.1093/molbev/msh244openalex-snapshot
A Broad Survey of Recombination in Animal Mitochondria
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a004049openalex-snapshot
Heteroplasmy and Evidence for Recombination in the Mitochondrial Control Region of the Flatfish Platichthys flesus
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025848openalex-snapshot
Sequence variation in the guillemot (Alcidae: Cepphus) mitochondrial control region and its nuclear homolog
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a040115openalex-snapshot
Contrasting population structure from nuclear intron sequences and mtDNA of humpback whales.
inferredcites →https://doi.org/10.1098/rspb.2002.1961openalex-snapshot
Complete mitochondrial DNA genome sequences show that modern birds are not descended from transitional shorebirds
inferredcites →https://doi.org/10.1111/j.1365-294x.2004.02264.xopenalex-snapshot
Temporal changes in allele frequencies and low effective population size in greater prairie‐chickens
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02672.xopenalex-snapshot
An unusual source of apparent mitochondrial heteroplasmy: duplicate mitochondrial control regions in Thalassarche albatrosses
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02713.xopenalex-snapshot
A role for nonphysical barriers to gene flow in the diversification of a highly vagile seabird, the masked booby (Sula dactylatra)
inferredcites →https://doi.org/10.1111/j.1471-8286.2004.00628.xopenalex-snapshot
Microsatellite loci from the five‐lined skink (Eumeces fasciatus)
inferredcites →https://doi.org/10.1139/g03-034openalex-snapshot
Characterization of the red knot (Calidris canutus) mitochondrial control region
inferredcites →https://doi.org/10.1201/9781315735368-14openalex-snapshot
Energy Conversion: Mitochondria and Chloroplasts
inferredcites →https://doi.org/10.1515/bc.1999.107openalex-snapshot
Mitochondria Harbouring Mutant mtDNA a Cuckoo in the Nest?
inferredcites →https://doi.org/10.1642/0004-8038(2002)119[0820:msfsso]2.0.co;2openalex-snapshot
Molecular Support for Species Status of the Nazca Booby (Sula granti)
inferredcites →https://doi.org/10.2307/4089130openalex-snapshot
Numts: A Challenge for Avian Systematics and Population Biology
inferredcites →https://doi.org/10.5860/choice.35-1515openalex-snapshot
Avian molecular evolution and systematics
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3853/j.2201-4349.67.2015.1634zenodo-depositor-declared
Phylogeny for the tribe Thophini (Cicadoidea: Cicadidae) with the description of a new subspecies of Thopha sessiliba Distant from Western Australia
inferred← citeshttps://doi.org/10.1002/ece3.10135openalex-snapshot
Development of short‐target primers for species identification in biological studies of Carnivora
inferred← citeshttps://doi.org/10.1007/s00294-010-0331-1openalex-snapshot
The occurrence of mtDNA heteroplasmy in multiple cetacean species
inferred← citeshttps://doi.org/10.1007/s10144-015-0505-2openalex-snapshot
Large‐scale population genetics of the mountain ant Proformica longiseta (Hymenoptera: Formicidae)
inferred← citeshttps://doi.org/10.1007/s10493-016-0086-6openalex-snapshot
Haplotype identification and detection of mitochondrial DNA heteroplasmy in Varroa destructor mites using ARMS and PCR–RFLP methods
inferred← citeshttps://doi.org/10.1007/s10592-016-0886-6openalex-snapshot
Population expansion, current and past gene flow in Gould’s petrel: implications for conservation
inferred← citeshttps://doi.org/10.1016/j.mito.2010.10.004openalex-snapshot
Preventing the pollution of mitochondrial datasets with nuclear mitochondrial paralogs (numts)
inferred← citeshttps://doi.org/10.1016/j.mito.2020.06.007openalex-snapshot
