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| Name | Authors | DOI | Group |
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Vandy - Exercise Stress Test Resource Report Resource Website |
Louise Lantier | DOI:10.17504/protocols.io.yxcfxiw | Mouse Metabolic Phenotyping Centers | Summary: The exercise stress test is a maximal exercise test used to calculate VO2 max. Mice are run to complete exhaustion as the treadmill speed is increased every three minutes (See table 1). During the test, direct measurements of the oxygen consumption and carbon dioxide output by the mouse are made, which are then used to calculate VO2 max, VCO2, and RER. VO2 max refers to the maximum amount of oxygen that the mouse can utilize during maximal exercise. | Vanderbilt University | https://mmpc.org/shared/document.aspx?id=237&docType=Protocol | 1 | 2019 | Louise Lantier 2019. Vandy - Exercise Stress Test. protocols.io https://dx.doi.org/10.17504/protocols.io.yxcfxiw | 2021-04-15 09:15:52 | ||
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Cell DIVE™ Platform | Antibody Purification Chemistry Resource Report Resource Website |
Anup Sood, Eric Williams, Liz McDonough | DOI:10.17504/protocols.io.bpx9mpr6 | Human BioMolecular Atlas Program (HuBMAP) Method Development Community, GE Research | The purpose of the protocol is to purify antibodies that will be conjugated to Cy dyes as per the Cell DIVE™ technology. Affinity chromatography will be used to remove impurities from the vendor antibody to enable conjugation. | GE Research, GE Research, GE Research | 1 | 2021 | Anup Sood, Eric Williams, Liz McDonough 2021. Cell DIVE™ Platform | Antibody Purification Chemistry. protocols.io https://dx.doi.org/10.17504/protocols.io.bpx9mpr6 | 2021-04-15 09:15:53 | |||
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Restriction Digest of Plasmid DNA Resource Report Resource Website |
Addgene The Nonprofit Plasmid Repository | DOI:10.17504/protocols.io.63shgne | This protocol is for restriction digest of plasmid DNA. To see the full abstract and additional resources, please visit http://www.addgene.org/plasmid_protocols/restriction_digest/. | Addgene | http://www.addgene.org/plasmid_protocols/restriction_digest/ | 3 | 2019 | Addgene The Nonprofit Plasmid Repository 2019. Restriction Digest of Plasmid DNA. protocols.io https://dx.doi.org/10.17504/protocols.io.63shgne | 2021-04-15 09:15:53 | |||
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Protocol for sampling and transport of nose- and thoratsamples in the Fit Futures study Resource Report Resource Website |
Dina Stensen, Anne-Sofie Furberg, Karina Olsen, Gunnar Skov Simonsen, Johanna UE Sollid, Lars Småbrekke, Guri Grimnes, Cristopher Sievert Nielsen | DOI:10.17504/protocols.io.2j5gcq6 | The aim of the study is to evaluate prevalence of Staphylococcus aureus in a youth population. This samples will be connected to other possible riskfactors for Staphylococcus aureus carriage. | Stensen DB, Småbrekke L, Olsen K, Grimnes G, Nielsen CS, Simonsen GS, Sollid JUE, Furberg A (2019) Hormonal contraceptive use and Staphylococcus aureus nasal and throat carriage in a Norwegian youth population. PLoS ONE 14(7): e0218511. doi: 10.1371/journal.pone.0218511 | University hospital of North Norway, Department of Community Medicine, Faculty of Health Sciences, UiT The Arctic University of Norway, Department of Microbiology and Infection Control, University Hospital of North Norway, Department of Microbiology and Infection Control, University Hospital of North Norway, Research Group for Host-Microbe Interaction, Department of Medical Biology, Department of Pharmacy, Faculty of Health Sciences, UiT The Arctic University of Norway, Endocrinology Research Group, Department of Clinical Medicine, Faculty of Health Sciences, UiT The Arctic University of Norway, Division of Ageing and Health, Norwegian Institute of Public Health | https://doi.org/10.1371/journal.pone.0218511 | 2 | 2019 | Dina Stensen, Anne-Sofie Furberg, Karina Olsen, Gunnar Skov Simonsen, Johanna UE Sollid, Lars Småbrekke, Guri Grimnes, Cristopher Sievert Nielsen 2019. Protocol for sampling and transport of nose- and thoratsamples in the Fit Futures study. protocols.io https://dx.doi.org/10.17504/protocols.io.2j5gcq6 | 2021-04-15 09:15:58 | ||
