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2,848 results for “sequence data”
Fine-scale structure of the 2016-2017 Central Italy Seismic Sequence from data recorded at the Italian National Network
<p><strong>Data Set </strong></p> <p>Catalog of 33,983 earthquakes located during the 2016-2017 Central Italy seismic sequence. The velocity model used is the 1D gradient P- and S-wave velocity models (after Carannante et al., 2013). We used the highest quality P- and S-wave arrival times manually picked by analysts of the National Institute of Geophysics and Volcanology (INGV) seismic monitoring room, having an uncertainty lower than 0.6 s. </p> <p>Events were located by means of a 2-step procedure: the INGV routine absolute locations computation for all events with ML ≥ 1.5 that occurred in the study area between August 2016 and January 2018, using the method described in Chiaraluce et al. (2017); the determination of relative locations by applying the HypoDD code (Waldhauser, 2001) to the catalog picks and phase delay times measured from waveform cross correlation.</p> <p>The time domain cross-correlation method (Schaff et al., 2004; Schaff and Waldhauser, 2005) was applied to seismograms of all pairs of events separated by 3 km or less and recorded at common stations. Seismograms were filtered in the 1-15 Hz frequency range using a 4 pole, zero phase band‐pass Butterworth filter. The correlations measurements were performed on 0.7 s long window for P-waves and 1 s windows for S-waves. Only measurements with correlation coefficients greater than 0.7 were kept, resulting in a total of ~4.4 million P and ~1.1 million S wave delay times. </p> <p>We sub-divided the entire dataset in 18 rectangular boxes, containing a maximum of 6000 earthquakes, orthogonal to and centered on the mean strike of the seismic sequence. The overlap between neighboring boxes is 50% with respect to the NW-SE extension. HypoDD is run separately on each box. Resulting relative locations from all boxes were combined into a single catalog, computing the weighted mean of double hypocenters in the overlapping regions (Waldhauser and Schaff, 2008).</p> <p>The final double-difference catalog includes 33,982 events occurring between 24<sup>th</sup> of August 2016 and 18<sup>th</sup> of January 2018.</p> <p>The catalog is in csv format, semicolon separator, ordered by origin time and the header content is the following:</p> <ul> <li>Id-ingv: ingv eventid, useful to link to the QuakeML phase file through the INGV fdsnws/event webservice (<a href="https://meet.google.com/linkredirect?authuser=0&dest=http%3A%2F%2Fwebservices.ingv.it%2Fswagger-ui%2Fdist%2F%3Furl%3Dhttps%3A%2F%2Fingv.github.io%2Fopenapi%2Ffdsnws%2Fevent%2F0.0.1%2Fevent.yaml">http://webservices.ingv.it/swagger-ui/dist/?url=https://ingv.github.io/openapi/fdsnws/event/0.0.1/event.yaml</a>) and to the reported magnitude;</li> <li>Latitude(°) expressed in decimal degrees;</li> <li>Longitude(°) expressed in decimal degrees;</li> <li>Depth(km) hypocentral depth expressed in kilometers;</li> <li>Year of origin time in the format yyyy;</li> <li>Month of origin time in the format mm;</li> <li>Day of origin time in the format dd; </li> <li>Hour of origin time in the format hh;</li> <li>Minute of origin time in the format min;</li> <li>Second of origin time in the format ??.?????? s;</li> <li>Magnitude: the value available at the phases downloading time (see Id-ingv fdsnws/event)</li> </ul> <p> </p> <p> </p> <p> </p> <p><br> </p>
Strong sequence dependence in RNA/DNA hybrid strand displacement kinetics supplementary data and code
<p>Supplementary data and code needed to replicate figures and results for the paper: Strong sequence-dependence in RNA/DNA hybrid strand displacement kinetics - Francesca G. Smith, John P. Goertz, Molly M. Stevens and Thomas E. Ouldridge. README is included to explain each folder and file in the repository.</p>
Supporting data for publication: The role of the three-dimensional geometry of fault steps on event migration during fluid-induced seismic sequences.
