Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
11,177
datasets available to search
ShareScore release 0.9.0
Dataset results
11,177 results for “identify”
Subspecies and Distribution. L.o.obscurusMiller,1903—SouthPagaiI(offWSumatra). L.o.auroreusSody,1949—NorthPagaiI(offWSumatra). L. o. siberu Chasen & Kloss, 1928 — Siberut I (off W Sumatra). The species also occurs in Sipora I (off W Sumatra) but the collected specimens were identified only to species level. in Sciuridae
Subspecies and Distribution. L.o.obscurusMiller,1903—SouthPagaiI(offWSumatra). L.o.auroreusSody,1949—NorthPagaiI(offWSumatra). L. o. siberu Chasen & Kloss, 1928 — Siberut I (off W Sumatra). The species also occurs in Sipora I (off W Sumatra) but the collected specimens were identified only to species level.
Distribution. NE Mali, EC & SE Sudan, SE South Sudan, and NE Ethiopia. There is also a record from ancient Egypt in Thebes where a mummified individual has recently been identified, although status of the species there is uncertain considering no individuals have been observed there in recent times. in Soricidae
Distribution. NE Mali, EC & SE Sudan, SE South Sudan, and NE Ethiopia. There is also a record from ancient Egypt in Thebes where a mummified individual has recently been identified, although status of the species there is uncertain considering no individuals have been observed there in recent times.
Distribution. Nile Delta, NW Egypt. Ancient mummified remains have been identified in Thebes, SE Egypt. in Soricidae
Distribution. Nile Delta, NW Egypt. Ancient mummified remains have been identified in Thebes, SE Egypt.
Distribution. Known from SW China (Yunnan and Guizhou), adjacent N & W Myanmar, Laos, Thailand, and S Vietnam. Because both the Indochinese White-toothed Shrew and the Hainan White-toothed Shrew (C. wuchihensis) were identified as Horsfield's White-toothed Shrew (C. horsfieldiz) until recently, their distribution limits in China are not clear. in Soricidae
Distribution. Known from SW China (Yunnan and Guizhou), adjacent N & W Myanmar, Laos, Thailand, and S Vietnam. Because both the Indochinese White-toothed Shrew and the Hainan White-toothed Shrew (C. wuchihensis) were identified as Horsfield's White-toothed Shrew (C. horsfieldiz) until recently, their distribution limits in China are not clear.
Distribution. Widely distributed in mainland of C & S China (from SE Tibet [= Xizang] E through S Gansu and Shaanxi to Fujian) and Hainan I, also recorded in Nepal, NE India, Myanmar, Thailand, Laos, and Vietnam. Because many specimens previously identified as C. attenuata have been recognized as distinct species, its distribution range may be overestimated, and its limits are unclear. in Soricidae
Distribution. Widely distributed in mainland of C & S China (from SE Tibet [= Xizang] E through S Gansu and Shaanxi to Fujian) and Hainan I, also recorded in Nepal, NE India, Myanmar, Thailand, Laos, and Vietnam. Because many specimens previously identified as C. attenuata have been recognized as distinct species, its distribution range may be overestimated, and its limits are unclear.
Subspecies and Distribution. M.r.rufescensAlston,1877—NewBritainandNewIrelandIs. M.r.calidiorThomas,1911—lowlandsofSWNewGuinea. M.r.gracilisThomas,1906—SescarpmentoftheCentralCordilleraofNewGuineafromMtBosaviEtotheOwenStanleyRange. M.r.hageniTroughton,1937—mountainsofNewGuineafromCWestPapua(=IrianJaya])EtotheKratkeRange. M.r.niviventerTate,1951—lowerDigulandFlyriverbasins,SCNewGuinea. M.r.stalkeriThomas,1904—lowlandsofN&SENewGuinea. M. r. wisselensis Menzies, 1996 — known only from the Wissel Lakes area ofW New Guinea. Known also from islands of Waigeo, Salawati, Yapen, Blup Blup, Karkar, and Sideia (off NW, N & SE New Guinea), but subspecies involved not identified. in Muridae
Subspecies and Distribution. M.r.rufescensAlston,1877—NewBritainandNewIrelandIs. M.r.calidiorThomas,1911—lowlandsofSWNewGuinea. M.r.gracilisThomas,1906—SescarpmentoftheCentralCordilleraofNewGuineafromMtBosaviEtotheOwenStanleyRange. M.r.hageniTroughton,1937—mountainsofNewGuineafromCWestPapua(=IrianJaya])EtotheKratkeRange. M.r.niviventerTate,1951—lowerDigulandFlyriverbasins,SCNewGuinea. M.r.stalkeriThomas,1904—lowlandsofN&SENewGuinea. M. r. wisselensis Menzies, 1996 — known only from the Wissel Lakes area ofW New Guinea. Known also from islands of Waigeo, Salawati, Yapen, Blup Blup, Karkar, and Sideia (off NW, N & SE New Guinea), but subspecies involved not identified.
