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13,117 results for “Maps”
A Single-Cell Transcriptomic Map of the Human and Mouse Pancreas Reveals Inter- and Intra-cell Population Structure.
<p>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE84133</p>
NESEA-Rice10: high-resolution annual paddy rice maps for Northeast and Southeast Asia from 2017 to 2019
<p>This dataset provides annual paddy rice maps of Northeast and Southeast Asia from 2017 to 2019.</p> <p>*** The data file is in “.tif" format</p> <p>*** Spatial extent: Northeast and Southeast Asia</p> <p>*** Temporal Resolution: Yearly</p> <p>*** Pixel size: 10 m</p> <p>*** Projection information: EPSG: 4326</p> <p>*** CropType: Paddy rice.</p> <p>*** Year: Values from 2017 to 2019</p> <p>*** The file name consists of year (Y), latitude range (N/S), and longitude range (E). For example, the file name '2019Y_40_45N_140_145E' means the map of paddy rice in the range of 40-50 degrees North and 140-145 degrees East for 2019.</p>
Distribution. Discontinuous and limited to wetland environments in SE Sudan, perhaps the Rift Valley of Ethiopia, W Kenya surrounding Lake Victoria (two locations, very rare), Uganda, Burundi, Rwanda, NW Tanzania, and NE DR Congo. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in SE Sudan, perhaps the Rift Valley of Ethiopia, W Kenya surrounding Lake Victoria (two locations, very rare), Uganda, Burundi, Rwanda, NW Tanzania, and NE DR Congo. Maps and distributional information here are provisional pending future research.
Open-Source Low-Cost Cardiac Optical Mapping System
<p>Optical fluorescence imaging data for <strong>Open-Source Low-Cost Cardiac Optical Mapping System </strong>PLOS ONE paper submission</p>
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in the Congo Basin N and W of the range of the Zambezi Sitatunga in S Benin (Porto Novo), S Nigeria, Cameroon, Central African Republic, Equatorial Guinea, Gabon, Republic of the Congo, N DR Congo; also several isolated populations in W Africa (Senegal, Gambia & Guinea-Bissau), NE Nigeria and W Chad, and perhaps extreme S Ghana. Maps and distributional information here are provisional pending future research.
Distribution. Discontinuous and limited to wetland environments in two areas of S Sudan: small swamps in SW Sudan near the DR Congo border, where the type specimen was collected, and the Sudd Swamps (Bahr-el-Ghazal) of the upper White Nile. Maps and distributional information here are provisional pending future research. in Bovidae
Distribution. Discontinuous and limited to wetland environments in two areas of S Sudan: small swamps in SW Sudan near the DR Congo border, where the type specimen was collected, and the Sudd Swamps (Bahr-el-Ghazal) of the upper White Nile. Maps and distributional information here are provisional pending future research.
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear. in Tragulidae
Subspecies and Distribution. T.n.napuF.Cuvier,1822—SMyanmar,Thai/MalayPeninsula,islandsoffWMalayPeninsula(Langkawi&Pangkor),Borneo,SSumatra,BangkaI,islandsoffBorneo(Laut&Serasan). T.n.bangue:Chasen&Kloss,1931—BanggiIandBalembanganI,offNBorneo. T.n.bunguranensisMiller,1901—NatunaIs(=Bunguran),oftWBorneo. T.n.neubronneriSody,1931—NSumatra. T.n.nmiasisLyon,1916—NiasI,offWSumatra. T.n.rufulusMiller,1900—TiomanI,offEMalayPeninsula,RiauandLinggaArchipelagos. T. n. terutus Thomas & Wroughton, 1909 — Terutau I, off W Malay Peninsula. The species was recently reconfirmed for Singapore. Maps that include Vietnam, Cambodia, and Laos in the distribution range are based on the earlier assumption that 7. versicolor was a subspecies of 1. napu. Subsequent studies have indicated that 7. versicolor is a distinct species, and that the range of 1. napu therefore does not extend into Cambodia, Laos, and Vietnam. The northern limit on the Thai-Malay peninsula is not well defined. Specimens of 1. napu have been collected from as far north as Bankachon in southern Myanmar (10° 08" N), but despite fairly intensive camera-trapping in Kui Buri National Park, Thailand (12° N), 7. napu has not been photographed there. At the northern margin ofits range, it is generally rare. It has been reported, for example, that during the flooding of the Chiew Larn Reservoir (Surat Thani Province; about 9° N, 98° 45' E), only six 7. napu were rescued compared with 172 71. kanchil. This area is the transition zone from wetter evergreen forest to drier deciduous types, and it might be that 7° napu is not well adapted to the drier forest types towards the northern limit ofits range. There are unconfirmed reports of the species on Java, where it may have been confused with one of the two color morphs of 7. javanicus. As explained in the Taxonomy section, the subspecific status of the populations of several islands remains unclear.
