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172 results for “DART”

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zenodo36/100

Fig. 45. Character 60 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 45. Character 60, dark lower lip line. State

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 34. Character 49, pale paracloacal mark. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 34. Character 49, pale paracloacal mark. State 1, present (degranvillei, AMNH 90880).

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 32. Character 30, tarsal fringe. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 32. Character 30, tarsal fringe. State 1, present (Megaelosia goeldii, AMNH 103950).

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 38. Character 53, dorsolateral stripe B. State 1 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 38. Character 53, dorsolateral stripe B. State 1, present (femoralis, AMNH 140646).

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 29. Character 22 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 29. Character 22, male supracarpal pad

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 27. Character 19 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 27. Character 19, metacarpal ridge. State

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 14 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 14. Hypothesized phylogeny of anurans, redrawn from Lynch (1973).

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 15 in PHYLOGENETIC SYSTEMATICS OF DART-POISON FROGS AND THEIR RELATIVES (AMPHIBIA: ATHESPHATANURA: DENDROBATIDAE)

Fig. 15. Hypothesized phylogeny of neobatrachians, redrawn from Ford and Cannatella (1993).

opencc-by-4.0Aug 2006View details →
zenodo36/100

Fig. 2 in The Blue Dyeing Poison-Dart Frog, Dendrobates tinctorius (Dendrobates azureus, Hoogmoed 1969): extant in Suriname based on a rapid survey

Fig. 2. Dendrobates tinctorius from Sipaliwini savanna, Suriname.

opencc-by-4.0Dec 2019View details →
zenodo36/100

WACCMX+DART output files associated with the publication "The Impact of Assimilating COSMIC-2 Observations of Electron Density in WACCMX"

<p>WACCMX+DART output files that are associated with the publication &quot;The Impact of Assimilating COSMIC-2 Observations of Electron Density in WACCMX&quot;. Data files include DART diagnostics for the COSMIC-2 and Control experiments, as well as the vertical plasma drift velocities.</p>

opencc-by-4.0Aug 2021View details →
dryad36/100

DaRT-seq raw data of Eucalyptus spp for the genetic assessment of the value of restoration planting within an endangered eucalypt woodland

<p>Assessment of woodland restoration often focusses on stand demographics, but genetic factors likely influence long-term stand viability. We examined the genetic composition of Yellow Box (<em>Eucalyptus melliodora</em>) trees in endangered Box-Gum Grassy Woodland in SE Australia, some 30 years after planting with seeds of reportedly local provenance. Using DArT sequencing for 1406 SNPs, we compared genetic diversity and population structure of planted <em>E. melliodora</em> trees with remnant bushland trees, paddock trees, and natural recruits. Genetic patterns imply that natural stands and paddock trees had historically high gene flow (among group pairwise FST = 0.04–0.10). Genetic diversity was highest among relictual paddock trees (He = 0.17), while diversity of revegetated trees was identical to natural bushland trees (He = 0.14). Bayesian clustering placed the revegetated trees into six genetic groups with four corresponding to genotypes from paddock trees, indicating that revegetated stands are mainly of genetically diverse, local provenance. Natural recruits were largely derived from paddock trees with some contribution from planted trees. A few trees have likely hybridised with other local eucalypt species which are unlikely to compromise stand integrity. We show that paddock trees have high genetic diversity and capture historic genetic variety and provide important foci for natural recruitment of genetically diverse and outcrossed seedlings.</p>

opencc-zeroApr 2023View details →
zenodo36/100

Dart Pistol

A dart pistol inspired by Jurassic Park's dart rifle. Non-lethal... Mostly... Source: Objaverse 1.0 / Sketchfab

opencc-byApr 2021View details →
zenodo36/100

Broken stone dart point, La Sufricaya

This heavy dart point (SUF.pL10.01.04.02) looks like local chert mined at Hamontun. The tip is missing. The owner presumably recovered the dart after it hit the target and then replaced the point upon returning home... or the dart was in fact thrown at La Sufricaya and just stayed on the ground until the wood decomposed and only the point was left. Source: Objaverse 1.0 / Sketchfab

opencc-byFeb 2019View details →
dryad36/100

Data from: Does batrachotoxin autoresistance co-evolve with toxicity in Phyllobates poison-dart frogs?

