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1,696 results for “DNA sequence”
Figure 29–32 in DNA sequences corroborate Soesiladeepakius as a non-salticoid genus of jumping spiders: placement with lapsiines, phylogeny, and description of six new species (Araneae, Salticidae)
Figure 29–32. Soesiladeepakius gasnieri sp. nov., female. 29, ventral view. 30, lateral view. 31, epigyne, ventral view. 32, dorsal view, clarified.
Figure 22–28 in DNA sequences corroborate Soesiladeepakius as a non-salticoid genus of jumping spiders: placement with lapsiines, phylogeny, and description of six new species (Araneae, Salticidae)
Figure 22–28. Soesiladeepakius gasnieri sp. nov. 22, left male palp, retrolateral view. 23, ventral view. 24, dorsal view. 25, prolateral view. 26, bulb, retrolateral anterior view. 27, retrolateral view. 28, ventral view, clarified. ma?, putative median apophysis.
Figure 19–21 in DNA sequences corroborate Soesiladeepakius as a non-salticoid genus of jumping spiders: placement with lapsiines, phylogeny, and description of six new species (Araneae, Salticidae)
Figure 19–21. Soesiladeepakius gasnieri sp. nov. 19, male, dorsal view. 20, ventral view. 21, lateral view.
Figure 16–18 in DNA sequences corroborate Soesiladeepakius as a non-salticoid genus of jumping spiders: placement with lapsiines, phylogeny, and description of six new species (Araneae, Salticidae)
Figure 16–18. Soesiladeepakius retroversus sp. nov. 16, left male palp, prolateral view. 17, ventral view. 18, retrolateral view. ma?, putative median apophysis.
Figure 5–9 in DNA sequences corroborate Soesiladeepakius as a non-salticoid genus of jumping spiders: placement with lapsiines, phylogeny, and description of six new species (Araneae, Salticidae)
Figure 5–9. Soesiladeepakius lyra sp. nov., female. 5, chelicera, retrolateral view. 6, palpal claw. 7, prolateral tarsal claw. 8, retrolateral tarsal claw. 9, long spines on ventral tibia I and metatarsus I.
Figure 3 in Molecular dating and diversification of the South American lizard genus Liolaemus (subgenus Eulaemus) based on nuclear and mitochondrial DNA sequences
Figure 3. Posterior probability distributions for mean rates of evolution estimated from the combined data under a partitioned analysis for the mitochondrial (A) and nuclear genes (B). The middle line of each box plot represents mean rates and the top and bottom lines indicate the 95% credibility intervals. CMOS; MXRA-5.
Figure 2 in Molecular dating and diversification of the South American lizard genus Liolaemus (subgenus Eulaemus) based on nuclear and mitochondrial DNA sequences
Figure 2. Age posterior probability distributions for each of the Eulaemus crown groups. Vertical black line represents the Miocene-Pliocene boundary (5.33 Mya).
Figure 1 in Molecular dating and diversification of the South American lizard genus Liolaemus (subgenus Eulaemus) based on nuclear and mitochondrial DNA sequences
Figure 1. Fifty per cent majority rule phylogram from the partitioned BEAST analyses of the combined data set (cytochrome b, 12S, CMOS, and MXRA5). Numbers above and below the nodes represent posterior probability values and mean estimates of divergence dates (in millions of years), respectively.
Figure 9 in Systematic revision of Sabellariidae (Polychaeta) and their relationships with other polychaetes using morphological and DNA sequence data
Figure 9. Photographs of preserved specimens: A, nuchal spines (hooks), I. australiensis; B, thoracic segments with lateral lobes, I. australiensis; C, thoracic segments with lateral lobes, L. giardi; D, abdominal segments with 'proventricle', dorsal view, Sabellaria sp. nov. 2; E, abdominal segments with 'proventricle', ventral view, Sabellaria sp. nov. 2; F, posterior abdominal segments and cauda, Idanthyrsus australiensis. Abbreviations: b, branchia; ca, cauda; ll, lateral lobes; nh, nuchal spines (hooks); pv, proventricle.
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.
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.
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.
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.
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).
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.
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.
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.
FIGURE 1 in Reinstatement of Alysicarpus pokleanus (Leguminosae, Papilionoideae: Desmodieae) based on ITS sequences of nuclear ribosomal DNA
FIGURE 1. Best ML tree obtained after analyzing 41 accessions from previous study (Gholami et al. 2017) including 3 outgroups using RaXML (Stamatakis 2014) on CIPRES Science gateway (Miller et al. 2010).
FIGURE 4 in Phylogeny and taxonomy of Meeboldia, Sinodielsia and their relatives (Apiaceae: Apioideae) inferred from nrDNA ITS, plastid DNA intron (rpl16 and rps16) sequences and morphological characters
FIGURE 4. Mericarp morphology of Meeboldia yunnanensis, S. microloba, S. thibetica, Tongoloa zhongdianensis and Hymenidium apiolens (a–c, d–f, g–i, j–l and m–o). Fruit views are dorsal side, commissural side and transverse section for each row from left to right. Scale bars are 1 mm. Terminologies followed Kljuykov et al. (2004). cv = commissural vittae; lr = lateral rib; mar = marginal rib; mer = median rib; vv = vallecular vittae.
FIGURE 1 in Phylogeny and taxonomy of Meeboldia, Sinodielsia and their relatives (Apiaceae: Apioideae) inferred from nrDNA ITS, plastid DNA intron (rpl16 and rps16) sequences and morphological characters
FIGURE 1. Phylogenetic tree of Acronema clade (A) and Sinodielsia clade (B) derived from Bayesian inference analysis using the ITS dataset. The numbers above and below the nodes are BI-PP and ML-BS presented as percentages, respectively (> 50%). Those nodes not occurring in the ML tree are indicated by pound symbols (#). The names of the clades follow the study of Downie et al. (2010).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
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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.
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.
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.