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.
20
datasets available to search
ShareScore release 0.9.0
Dataset results
20 results for “western Uganda”
Supplementary data and code: Human–Wildlife Interactions Predict Febrile Illness in Park Landscapes of Western Uganda
<p>Data at code used for analyses.</p> <p>Salerno J, Ross N, Ghai R, et al (2017) Human–Wildlife Interactions Predict Febrile Illness in Park Landscapes of Western Uganda. EcoHealth. doi: 10.1007/s10393-017-1286-1<br> </p>
Figures 14–19 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figures 14–19. Automontage photographs of features of the Aleiodes buzurae-group. (14) Aleiodes kasenenei sp. n., habitus; (15)–(19) Aleiodes kanyawarensis sp. n., habitus, face, mesosoma, wings and metasoma, respectively.
Figure 3 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 3. Bootstrap consensus tree from analysis of CO1 sequence data for Aleiodes reared from suspended mummies in Uganda plus another member of the A. buzurae-group and outgroups.
Figures 20–25 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figures 20–25. Automontage photographs of features of Aleiodes trevelyanae sp. n. (20)–(24) Habitus, face, metasoma, mesosoma and wings of holotype; (25) metasoma of paratype.
Figures 10–13 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figures 10–13. Automontage photographs of features of Aleiodes busutai sp. n., habitus, head lateral aspect, metasoma and mesosoma, respectively.
Figure 2 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 2. Phylogram from analysis of CO1 DNA sequence data for individuals of the A. buzurae-group and related species, and also multiple representatives of four European species for comparison.
Figure 1 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 1. Photograph of a suspended mummy showing J-shaped configuration with silk thread (arrowed) arising near larval mouth.
Figure 4 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 4. Selected contiguous fragment of the CO1 gene in individuals of the Aleiodes buzurae-group from Uganda and Kenya with bold characters indicating substitutions. Asterisks show phylogenetically informative substitutions at species level; exclamation marks show apomorphies for individual species in the buzarae group and $ sites that have both unique and informative variation.
Getting Malaria "Off the Back" of Women and Children in Western Uganda
ClinicalTrials.gov study NCT04102592. IPD Sharing: YES. Countries: 1. Publications: 1.
Data from: How do patients and health workers interact around malaria rapid diagnostic testing, and how are the tests experienced by patients in practice? A qualitative study in western Uganda
Background: Successful scale-up in the use of malaria rapid diagnostic tests (RDTs) requires that patients accept testing and treatment based on RDT results and that healthcare providers treat according to test results. Patient-provider communication is a key component of quality care, and leads to improved patient satisfaction, higher adherence to treatment and better health outcomes. Voiced or perceived patient expectations are also known to influence treatment decision-making among healthcare providers. While there has been a growth in literature on provider practices around rapid testing for malaria, there has been little analysis of inter-personal communication around the testing process. We investigated how healthcare providers and patients interact and engage throughout the diagnostic and treatment process, and how the testing service is experienced by patients in practice. Methods: This research was conducted alongside a larger study which explored determinants of provider treatment decision-making following negative RDT results in a rural district (Kibaale) in mid-western Uganda, ten months after RDT introduction. Fifty-five patients presenting with fever were observed during routine outpatient visits at 12 low-level public health facilities. Observation captured communication practices relating to test purpose, results, diagnosis and treatment. All observed patients or caregivers were immediately followed up with in-depth interview. Analysis followed the 'framework' approach. A summative approach was also used to analyse observation data. Results: Providers failed to consistently communicate the reasons for carrying out the test, and particularly to RDT-negative patients, a diagnostic outcome or the meaning of test results, also leading to confusion over what the test can detect. Patients appeared to value testing, but were frustrated by the lack of communication on outcomes. RDT-negative patients were dissatisfied by the absence of information on an alternative diagnosis and expressed uncertainty around adequacy of proposed treatment. Conclusions: Poor provider communication practices around the testing process, as well as limited inter-personal exchange between providers and patients, impacted on patients' perceptions of their proposed treatment. Patients have a right to health information and may be more likely to accept and adhere to treatment when they understand their diagnosis and treatment rationale in relation to their perceived health needs and visit expectations.
On following pages: 154. Western Tsessebe (Damaliscus lunatus); 155. Bangweulu Tsessebe (Damaliscus superstes ugandae); 159. Ruaha Topi (Damaliscus eurus); 160. Serengeti Topi (Damaliscus jimela); 161. Coastal Topi (Damaliscus); 156. Korrigum (Damaliscus korrigum); 157. Tiang (Damaliscus tiang); 158. Uganda Topi (Damaliscus top). in Bovidae
On following pages: 154. Western Tsessebe (Damaliscus lunatus); 155. Bangweulu Tsessebe (Damaliscus superstes ugandae); 159. Ruaha Topi (Damaliscus eurus); 160. Serengeti Topi (Damaliscus jimela); 161. Coastal Topi (Damaliscus); 156. Korrigum (Damaliscus korrigum); 157. Tiang (Damaliscus tiang); 158. Uganda Topi (Damaliscus top).
