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.
184
datasets available to search
ShareScore release 0.9.0
Dataset results
184 results for “298”
GROMOS-CKP POPS simulations (versions 1 and 2) 298 K with GROMOS NH3 charges and PME
<p>GROMOS-CKP POPS simulations (298 K, starting structure from the CHARMM-GUI with the appropriate hydrogen atoms removed) performed with 1.4 nm cut-offs, PME and a long range dispersion correction. The charges for the NH3 part of the head group are taken from the standard GROMOS force field parameters. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
Slipids POPS simulations (versions 1 and 2) 298 K 1.0 nm cut-off with LJ-PME
<p>Slipids POPS simulations (298 K, starting structure from the CHARMM-GUI) performed with 1.0 nm cut-offs, PME and LJ-PME. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
CHARMM36 POPS simulations (versions 1 and 2) 298 K 1.0 nm LJ switching
<p>CHARMM36 POPS simulations (298 K, starting structure from the CHARMM-GUI) performed with a 1.0 nm point at which to switch off the van der Waals interactions. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
CHARMM36-UA POPS simulations (versions 1 and 2) 298 K 1.0 nm LJ switching
<p>CHARMM36-UA POPS simulations (298 K, starting structure from the CHARMM-GUI) performed with a 1.0 nm point at which to switch off the van der Waals interactions. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
Berger POPS simulations (versions 1 and 2) 298 K 1.0 nm cut-off
<p>Berger POPS simulations (298 K, starting structure from the CHARMM-GUI with the appropriate hydrogen atoms removed) performed with 1.0 nm cut-offs and no long range dispersion correction. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
GROMOS-CKP POPS simulations (versions 1 and 2) 298 K with Berger/Chiu NH3 charges and PME
<p>GROMOS-CKP POPS simulations (298 K, starting structure from the CHARMM-GUI with the appropriate hydrogen atoms removed) performed with 1.4 nm cut-offs, PME and a long range dispersion correction. The charges for the NH3 part of the head group are the same as in the Berger PS simulations (originally taken from the Berger/Chiu PC head group). Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
CHARMM36 POPS/POPC simulations (versions 1 and 2) 298 K 1.0 nm LJ switching with Na ions
<p>CHARMM36 mixed POPS and POPC bilayer simulations (298 K, starting structure from the CHARMM-GUI with 22 POPS and 110 POPC lipids) performed with a 1.0 nm point at which to switch off the van der Waals interactions. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small. These simulations were performed with Na ions used to neutralise the system.</p>
CHARMM36 POPS/POPC simulations (versions 1 and 2) 298 K 1.0 nm LJ switching with K ions
<p>CHARMM36 mixed POPS and POPC bilayer simulations (298 K, starting structure from the CHARMM-GUI with 22 POPS and 110 POPC lipids) performed with a 1.0 nm point at which to switch off the van der Waals interactions. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small. These simulations were performed with K ions used to neutralise the system.</p>
CHARMM36 POPS simulations (versions 1 and 2) 298 K 1.0 nm LJ switching with K ions
<p>CHARMM36 POPS simulations (298 K, starting structure from the CHARMM-GUI) performed with a 1.0 nm point at which to switch off the van der Waals interactions. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small. These simulations were performed with K ions used to neutralise the system.</p>
FIGURES 298–302. Female postabdomens. 298–300 in Key to Adults of North American Genera of the Subfamily Cecidomyiinae (Diptera: Cecidomyiidae)
FIGURES 298–302. Female postabdomens. 298–300, Endaphis fugitiva Gagné: 298, 7th segment to cerci; 299, 8th segment to cerci (lateroventral); 300, cerci and hypoproct (lateral). 301, Harmandiola amisae Gagné, 6th segment to cerci with detail (lateral). 302, Lopesia licaniae Gagné, 7th segment to cerci with detail (lateral).