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Transfection of Naegleria gruberi Resource Report Resource Website |
Anastasios Tsaousis | DOI:10.17504/protocols.io.hpub5nw | Protist Research to Optimize Tools in Genetics (PROT-G) | Faktorová D, Nisbet RER, Robledo JAF, Casacuberta E, Sudek L, Allen AE, Ares M, Aresté C, Balestreri C, Barbrook AC, Beardslee P, Bender S, Booth DS, Bouget F, Bowler C, Breglia SA, Brownlee C, Burger G, Cerutti H, Cesaroni R, Chiurillo MA, Clemente T, Coles DB, Collier JL, Cooney EC, Coyne K, Docampo R, Dupont CL, Edgcomb V, Einarsson E, Elustondo PA, Federici F, Freire-Beneitez V, Freyria NJ, Fukuda K, García PA, Girguis PR, Gomaa F, Gornik SG, Guo J, Hampl V, Hanawa Y, Haro-Contreras ER, Hehenberger E, Highfield A, Hirakawa Y, Hopes A, Howe CJ, Hu I, Ibañez J, Irwin NAT, Ishii Y, Janowicz NE, Jones AC, Kachale A, Fujimura-Kamada K, Kaur B, Kaye JZ, Kazana E, Keeling PJ, King N, Klobutcher LA, Lander N, Lassadi I, Li Z, Lin S, Lozano J, Luan F, Maruyama S, Matute T, Miceli C, Minagawa J, Moosburner M, Najle SR, Nanjappa D, Nimmo IC, Noble L, Vanclová AMGN, Nowacki M, Nuñez I, Pain A, Piersanti A, Pucciarelli S, Pyrih J, Rest JS, Rius M, Robertson D, Ruaud A, Ruiz-Trillo I, Sigg MA, Silver PA, Slamovits CH, Smith GJ, Sprecher BN, Stern R, Swart EC, Tsaousis AD, Tsypin L, Turkewitz A, Turnšek J, Valach M, Vergé V, Dassow Pv, Haar Tvd, Waller RF, Wang L, Wen X, Wheeler G, Woods A, Zhang H, Mock T, Worden AZ, Lukeš J, Genetic tool development in marine protists: emerging model organisms for experimental cell biology. Nature Methods 17(5). doi: 10.1038/s41592-020-0796-x | University of Kent | https://doi.org/10.1038/s41592-020-0796-x | 1 | 2017 | Anastasios Tsaousis 2017. Transfection of Naegleria gruberi. protocols.io https://dx.doi.org/10.17504/protocols.io.hpub5nw | 2021-04-15 09:15:53 | ||
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UTK Laboratory Orientation/Training Resource Report Resource Website |
Gary Lecleir, Steven Wilhelm | DOI:10.17504/protocols.io.6c3hayn | The Aquatic Microbial Ecology Research Group - AMERG (The Buchan, Zinser and Wilhelm labs) | Welcome to the Wilhelm Lab. This short training is to help orient those that are learning how to work in a laboratory environment as well as help those that are joining our lab to become acquainted with our procedures. | University of Illinois at Urbana-Champaign, The University of Tennessee, Knoxville | 1 | 2019 | Gary Lecleir, Steven Wilhelm 2019. UTK Laboratory Orientation/Training. protocols.io https://dx.doi.org/10.17504/protocols.io.6c3hayn | 2021-04-15 09:15:50 | |||
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Cell counting with a haemocytometer (with mouse bone marrow example) Resource Report Resource Website |
Thomas Ashhurst, Darren A. Cox, Adrian L. Smith, Nicholas J. C. King | DOI:10.17504/protocols.io.btqgnmtw | Immune Dynamics | Cell counting is a critical step to determine the number of live leukocytes (white blood cells, WBC) and erythrocytes (red blood cells, RBC) per femur, and is accurately performed using a microscope and haemocytometer. This step allows enables the distribution of a specific number of cells per well in the staining plate. Some researchers prefer to perform an erythrocyte (or red blood cell, RBC) lysis prior to counting, as some researchers are concerned about misidentifying erythrocytes as leukocytes during counting. This RBC lysis removes all erythrocytes prior to counting, resulting in easier counting of leukocytes. However, we have found that differentiating leukocytes from erythrocytes is straight forward at a higher magnification based on size (erythrocytes are smallest), colour (erythrocytes are red in colour), and birefringence (leukocytes exhibit birefringence, erythrocytes do not). Additionally, RBC lysis prior to cell staining will have a small impact on CD115 staining levels (see protocol notes). To circumvent the need for RBC lysis prior to staining, we count the number of leukocytes (and erythrocytes) in the centre square only, at a high magnification. Alternatively, an automated cell counter can be used to speed up counting. However, care must be taken to ensure that any automated cell counter is accurately performing counts, as most automated cell counters are calibrated to human blood cells. | The University of Sydney, The University of Sydney, The Centenary Institute, The University of Sydney | https://link.springer.com/protocol/10.1007/978-1-4939-9454-0_12 | 1 | 2021 | Thomas Ashhurst, Darren A. Cox, Adrian L. Smith, Nicholas J. C. King 2021. Cell counting with a haemocytometer (with mouse bone marrow example). protocols.io https://dx.doi.org/10.17504/protocols.io.btqgnmtw | 2021-04-15 09:15:50 | ||
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Determination of florfenicol and florfenicol amine in fish plasma (Salmo salar) through HPLC MS/MS Resource Report Resource Website |
Betty San Martín, Lisette Lapierre, Marcela Fresno, Javiera Cornejo | DOI:10.17504/protocols.io.zhdf326 | Martín BS, Fresno M, Cornejo J, Godoy M, Ibarra R, Vidal R, Araneda M, Anadón A, Lapierre L (2019) Optimization of florfenicol dose against Piscirickettsia salmonis in Salmo salar through PK/PD studies. PLoS ONE 14(5): e0215174. doi: 10.1371/journal.pone.0215174 | Universidad de Chile, Universidad de Chile, Universidad de Chile, Universidad de Chile | https://doi.org/10.1371/journal.pone.0215174 | 1 | 2019 | Betty San Martín, Lisette Lapierre, Marcela Fresno, Javiera Cornejo 2019. Determination of florfenicol and florfenicol amine in fish plasma (Salmo salar) through HPLC MS/MS. protocols.io https://dx.doi.org/10.17504/protocols.io.zhdf326 | 2021-04-15 09:15:50 | |||
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ClampFISH Resource Report Resource Website |
Sara H Rouhanifard, Ian A Mellis, Margaret Dunagin, Sareh Bayatpour, Orsolya Symmons, Allison Cote, Arjun Raj | DOI:10.17504/protocols.io.qeydtfw | Human Cell Atlas Method Development Community | Non-enzymatic, high-gain signal amplification methods with single-cell, single-molecule resolution are in great need. We present click-amplifying FISH (clampFISH) for the fluorescent detection of RNA that combines the specificity of oligonucleotides with bioorthogonal click chemistry in order to achieve high specificity and extremely high-gain (>400x) signal amplification. We show that clampFISH signal enables detection with low magnification microscopy and separation of cells by RNA levels via flow cytometry. Additionally, we show that the modular design of clampFISH probes enables multiplexing, that the locking mechanism prevents probe detachment in expansion microscopy, and that clampFISH works in tissue samples. | University of Pennsylvania, University of Pennsylvania, University of Pennsylvania, University of Pennsylvania, University of Pennsylvania, University of Pennsylvania, University of Pennsylvania | https://www.biorxiv.org/content/early/2018/05/07/222794 | 1 | 2018 | Sara H Rouhanifard, Ian A Mellis, Margaret Dunagin, Sareh Bayatpour, Orsolya Symmons, Allison Cote, Arjun Raj 2018. ClampFISH . protocols.io https://dx.doi.org/10.17504/protocols.io.qeydtfw | 2021-04-15 09:15:53 | ||
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Creating sci-Space Grids for Spatial Barcoding Resource Report Resource Website |
Sanjay Srivatsan, Mary Regier | University of Washington, University of Washington | 1 | 2021 | Sanjay Srivatsan, Mary Regier 2021. Creating sci-Space Grids for Spatial Barcoding. protocols.io https:// | 2021-04-15 09:15:50 | ||||||
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Test-serology-protocol Resource Report Resource Website |