Subspecies and Distribution. L. ¢c. capensis Linnaeus, 1758 — Western Cape Province (South Africa). L.c.aegyptiusDesmarest,1822—Egypt,Sudan,Palestine. L.c.aquiloThomas&Wroughton,1907—SMozambique. L. c. arabicus Hemprich & Ehrenberg, 1832 — Middle East, Arabian Peninsula, Iran, SW Pakistan (Baluchistan), and SW Afghanistan. . ¢. atlanticus de Winton, 1898 — Morocco. ¢. carpi Lundholm, 1955 — NW Namibia. granti Thomas & Schwann, 1904 — Northern Cape Province (South Africa). MDDnop hawker: Thomas, 1901 — W Sudan, Eritrea. isabellinus Cretzschmar, 1826 — Egypt, Sudan, Eritrea. Ean mediterraneus Wagner, 1841 — Sardinia. schlumberger: Remy Saint-Loup, 1894 — NE Morocco. sinaiticus Hemprich & Ehrenberg, 1832 — Egypt, Iraq. S whitakeri Thomas, 1902 — Libya, Niger and Algeria. The Cape Hare occurs in the Mediterranean I of Sardinia and in isolated populations scattered throughout most of the Arabian Peninsula and the Middle East and E to W Himalayas. This species has an extensive range in Africa which is separated in two distinct regions. First, in Egypt, Sudan, South Sudan, Eritrea, Ethiopia, Uganda, Kenya, and Tanzania, and throughout most of the dry savanna regions of C, W & N Africa, including parts of the Sahara Desert. Second, in savanna and semi-desert regions of Namibia, Botswana, S Zimbabwe, SW Mozambique, South Africa, Swaziland, and Lesotho. in Leporidae
Subspecies and Distribution. L. ¢c. capensis Linnaeus, 1758 — Western Cape Province (South Africa). L.c.aegyptiusDesmarest,1822—Egypt,Sudan,Palestine. L.c.aquiloThomas&Wroughton,1907—SMozambique. L. c. arabicus Hemprich & Ehrenberg, 1832 — Middle East, Arabian Peninsula, Iran, SW Pakistan (Baluchistan), and SW Afghanistan. . ¢. atlanticus de Winton, 1898 — Morocco. ¢. carpi Lundholm, 1955 — NW Namibia. granti Thomas & Schwann, 1904 — Northern Cape Province (South Africa). MDDnop hawker: Thomas, 1901 — W Sudan, Eritrea. isabellinus Cretzschmar, 1826 — Egypt, Sudan, Eritrea. Ean mediterraneus Wagner, 1841 — Sardinia. schlumberger: Remy Saint-Loup, 1894 — NE Morocco. sinaiticus Hemprich & Ehrenberg, 1832 — Egypt, Iraq. S whitakeri Thomas, 1902 — Libya, Niger and Algeria. The Cape Hare occurs in the Mediterranean I of Sardinia and in isolated populations scattered throughout most of the Arabian Peninsula and the Middle East and E to W Himalayas. This species has an extensive range in Africa which is separated in two distinct regions. First, in Egypt, Sudan, South Sudan, Eritrea, Ethiopia, Uganda, Kenya, and Tanzania, and throughout most of the dry savanna regions of C, W & N Africa, including parts of the Sahara Desert. Second, in savanna and semi-desert regions of Namibia, Botswana, S Zimbabwe, SW Mozambique, South Africa, Swaziland, and Lesotho.
Subspecies and Distribution. L.v.victoriaeThomas,1893—Tanzania. L.v.angolensisThomas,1904—Angola. L.v.senegalensisRochebrune,1883—Senegal,TheGambia. L. v. whyte: Thomas, 1894 — Malawi. The African Savanna Hare is present from the Atlantic coast of NW Africa (Western Sahara S to Guinea), E across the Sahel to Sudan and the extreme W Ethiopia, S through E Africa (E DR Congo, Uganda, W Kenya, Rwanda, Burundi, and Tanzania) to most of Angola, Zambia, Malawi, NE Namibia, Botswana, Zimbabwe, Mozambique, E South Africa, Swaziland, and Lesotho; a small isolated population exists near Beni Abbas in the Sahara Desert in W Algeria. in Leporidae
Subspecies and Distribution. L.v.victoriaeThomas,1893—Tanzania. L.v.angolensisThomas,1904—Angola. L.v.senegalensisRochebrune,1883—Senegal,TheGambia. L. v. whyte: Thomas, 1894 — Malawi. The African Savanna Hare is present from the Atlantic coast of NW Africa (Western Sahara S to Guinea), E across the Sahel to Sudan and the extreme W Ethiopia, S through E Africa (E DR Congo, Uganda, W Kenya, Rwanda, Burundi, and Tanzania) to most of Angola, Zambia, Malawi, NE Namibia, Botswana, Zimbabwe, Mozambique, E South Africa, Swaziland, and Lesotho; a small isolated population exists near Beni Abbas in the Sahara Desert in W Algeria.