<p><span>This repository contains the supplementary data used in the publication Roche et al., 2024 (The role of the three-dimensional geometry of fault steps on event migration during fluid-induced seismic sequences), including (1) the seismicity catalogues from Cahuilla, Yellowstone and West Bohemia, modified from Ross et al. (2020), Shelly et al. (2013) and Hainzl et al. (2016), and (2) the pictures series used to build isochrone contour maps.</span></p> <p><span><span>1.<span> </span></span></span><span>Seismicity catalogues</span></p> <p><span>The seismicity catalogues from Cahuilla, Yellowstone and West Bohemia are modified from Ross et al. (2020), Shelly et al. (2013) and Hainzl et al. (2016). The catalogues include the hypocentre location, relative time, and magnitude for non-filtered and filtered data. General information on each catalogue and filtering and modifications can be found in the associated publication.</span></p> <p><span> Dataset list:</span></p> <ul> <li><span>Cahuilla Catalogues (modified from Ross et al., 2019): </span></li> <ul> <li><span>Original data: File name: VR_sup_0021_Cah_All</span></li> <li><span>Filtered data: File name: VR_sup_0022_Cah_Filter</span></li> </ul> <li><span>Bohemia 2008 Catalogues (modified from Haintzl et al., 2016): </span></li> <ul> <li><span>Original data: File name: VR_sup_0023_Boh_08_All</span></li> <li><span>Filtered data: File name: VR_sup_0024_Boh_08_Filter</span></li> </ul> <li><span>Bohemia 2014 Catalogues (modified from Haintzl et al., 2016): </span></li> <ul> <li><span>Original data: File name: VR_sup_0025_Boh_14_All</span></li> <li><span>Filtered data: File name: VR_sup_0026_Boh_14_Filter</span></li> </ul> <li><span>Yellowstone Catalogs (modified from Shelly et al., 2013): </span></li> <ul> <li><span>Original data: File name: VR_sup_0027_Yell_14_All</span></li> <li><span>Filtered data: File name: VR_sup_0028_Yell_14_Filter</span></li> </ul> </ul> <p><span>The files are text files tab-delimited, with the following headers:</span></p> <ul> <li><span>Index: 1 by default</span></li> <li><span>Easting(m): hypocenter Easting in meters </span></li> <li><span>Northing(m): hypocenter Northing in meters </span></li> <li><span>Depth(m): hypocenter depth in meters </span></li> <li><span>Mw: magnitude</span></li> <li><span>Relative Time(s): date of the origin time in the format </span></li> </ul> <p><span><span>2.<span> </span></span></span><span>Seismicity catalogues</span></p> <p><span>The pictures series are images of seismicity at a regular time interval for each studied step.</span></p> <p><span>Dataset list:</span></p> <ul> <li><span>Step C1: File name: VR-sup-0012-Pictures_C1.</span></li> <li><span>Step C2: File name: VR-sup-0013-Pictures_C2.</span></li> <li><span>Step C3: File name: VR-sup-0014-Pictures_C3.</span></li> <li><span>Step C4: File name: VR-sup-0015-Pictures_C4.</span></li> <li><span>Step Y1: File name: VR-sup-0016-Pictures _Y1.</span></li> <li><span>Step B1I: File name: VR-sup-0017-Pictures _B1I.</span></li> <li><span>Step B1II: File name: VR-sup-0018-Pictures _B1II.</span></li> <li><span>Step B2: File name: VR-sup-0019-Pictures _B2.</span></li> <li><span>Step B3: File name: VR-sup-0020-Pictures _B3.</span></li> </ul> <p><span>Each file contains a series of pictures in JPEG format. For each picture, events in the overlying and underlying segments are indicated in blue and red. The full circles represent the events occurring during the last interval. The empty circles represent the events occurring in the previous intervals.</span></p> <p><span>If you find these data useful in your research, please cite Roche et al. (2024), as well as the relevant papers Ross et al. (2020), Shelly et al. (2013) and Hainzl et al. (2016).</span></p>
RNA sequencing data for bleomycin exposed THP-1 macrophages
<p>This dataset contains normalized counts matrices, from dds_deseq objects, from DeSeq2 analysis of RNA sequencing data, from THP-1 macrophages exposed to multiple doses of bleomycin in the range of 0-100µg/ml for 24H, 48H or 72H.</p>
Variant Data from Pooled Sequencing of Hybrid Kiwifruit
<p>Variant data from pooled sequencing of hybrid <em>Actinidia</em> families segregating for fruit size and Vitamin C Content.</p>