Dr. John Smith | DOI:10.17504/protocols.io.bewejfbe | This is an assay describing indirect sandwich ELISA for RDP Ag of SARS-CoV-2. Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda, Yadda, yadda, yadda. | Stanford University | 1 | 2020 | Dr. John Smith 2020. Test-serology-protocol. protocols.io https://dx.doi.org/10.17504/protocols.io.bewejfbe | 2021-04-15 09:15:57 | ||||
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Quality Control of Reads Using Trimmomatic (Cyverse) Resource Report Resource Website |
Benjamin Bolduc | DOI:10.17504/protocols.io.gvybw7w | VERVE Net, Sullivan Lab, iVirus | A collection of protocols designed to guide the user in processing a viral metagenome from raw sequence data to assembly, and subsequent analysis. The user uses actual reads from Ocean Sampling Day (2014) and processes them entirely within Cyverse, a NSF-supported cyberinfrastructure.Quality trimming of reads is important! | The Ohio State University | 1 | 2016 | Benjamin Bolduc 2016. Quality Control of Reads Using Trimmomatic (Cyverse). protocols.io https://dx.doi.org/10.17504/protocols.io.gvybw7w | 2021-04-15 09:15:58 | |||
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Mild Hypothermia to prevent Acute kidney injury in Liver Transplantation (MHALT) Trial - Statistical Analysis Plan for the Interim Analysis, v1.0 Resource Report Resource Website |
Michael Bokoch, Claus Niemann, Dieter Adelmann, Rishi Kothari | DOI:10.17504/protocols.io.bf5kjq4w | UCSF Transplant Anesthesia Research Group (TARG) | Acute kidney injury (AKI), or worsening kidney function, is a common complication after liver transplantation (20-90% in published studies). Patients who experience AKI after liver transplantation have higher mortality, increased graft loss, longer hospital and intensive care unit stays, and more progression to chronic kidney disease compared with those who do not. In this study, half of the participants will have their body temperature cooled to slightly lower than normal (mild hypothermia) for a portion of the liver transplant operation, while the other half will have their body temperature maintained at normal. The study will evaluate if mild hypothermia protects from AKI during liver transplantation.This study is a single-blinded, randomized controlled trial of mild hypothermia during liver transplantation to provide protection from AKI. Participants will be randomized to normothermia (36.5-37.5 °C) versus mild hypothermia (34-35 °C) during a portion of the liver transplant operation. The protocol is based on preliminary data from rodent models showing that hypothermia protects the kidneys from ischemia-reperfusion injury, as well as studies in deceased organ donors showing that cooling improves post-transplant organ function. Temperature will be maintained with standard techniques plus a minimally-invasive esophageal cooling device that is approved by the U.S. Food and Drug Administration. The investigators hypothesize that mild hypothermia will reduce the incidence and severity of AKI after LTx. Standard surrogates (e.g., change in serum creatinine, need for initiation of dialysis) and biomarkers will be used to assess the severity of kidney injury. | University of California, San Francisco, University of California, San Francisco, University of California, San Francisco, University of California, San Francisco | 1 | 2020 | Michael Bokoch, Claus Niemann, Dieter Adelmann, Rishi Kothari 2020. Mild Hypothermia to prevent Acute kidney injury in Liver Transplantation (MHALT) Trial - Statistical Analysis Plan for the Interim Analysis, v1.0 . protocols.io https://dx.doi.org/10.17504/protocols.io.bf5kjq4w | 2021-04-15 09:15:53 | |||
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Double digested Resource Report Resource Website |
Jiaxin Li | DOI:10.17504/protocols.io.bni6mche | South China University of Technology | 1 | 2020 | Jiaxin Li 2020. Double digested. protocols.io https://dx.doi.org/10.17504/protocols.io.bni6mche | 2021-04-15 09:15:58 | |||||