AMR Benchmarking dataset - Mapped ReadSets - 4
<p>Benchmarking dataset for AMR detection pipelines for assemblies focusing on ESKAPE pathogens in addition to Salmonella. This dataset consists of closed genomes from NCBI where paired-end Illumina data was available. The closed genomes from NCBI are provided in addition to assemblies based on the raw uploaded to NCBI, along with assemblies based on just the reads which mapped correctly to the closed assemblies. Reads were assembled using shovill v. 1.1.0 using SKESA and SPADES. Variants were called using snippy v. 4.6.0 and the mapped reads were extracted bedtools bamtofastq v2.29.2.</p>
Subspecies and Distribution. C.s.simumBurchell,1817—SEAngola,NENamibia,Botswana,Zimbabwe,SMozambique,Swaziland,SouthAfrica,andperhapsformerlyinextremeSWZambia. C. s. cottoni Lydekker, 1908 — historically present in S Chad, Central African Republic, S Sudan, NE DR Congo, and Uganda; last individuals occurred in DR Congo, but possibly extinct in the wild. The "Southern White Rhino," race simum, has been introduced into Kenya, Uganda, and Zambia. Especially vague range map for conservation reasons. in Rhinocerotidae
Subspecies and Distribution. C.s.simumBurchell,1817—SEAngola,NENamibia,Botswana,Zimbabwe,SMozambique,Swaziland,SouthAfrica,andperhapsformerlyinextremeSWZambia. C. s. cottoni Lydekker, 1908 — historically present in S Chad, Central African Republic, S Sudan, NE DR Congo, and Uganda; last individuals occurred in DR Congo, but possibly extinct in the wild. The "Southern White Rhino," race simum, has been introduced into Kenya, Uganda, and Zambia. Especially vague range map for conservation reasons.
Subspecies and Distribution. D.b.bicornisLinnaeus,1758—Namibia,W&SESouthAfrica. D.b.longipesZukowsky,1949—historicallyinNigeria,Cameroon,Chad,Sudan,andCentralAfricanRepublic(couldbeextinct). D. b. michaeli Zukowsky, 1965 — Kenya, Rwanda (could be extinct by now), and N Tanzania; historically also in Sudan, Ethiopia, and Uganda. D. b. minor Drummond, 1876 — C Tanzania, Zambia, Zimbabwe, Malawi, Botswana, and Mozambique (possibly extinct), to N and CE South Africa. Especially vague range map for conservation reasons. in Rhinocerotidae
Subspecies and Distribution. D.b.bicornisLinnaeus,1758—Namibia,W&SESouthAfrica. D.b.longipesZukowsky,1949—historicallyinNigeria,Cameroon,Chad,Sudan,andCentralAfricanRepublic(couldbeextinct). D. b. michaeli Zukowsky, 1965 — Kenya, Rwanda (could be extinct by now), and N Tanzania; historically also in Sudan, Ethiopia, and Uganda. D. b. minor Drummond, 1876 — C Tanzania, Zambia, Zimbabwe, Malawi, Botswana, and Mozambique (possibly extinct), to N and CE South Africa. Especially vague range map for conservation reasons.
