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Sources of inversion variation in the small single copy (SSC) region of chloroplast genomes
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mpev.1996.0038openalex-snapshot
The Distribution and Phylogenetic Significance of a 50-kb Chloroplast DNA Inversion in the Flowering Plant Family Leguminosae
inferredcites →https://doi.org/10.1007/bf00018459openalex-snapshot
Structural organization of the chloroplast genome of the chromophytic algaVaucheria bursata
inferredcites →https://doi.org/10.1007/bf00418530openalex-snapshot
Structural evolution and flip-flop recombination of chloroplast DNA in the fern genus Osmunda
inferredcites →https://doi.org/10.1007/bf00420317openalex-snapshot
Recombination within the inverted repeat sequences of the Chlamydomonas reinhardii chloroplast genome produces two orientation isomers
inferredcites →https://doi.org/10.1007/s11105-015-0853-2openalex-snapshot
Comparative Analysis of Asteraceae Chloroplast Genomes: Structural Organization, RNA Editing and Evolution
inferredcites →https://doi.org/10.1016/j.gene.2014.07.041openalex-snapshot
Complete chloroplast genome sequences of Praxelis (Eupatorium catarium Veldkamp), an important invasive species
inferredcites →https://doi.org/10.1016/j.jmb.2003.11.020openalex-snapshot
Most Chloroplast DNA of Maize Seedlings in Linear Molecules with Defined Ends and Branched Forms
inferredcites →https://doi.org/10.1038/301092a0openalex-snapshot
Chloroplast DNA exists in two orientations
inferredcites →https://doi.org/10.1073/pnas.0709121104openalex-snapshot
Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns
inferredcites →https://doi.org/10.1073/pnas.89.16.7722openalex-snapshot
Chloroplast DNA inversions and the origin of the grass family (Poaceae).
inferredcites →https://doi.org/10.1093/dnares/dsr002openalex-snapshot
The Complete Chloroplast Genome of 17 Individuals of Pest Species Jacobaea vulgaris: SNPs, Microsatellites and Barcoding Markers for Population and Phylogenetic Studies
inferredcites →https://doi.org/10.1111/j.0022-3646.1992.00347.xopenalex-snapshot
ORGANIZATION OF THE CHLOROPLAST GENOME OF THE FRESHWATER CENTRIC DIATOM CYCLOTELLA MENEGHINIANA1
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03195.xopenalex-snapshot
Recombination and the maintenance of plant organelle genome stability
inferredcites →https://doi.org/10.1146/annurev.ge.19.120185.001545openalex-snapshot
COMPARATIVE ORGANIZATION OF CHLOROPLAST GENOMES
inferredcites →https://doi.org/10.1186/1471-2164-9-211openalex-snapshot
Chloroplast genome sequencing analysis of Heterosigma akashiwo CCMP452 (West Atlantic) and NIES293 (West Pacific) strains
inferredcites →https://doi.org/10.1266/ggs.81.311openalex-snapshot
Complete Nucleotide Sequence of the Cotton (Gossypium barbadense L.) Chloroplast Genome with a Comparative Analysis of Sequences among 9 Dicot Plants
inferredcites →https://doi.org/10.1371/journal.pone.0012762openalex-snapshot
The Complete Chloroplast Genome Sequence of Date Palm (Phoenix dactylifera L.)
inferredcites →https://doi.org/10.1371/journal.pone.0036869openalex-snapshot
Complete Chloroplast Genome Sequence of a Major Invasive Species, Crofton Weed (Ageratina adenophora)
inferredcites →https://doi.org/10.1371/journal.pone.0057533openalex-snapshot
Complete Chloroplast Genome Sequences of Mongolia Medicine Artemisia frigida and Phylogenetic Relationships with Other Plants
inferredcites →https://doi.org/10.1600/0363644042451008openalex-snapshot
Recombination, Heteroplasmy, Haplotype Polymorphism, and Paralogy in Plastid Genes: Implications for Plant Molecular Systematics
inferredcites →https://doi.org/10.3732/ajb.1400049openalex-snapshot
Comparative analysis of complete chloroplast genome sequence and inversion variation in Lasthenia burkei (Madieae, Asteraceae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Complete chloroplast genome sequence of Xanthium sibiricum provides useful DNA barcodes for future species identification and phylogeny
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Plastid phylogenomics of the Sansevieria Clade of Dracaena (Asparagaceae) resolves a recent radiation
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Gene losses and partial deletion of small single-copy regions of the chloroplast genomes of two hemiparasitic Taxillus species
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IRscope: an online program to visualize the junction sites of chloroplast genomes
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Long-reads reveal that the chloroplast genome exists in two distinct versions in most plants
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The structure of mitochondrial genomes is associated with geography in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1101/692798openalex-snapshot
Stable and widespread structural heteroplasmy in chloroplast genomes revealed by a new long-read quantification method
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Strategies for complete plastid genome sequencing
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inferred← citeshttps://doi.org/10.1111/jpy.12811openalex-snapshot
Flip‐flop organization in the chloroplast genome of Capsosiphon fulvescens (Ulvophyceae, Chlorophyta)
inferred← citeshttps://doi.org/10.1155/2019/4370258openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12859-020-3475-0openalex-snapshot
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Comparative analysis of codon usage bias in chloroplast genomes of ten medicinal species of Rutaceae
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Additional file 1 of The complete mitochondrial genome of okra (Abelmoschus esculentus): using nanopore long reads to investigate gene transfer from chloroplast genomes and rearrangements of mitochondrial DNA molecules
inferred← citeshttps://doi.org/10.6084/m9.figshare.20193849openalex-snapshot
Additional file 2 of The complete mitochondrial genome of okra (Abelmoschus esculentus): using nanopore long reads to investigate gene transfer from chloroplast genomes and rearrangements of mitochondrial DNA molecules
inferred← citeshttps://doi.org/10.6084/m9.figshare.26722848openalex-snapshot
Additional file 1 of Comparative analysis of codon usage bias in chloroplast genomes of ten medicinal species of Rutaceae
inferred← citeshttps://doi.org/10.7287/peerj.2540v0.1/reviews/1openalex-snapshot
Peer Review #1 of "The complete chloroplast genome sequence of Gentiana lawrencei var. farreri (Gentianaceae) and comparative analysis with its congeneric species (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2540v0.1/reviews/2openalex-snapshot
Peer Review #2 of "The complete chloroplast genome sequence of Gentiana lawrencei var. farreri (Gentianaceae) and comparative analysis with its congeneric species (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.2540v0.2/reviews/1openalex-snapshot
Peer Review #1 of "The complete chloroplast genome sequence of Gentiana lawrencei var. farreri (Gentianaceae) and comparative analysis with its congeneric species (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.7747v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Characterizing gene tree conflict in plastome-inferred phylogenies (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7747v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Characterizing gene tree conflict in plastome-inferred phylogenies (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7747v0.1/reviews/3openalex-snapshot
Peer Review #3 of "Characterizing gene tree conflict in plastome-inferred phylogenies (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.7747v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Characterizing gene tree conflict in plastome-inferred phylogenies (v0.2)"
inferred← citeshttps://doi.org/10.7287/peerj.7747v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Characterizing gene tree conflict in plastome-inferred phylogenies (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.2540openalex-snapshot
The complete chloroplast genome sequence of Gentiana lawrencei var . farreri (Gentianaceae) and comparative analysis with its congeneric species
inferred← citeshttps://doi.org/10.7717/peerj.7747openalex-snapshot
Characterizing gene tree conflict in plastome-inferred phylogenies
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