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Spectrophotometry method for the detection of Biochemical parameters Resource Report Resource Website |
Xiaohua Du, Xia Liu, Mawolo James Blackar, Yingjie Zhou, Haifeng Wang, Fayang Liu, Zhiqing He | DOI:10.17504/protocols.io.6wchfaw | Definition of key termsSpectrophotometry is an experimental technique that is used to measure the concentration of solutes in a specific solution by calculating the amount of light absorbed by those solutes.[1] This technique is powerful because certain compounds will absorb different wavelengths of light at different intensities. By analyzing the light that passes through the solution, you can identify particular dissolved substances in solution and how concentrated those substances are. A automatic analyser (7180) is the device used to analyze solutions in a laboratory research setting.Desecription of Automatic analyserThe Automatic analyser (7180) is a medium-sized biochemistry automatic analyzer.The minimum required amount of reaction solution is smaller due to a new optical design, and running cost is lower and working efficiency higher because the operating unit is usable in the same way as a general-purpose personal computer. Further, this analyzer features a wide range of applications including routine, stat and special analyses.Benefit of Spectrophotometry methodThe usage of Automatic analyser (Hitachi Ltd 7180 Serial, Tokyo, Japan) enabled us to obtained more samples result in less time and this prevented other factors from influencing our tested results. | Liu X, Mawolo JB, Du X, Zhou Y, Wang H, Liu F, He Z, Marela HA (2019) Investigation of biochemical and physiological parameters of the newborn Saiga antelope (Saiga tatarica) in Gansu Province, China. PLoS ONE 14(11): e0224822. doi: 10.1371/journal.pone.0224822 | Faculty of Veterinary Medicine, Gansu Agricultural University, Lanzhou City, Gansu Province, People's Republic of China, College of Life Science and Technology, Gansu Agricultural University, Lanzhou City, Gansu Province, People's Republic of China, College of Life Science and Technology, Gansu Agricultural University, Lanzhou City, Gansu Province, People's Republic of China , Gansu Endangered Animal Protection Center of State Forestry Administration, Wuwei City, Gansu Province, People's Republic of China, College of Life Science and Technology, Gansu Agricultural University, Lanzhou City, Gansu Province, People's Republic of China , College of Life Science and Technology, Gansu Agricultural University, Lanzhou City, Gansu Province, People's Republic of China, Gansu Endangered Animal Protection Center of State Forestry Administration, Wuwei City, Gansu Province, People's Republic of China | https://doi.org/10.1371/journal.pone.0224822 | 1 | 2019 | Xiaohua Du, Xia Liu, Mawolo James Blackar, Yingjie Zhou, Haifeng Wang, Fayang Liu, Zhiqing He 2019. Spectrophotometry method for the detection of Biochemical parameters. protocols.io https://dx.doi.org/10.17504/protocols.io.6wchfaw | 2021-04-15 09:15:53 | ||
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Diplonema Genomic DNA isolation Resource Report Resource Website |
Binnypreet Kaur1, 2, Drahomíra Faktorová1, 2, , Priscila Peña-Diaz1 and Julius Lukeš1, 2 | DOI:10.17504/protocols.io.hfyb3pw | Julius Lukes | E-mail: [email protected] | 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic, 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic, 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic, 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic, 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic, 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic, 1 Institute of Parasitology, Biology Centre, Czech Academy of Sciences, 37005, České Budějovice, Czech Republic 2 Faculty of Sciences, University of South Bohemia, 37005, České Budějovice, Czech Republic | 1 | 2018 | Binnypreet Kaur1, 2, Drahomíra Faktorová1, 2, , Priscila Peña-Diaz1 and Julius Lukeš1, 2 2018. Diplonema Genomic DNA isolation. protocols.io https://dx.doi.org/10.17504/protocols.io.hfyb3pw | 2021-04-15 09:15:58 | |||
