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6,383 results for “Isolation”
MRI data of 40 adult participants in response to a cue induced craving task following food fasting, social isolation and baseline (within-subject design)
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Root fungi isolated from common Louisiana marsh plants 2017-18.
Nearly all plants are colonized by fungal endophytes, and a growing body of work shows that both environment and host species shape plant-associated fungal communities. However, few studies place their work in a phylogenetic context to understand endophyte community assembly through an evolutionary lens. Here we collected data to investigate environmental and host effects on root endophyte assemblages in coastal Louisiana marshes. We isolated and sequenced culturable fungal endophytes from roots of three-four dominant plant species from each of three sites of varying salinity. We provide data on abundance and taxonomy of the isolated fungal taxa as well as phylogenetic diversity (mean phylogenetic distance, MPD) and phylogenetic composition (based on MPD).
Human intestinal Bacteria Collection (HiBC): Isolates and genomes metadata
<p>The <a href="https://hibc.rwth-aachen.de/" target="_blank" rel="noopener">Human intestinal Bacteria Collection (HiBC)</a> is a collection of bacterial strains, isolated from the human gut for which 16S rRNA gene sequences, genome sequences and culture conditions are made available to the research community. In addition to previously described bacteria, we include strains that represent novel species which have been taxonomically described and validly named, or will be in the future. This collection will be updated regularly.</p> <p>This dataset includes the taxonomy of the isolates, as well as metadata regarding their cultivation and isolation. We also provide metadata regarding the sequencing, genome assembly process and the biological sequences.</p> <p><strong>UPDATE v7</strong>: INSDC accession for <em>Segatella sinensis</em> CLA-AA-H117 was a missing value and is now the correct value of GCA_040324585.2.</p> <p><strong>UPDATE v6: </strong>The growth atmosphere is now indicated by anaerobic or aerobic instead of "Anaerobe/Aerobe" that was a misleading term. The risk group of these two isolates went from 1 to 2:</p> <ul> <li>CLA-AA-H205: <em>Anaerostipes caccae </em></li> <li>CLA-AA-H83: <em>Bacteroides fragilis</em></li> </ul> <p>The risk group of the following isolates has been updated (usually from unknown to 1, or from 2 to 1):</p> <ul> <li>CLA-SR-H026: <em>Aedoeadaptatus acetigenes</em></li> <li>CLA-KB-H139:<em> Bacteroides xylanisolvens</em></li> <li>CLA-SR-H015: <em>Bacteroides xylanisolvens</em></li> <li>CLA-AA-H187: <em>Blautia fusiformis</em></li> <li>CLA-AA-H274: <em>Brotaphodocola catenula</em></li> <li>CLA-AA-H286: <em>Butyricimonas faecihominis</em></li> <li>CLA-AA-H278:<em> Clostridium fessum</em></li> <li>CLA-AA-H147: <em>Dorea ammoniilytica</em></li> <li>CLA-SR-H027: D<em>orea formicigenerans</em></li> <li>CLA-KB-H89: <em>Dorea longicatena</em></li> <li>CLA-KB-H94: <em>Dorea longicatena</em></li> <li>CLA-SR-H022: <em>Enterococcus lactis</em></li> <li>CLA-AA-H250: <em>Hominenteromicrobium mulieris</em></li> <li>CLA-AA-H232: H<em>ominilimicola fabiformis</em></li> <li>CLA-AA-H246: <em>Hominisplanchenecus faecis</em></li> <li>CLA-AA-H276:<em> Hominiventricola filiformis</em></li> <li>CLA-AA-H213:<em> Oliverpabstia intestinalis</em></li> <li>CLA-AA-H241: <em>Oliverpabstia intestinalis</em></li> <li>CLA-AA-H58: <em>Pilosibacter fragilis</em></li> <li>CLA-KB-H110: <em>Ruthenibacterium lactatiformans</em></li> <li>CLA-AA-H174: <em>Segatella sinensis</em></li> <li>CLA-AA-H2: <em>Veillonella parvula</em></li> <li>CLA-AA-H273: <em>Waltera acetigignens</em></li> </ul> <p>Typos in media list have been fixed. </p> <p><strong>UPDATE v5</strong>: The accessions number for the genomes on INSDC databases are added under the column Accession. Plus two typos in the risk group column have been corrected as follow:</p> <ul> <li>CLA-AA-H173: from Risk Group 4 (!) to 2 like the other strain of <em>Sutterella wadsworthensis</em></li> <li>CLA-AA-H198: from Risk Group 4 (!) to 1 like the other <em>Bifidobacterium </em>species.