Open the record for dataset details and reuse information.

publicDec 2018View details →
dryad36/100

DaRT-seq raw data of Eucalyptus spp for the genetic assessment of the value of restoration planting within an endangered eucalypt woodland

Open the record for dataset details and reuse information.

publicApr 2023View details →
dryad36/100

An advancement in developmental and reproductive toxicity (DART) risk assessment: evaluation of a bioactivity and exposure-based NAM toolbox

Open the record for dataset details and reuse information.

publicAug 2025View details →
zenodo32/100

BSF DART - demo trio

<p>This dataset is a trio variant calling cohort to use as demonstration in the BSF DART software.</p> <p>The trio comprises the exome data from the&nbsp;Ashkenazim GIAB dataset (<a href="https://www.nature.com/articles/sdata201625">https://www.nature.com/articles/sdata201625</a>):</p> <ul> <li>HG002_NA24385_son (<a href="https://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/HG002_NA24385_son/OsloUniversityHospital_Exome/">ftp data</a>)</li> <li>HG003_NA24149_father&nbsp;(<a href="https://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/HG003_NA24149_father/OsloUniversityHospital_Exome/">ftp data</a>)</li> <li>HG004_NA24143_mother (<a href="https://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/HG004_NA24143_mother/OsloUniversityHospital_Exome/">ftp data</a>)</li> </ul> <p>We re-aligned the original bam files to the GRCh38 genome, ran variant calling using GATK v4 HaplotypeCaller on each sample, merged the resulting gVCF files into a single cohort, generated VCF files for each sample and annotated them using ENSEMBL VEP v100 (you can find below the exact command line).</p> <p>Moreover, in order to inform users regarding variant calling quality, we ran the GATK v3.8 CallableLoci analysis on each bam file using a list of exome targets as target intervals.</p> <p>Finally, for each sample we produced:</p> <ul> <li>a bigBed track ({sample}_callable_loci.bb) with callability information for each exome region</li> <li>a file ({sample}_non_callable_regions.tsv) containing annotations for the regions which are not &quot;CALLABLE&quot; calculated using the&nbsp;<a href="http://github.com/mkschuster/bsfR/blob/master/exec/bsf_variant_calling_coverage.R">bsf_variant_calling_coverage.R</a>&nbsp;script</li> </ul> <p>Please note, that the bam files in the archive have been downsampled to 30% of the original coverage for illustrative purposes but the variant calling has been run using full coverage.</p> <p><strong>VEP command line:</strong></p> <pre><code class="language-bash">vep \ --allele_number --allow_non_variant \ --assembly GRCh38 \ --cache --dir_cache ${path_to_cache} --offline \ --dir_plugins ${path_to_plugins} \ --dont_skip --everything --failed 1 \ --fasta ${path_to_hg38_fasta}\ --flag_pick_allele_gene --force_overwrite --format vcf \ --gencode_basic --hgvsg --exclude_predicted \ --plugin CADD,${path_to_CADD_resources}/hg38/1.6/whole_genome_SNVs.tsv.gz,${path_to_CADD_resources}/hg38/1.6/gnomad.genomes.r3.0.indel.tsv.gz \ --species homo_sapiens --merged \ --tmpdir ./tmp \ --vcf --compress_output bgzip --fork 16 \ --input_file ./BSA_0000_DART_Demo_Trio_cohort.vcf.gz \ --output_file ./BSA_0000_DART_Demo_Trio_cohort.vep.vcf.gz \ --stats_file ./BSA_0000_DART_Demo_Trio_cohort.vep.html \ --warning_file ./BSA_0000_DART_Demo_Trio_cohort.vep.warning.txt;</code></pre> <p>&nbsp;</p>

opencc-by-4.0Dec 2020View details →
zenodo32/100

Daedric Dart from Morrowind

Source: Objaverse 1.0 / Sketchfab

opencc-byFeb 2022View details →
zenodo32/100

FIGURE 9 in A new species of poison-dart frog (Anura: Dendrobatidae) from Manu province, Amazon region of southeastern Peru, with notes on its natural history, bioacoustics, phylogenetics, and recommended conservation status

FIGURE 9. Currently known distribution of Ameerega shihuemoy (orange circles). The main natural protected areas in the Madre de Dios region are shown in green. Amarakaeri Communal Reserve covers an area of 402.335,62 ha; A. shihuemoy has been found at six localities inside this reserve.

opennotspecifiedDec 2017View details →
zenodo32/100

FIGURE 10. A in A new species of poison-dart frog (Anura: Dendrobatidae) from Manu province, Amazon region of southeastern Peru, with notes on its natural history, bioacoustics, phylogenetics, and recommended conservation status

FIGURE 10. A, dorsal, and B, ventral view of the body; C, lateral view of head; and D, ventral view of the hand, of the adult holotype CBF 3900 of Ameerega yungicola. Scale on every picture. Photos by Daniela Rössler.

opennotspecifiedDec 2017View details →

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International Brain Laboratory public data

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OpenNeuro

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