AMR Benchmarking dataset - Mapped ReadSets - 5
<p>Benchmarking dataset for AMR detection pipelines for assemblies focusing on ESKAPE pathogens in addition to Salmonella. This dataset consists of closed genomes from NCBI where paired-end Illumina data was available. The closed genomes from NCBI are provided in addition to assemblies based on the raw uploaded to NCBI, along with assemblies based on just the reads which mapped correctly to the closed assemblies. Reads were assembled using shovill v. 1.1.0 using SKESA and SPADES. Variants were called using snippy v. 4.6.0 and the mapped reads were extracted bedtools bamtofastq v2.29.2.</p>
Multivocal Literature Mapping on DSLs and Tools for Entity-Relationship Modeling
<p><strong>[ERES 2021 - Fórum de Pós-Graduação]</strong></p> <p><strong>Abstract:</strong> The variety of database system technologies that became available in recent years makes difficult the selection of tools for modeling entity-relationship (ER). In this sense, we contribute with an overview of the recent innovations through a systematic literature mapping complemented by research in the gray literature. This paper scopes ten (10) primary studies focused on Domain-Specific Languages (DSL) and identifies fifty-five (55) tools already applied in industry and academia for ER modeling at the conceptual, logical, and physical level. Hence, as a significant increment to existing mapping studies, this presents the state of the art and practice for ER modeling, including its characterization and research gaps.</p>
Map 1 in New species, synonymies, combinations, and records of micropterous Athetini from China (Coleoptera: Staphylinidae: Aleocharinae)
Map 1: Distributions of micropterous Bellatheta species in China: B. qiliana (black circles); B. proiecta (black diamond); B. daxuensis (white circles); B. aucticeps (black triangle); B. smetanai (white triangles); B. excaecata (white diamond); B. diacangica (black star).
Map 3 in The Cephennium fauna of Turkey and the Middle East (Coleoptera: Staphylinidae: Scydmaeninae)
Map 3: Distributions of the species of the Cephennium jonicum and C. corruptum groups in Turkey: C. unguicum (grey stars); C. deplectens (white stars); C. sicaferum (grey triangles); C. duplum (grey diamonds); C. geminum (grey circles); C. reductum (black triangles); C. corruptum (black circles); C. fimbriatum (white square); C. besucheti (black square); C. affimbriatum (white circles); C. marasicum (black diamonds); C. dolucanum (white triangle); C. kartalicum (black star); C. nemruticum (white diamond).
Map 1 in The Cephennium fauna of Turkey and the Middle East (Coleoptera: Staphylinidae: Scydmaeninae)
Map 1: Distributions of species of the Cephennium perispinctum group: C. bodemeyeri (black circles); C. liguliferum (white star); C. infractum (white triangle); C. immutatum (white circles).
Maps 2–5 in The Staphylinidae of Armenia and Nagorno-Karabakh (Coleoptera)
Maps 2–5: Distributions of endemic species and species groups.Map 2 (upper left): regionally endemicGeostiba species (all species pooled;G. sororcula omitted) (black circles) and the locally endemicBellatheta khustupica (white circle).Map 3(upper right):Atheta meghruica (white symbols) and regionally endemic Pselaphinae (black symbols):Bryaxis armeniacus (black circle),B. meghruicus (black triangle), B. seductus (black diamonds), Tychus milvus (black square). Map 4 (lower left): Oxypoda grandecristata (white circle) and regionally endemic Scydmaeninae (black symbols): Euconnus karabakhus (black circles),E. longilaminatus (black square), E. tavushus (black triangle),Neuraphes gomarantsus (black star), N. syunikus (black diamonds).Map 5(lower right):Xantholinus adustus (white circles), a regional endemic of South Armenia, and X. kirschenblati (black circles), a species currently known only from Armenia and Nagorno-Karabakh, but probably present also in adjacent regions.
Map 7 in Revision of theBaeoglena species of the West Palaearctic Region (Coleoptera: Staphylinidae: Aleocharinae)
Map 7: Distributions ofOxypoda caucasica (black circles) andO. derecta (white triangles) in the Caucasus region, based on revised
Map 2 in Revision of theBaeoglena species of the West Palaearctic Region (Coleoptera: Staphylinidae: Aleocharinae)
Map 2: Distribution ofOxypoda praecox in Europe, based on revised male-based records (black circles), female-based records (white
Map 4 in Revision of theBaeoglena species of the West Palaearctic Region (Coleoptera: Staphylinidae: Aleocharinae)
Map 4: Distribution ofOxypoda fusina in the West Mediterranean, based on revised records (white circle: doubtful female-based
Map 5 in Revision of theBaeoglena species of the West Palaearctic Region (Coleoptera: Staphylinidae: Aleocharinae)
Map 5: Distributions ofOxypoda nova (black circles) andO. kuehnelti (white diamonds) in the East Mediterranean, based on revised
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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)
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.
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.