</li> </ul> <p><strong>UPDATE v4</strong>: Only the taxonomy of a couple of isolates has been changed, as follow:</p> <ul> <li>CLA-ER-H4: <em>Collinsella sp900547855</em> instead of <em>Collinsella sp900544645</em></li> <li>CLA-AA-H142: <em>Pilosibacter fragilis</em> (<em>f__Clostridiaceae</em>) instead of <em>Sakamotonia hominis gen. nov.</em> (<em>f__Lachnospiraceae</em>)</li> <li>CLA-AA-H58: <em>Pilosibacter fragilis </em>(<em>f__Clostridiaceae</em>) instead of <em>Sakamotonia hominis gen. nov. </em>(<em>f__Lachnospiraceae</em>)</li> <li>CLA-AA-H89B: <em>Lachnospira intestinalis sp. nov.</em> instead of <em>Lachnospira hominis sp. nov.</em></li> <li>CLA-JM-H10: <em>Lachnospira hominis sp. nov.</em> instead of <em>Lachnospira intestinalis sp. nov.</em></li> <li>CLA-JM-H7B: <em>Faecalibacterium taiwanense</em> instead of <em>Faecalibacterium faecis sp. nov.</em></li> <li>CLA-JM-H45: <em>Merdimmobilis hominis</em> instead of <em>Hominicola intestinalis gen. nov.</em></li> </ul> <p><strong>UPDATE v3</strong>: The genome of one of our isolate had been unfortunately swapped. This mistake has been now corrected on Zenodo and Coscine. The genome of <em>Segatella sinensis</em> CLA-AA-H117 should be considered correct with 103 contigs and 3 671 232 nt. Please note that the genome available at the NCBI is the correct one (GCA_040324585.2). Two typos regarding taxonomy have been corrected as well: <em>Maccoya intestinihominis</em> has been corrected to <em>Maccoyia intestinihominis</em> and <em>Faecousia faecis</em> to <em>Faecousia intestinalis</em>.</p>
Infection Inspection: Classifications and images of ciprofloxacin-treated Escherichia coli clinical isolates
<p>This dataset includes a .csv file with the image metadata and a folder of RGB images of <i>E. coli</i> grown from clinical isolates with varying concentrations of the antibiotic ciprofloxacin and varying minimum inhibitory concentrations. The <i>E. coli</i> cell membranes are stained with Nile Red and the DNA is stained with DAPI. The details of the image data collection are included in: https://doi.org/10.1038/s42003-023-05524-4. The classification data come from a Zooniverse citizen science project, Infection Inspection. (https://www.zooniverse.org/projects/conor-feehily/infection-inspection) Volunteers learned how to interpret ciprofloxacin response phenotypes as antibiotic-sensitive or antibiotic-resistant, and their classifications are included in the Metadata.csv file.</p><p>This dataset could be used for further analysis into the volunteer classifications, or the image data could be used for further image feature analysis of the ciprofloxacin response phenotypes.</p>
MAMEM EEG SSVEP Dataset I (256 channels, 11 subjects, 5 frequencies presented in isolation)
<p>EEG signals with 256 channels captured from 11 subjects executing a SSVEP-based experimental protocol. Five different frequencies (6.66, 7.50, 8.57, 10.00 and 12.00 Hz) have been used for the visual stimulation, and the EGI 300 Geodesic EEG System (GES 300), using a 256-channel HydroCel Geodesic Sensor Net (HCGSN) and a sampling rate of 250 Hz has been used for capturing the signals. </p>
An acoustically isolated European starling song library
<p>A dataset of song collected from 14 European starlings individually recorded in acoustically isolated chambers. Each folder contains vocalizations for one bird.</p> <p>These data were used for the publication, "<em>Parallels in the sequential organization of birdsong and human speech</em>". Nature Communications (2019). If you use this dataset, please cite this publication and this repository.</p> <p>Work supported by NSF Graduate Research Fellowship 2017216247 to TS and an NIH R56DC016408 to TQG.</p>
Genome drafts of Lotmaria passim strains C2 and C3 isolated from honeybees in Spain
<p>Lotmaria passim is a highly prevalent parasite of honeybees. Herein is reported the draft genome sequences of L. passim C2 and C3 strains of 27.15 Mbp and 26.94 Mbp, respectively. The genomes were sequenced using Illumina MiSeq platform and will allow for further comparative and functional genomics studies.</p>