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Isolation of single nuclei from postmortem fresh frozen human brain and immunostaining for NeuN Resource Report Resource Website |
Marcos Otero-Garcia, Inma Cobos | DOI:10.17504/protocols.io.6tuhenw | Neurodegeneration Method Development Community | - Protocol based on Krishnaswami et al., Nat Protoc. 2016, 3:499-524- Used routinely in our lab for the isolation of single nuclei from fresh frozen postmortem brains from subjects with neurodegenerative disorders and healthy controls for single-nucleus RNA-seq- Works also for isolation of nuclei from fresh frozen mouse brains - Used for isolation of all nuclei or antibody-enriched populations (i.e., NeuN+ nuclei)- We always perform and strongly recommend FACS if used for single-nucleus RNA-seq | Stanford University, Stanford University | 1 | 2019 | Marcos Otero-Garcia, Inma Cobos 2019. Isolation of single nuclei from postmortem fresh frozen human brain and immunostaining for NeuN. protocols.io https://dx.doi.org/10.17504/protocols.io.6tuhenw | 2021-04-15 09:15:53 | |||
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Flow cytometry Resource Report Resource Website |
Yuan Yao, morigen | DOI:10.17504/protocols.io.p9ndr5e | Yao Y, Ma Y, Chen X, Bade R, Lv C, Zhu R (2018) Absence of RstA results in delayed initiation of DNA replication in Escherichia coli. PLoS ONE 13(7): e0200688. doi: 10.1371/journal.pone.0200688 | Inner Mongolia People's Hospital, Inner Mongolia University | https://doi.org/10.1371/journal.pone.0200688 | 1 | 2018 | Yuan Yao, morigen 2018. Flow cytometry. protocols.io https://dx.doi.org/10.17504/protocols.io.p9ndr5e | 2021-04-15 09:15:53 | |||
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Measuring spectral reflectance and transmittance (350-2500 nm) of small and/or narrow leaves using the Spectra Vista Corporation (SVC) DC-R/T Integrating Sphere Resource Report Resource Website |
Etienne Laliberté, Raymond Soffer | DOI:10.17504/protocols.io.qp7dvrn | Canadian Airborne Biodiversity Observatory | Here we describe the standardised protocol used by the Canadian Airborne Biodiversity Observatory (CABO) to measure leaf spectral reflectance and transmittance, using an integrating sphere fitted to a portable full-range field spectroradiometer, for the special case where an individual leaf is too small and/or too narrow to entirely cover the reflectance or transmission port of the integrating sphere. Briefly, three arrays of mature, healthy and sunlit leaves from a canopy plant are arranged on a custom sample mount, and are then used for measurements of adaxial reflectance and transmittance. Reflectance measurements are referenced to a calibrated Spectralon® disk and corrected for stray light. Our leaf spectroscopy protocol is an adaptation of that of Noda et al. (2013) to the SVC DC-R/T sphere, and also builds from protocols by the Carnegie Airborne Observatory and the SVC integrating sphere user manual. | Université de Montréal, National Research Council | 2 | 2018 | Etienne Laliberté, Raymond Soffer 2018. Measuring spectral reflectance and transmittance (350-2500 nm) of small and/or narrow leaves using the Spectra Vista Corporation (SVC) DC-R/T Integrating Sphere. protocols.io https://dx.doi.org/10.17504/protocols.io.qp7dvrn | 2021-04-15 09:15:58 | |||
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During Data Acquisition Resource Report Resource Website |
Lukas Snoek | DOI:10.17504/protocols.io.jrbcm2n | Spinoza Centre, REC-L | This is a test | Spinoza Centre, REC-L | 1 | 2017 | Lukas Snoek 2017. During Data Acquisition. protocols.io https://dx.doi.org/10.17504/protocols.io.jrbcm2n | 2021-04-15 09:15:54 |
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