Supplementary dataset to publication: Oxford nanopore technologies - a valuable tool to generate whole-genome sequencing data for in silico serotyping and the detection of genetic markers in Salmonella, Thomas et al 2023
<p>Bacteria of the genus <em>Salmonella</em> pose a major risk to livestock, the food economy, and public health. <em>Salmonella</em> infections are one of the leading causes of food poisoning. The identification of serovars of <em>Salmonella</em> achieved by their diverse surface antigens is essential to gain information on their epidemiological context. Traditionally, slide agglutination has been used for serotyping. In recent years, whole-genome sequencing (WGS) followed by <em>in silico</em> serotyping has been established as an alternative method for serotyping and the detection of genetic markers for <em>Salmonella</em>. Until now, WGS data generated with Illumina sequencing are used to validate <em>in silico</em> serotyping methods. Oxford Nanopore Technologies (ONT) opens the possibility to sequence ultra-long reads and has frequently been used for bacterial sequencing. In this study, ONT sequencing data of 28 <em>Salmonella</em> strains of different serovars with epidemiological relevance in humans, food, and animals were taken to investigate the performance of the <em>in silico</em> serotyping tools SISTR and SeqSero2 compared to traditional slide agglutination tests. Moreover, the detection of genetic markers for resistance against antimicrobial agents, virulence, and plasmids was studied by comparing WGS data based on ONT with WGS data based on Illumina. Based on the ONT data from flow cell version R9.4.1, <em>in silico</em> serotyping achieved an accuracy of 96.4 and 92% for the tools SISTR and SeqSero2, respectively. Highly similar sets of genetic markers comparing both sequencing technologies were identified. Taking the ongoing improvement of basecalling and flow cells into account, ONT data can be used for <em>Salmonella in silico</em> serotyping and genetic marker detection.</p>
Data from: Complex population structure and haplotype patterns in Western Europe honey bee from sequencing a large panel of haploid drones
<p>This vcf file contains 7.023.689 SNPs and 870 honey bee samples, as described in the paper "Complex population structure and haplotype patterns in Western Europe honey bee from sequencing a large panel of haploid drones" by Wragg et al., available at https://doi.org/10.1101/2021.09.20.460798 as preprint.</p> <p>Eight hundred and seventy haploid drone samples from several honey bee subspecies hybrids were sequenced and aligned to the HAv3.1 reference genome. Sequence read alignment and genotyping quality filters were used to obtain a selection of 7.023.689 high-quality SNPs. The file Diversity_Study_629_Samples.txt corresponds to the 629 unique samples that were used for the diversity study described in the paper and can be used to recreate the restricted diversity dataset using bcftools or an equivalent software.</p> <p>Having sequenced haploid drones, heterozygous SNPs resulting from duplicated regions could be filtered out and the data is phased.</p>
Magnetic resonance spectroscopy data acquired in tinnitus subjects and healthy volunteers using PRESS sequence
<p>This dataset contains raw free induction decay (FID) signals collected during 1H magnetic resonance spectroscopy (MRS) study in 52 individuals with tinnitus (24 with unilateral and 28 with bilateral tinnitus) and 25 healthy volunteers (described in detail in a separate article doi:10.1038/s41598-023-45024-3).</p><p>Data acquisition was performed using 3T Siemens Prisma Fit scanner with a 20-channel receiver head-coil. A single voxel spectroscopy (SVS) PRESS (Point-Resolved Spectroscopy Sequence) sequence was applied for collection of MRS data, using standard Siemens water suppression (water saturation, 50 Hz bandwidth) and no lipid suppression. MRS data was collected from four cubic 3.75 cm3 (1.5 cm x 1.5 cm x 1.5 cm) regions-of-interest in the brain, placed in the left temporal lobe, right temporal lobe, left frontal lobe, and right frontal lobe. The MRS sequence parameters were: TR (time of repetition) = 2000 ms, TE (time of echo) = 40 ms, TA (time of acquisition) = 4 min 26 s, 128 averages with 1024 time points and 1200 Hz bandwidth.