Scanning electron microscope images of spruce needle homogenate and scanning electron microscope images of isolated small cellular particles from spruce needle homogenate
<p>Scanning electron microscope images of spruce needle homogenate and of isolated small cellular particles from spruce needle homogenate are presented. Each image is supplemented by description of the preparation of the sample and the data on the imaging technique and equipment. The data are curated by Veronika Kralj-Iglic and University of Ljubljana, Faculty of Health Sciences, Laboratory of Clinical Biophysics, and Anna Romolo, presently at University of Ljubljana, Faculty of Electrical Engineering, Laboratory of Physics, Ljubljana, Slovenia. Present address of Marko Jeran is: Department of Inorganic Chemistry and Technology, “Jožef Stefan” Institute, Ljubljana, Slovenia.</p>
Data set for publication: Determination of Virulence-Associated Genes and Antimicrobial Resistance Profiles in Brucella Isolates Recovered from Humans and Animals in Iran Using NGS Technology
<p>This dataset includes information on resistance profiling, as well as antimicrobial resistance (AMR) genes and virulence-related factors that were identified in <em>Brucella</em> isolates recovered from humans and animals in different regions of Iran using classical phenotyping and next-generation sequencing (NGS) technology.</p>
Dataset containing binominal lexemes in Harakmbut (isolate, Peru), for "The derivational use of classifiers in Western Amazonia" and "When the alienability contrast fails to surface in adnominal possession: Bound nouns in Harakmbut"
<p>This is the dataset used, amongst others, in the paper: Van linden, An. Forthcoming. When the alienability contrast fails to surface in adnominal possession: Bound nouns in Harakmbut. Special Issue “Re-assessing the explanatory potential of alienability contrasts”, guest-edited by Françoise Rose & An Van linden. <em>Linguistics – An Interdisciplinary Journal of the Language Sciences</em>. [<a href="https://doi.org/10.1515/ling-2022-0039">https://doi.org/10.1515/ling-2022-0039</a>]</p> <p>For more details, see the ReadMe file.</p>
OrchideaSOL: an audio dataset of isolated musical notes, including mutes and extended playing techniques
<p>OrchideaSOL<br> ==========<br> Version 2.0, April 2020.<br> </p> <p> </p> <p>Created By<br> --------------</p> <p>Carmine-Emanuele Cella (1), Daniele Ghisi (1), Vincent Lostanlen (2), Fabien Lévy (3), Joshua Fineberg (4), Yan Maresz (5)<br> <br> (1): UC Berkeley<br> (2): New York University<br> (3): Columbia University<br> (4): Boston University<br> (5): Conservatoire de Paris</p> <p> </p> <p>Description<br> ---------------</p> <p><br> OrchideaSOL is a dataset of 13265 samples, each containing a single musical note from one of 14 different instruments:</p> <ol> <li>Bass Tuba</li> <li>French Horn</li> <li>Trombone</li> <li>Trumpet in C</li> <li>Accordion</li> <li>Contrabass</li> <li>Violin</li> <li>Viola</li> <li>Violoncello</li> <li>Bassoon</li> <li>Clarinet in B-flat</li> <li>Flute</li> <li>Oboe</li> <li>Alto Saxophone</li> </ol> <p> </p> <p>These sounds were originally recorded at Ircam in Paris (France) between 1996 and 1999, as part of a larger project named Studio On Line (SOL). One asset of OrchideaSOL is that it contains many combinations of mutes and extended playing techniques.<br> <br> The OrchideaSOL audio data can be used for creative purposes insofar at the use complies with the Ircam Forum License. Please visit: https://forum.ircam.fr/legal/contrat-de-licence-forum-ircam/</p> <p><br> The OrchideaSOL metadata can be used for creative purposes insofar at the use complies with the Creative Commons Attribution 4.0 International license (see below).