Subspecies and Distribution. E.p.patasSchreber,1774—sub-SaharanAfricafromSMauritaniaandSenegaltoChadandCentralAfricanRepublic;isolatedpopulationsinhabittherockyAirMassifofNNigerandtheEnnediMassif,Chad. E.p.baumstarkiMatschie,1905—NCTanzania(SerengetiandAthiPlainsandtheWsideofMt.Kilimanjaro),butthedistributionisnotwelldocumented. E. p. pyrrhonotus Hemprich & Erhenburg, 1829 — Sudan (N to Nubia), South Sudan, W Ethiopia, N DR Congo, N Uganda, and Kenya. Introduced into south-western Puerto Rico in the Caribbean Islands. in Cercopithecidae
Subspecies and Distribution. E.p.patasSchreber,1774—sub-SaharanAfricafromSMauritaniaandSenegaltoChadandCentralAfricanRepublic;isolatedpopulationsinhabittherockyAirMassifofNNigerandtheEnnediMassif,Chad. E.p.baumstarkiMatschie,1905—NCTanzania(SerengetiandAthiPlainsandtheWsideofMt.Kilimanjaro),butthedistributionisnotwelldocumented. E. p. pyrrhonotus Hemprich & Erhenburg, 1829 — Sudan (N to Nubia), South Sudan, W Ethiopia, N DR Congo, N Uganda, and Kenya. Introduced into south-western Puerto Rico in the Caribbean Islands.
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996). in Muridae
Lophuromys medicaudatus, L. woosnami, and L. luteogaster are in subgenus Kivumys and woosnami species group. Monotypic. Distribution. Endemic to the Albertine Rift, occurring around Lake Kivu in E DR Congo and Rwanda and SW Uganda (Bwindi). Descriptive notes. Head—body 92-112 mm, tail 73-95 mm, ear 15-19 mm, hindfoot 18-23 mm; weight 29-43 g. Similar to other species in subgenus Kivumys, the Western Rift Brush-furred Rat has unspeckled pelage, and tail ¢.85% of head-body length. Dorsum is uniform dark brown-olive, and venter is orange. Females have three pairs of mammae. Habitat. Mountain swamps and mountain forests at elevations of 1850-2500 m. Food and Feeding. The Western Rift Brush-furred Rat is omnivorous; diets contain 30-100% arthropods, mollusks, seeds, and fruits. Breeding. Female Western Rift Brush-furred Rats can have 1-2 embryos. Pregnant females were observed in February, April, and July. Activity patterns. The Western Rift Brush-furred Rat is terrestrial. Movements, Home range and Social organization. No information. Status and Conservation. Classified as Vulnerable on The IUCN Red List. The Western Rift Brush-furred Rat has never been found in modified secondary environment and is quite rare. Bibliography. Dieterlen (1976b, 1987 2013g), Kasangaki et al. (2003), Verheyen et al. (1996).
Improving the Nutrition Status of Infants in South-Western Uganda
ClinicalTrials.gov study NCT02098031. IPD Sharing: Not stated. Countries: 1. Publications: 5.
Genetic Patterns of Common-Bean Seed Acquisition and Early-stage Adoption among Farmer Groups in Western Uganda
Open the record for dataset details and reuse information.
Data from: How do patients and health workers interact around malaria rapid diagnostic testing, and how are the tests experienced by patients in practice? A qualitative study in western Uganda
Open the record for dataset details and reuse information.
Figures 6–9 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figures 6–9. Automontage photographs of features of the Aleiodes buzurae-group. (6) A. buzurae, metasoma. (7)– (9) A. barnardae sp. n., habitus, face and metasoma, respectively.
Figure 5 in Suspended mummies in Aleiodes species (Hymenoptera: Braconidae: Rogadinae) with descriptions of six new species from western Uganda based largely on DNA sequence data
Figure 5. Two fragments of the ITS2 region aligned by eye showing marked differences between species in the Aleiodes buzurae-group. Asterisks and bold font indicate substitutions in length-conserved regions and lines show regions of length variation. Xs indicate uncertainty about number and identity of bases.
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.