Large-scale human tissue analysis identifies Uroplakin 3B as a useful diagnostic marker for mesothelioma and normal meso-thelial cells
<p><strong>Supplement Figure 1:</strong> IHC validation by comparison of antibodies. Using MSVA-736M, an apical membranous Upk3b positivity is seen in mesothelial cells covering an appendix (A), amnion cells of a placenta (B), and umbrella cells of the renal pelvis urothelium (C), while staining is absent in adrenal gland (D). Using clone C362, a similar membranous staining is seen in mesothelial cells of the appendix (E), amnion cells (F), and urothelial umbrella cells (G) despite of a higher level of background staining. Clone C362 results in a significant nuclear staining of adrenocortical cells (H) which was not seen by MSVA-736M.</p>
A new gene set identifies senescent cells and predicts senescence-associated pathways across tissues
<p>Although cellular senescence drives multiple age-related co-morbidities through the senescence-associated secretory phenotype (SASP), <em>in vivo</em> senescent cell identification remains challenging. Here, we generated a gene set (SenMayo) and validated its enrichment in bone biopsies from two aged human cohorts. We further demonstrated reductions in SenMayo in bone following genetic clearance of senescent cells in mice and in adipose tissue from humans following pharmacological senescent cell clearance. We next used SenMayo to identify senescent hematopoietic or mesenchymal cells at the single cell level from human and murine bone marrow/bone scRNA-seq data. Thus, SenMayo identifies senescent cells across tissues and species with high fidelity. Using this senescence panel, we were able to characterize senescent cells at the single-cell level and identify key intercellular signaling pathways. SenMayo also represents a potentially clinically applicable panel for monitoring senescent cell burden with aging and other conditions as well as in studies of senolytic drugs.</p>
Machine learning on large-scale proteomics data identifies tissue- and cell type-specific proteins
<p>Using data from 183 public human data sets from PRIDE, a machine learning model was trained to identify tissue and cell-type specific protein patterns. PRIDE projects were searched with ionbot and tissue/cell type annotation was manually added. Data from physiological samples were used to train a Random Forest model on protein abundances to classify samples into tissues and cell types. Subsequently, a one-vs-all classification and feature importance were used to analyse the most discriminating protein abundances per class. Based on protein abundance alone, the model was able to predict tissues with 98% accuracy, and cell types with 99% accuracy. The F-scores describe a clear view on tissue-specific proteins and tissue-specific protein expression patterns. In-depth feature analysis shows slight confusion between physiologically similar tissues, demonstrating the capacity of the algorithm to detect biologically relevant patterns. These results can in turn inform downstream uses, from identification of the tissue of origin of proteins in complex samples such as liquid biopsies, to studying the proteome of tissue-like samples such as organoids and cell lines</p>
Dataset: Architecture-based Attack Propagation and Variation Analysis for Identifying Confidentiality Issues in Industry 4.0
<p>Dataset for the publication <em>Architecture-based Attack Propagation and Variation Analysis for Identifying Confidentiality Issues in Industry 4.0</em></p> <p>More Information can be found in the zipped Readme</p>
Figure 5 in Actionable, long-term stable and semantic web compatible identifiers for access to biological collection objects
Figure 5. The Wallich Catalogue. Screenshot of Wallich Catalogue hosted by Royal Botanic Garden Edinburgh showing popup for stable URI containing information hosted at Botanic Garden and Botanical Museum Berlin-Dahlem.