<br> <br> OrchideaSOL can be used for education and research purposes. In particular, it can be employed as a dataset for training and/or evaluating music information retrieval (MIR) systems, for tasks such as instrument recognition, playing technique recognition, or fundamental frequency estimation. For this purpose, we provide an official 5-fold split of OrchideaSOL. This split has been carefully balanced in terms of instrumentation, pitch range, and dynamics. For the sake of research reproducibility, we encourage users of OrchideaSOL to adopt this split and report their results in terms of average performance across folds.</p> <p> </p> <p>Data Files<br> --------------</p> <p>OrchideaSOL contains 13265 audio clips as WAV files, sampled at 44.1 kHz, with a single channel (mono), at a bit depth of 16. This is equivalent to the audio quality of a compact disc. Audio clips vary in duration between two and ten seconds.</p> <p>Every audio file has a file path of the form:<br> <FAMILY>/<INSTRUMENT><+MUTE>/<TECHNIQUE>/<INSTR><+M>-<TECH>-<PITCH>-<DYN>-<INSTANCE>-<MISC>.wav</p> <p><br> where:</p> <ul> <li><FAMILY> corresponds to the instrument family: "Brass", "Keyboards" (includes accordion), "Strings", and "Winds" (i.e., woodwinds).</li> <li><INSTRUMENT> is the full name of the instrument.</li> <li><+MUTE> is the type of mute being used, such as "wah", "harmon", "piombo", or "sordina". If there is no mute, this field is absent.</li> <li><TECHNIQUE> is the type of playing technique.</li> <li><INSTR> is the abbreviation of the instrument.</li> <li><+M> is the abbreviation of the type of mute, if applicable.</li> <li><TECH> is the abbreviation of playing technique.</li> <li><PITCH> denotes the pitch of the musical note. This pitch is encoded in the American standard pitch notation: pitch class (C means "do") followed by pitch octave. According to this convention, A4 has a fundamental frequency of 440 Hz.</li> <li><DYN> denotes the intensity dynamics, ranked from pp (pianissimo) to ff (fortissimo).</li> <li><INSTANCE> contains additional information, when applicable. For example, for bowed string instruments, the same pitch may sometimes be achieved on different positions and different strings, resulting in small timbre differences. In this case the label "1c", "2c", "3c", or "4c" denotes the string which is being bowed. (The letter c originates from the word "corde", which means string in French.) By convention, the first string is the one with the highest pitch when played as an open string. Furthermore, on some wind instruments, the same note was played multiple times, e.g. at multiple durations. In this case, we use the label "alt1", "alt2", etc. to denote alternative instances of the note. If none of these tags apply, the <INSTANCE> field becomes "N", which stands for "Not Applicable".</li> <li><MISC> contains additional information, if applicable. In OrchideaSOL, some pitches were never recorded, and thus missing from the chromatic scale. In this case, the <MISC> tag contains a letter "R", to denote the fact that the corresponding WAV file has been obtained by transforming a different audio clip via some digital frequency transposition (similar to Auto-Tune). The letter "R" stands for "resampled". Furthermore, some pitches were slightly out of tune in comparison with the A440 tuning standard. Again, we applied some digital frequency transposition to correct them and put them exactly in tune. The amount of frequency transposition is measured in "cents" of an equal-tempered semitone. The letter "T" stands for "tuned". Because we employed a high-fidelity algorithm for frequency transposition, and because the amount of digital frequency transposition is small, the timbre of pitch-corrected notes remains faithful to the instrument. If none of these tags apply, the <MISC> field becomes "N", which stands for "natural"; in this case, the note is distributed exactly as it was recorded in the studio.</li> </ul> <p>For example, "Strings/Violin+sordina/tremolo/Vn+S-trem-A4-mf-4c-T13d_R200d.wav" corresponds to:</p> <ul> <li>a violin sound;</li> <li>equipped with a sordina mute;</li> <li>played in the tremolo playing technique;</li> <li>at pitch A4 (440 Hz);</li> <li>with mezzoforte dynamics;</li> <li>on the fourth string (i.e. the lowest);</li> <li>resampled from a B4 by lowering pitch by a semitone, i.e. 100 cents (R100d)</li> <li>lowered by 13 cents (T22d) to match the A440 tuning standard.