Mitochondrial DNA intra-individual variation in a bumblebee species: A challenge for evolutionary studies and molecular identification
inferred← citeshttps://doi.org/10.1016/j.ympev.2008.12.008openalex-snapshot
False phylogenies on wood mice due to cryptic cytochrome-b pseudogene
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.09.025openalex-snapshot
A phylogenetic test of sympatric speciation in the Hydrobatinae (Aves: Procellariiformes)
inferred← citeshttps://doi.org/10.1080/24701394.2020.1844677openalex-snapshot
Mitochondrial heteroplasmy and pseudogenes in the freshwater prawn, Macrobrachium amazonicum (Heller, 1862): DNA barcoding and phylogeographic implications
inferred← citeshttps://doi.org/10.1093/gbe/evaf174openalex-snapshot
Mitochondrial Impostors: Prevalence and Impacts of NUMTs on Genetic and Evolutionary Studies in Carnivora
inferred← citeshttps://doi.org/10.1093/jhered/esr104openalex-snapshot
Short Reads, Circular Genome: Skimming SOLiD Sequence to Construct the Bighorn Sheep Mitochondrial Genome
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2009.04155.xopenalex-snapshot
Glacial refugia in a maritime temperate climate: Cicada (Kikihia subalpina) mtDNA phylogeography in New Zealand
inferred← citeshttps://doi.org/10.1111/j.1439-0469.2008.00492.xopenalex-snapshot
Incorporation of mitochondrial fragments in the nuclear genome (Numts) of the longhorned beetleMonochamus galloprovincialis(Coleoptera, Cerambycidae)
inferred← citeshttps://doi.org/10.1111/jzs.12446openalex-snapshot
Mind thenumt: Finding informative mitochondrial markers in a giant grasshopper genome
inferred← citeshttps://doi.org/10.1186/1471-2148-10-238openalex-snapshot
Time and time again: unisexual salamanders (genus Ambystoma) are the oldest unisexual vertebrates
inferred← citeshttps://doi.org/10.1186/1471-2148-10-372openalex-snapshot
Haplowebs as a graphical tool for delimiting species: a revival of Doyle's "field for recombination" approach and its application to the coral genus Pocillopora in Clipperton
inferred← citeshttps://doi.org/10.1186/s12859-015-0682-1openalex-snapshot
Odintifier - A computational method for identifying insertions of organellar origin from modern and ancient high-throughput sequencing data based on haplotype phasing
inferred← citeshttps://doi.org/10.1371/journal.pone.0037142openalex-snapshot
Selective Enrichment and Sequencing of Whole Mitochondrial Genomes in the Presence of Nuclear Encoded Mitochondrial Pseudogenes (Numts)
inferred← citeshttps://doi.org/10.1371/journal.pone.0226860openalex-snapshot
Voluntary wheel running has no impact on brain and liver mitochondrial DNA copy number or mutation measures in the PolG mouse model of aging
inferred← citeshttps://doi.org/10.1525/auk.2011.11011openalex-snapshot
Rangewide population genetic structure of Xantus's Murrelet (Synthliboramphus hypoleucus)
inferred← citeshttps://doi.org/10.1525/cond.2013.120031openalex-snapshot
Minimal Genetic Structure in the Cerulean Warbler Despite Evidence for Ecological Differentiation among Populations
inferred← citeshttps://doi.org/10.1603/008.102.0509openalex-snapshot
Evolution of Flight-Muscle Polymorphism in the Dung Beetle Phelotrupes laevistriatus (Coleoptera: Geotrupidae): A Phylogeographic Analysis
inferred← citeshttps://doi.org/10.1675/063.032.0212openalex-snapshot
Molted Feathers as a Source of DNA for Genetic Studies in Waterbird Populations
inferred← citeshttps://doi.org/10.4238/vol10-3gmr1217openalex-snapshot
Genetic status of the wood stork (Mycteria americana) from the southeastern United States and the Brazilian Pantanal as revealed by mitochondrial DNA analysis
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