Searching the RRID Resource Information Network
Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.
| Name | Authors | DOI | Group |
Summary |
Associated Publications |
RRIDs used | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Diatom Transformation via Bacterial Conjugation Resource Report Resource Website |
Jeric Harper | DOI:10.17504/protocols.io.hgpb3vn | Protist Research to Optimize Tools in Genetics (PROT-G), Alverson Lab | protocols.io | http://www.nature.com/articles/ncomms7925 | 3 | 2017 | Jeric Harper 2017. Diatom Transformation via Bacterial Conjugation. protocols.io https://dx.doi.org/10.17504/protocols.io.hgpb3vn | 2021-04-15 09:15:09 | |||
|
Fabrication of DNA constructs by Gibson Assembly and Golden Gate reactions Resource Report Resource Website |
Tamara Matute, Isaac Nuñez, Peter Von Dassow, Fernan Federici | DOI:10.17504/protocols.io.hpib5ke | Protist Research to Optimize Tools in Genetics (PROT-G), Laboratorio de Tecnologias Libres | , , , | 1 | 2017 | Tamara Matute, Isaac Nuñez, Peter Von Dassow, Fernan Federici 2017. Fabrication of DNA constructs by Gibson Assembly and Golden Gate reactions. protocols.io https://dx.doi.org/10.17504/protocols.io.hpib5ke | 2021-04-15 09:14:46 | ||||
|
Staining protocol for unicellular protists: Lysotracker and Dapi Resource Report Resource Website |
Maria Rubio-Brotons | DOI:10.17504/protocols.io.gg4btyw | Protist Research to Optimize Tools in Genetics (PROT-G), Multicellgenomelab | IBE CSIC-UPF | 3 | 2016 | Maria Rubio-Brotons 2016. Staining protocol for unicellular protists: Lysotracker and Dapi. protocols.io https://dx.doi.org/10.17504/protocols.io.gg4btyw | 2021-04-15 09:15:05 | ||||
|
Establishment of clonal algal cultures by flow cytometry sorting Resource Report Resource Website |
Marie D., Le Gall F., Edern R., Gourvil P., Vaulot, D. | DOI:10.17504/protocols.io.hdib24e | Ecology of Marine Plankton (ECOMAP) team - Roscoff, Protist Research to Optimize Tools in Genetics (PROT-G), Roscoff Culture Collection | This protocol can be used :to isolate novel cultures from natural samplesto isolate novel cultures from enriched samplesto purify existing cultures and remove contaminantsto obtain clonal cultures from a unialgal strainReference : Marie, D., Le Gall, F., Edern, R., Gourvil, P. & Vaulot, D. 2017. Improvement of phytoplankton culture isolation using single cell sorting by flow cytometry. J. Phycol. in press. | CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff | http://doi.wiley.com/10.1111/jpy.12495 | 1 | 2017 | Marie D., Le Gall F., Edern R., Gourvil P., Vaulot, D. 2017. Establishment of clonal algal cultures by flow cytometry sorting. protocols.io https://dx.doi.org/10.17504/protocols.io.hdib24e | 2021-04-15 09:14:44 | ||
|
Culturing Euplotes crassus to high densities using a combination of algae and bacteria as the food source. Resource Report Resource Website |
Lawrence A. Klobutcher | DOI:10.17504/protocols.io.gw2bxge | Protist Research to Optimize Tools in Genetics (PROT-G) | This procedure was developed to investigate the possible use of RNAi through bacterial feeding as a means of knocking down expression of particular genes.While the utility of RNAi is still being investigated, the method is effective in growing Euplotes crassus to higher densities than is possible using algae alone. Using moderately dense cultures of algae, we typically achieve cell densities of 500-1,000 cells/ml, while with the E. coli supplemented cultures we describe here, Euplotes cell densities exceed 3,000 cells/ml. In fact, preliminary studies mixing a volume of a Euplotes culture with an equal volume of resuspended E. coli have produced a density of ~8,000 cells/ml.While the described procedure involves small cultures, it can likely be scaled up as required.For some species of Euplotes, long-term culture using bacteria as a food source has not been successful (C. Miceli, personal communication), suggesting that some essential nutrient is not being provided in sufficient quantitities | University of Connecticut Health Center | 1 | 2017 | Lawrence A. Klobutcher 2017. Culturing Euplotes crassus to high densities using a combination of algae and bacteria as the food source.. protocols.io https://dx.doi.org/10.17504/protocols.io.gw2bxge | 2021-04-15 09:15:11 | |||