</li> </ul> <p> </p> <p>The audio data for OrchideaSOL is not directly downloadable on Zenodo. Rather, it can be downloaded for free after registering to the Ircam forum. Please visit: https://forum.ircam.fr/</p> <p> </p> <p>Metadata File<br> -------------------</p> <p>The OrchideaSOL_metadata.csv file contains 13265 rows, one for each audio clip. It can be opened by a text editor or by a spreadsheet software application. It contains 13 columns:</p> <ol> <li>Path to the WAV file, in UNIX filesystem format. For Windows compatibility, replace the slashes ("/") by backslashes ("\"). Ex: "Strings/Violin+sordina/tremolo/Vn+S-trem-A4-mf-4c-T13d_R200d.wav"</li> <li>Fold ID. Either equal to 0, 1, 2, 3, or 4.</li> <li>Family. Ex: "Brass"</li> <li>Instrument abbreviation. Ex: "BTb"</li> <li>Instrument name in full. Ex: "Bass Tuba"</li> <li>Technique abbreviation.</li> <li>Technique name in full.</li> <li>Pitch. Ex: "A#1"</li> <li>Pitch ID in MIDI format. Ex: 34. Integer in the range 0-127.</li> <li>Dynamics. Ex: "ff".</li> <li>Dynamics ID. Integer. pp maps to 0 and ff maps to 4. The higher, the louder.</li> <li>Instance ID. Integer in the range 0-4</li> <li>String ID. Equal to 1, 2, 3, 4, or empty if not applicable.</li> <li>"Needed digital retuning". TRUE if the file has been pitch-shifted with digital audio effects; FALSE otherwise.</li> </ol> <p> </p> <p>Conditions of Use<br> ------------------------</p> <p>OrchideaSOL was created in 2020 by Carmine-Emanuele Cella, Daniele Ghisi, Vincent Lostanlen, Fabien Lévy, Joshua Fineberg, and Yan Maresz.</p> <p>OrchideaSOL is a derivative of SOL. We wish to thank Hugues Vinet, Greg Beller, and all coordinators of the Ircam Forum for their authorization to upload the metadata of OrchideaSOL to Zenodo.</p> <p>The audio samples in OrchideaSOL are offered free of charge under the Ircam Forum License. Please visit: https://forum.ircam.fr/legal/contrat-de-licence-forum-ircam/</p> <p>The dataset and its contents are made available on an "as is" basis and without warranties of any kind, including without limitation satisfactory quality and conformity, merchantability, fitness for a particular purpose, accuracy or completeness, or absence of errors. Subject to any liability that may not be excluded or limited by law, the authors are not liable for, and expressly exclude all liability for, loss or damage however and whenever caused to anyone by any use of the OrchideaSOL dataset or any part of it.</p> <p> </p> <p>Versions<br> -----------<br> 1.0 was released on February 24th, 2020.<br> 2.0 was released on April 4th, 2020. It fixes a bug in the instance IDs of oboe sounds in the "blow without reed" technique.</p> <p> </p> <p>Feedback<br> -------------</p> <p>Please help us improve OrchideaSOL by sending your feedback to:<br> carmine.cella@berkeley.edu</p> <p>For issues regarding the metadata encoding, the five-fold split, or the OrchideaSOL module in mirdata, please write to:<br> vincent.lostanlen@nyu.edu</p> <p>In case of a problem, please include as many details as possible.</p>
Dataset of BattLeDIM: Battle of the Leakage Detection and Isolation Methods
<p>Drinking Water Distribution Networks (DWDN) are susceptible to infrastructure failures, which may lead to water losses. Typically, these water losses are due to background leakages and pipe bursts which may occur anywhere within the distribution network. Background leakages are normally difficult to detect due to their small size, whereas pipe bursts are easier to locate as they are of larger size and may appear on the surface. The early detection and localization of some leakage event is extremely important, as this would reduce the time required for accommodating the event and therefore reducing the risk of further infrastructure degradation, contamination events and consumer complaints.