Figure 4 in Actionable, long-term stable and semantic web compatible identifiers for access to biological collection objects
Figure 4. The CETAF Specimen URI Tester provides for any given Specimen URI an overview of the redirection process as well as a preview of machine-readable and human-readable data associated with the URI.
Figure 3 in Actionable, long-term stable and semantic web compatible identifiers for access to biological collection objects
Figure 3. CETAF stable HTTP URIs in the GBIF data portal. The Global Biodiversity Information Facility (GBIF) publishes CETAF stable HTTP URIs via their data portal.
Figure 2 in Actionable, long-term stable and semantic web compatible identifiers for access to biological collection objects
Figure 2. Basic redirection mechanisms. Human users are redirected to a human-readable web-representation of the specimens. Software systems are re-directed to a machine-readable metadata record.
Fig. 4 in The ''Lembeh Frogfish'' Identified: Redescription of Nudiantennarius subteres (Smith and Radcliffe, in Radcliffe, 1912) (Teleostei: Lophiiformes: Antennariidae)
Fig. 4. Nudiantennarius subteres, uncollected specimens: (A) Dauin, Negros Island, Philippines, 7 March 2017 (photo by Daniel Geary); (B) Ambon, Indonesia, October 1996 (photo by Scott Michael); (C) Lembeh Strait, Sulawesi, Indonesia, 2005 (photo by Teresa Zuberbühler); (D) Dauin, Negros Oriental, Philippines, 11 May 2015 (photo by Daniel Geary); (E) juvenile, Dauin, Negros Oriental, Philippines, 12 April 2016 (photo by Daniel Geary); (F) Lembeh Strait, Sulawesi, Indonesia, 27 September 2013 (photo by Colin Marshall).
Fig. 1 in The ''Lembeh Frogfish'' Identified: Redescription of Nudiantennarius subteres (Smith and Radcliffe, in Radcliffe, 1912) (Teleostei: Lophiiformes: Antennariidae)
Fig. 1. Nudiantennarius subteres (Smith and Radcliffe, in Radcliffe, 1912), the holotype, USNM 70268, 42 mm SL, collected off Luzon, Philippines, 10 May 1909 (pectoral and pelvic fins retouched).
Fig. 3 in The ''Lembeh Frogfish'' Identified: Redescription of Nudiantennarius subteres (Smith and Radcliffe, in Radcliffe, 1912) (Teleostei: Lophiiformes: Antennariidae)
Fig. 3. Nudiantennarius subteres, uncollected specimens: (A) Pantar Island, Alor Archipelago, Indonesia, 29 November 2006 (2006 David Hall); (B) Secret Bay, Anilao, Philippines, 18 April 2009 (photo by Stephane Bailliez); (C) Dauin, Negros Island, Philippines, 29 April 2015 (photo by Daniel Geary); (D) Ambon, Indonesia, 28 October 2015 (photo by Linda Ianniello); (E) hypothesized mated pair, male on the left, female on the right; Seraya Bay, northeast Bali, Indonesia, 1 November 2012 (photo by Vincent Chalias); (F) Secret Bay, Anilao, Philippines, ca. 2 m depth, 19 April 2009 (photo by Stephane Bailliez).
Fig. 5 in The ''Lembeh Frogfish'' Identified: Redescription of Nudiantennarius subteres (Smith and Radcliffe, in Radcliffe, 1912) (Teleostei: Lophiiformes: Antennariidae)
Fig. 5. Fifty percent majority rule phylogeny of the cytochrome oxidase I (COI) gene, from trees sampled in the posterior, generated from Bayesian analysis. Branch lengths are measured in expected substitutions per site and are proportional to length. Numbers above nodes are posterior probabilities.
Fig. 2 in The ''Lembeh Frogfish'' Identified: Redescription of Nudiantennarius subteres (Smith and Radcliffe, in Radcliffe, 1912) (Teleostei: Lophiiformes: Antennariidae)
Fig. 2. Esca of Nudiantennarius subteres, BMNH 1866.8.14.108, 64 mm SL (after Pietsch and Grobecker, 1987).
Identifying volatile metabolite signatures for the diagnosis of bacterial respiratory tract infection using electronic nose technology: a pilot study
<p>Datasets for the <strong>Identifying volatile metabolite signatures for the diagnosis of bacterial respiratory tract infection using electronic nose technology: a pilot study. </strong></p>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.