| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S10577-011-9246-Z |
| P698 | PubMed publication ID | 21987187 |
| P50 | author | Laura J. Kelly | Q64883831 |
| Ilia J. Leitch | Q42056872 | ||
| P2860 | cites work | Doubling genome size without polyploidization: dynamics of retrotransposition-driven genomic expansions in Oryza australiensis, a wild relative of rice | Q22065740 |
| Differential lineage-specific amplification of transposable elements is responsible for genome size variation in Gossypium | Q22065742 | ||
| The B73 Maize Genome: Complexity, Diversity, and Dynamics | Q22065899 | ||
| Evolution of DNA amounts across land plants (embryophyta) | Q22066091 | ||
| The Arabidopsis lyrata genome sequence and the basis of rapid genome size change | Q22122056 | ||
| The genome of woodland strawberry (Fragaria vesca) | Q22122058 | ||
| The genome of Theobroma cacao | Q22122059 | ||
| The genome of the domesticated apple (Malus × domestica Borkh.) | Q22122060 | ||
| The genome of the cucumber, Cucumis sativus L | Q22122061 | ||
| Draft genome sequence of the oilseed species Ricinus communis | Q22122119 | ||
| Genome sequencing and analysis of the model grass Brachypodium distachyon | Q22122196 | ||
| Genome sequence of the palaeopolyploid soybean | Q22122200 | ||
| Analysis of the genome sequence of the flowering plant Arabidopsis thaliana | Q22122387 | ||
| Sequencing technologies - the next generation | Q27860568 | ||
| Nuclear DNA content and genome size of trout and human | Q28204636 | ||
| Next-generation DNA sequencing methods | Q28285066 | ||
| The origin, evolution and proposed stabilization of the terms 'genome size' and 'C-value' to describe nuclear DNA contents | Q28298127 | ||
| Genome Size and Species Diversification | Q28742138 | ||
| Repetitive DNA in the pea (Pisum sativum L.) genome: comprehensive characterization using 454 sequencing and comparison to soybean and Medicago truncatula | Q28755920 | ||
| Transposable elements and the evolution of regulatory networks | Q28756349 | ||
| Next-generation DNA sequencing | Q29547447 | ||
| ChIP-seq: advantages and challenges of a maturing technology | Q29615336 | ||
| Genome size and transposable element content as determined by high-throughput sequencing in maize and Zea luxurians | Q42707286 | ||
| Genomic and small RNA sequencing of Miscanthus x giganteus shows the utility of sorghum as a reference genome sequence for Andropogoneae grasses | Q42776729 | ||
| Evolutionary conservation, diversity and specificity of LTR-retrotransposons in flowering plants: insights from genome-wide analysis and multi-specific comparison | Q43044106 | ||
| A whole-genome snapshot of 454 sequences exposes the composition of the barley genome and provides evidence for parallel evolution of genome size in wheat and barley | Q47183283 | ||
| Mechanisms and rates of genome expansion and contraction in flowering plants. | Q52115877 | ||
| The largest eukaryotic genome of them all? | Q56048669 | ||
| Estimation of nuclear DNA content in plants using flow cytometry | Q57014941 | ||
| Genome Size and its Uses: The Impact of Flow Cytometry | Q57067644 | ||
| Genome Size Evolution in Plants | Q57067654 | ||
| Next Generation Sequencing Reveals Genome Downsizing in Allotetraploid Nicotiana tabacum, Predominantly through the Elimination of Paternally Derived Repetitive DNAs | Q60534772 | ||
| The epigenetic landscape of plants | Q81152836 | ||
| Variation in nuclear DNA content in Malus species and cultivated apples | Q82164294 | ||
| The development and impact of 454 sequencing | Q82255359 | ||
| DNA transposons and the evolution of eukaryotic genomes | Q29617153 | ||
| A unified classification system for eukaryotic transposable elements | Q29617222 | ||
| Transposable elements and the epigenetic regulation of the genome | Q29617224 | ||
| The map-based sequence of the rice genome | Q29617329 | ||
| Graph-based clustering and characterization of repetitive sequences in next-generation sequencing data. | Q30495793 | ||
| Nuclear DNA C-values in 30 species double the familial representation in pteridophytes | Q30845029 | ||
| Transposable elements and an epigenetic basis for punctuated equilibria | Q33453627 | ||
| Small RNAs, DNA methylation and transposable elements in wheat | Q33618598 | ||
| The Pinus taeda genome is characterized by diverse and highly diverged repetitive sequences | Q33627050 | ||
| The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). | Q33719213 | ||
| Diverse retrotransposon families and an AT-rich satellite DNA revealed in giant genomes of Fritillaria lilies. | Q33771655 | ||
| Nuclear DNA amounts in angiosperms: targets, trends and tomorrow | Q33800794 | ||
| Field guide to next-generation DNA sequencers | Q33904607 | ||
| Patching gaps in plant genomes results in gene movement and erosion of colinearity | Q34085145 | ||
| A window into third-generation sequencing | Q34139314 | ||
| Comparisons with Caenorhabditis (approximately 100 Mb) and Drosophila (approximately 175 Mb) using flow cytometry show genome size in Arabidopsis to be approximately 157 Mb and thus approximately 25% larger than the Arabidopsis genome initiative est | Q34184796 | ||
| Nuclear DNA amounts in angiosperms: progress, problems and prospects. | Q34582822 | ||
| Genome evolution in the genus Sorghum (Poaceae) | Q34582856 | ||