</p> <p>In previous years, a number of methodologies have been proposed to detect and isolate the location of leakage events using various types of sensor measurements. These methods were commonly evaluated on private commercial datasets, and as a result, it is not possible to objectively compare these methods in their ability to detect and isolate leaks. In the past year, a leakage detection dataset has been proposed, LeakDB, based on benchmark networks and created using the WNTR tool, using pressure-driven demands and realistic leakage modelling. Inspired by the “BATtle of the Attack Detection ALgorithms” (BATADAL), which focused on the detection of cyber-physical attacks, our team decided to organize a similar “battle” focusing on leakage events.</p> <p>The Battle of the Leakage Detection and Isolation Methods (BattLeDIM), aims at objectively comparing the performance of methods for the detection and localization of leakage events, relying on SCADA measurements of flow and pressure sensors installed within water distribution networks. Participants may use different types of tools and methods, including (but not limited to) engineering judgement, machine learning, statistical methods, signal processing, and model-based fault diagnosis approaches.</p>
Genomes and full-length 16S reference sequences for 27 Alpha- and Gamma-Proteobacterial isolates from Red Sea Acropora corals
<p>Coral-associated bacteria contribute to the biology of their host, but the underlying molecular interactions are largely unknown. To further our functional understanding, we obtained 27 alpha- and gamma-proteobacterial isolates, many of which are Rhodobacteraceae, from three coral species of the genus <em>Acropora </em>and assembled/annotated their genomes as a resource for further functional studies. Our results reveal the immense taxonomic and genetic diversity of common alpha- and gamma-proteobacterial coral-associated bacteria. We hope these data provide a framework to study the function of specific bacteria in the coral holobiont. Isolates are available upon request.</p>
CLDF dataset derived from Ugarte et al.'s "NorthPeruLex - A Lexical Dataset of Small Language Families and Isolates from Northern Peru (forthcoming).
<p>Cite the source of the dataset as:</p> <blockquote> <p>Ugarte, Carlos and Blum, Frederic and Ingunza, Adriano and Gonzales, Rosa and Peña, Jaime. Forthcoming. NorthPeruLex - A Lexical Dataset of Small Language Families and Isolates from Northern Peru.</p> </blockquote>
Exploring the Exclusive Isolation of Pseudomonas syringae in Peltigera Lichens via metabolite analysis and growth assays - Appendix
<p>Lichen samples from Iceland were collected from the genera Peltigera, Cladonia, and Stereocaulon in March 2023 at Heidmork forest, Oskjuhlid hill, and the shores of Ellidaa in Arbaejarstifla. All specimens underwent morphological analysis, and corresponding vouchers have been deposited at the Icelandic Institute of Natural History.</p>
Data from: Absence of genetic isolation across highly fragmented landscape in the ant Temnothorax nigriceps
<p><strong>This README accompanies data_genotyping.txt</strong></p> <p> </p> <p><strong><em>Associate publication : </em></strong></p> <p>Absence of genetic isolation across highly fragmented landscape in the ant Temnothorax nigriceps</p> <p>M. Cordonnier<sup>a</sup>, D. Felten<sup>a</sup>, A. Trindl<sup>a</sup>, J. Heinze<sup>a</sup>*, A. Bernadou<sup>a</sup>*</p> <p><sup>a</sup>Lehrstuhl für Zoologie / Evolutionsbiologie, Univ. Regensburg</p> <p>*Equal contribution</p> <p> </p> <p>****************************** CONTENTS *******************************</p> <p>The data can be readily imported in any statistical package or spreadsheet program. Please, contact me if you need the file formatted in other ways.</p> <p> </p> <p>This file includes a description of the variables.