</p><p>MRS data is stored in RDA file format, developed by Siemens (see doi:10.1002/nbm.4257, Table 1). Each RDA file contains a text header (which can be viewed using a standard notepad application) and binary FID signal under the header. Data can be imported for analysis using several open-source packages (tested with FID-A doi:10.1002/mrm.26091 and spant doi:10.21105/joss.03646). </p><p>Naming scheme of files is as follows:</p><p><participant ID>_<hemisphere: L or R>_<region: F (frontal) or T (temporal)>.rda</p><p>For example: <i>001_L_F.rda</i> is data from participant 001 collected from a voxel placed in a ROI in the left frontal lobe.</p><p>In order to allow replication of the results from the original article, we also added information about the group of each of the subjects. This information is stored in a TSV file containing two columns: <i>participant_ID</i> and<i> group</i> (C – control, TU – unilateral tinnitus, TB – bilateral tinnitus).</p><p>Aside from replication of our results this dataset may be used e.g. for testing of different MRS data processing pipelines.</p>
MACREL software benchmark data set: Simulated metagenomes with sequencing quality, errors profile and abundance distributions derived from real samples
<p>These metagenomes were used in the benchmarking of FACS pipeline, and were designed after NGLess benchmark dataset (doi.org/10.5281/zenodo.2560288). Metagenomes were simulated with <a href="https://www.niehs.nih.gov/research/resources/software/biostatistics/art/index.cfm">ART-bin-MountRainier-2016.06.05</a> using real abundance profiles (.abund files) available <a href="https://doi.org/10.5281/zenodo.2560288">elsewhere</a>, and <a href="http://progenomes1.embl.de/data/repGenomes/representatives.contigs.fasta.gz">proGenomes' representative contigs</a> as reference genomes. There are available metagenomes with 40, 60 and 80 M (million of reads) based in the reference genomes and abundances of the following samples:</p> <pre><code>SAMEA2466916 SAMEA2466953 SAMEA2466965 SAMEA2621107 SAMEA2621229 SAMEA2621247</code></pre> <p>To convert them from the CRAM format back to fastq files:</p> <pre><code> ## 1. converting from cram to bam format: samtools view -b -T refgenome.fa -o file.bam file.cram ## 2. sorting the bam file: samtools sort -n file.bam -o input_sorted.bam # sort reads by identifier-name (-n) ## 3. converting from bam to fastq format: bedtools bamtofastq -i input_sorted.bam -fq output_r1.fastq -fq2 output_r2.fastq </code></pre> <p> </p>
A Bayesian Approach to Detect Pedestrian Destination-Sequences from WiFi Signatures: Data (Transp. Res. Part C, 2014)
<p>This dataset contains and describes the data used in</p> <p>Danalet, A., Farooq, B., & Bierlaire, M. (2014). A Bayesian approach to detect pedestrian destination-sequences from WiFi signatures. <em>Transportation Research Part C: Emerging Technologies</em>, <strong>44</strong>, 146-170. doi:10.1016/j.trc.2014.03.015</p> <p>Specifically it contains WiFi traces, pedestrian Semantically-Enriched Routing Graph (SERG), and Potential Attractivity measure (PAM).</p>
SNP and indel discovery and genotyping in next-generation sequencing data
<p>Code, logs and data for discovery and genotyping of SNPs and indels, in the the D.melanogaster genome, using GATK HaplotypeCaller. Code is in the zipped folder named code.zip. Run logs for this code as in the zipped folder named logs.zip. The unfiltered vcf genotypes file is named lhm_rg_HC_2015-09-15.vcf.gz. The filtered vcf genotypes file is named f1.lhm_rg_HC_raw.vcf.gz. The vcf submitted to NCBI dbSNP (filtered, and with indels >50bp and variants with null alternate alleles both removed) is named dbSNP.lhm_rg_HC_raw.vcf.gz. The folder local_reference.zip contains the reference assembly files against which genotypes were called against, and includes the code used to format the data prior to use. Also included is genotypes data from the two in-house reference line samples sequenced (BDGP6+ISO1 mito/dm6, Bloomington <em>Drosophila</em> Stock Center no. 2057)</p> <p>Samples are 220 Sussex-LH<sub>M</sub> hemiclones, and 2 RG. The first run did not include chromosome 4 and the mitochondrial genome, so these were genotyped separately, and then added to the rest of the results.</p> <p>The link for the NCBI dbSNP record is currently https://www.ncbi.nlm.nih.gov/projects/SNP/snp_viewBatch.cgi?sbid=1062461and the submitter handle is MORROW_EBE_SUSSEX.</p> <p>At the time of writting, the NCBI D.melanogaster build is still being updated, and therefore ss identifiers, but not rs identifers are available.</p> <p>The pre-print manuscript for this data is available on biorxiv: "Whole genome resequencing of a laboratory-adapted Drosophila melanogaster population sample" http://biorxiv.org/content/early/2016/10/17/081554 doi: http://dx.doi.org/10.1101/081554</p>
