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521 results for “DNA sequence data”

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zenodo32/100

Figure 8 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 8. Photographs of preserved specimens: A, operculum and anterior segments, lateral view, Sabellaria sp. nov. 2; B, operculum and anterior segments, lateral view, Lygdamis giardi; C, detail of opercular papillae, Lygdamis indicus; D, head and thoracic appendices, Idanthyrsus australiensis; E, head and thoracic appendices, Sabellaria sp. nov. 2; F, operculum and anterior segments, ventral view, Phalacrostemma sp. nov.; G, head and thoracic appendices, L. giardi; H, head and thoracic appendices, L. giardi; I, median organ with lateral ocelli, I. australiensis; J, head and thoracic appendices, Bathysabellaria spinifera; K, operculum and paleae, dorsal view, Tetreres robustus; L, operculum and thoracic segments, lateral view, B. spinifera; M, operculum and anterior segments, lateral view, T. robustus. Abbreviations: b, branchia; b2, branchia segment 2; bo, building organ; cn 1, cirrus neuropodia segment 1; chn1, chaetae neuropodium segment 1; dap, dorsal papilla; es, eyespots; ip; inner paleae; li, lips; mo, mouth; mor; median organ; mr, median ridge; ns, nuchal spines (hooks); op, outer paleae; opa, opercular papillae; p, paleae; pa, palp; pl, oral plates; tf, tentacular filaments.

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 4 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 4. Schematic representation of sabellariid relationships based on maximum-parsimony analyses of the morphological data (constant of concavity k = 4–6) and stylized drawing of opercula from top view, modified from Kirtley (1994). See text for further details.

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 6 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 6. Photographs of Idathyrsus australiensis alive: A, complete specimen, dorsal view; B, anterior end, dorsal view; C, anterior end, central view. Abbreviations: ab, abdomen; b, branchia; ca, cauda; g, gut; ip, inner paleae; nh, nuchal hooks; p, paleae; o, operculum; op, outer paleae; tf, tentacular filaments; pa, parathorax.

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 5 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 5. Stylized drawing of a sabellariid indicating the body regions and some of the morphological features described in Appendix 2: A, dorsal view; B, ventral view.

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 3 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 3. Trees resulting from parsimony analyses of morphological data of members of Sabellariidae and rooted with Spionidae, implementing implied weighting. Unambiguous changes are marked on the topology; black dots: synapomorphies, white dots: homoplastic character states. A, strict consensus of three most-parsimonious trees (constant of concavity k = 3); B, most-parsimonious tree (constant of concavity k = 4–6).

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 10 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 10. Scanning electron micrographs: A, arrangement of paleae in two rows, Idanthyrsus australiensis; B, paleae giving the appearance of being arranged in three rows with the mid and inner row directed in opposite directions, Sabellaria sp. nov. 2; C, paleae with cylindrical and straight blades, Phalacrostemma sp. nov.; D, paleae with flat, straight and smooth edges blades, Lygdamis giardi; E, paleae with flat, straight blades and denticulated margins, Idanthyrsus sp. nov. 1; F, paleae with flat, straight blades and denticulated margins, Idanthyrsus australiensis; G, paleae with flat, straight blades with smooth lateral margings but denticulated distal margins, Sabellaria sp. nov. 2; H, geniculate and concave paleae, Sabellaria sp. nov. 2; I, bent nuchal spines (hooks) without limbation I. australiensis; J, bent nuchal spines (hooks) without limbation Phalacrostemma sp.; K, parathoracic notopodia with lanceolate and capillary chaetae, I. australiensis; L, parathoracic neuropodia with lanceolate chaetae, of two sizes, I. australiensis; M, mid abdominal neurochaetae, I. australiensis; N, abdominal uncini with double rows of teeth, I. australiensis.

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 1 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 1. Trees resulting from parsimony analyses of Sabellariidae and previously related taxa (including members of Sabellida, Terebellida and Spionida). A, strict consensus after analyses based on 99 morphological features with jackknife support values. B, first of 25 most-parsimonious trees (TL 177, CI 0.58, RI 0.74) after analyses of morphological data with unambiguous changes marked on the topology. Numbers under nodes indicate jackknife values; black dots: synapomorphies, white dots: homoplastic character states. C, shortest tree (TL 9215, CI 0.54, RI 0.36) resulting from analysis of partial 18S, 28S and EF-1a sequences with jackknife support values. D, strict consensus of two most-parsimonious trees (TL 9434, CI 0.54 RI 0.37) of the combined dataset, with jackknife support values.

opennotspecifiedJan 2012View details →
zenodo32/100

Figure 2 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data

Figure 2. Strict consensus of 429 most-parsimonious trees after maximum-parsimony analysis of morphological data of members of Sabellariidae rooted with Spionidae (TL 73, CI 0.55, RI 0.86). Numbers under nodes indicate jackknife support values.

opennotspecifiedJan 2012View details →
zenodo32/100

FIGURE. Median network analyses (MNA) of a subset of the C. trilobus aggregate (i.e. those in the clade A from Fig. 11) based on concatenated DNA sequence data from ITS, trnL-trnF and psbJ-petA. Stars and arrow indicate accessions discussed in the text. NI: North Island, SI: South Island. in Five new species of Corybas (Diurideae, Orchidaceae) endemic to New Zealand and phylogeny of the Nematoceras clade