| Smallest angiosperm genomes found in lentibulariaceae, with chromosomes of bacterial size | Q34597826 | ||
| Genome-wide comparative analysis of copia retrotransposons in Triticeae, rice, and Arabidopsis reveals conserved ancient evolutionary lineages and distinct dynamics of individual copia families | Q34635609 | ||
| Punctuated genome size evolution in Liliaceae. | Q34705660 | ||
| Transposable elements and the evolution of genome size in eukaryotes | Q34790131 | ||
| Analysis of retrotransposon structural diversity uncovers properties and propensities in angiosperm genome evolution | Q35214955 | ||
| Intraspecific variation in genome size in angiosperms: identifying its existence | Q35982449 | ||
| Turning junk into gold: domestication of transposable elements and the creation of new genes in eukaryotes | Q36579703 | ||
| Epigenetic regulation of transposable elements in plants | Q37324789 | ||
| Rapid DNA loss as a counterbalance to genome expansion through retrotransposon proliferation in plants | Q37394386 | ||
| Transposable elements: powerful facilitators of evolution | Q37470360 | ||
| Do genetic recombination and gene density shape the pattern of DNA elimination in rice long terminal repeat retrotransposons? | Q37471851 | ||
| Insights from the comparison of plant genome sequences | Q37742162 | ||
| Assembly of large genomes using second-generation sequencing | Q37761251 | ||
| Crop genome sequencing: lessons and rationales | Q37809918 | ||
| Nuclear DNA amounts in angiosperms | Q39100593 | ||
| Genome size reduction through illegitimate recombination counteracts genome expansion in Arabidopsis | Q39860924 | ||
| P4510 | describes a project that uses | massive parallel sequencing | Q6784807 |
| P433 | issue | 7 | |
| P304 | page(s) | 939-953 | |
| P577 | publication date | 2011-10-01 | |
| P1433 | published in | Chromosome Research | Q15765850 |
| P1476 | title | Exploring giant plant genomes with next-generation sequencing technology | |
| P478 | volume | 19 |
| Q46964358 | A universe of dwarfs and giants: genome size and chromosome evolution in the monocot family Melanthiaceae |
| Q38276082 | Analysis of the giant genomes of Fritillaria (Liliaceae) indicates that a lack of DNA removal characterizes extreme expansions in genome size |
| Q41274387 | Bioinformatics resources for deciphering the biogenesis and action pathways of plant small RNAs |
| Q36732449 | CHH islands: de novo DNA methylation in near-gene chromatin regulation in maize |
| Q34561490 | Characterization of the basal angiosperm Aristolochia fimbriata: a potential experimental system for genetic studies. |
| Q34586452 | Consequences of normalizing transcriptomic and genomic libraries of plant genomes using a duplex-specific nuclease and tetramethylammonium chloride |
| Q39314475 | Effects of introgression on the genetic population structure of two ecologically and economically important conifer species: lodgepole pine (Pinus contorta var. latifolia) and jack pine (Pinus banksiana). |
| Q42186981 | Endogenous pararetrovirus sequences associated with 24 nt small RNAs at the centromeres of Fritillaria imperialis L. (Liliaceae), a species with a giant genome |
| Q50068308 | Evolutionary Epigenomics of Retrotransposon-Mediated Methylation Spreading in Rice |
| Q46852087 | Evolutionary relationships in the medicinally important genus Fritillaria L. (Liliaceae). |
| Q39487869 | Genome size and chromosome number in velvet worms (Onychophora). |
| Q46268440 | Genome size and identification of abundant repetitive sequences in Vallisneria spinulosa |
| Q45800365 | Genome size evolution: patterns, mechanisms, and methodological advances |
| Q91286646 | Identification and characterization of abundant repetitive sequences in Allium cepa |
| Q35852303 | In Depth Characterization of Repetitive DNA in 23 Plant Genomes Reveals Sources of Genome Size Variation in the Legume Tribe Fabeae. |
| Q37187492 | Isolation and characterization of reverse transcriptase fragments of LTR retrotransposons from the genome of Chenopodium quinoa (Amaranthaceae). |
| Q34613169 | LTR-retrotransposons in R. exoculata and other crustaceans: the outstanding success of GalEa-like copia elements |
| Q31103141 | Long Terminal Repeat Retrotransposon Content in Eight Diploid Sunflower Species Inferred from Next-Generation Sequence Data |
| Q57067594 | Molecular phylogenetics of Paphiopedilum (Cypripedioideae; Orchidaceae) based on nuclear ribosomal ITS and plastid sequences |
| Q42814151 | Next-generation sequencing reveals the impact of repetitive DNA across phylogenetically closely related genomes of Orobanchaceae. |
| Q38746884 | PlanTEnrichment: A tool for enrichment analysis of transposable elements in plants |
| Q58803219 | Satellite DNA in Paphiopedilum subgenus Parvisepalum as revealed by high-throughput sequencing and fluorescent in situ hybridization |
| Q91871010 | TEffectR: an R package for studying the potential effects of transposable elements on gene expression with linear regression model |
| Q34863106 | Transposon fingerprinting using low coverage whole genome shotgun sequencing in cacao (Theobroma cacao L.) and related species |
| Q36064318 | What's in a genome? The C-value enigma and the evolution of eukaryotic genome content |
| Q57067604 | Why size really matters when sequencing plant genomes |
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