</p> <p>***********************************************************************</p> <p>Variable names and descriptions</p> <p> </p> <p><strong>Sample:</strong> ID of the sampled nest</p> <p><strong>Location:</strong> Population of the sampled nest</p> <p> </p> <p><strong>List of genotypes </strong></p> <p>Microsatellite primers used in the study</p> <table> <tbody> <tr> <td> </td> <td> <p>Annealing temperature [°C]</p> </td> <td> <p>Orientation</p> </td> <td> <p>Sequence of primers</p> </td> </tr> <tr> <td> <p>LX GT218</p> </td> <td> <p>57</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-GTTCTTGCGCGGATGCATAC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-TGTACTCGCGTGTCTATCGG-3’</p> </td> </tr> <tr> <td> <p>Ant3993</p> </td> <td> <p>57</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-TGATCCGCTCTTAAAATTTAGATGGA-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-ACTTTCCGCRGCATTAAACATTTTCTT-3’</p> </td> </tr> <tr> <td> <p>L-18</p> </td> <td> <p>57</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-TGAATTTGGATGGCGGTAGAC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-ACCTAATGCACGCTTTAGAAT-3’</p> </td> </tr> <tr> <td> <p>LXA GT1</p> </td> <td> <p>57</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-GTGGCGACCAATTCTGCAAG-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-GCAGGACCAGCATCAAATGACAG-3’</p> </td> </tr> <tr> <td> <p>2MS17</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-CAGCCTCTATTTTGTTCGAAG-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-TTTACTGCGGCTCCATAATC-3’</p> </td> </tr> <tr> <td> <p>2MS46</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-GCTCACTACTATGCTGCCAGC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-CTTTCCTGCAAACCACGTGT-3’</p> </td> </tr> <tr> <td> <p>2MS60</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-TATGCGCCGGACAATAATCGC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-GTTCATTGTCCGAGGCGCAGC-3’</p> </td> </tr> <tr> <td> <p>2MS67</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-GAAGATTCGTCAGGATGCAGC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-AACTCTCGCTGGCAAGCGAGC-3’</p> </td> </tr> <tr> <td> <p>2MS82</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-AAAAGAGCATGCAACAGGTCAGC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-TTTCTTAAGTCGCAAGCGAGC-3’</p> </td> </tr> <tr> <td> <p>2MS87</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-GGAACCTCACTCAACCTCGGT-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-ACGCGGACTACTTTAACCGGA-3’</p> </td> </tr> <tr> <td> <p>2MS91</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-AAAGTCTCGGAGTGGCTTTGC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-ATTCTCGTCCATTTGTTCTAA-3’</p> </td> </tr> <tr> <td> <p>Ant11893</p> </td> <td> <p>55</p> </td> <td> <p>Forward</p> </td> <td> <p>5’-CAGGCTCGGRACGTTAATGC-3’</p> </td> </tr> <tr> <td> <p>Reverse</p> </td> <td> <p>5’-GGTGCCGACGTCTAGCTAGC-3’</p> </td> </tr> </tbody> </table> <p> </p> <p>Missing data are encoded “-9”.</p> <p> </p> <p>****************************** CONTACTING *****************************</p> <p>Contact me at:</p> <p> </p> <p>Marion Cordonnier</p> <p>e-mail: marion.cordonnier@hotmail.com</p> <p> </p> <p>***********************************************************************</p> <p> </p>
RNASeq data of isolated murine glomeruli treated with Vitamin D3 and DMSO
<p>RNASeq data of isolated murine glomeruli (as described here <a href="https://dx.doi.org/10.1111%2Fbph.13667">10.1111/bph.13667</a>) treated with Vitamin D3 (100 nM) and DMSO (0.1%) for 6 days. </p>
Controlled Formation of Dimers and Spatially Isolated Atoms in Bimetallic Au-Ru Catalysts via Carbon-Host Functionalization
<p>Enclosed we report the data in the article: "Controlled Formation of Dimers and Spatially Isolated Atoms in Bimetallic Au-Ru Catalysts via Carbon-Host Functionalization" by Pérez-Ramírez et al.</p>
Supporting Information for Disclosing Spin-Polarized Bonds on Isolable Molecules
<p>The file corresponds to the Bachelor Thesis of Ms. Elena Paulus. It contains the xyz coordinates of all optimized structures and their corresponding electronic energy in Hartree.</p>
Pre-processed AMR data on S. aureus isolates from PATRIC database
<p>Pre-processed AMR data on S. aureus isolates from PATRIC database. The majority class size was decreased to reach the class ratio of 1:1 when the susceptible/resistant or resistant/susceptible class ratio exceeded 3.5.</p>
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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
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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
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