FIGURE. Median network analyses (MNA) of a subset of the C. trilobus aggregate (i.e. those in the clade A from Fig. 11) based on concatenated DNA sequence data from ITS, trnL-trnF and psbJ-petA. Stars and arrow indicate accessions discussed in the text. NI: North Island, SI: South Island.

opennotspecifiedAug 2016View details →
zenodo32/100

FIGURE. Bayesian tree of New Zealand spider orchids (Corybas) based on DNA sequence data from ITS, trnL-trnF and psbJ-petA. Major clades are indicated by open bars and capital letters, members of the C. trilobus aggregate are shaded, and posterior probabilities/ bootstrap percentages (≥50) indicated by numbers near each node. NI: North Island, SI: South Island, MCQI: Macquarie Island, CHI: Chatham Island in Five new species of Corybas (Diurideae, Orchidaceae) endemic to New Zealand and phylogeny of the Nematoceras clade

FIGURE. Bayesian tree of New Zealand spider orchids (Corybas) based on DNA sequence data from ITS, trnL-trnF and psbJ-petA. Major clades are indicated by open bars and capital letters, members of the C. trilobus aggregate are shaded, and posterior probabilities/ bootstrap percentages (≥50) indicated by numbers near each node. NI: North Island, SI: South Island, MCQI: Macquarie Island, CHI: Chatham Island

opennotspecifiedAug 2016View details →
zenodo32/100

FIGURE 1. A in A note on the identity of the spikenard (Nardostachys jatamansi, Caprifoliaceae) based on DNA sequence data

FIGURE 1. A photograph of N. jatamansi with pink-colored flowers. Inset shows close-up of flowers. bar=10cm.

opennotspecifiedJan 2023View details →
dryad32/100

Complete organelle genomes of Korean fir, Abies koreana and phylogenomics of the gymnosperm genus Abies using nuclear and cytoplasmic DNA sequence data

<span>Background</span> <p><em><span>Abies koreana</span></em><span> E. H. Wilson is an endangered evergreen coniferous tree that is native to high altitudes in South Korea and susceptible to the effects of climate change. Hybridization and reticulate evolution have been reported in the genus; therefore, multigene datasets from nuclear and cytoplasmic genomes are needed to better understand its evolutionary history.</span></p> <span>Results</span> <p><span>Using Illumina NovaSeq6000 and Oxford Nanopore Technologies (ONT) PromethION platforms, we generated complete mitochondrial (1,174,803 bp) and plastid (121,341 bp) genomes from <em>A. koreana</em>. The mitochondrial genome is highly dynamic, transitioning from cis- to trans-splicing and breaking the conserved gene clusters. In the case of the plastome, the ONT reads revealed two structural conformations of <em>A. koreana</em>. The short inverted repeats (1,186 bp) of the <em>A. koreana</em> plastome are associated with the different structural types. Transcriptomic sequencing revealed 1,356 sites of C-to-U RNA editing in the 41 mitochondrial genes. Using <em>A. koreana</em> as a reference, we additionally produced nuclear ribosomal DNA and organelle genomic sequences from eight Abies species and generated multiple datasets for maximum likelihood and network analyses. Three sections (<em>Balsamea</em>, <em>Momi</em>, and <em>Pseudopicea</em>) were well grouped in the nuclear phylogeny, but the phylogenomic relationships showed conflicting signals in the mitochondrial and plastid genomes, indicating a complicated evolutionary history that may have included introgressive hybridization.</span></p> <span>Conclusions</span> <p><span>These results illustrate that phylogenomic analyses based on the sequences from differently inherited organelle genomes resulted in conflicting trees. Organellar capture, organellar genome recombination, and incomplete lineage sorting in an ancestral heteroplasmic individual can contribute to phylogenomic discordance. We provide strong support for the relationships within <em>Abies</em> and new insights into the phylogenomic complexity of this genus.</span></p>

opencc-zeroApr 2023View details →
dryad32/100

Data from: High-throughput sequencing of nematode communities from total soil DNA extractions

Open the record for dataset details and reuse information.

publicFeb 2015View details →
dryad32/100

Data from: Congruent species delimitation of two controversial gold-thread nanmu tree species based on morphological and restriction site-associated DNA sequencing data

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publicMay 2018View details →
dryad32/100

Data from: A cost-efficient and simple protocol to enrich prey DNA from extractions of predatory arthropods for large-scale gut content analysis by Illumina sequencing

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publicOct 2016View details →
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Data from: Sequencing historical specimens: successful preparation of small specimens with low amounts of degraded DNA

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publicFeb 2017View details →
dryad32/100

Data from: Targeted re-sequencing of coding DNA sequences for SNP discovery in non-model species

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publicJun 2018View details →
dryad32/100

Data from: Changes in soil microbial communities in post mine ecological restoration: implications for monitoring using high throughput DNA sequencing

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publicJan 2021View details →
dryad32/100

Analysis of RNA-seq, DNA target enrichment, and Sanger nucleotide sequence data resolves deep splits in the phylogeny of cuckoo wasps (Hymenoptera: Chrysididae)

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publicOct 2021View details →
dryad32/100

Data from: Deep-sea, deep-sequencing: metabarcoding extracellular DNA from sediments of marine canyons

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publicSep 2016View details →

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Allen Brain Atlas

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neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

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Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record