Structural variant discovery and genotyping in next-generation sequencing data
<p>Code, logs, data, and summaries for detection and genotyping of genomic structural variants in the D.melanogaster Sussex LHM hemiclones (and one in-house reference line individual), using Genomestrip/2.0</p> <p>The unfiltered CNV pipleline results are lhm_gs.cnvs.raw.vcf.gz</p> <p>Filtered CNV results (including removal of bad samples) are filtered.goodS.lhm_gs.cnvs.raw.vcf.gz</p> <p>The file uploaded to NCBI dbVAR (which comprises of the filtered CNVs and indels >50bp from the HaplotypeCaller method) is lhm_sx16.dbVAR.vcf.gz</p> <p>The NCBI dbVAR accession number is nstd134. Code, logs and summary data are in the zipped archives, named accordingly. The archive reference_data.zip contains additional input files required for Genomestrip, including a shell script for making some of them. The file gstrip_lhm_RG_bams.list is also an input for Genomestrip, indicating bam file names and paths.</p> <p>The pre-print manuscript for this data is available on biorxiv: "Whole genome resequencing of a laboratory-adapted Drosophila melanogaster population sample" http://biorxiv.org/content/early/2016/10/17/081554 doi: http://dx.doi.org/10.1101/081554</p> <p> </p>
Flow diagram for analysis of high-throughput sequencing data
<p>Tex code and resulting pdf image, summarising the data processing pipeline of high-throughput sequencing data (fastq format files), through mapping the data to a reference genome, and then discovery and genotyping of sequence variants. The latter stage uses both 'GATK Haplotype Caller' for smaller variants, such as single-nucleotide polymorphisms and insertion-deletion polymorphisms, and Genomestrip for variants such as deletions and duplications greater than 1000 nucelotide bases in length. Note that the flow diagram is intended to represent what steps were take in the study, and does not necessarily represent the current optimum methods.</p> <p>The manuscript for which this image is a part of can be found open-access at F1000 Research "Whole genome resequencing of a laboratory-adapted <em>Drosophila melanogaster </em>population sample" https://f1000research.com/articles/5-2644/v1 doi: 10.12688/f1000research.9912.1</p> <p> </p>
Data and configuration files for "Expansion of accreting main-sequence stars during rapid mass transfer"
<p>Data and configuration files that can be used to reproduce results from the paper <a href="https://ui.adsabs.harvard.edu/abs/2024ApJ...966L...7L/abstract">Expansion of Accreting Main-sequence Stars during Rapid Mass Transfer</a>. This directory contains MESA inlists and starting models used for calculations performed with MESA r15140, and YAML configuration files for calculations performed with COMPAS v02.41.04.</p> <p>See README.txt for a description of all files.</p> <p> </p> <p>Any work making use of these files should cite</p> <p>Lau, M., Hirai, R., Mandel, I., Tout, C., 2024, Expansion of Accreting Main-sequence Stars during Rapid Mass Transfer, ApJL, 966, 1</p> <div></div>
Supplementary Data Files for the paper "Intrinsically disordered compositional bias in proteins: Sequence traits, region clustering, and generation of hypothetical functional associations"
<div> <div> <div> <div> <p><strong>Supplementary data files relating to <a href="https://doi.org/10.1177/11779322241287485">https://doi.org/10.1177/11779322241287485. </a></strong></p> <p><strong><span>Suppl. File 1: Protein Family Clusters.</span></strong></p> <p><strong><span>Suppl. File 2: Cluster GO enrichments/depletions. </span></strong></p> <p><strong><span>Suppl. File 3: The raw ID-CBR data with annotations. </span></strong></p> <p><strong><span>Suppl. File 4: ­ID-CBR Cluster membership.</span></strong></p> <p><strong><span>Each file has an explanatory header. </span></strong></p> <p> </p> </div> </div> </div> </div>