GROMOS-CKP POPS/POPC simulations (versions 1 and 2) 298 K with GROMOS NH3 charges and PME
<p>GROMOS-CKP POPS/POPC simulations (298 K, starting structure from the CHARMM-GUI with the appropriate hydrogen atoms removed and with 22 POPS and 110 POPC lipids) performed with 1.4 nm cut-offs, PME and a long range dispersion correction. The charges for the NH3 part of the head group are taken from the standard GROMOS force field parameters. Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
MacRog POPS simulations (versions 1 and 2) 298 K with corrected PO not OP tails
<p>MacRog POPS simulations (298 K, starting structure from the CHARMM-GUI) performed with 1.0 nm cut-offs, PME and a dispersion correction. Two simulations were performed with differently assigned random starting velocities. Note that unlike the original MacRog simulations, these have the correct PO and not OP tails. </p>
GROMOS-CKP POPS/POPC simulations (versions 1 and 2) 298 K with Berger/Chiu NH3 charges and PME
<p>GROMOS-CKP POPS/POPC simulations (298 K, starting structure from the CHARMM-GUI with the appropriate hydrogen atoms removed and with 22 POPS and 110 POPC lipids) performed with 1.4 nm cut-offs, PME and a long range dispersion correction. The charges for the NH3 part of the head group are the same as in the Berger PS simulations (originally taken from the Berger/Chiu PC head group). Two different simulations generated with different starting velocities are provided (the files are named v1 and v2 for these different simulations). The trajectories contain only the data from 400-500 ns of the simulations (as per the analysis provided on the nmrlipids blog) and additionally they have been processed with trjconv -skip 10 to keep the upload small.</p>
PowerTAC 2018-07 Finals Game 298
Log and boot files of game 298
FIGURES 293–298 in New state and host records for Agromyzidae (Diptera) in the United States, with the description of thirty new species
FIGURES 293–298. Liriomyza ivorcutleri spec. nov., male genitalia; 293: external components, left lateral; 294: same, ventral; 295: hypandrium, ventral; 296: ejaculatory apodeme; 297: phallus, ventral; 298: phallus, left lateral.
FIGURES 295–298. Barsine spp., male genitalia. 295, B in A review of the Barsine hypoprepioides (Walker, 1862) species-group, with descriptions of fifteen new species and a new subspecies (Lepidoptera, Erebidae, Arctiinae)
FIGURES 295–298. Barsine spp., male genitalia. 295, B. honbaensis, holotype, Vietnam, slide AV2538 Volynkin (ex prep. Dubatolov); 296, ditto, Taiwan, slide MWM 31455 Volynkin; 297, ditto, N Myanmar, slide MWM 34587 Volynkin; 298, B. dentata, Taiwan, slide MWM 34595 Volynkin.
finals_2019_07_298
Log and boot files of game 298
FIGURES 298–301. SEM. 298 in The diatom genus Gomphonema Ehrenberg in Lake Baikal. II. Revision of taxa from Gomphonema acuminatum and Gomphonema truncatum-capitatum complexes
FIGURES 298–301. SEM. 298. Gomphonema capitatum, external view, footpole with apical pore field restricted almost entirely to the valve mantle. Pore field bisected by deflected distal raph end. C–shaped areolae evident. 299–301. Gomphonema cf. capitatum, external views. 299. General valve view. 300. Headpole with distal raphe end deflected onto mantle. Striae with C-shaped areolae continue from valve all around the mantle. 301. Central area. Undulate raphe is distinct. Striae formed of C-shaped areolae. Scale bars = 2 μm in Figs 298, 300, 301; 5 μm in Fig. 299.
FIGURES 295–304. Figures 295–298 in Rearing mining flies (Diptera: Agromyzidae) from host plants as an instrument for associating females with males, with the description of seven new species
FIGURES 295–304. Figures 295–298: Agromyza hendeli Griffiths; 295: cephalopharyngeal skeleton; 296: frontal view of head; 297: head viewed from the side; 298: spermatheca. Figure 299: cephalopharyngeal skeleton of A. igniceps Hendel; Figures 300–304: A. reptans Fallén; 300: cephalopharyngeal skeleton; 301: parastomal bar and anterior portion of pharyngeal sclerite viewed from below; 302: frontal view of head; 303: head viewed from the side; 304: spermathecae.
FIGURES 292–301. Pinodytes capizzii. 292. Male right antenna, dorsal. 293. Male right protibia and protarsus. 294. Male right mesotibia. 295. Male right metafemur and metatibia. 296. Aedeagus, lateral. 297. Aedeagus, dorsal. 298 in Systematics, distributions and bionomics of the Catopocerini (eyeless soil fungivore beetles) of North America (Coleoptera: Leiodidae: Catopocerinae) 3077
FIGURES 292–301. Pinodytes capizzii. 292. Male right antenna, dorsal. 293. Male right protibia and protarsus. 294. Male right mesotibia. 295. Male right metafemur and metatibia. 296. Aedeagus, lateral. 297. Aedeagus, dorsal. 298. Variation in apex of aedeagus, dorsal (Lane Co., Oregon). 299. Variation in apex of aedeagus, dorsal (Columbia Co., Oregon). 300. Spermatheca. 301. Mesoventrite, lateral. Scale bar = 0.1 mm (Fig. 300), 0.3 mm (Figs. 292–299, 301).
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.