GWAS Summary Statistics for Publication: Identifying novel genetic and phenotypic associations to genomic features by leveraging off-target reads in exome sequencing data
<p>This dataset contains summary statistics for genome-wide association studies (GWAS) conducted on genomic features derived from off-target reads in whole-exome sequencing (WES) data. The study utilized tools like Seeing Beyond the Target (SBT) and ImReP to construct novel phenotypic features from unmapped reads in ~50,000 participants in the UK Biobank. Features include mitochondrial DNA (mtDNA) copy number, ribosomal DNA (rDNA) copy number (5S, 18S, 28S), immune repertoire metrics (e.g., T-cell receptor alpha diversity), and microvial genome load (viral and fungal).</p> <p>Summary statistics can be used for replication studies, meta-analyses, or further exploration of these phenotypes.</p>
Sequence-based microsatellite data of Anadenanthera colubrina (Leguminosae)
<p>The file contains SSRseq genotyping data of <em>Anadenanthera colubrina</em> populations. Individuals from two life stages were scored at 25 SSRseq loci. Goncalves AL, García MV, Chancerel E, Lepais O, Heuertz M. High-throughput sequence-based microsatellite genotyping for the non-model Neotropical tree species <em>Anadenanthera colubrina</em> (Leguminosae).</p> <p>The file contains</p> <p>- Two different data sets:</p> <p>GS: Genotypes based on sequence identity.<br>GL: Genotypes based on amplicon length.</p> <p>- Allele sequence information</p>
Supplementary data for "Single extreme storm sequence can offset decades of predicted shoreline retreat by sea-level rise"
<p>This dataset comprises topography and bathymetric data at three coastal locations in Australia (Narrabeen), UK (Perranporth) and used for the publication "Single extreme storm sequence can offset decades of predicted shoreline retreat by sea-level rise". Please refer to readme files for metadata</p>
VirHunter: a deep learning-based method for detection of novel RNA viruses in plant sequencing data
<p>This storage contains 2 archives: toy datasets to test the training of the VirHunter and weights of the fully trained VirHunter models for 3 host species (peach, grapevine, sugar beet) and for fragment sizes 500 and 1000. .</p> <p>The toy dataset consists of 3 archived files: 'viruses.fasta', 'host.fasta', 'bacteria.fasta'.</p> <p>'viruses.fasta' contains 10000 randomly selected plant viruses from the virus dataset described in the paper.</p> <p>'host.fasta' consists of peach chromosome 2.</p> <p>'bacteria.fasta' consists of 10 bacterial genomes selected randomly: GCF_000284415, GCF_000590555, GCF_001548055, GCF_002795265, GCF_003330825, GCF_003957805, GCF_005845345, GCF_009176625, GCF_010748935, GCF_014681765</p> <p> </p>
Simulation Data for "Community-Driven Code Comparisons for Three-Dimensional Dynamic Modeling of Sequences of Earthquakes and Aseismic Slip"
<p>Simulation data from Jiang et al. (2022), "Community-Driven Code Comparisons for Three-Dimensional Dynamic Modeling of Sequences of Earthquakes and Aseismic Slip," <em>Journal of Geophysical Research: Solid Earth</em><em>.</em></p> <p>The archive includes simulation data for 3D SEAS benchmarks BP4-QD and BP5-QD that are analyzed in our paper (descriptions in NOTES.txt) </p> <p><strong>BP4-QD Benchmark Simulations:</strong><br>1000 m: jiang.5, lambert.8, barbot.3, barbot.2, dliu.2, li.4<br>500 m: jiang.3, lambert.3, barbot.5, barbot.7, ozawa</p> <p><strong>BP5-QD Benchmark Simulations:</strong><br>2000 m: jiang.6, lambert.8, liu.4, cattania.5, dli.7, barbot.3, dliu.10, li.3<br>1000 m: jiang.2, lambert.7, liu.5, cattania.3, ozawa, dli.5, barbot, dliu.6, li.2<br>500 m: jiang.4, lambert.9, liu.6, cattania.4, ozawa.2, dli.6, barbot.2, dliu.8<br>250 m: lambert.10, liu.7</p> <p><strong>BP5-QD with Off-Fault Data:</strong><br>1000 m: lambert.7, dli.5, barbot, dliu.6, li.2<br>500 m: lambert.9, dli.6, barbot.2, dliu.8</p> <p>Tables 2–4 in our paper summarizes details of numerical codes and selected simulations.</p> <p>The benchmark descriptions and the full suite of simulation data are available at SEAS online platform https://strike.scec.org/cvws/seas/.</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.