|
Euplotes crassus transformation using Lipofectamine 2000 as vehicle Resource Report Resource Website |
RACHELE CESARONI | DOI:10.17504/protocols.io.g42byye | Protist Research to Optimize Tools in Genetics (PROT-G) | University of Bern, Institute of Biology | 3 | 2017 | RACHELE CESARONI 2017. Euplotes crassus transformation using Lipofectamine 2000 as vehicle. protocols.io https://dx.doi.org/10.17504/protocols.io.g42byye | 2021-04-15 09:14:47 | ||||
|
Transfection of Crypthecodinium cohnii using labelled DNA Resource Report Resource Website |
José A. Fernández Robledo | DOI:10.17504/protocols.io.z26f8he | Protist Research to Optimize Tools in Genetics (PROT-G) | José A. Fernández Robledo Nastasia J. Freyria Bigelow Laboratory for Ocean Sciences | 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 | Bigelow Laboratory for Ocean Sciences | https://doi.org/10.1038/s41592-020-0796-x | 1 | 2019 | José A. Fernández Robledo 2019. Transfection of Crypthecodinium cohnii using labelled DNA. protocols.io https://dx.doi.org/10.17504/protocols.io.z26f8he | 2021-04-15 09:15:11 | |
|
RNA-seq Library Construction with the KAPA mRNA HyperPrep Kit Resource Report Resource Website |
Amanda Scholes | DOI:10.17504/protocols.io.uueewte | Protist Research to Optimize Tools in Genetics (PROT-G), Lewis Lab | A protocol for making multiplexed RNA-seq libraries using KAPA Biosystems mRNA HyperPrep Kit, optimized for Saccharomyces cerevisiae. | Scholes AN, Lewis JA, Comparison of RNA isolation methods on RNA-Seq: implications for differential expression and meta-analyses. BMC Genomics doi: 10.1186/s12864-020-6673-2 | University of Arkansas - Fayetteville | https://doi.org/10.1186/s12864-020-6673-2 | 1 | 2019 | Amanda Scholes 2019. RNA-seq Library Construction with the KAPA mRNA HyperPrep Kit. protocols.io https://dx.doi.org/10.17504/protocols.io.uueewte | 2021-04-15 09:15:08 | |
|
Quick staining procedure of nuclei in Euplotes using DAPI Resource Report Resource Website |
Rachele Cesaroni | DOI:10.17504/protocols.io.hjfb4jn | Protist Research to Optimize Tools in Genetics (PROT-G) | 5 | 2017 | Rachele Cesaroni 2017. Quick staining procedure of nuclei in Euplotes using DAPI. protocols.io https://dx.doi.org/10.17504/protocols.io.hjfb4jn | 2021-04-15 09:14:48 | |||||
|
Plasmids for transformation of Bigelowiella, Pyramimonas, Eutreptiella and Chromera Resource Report Resource Website |
Pavel Doležal and Vladimir Hampl | DOI:10.17504/protocols.io.hh6b39e | Protist Research to Optimize Tools in Genetics (PROT-G) | In this protocol we publish the maps and sequences of specific plasmids designed for the transformation of Bigelowiella natans, Pyramimonas parkeae, Eutreptiella gymnastica, Chromera velia and Pseudonitzchia delicatissima. All these plasmids contain gene for firefly lucipherase as a reporter, some of them contain PAC (puromycin) or G418 (neomycin) resistance gene. All genes are flanked by organism specific up- and downstream gene regions extracted from genomic and transcriptomic data. It should be noted that we were not successful in any transformation by these plasmids, but it does not mean that the problem is in the plasmids. All plasmids are available upon request. The plasmid maps and sequences can be downloaded as a word file from More/Material section of this protocol. | Charles University, Prague | 1 | 2017 | Pavel Doležal and Vladimir Hampl 2017. Plasmids for transformation of Bigelowiella, Pyramimonas, Eutreptiella and Chromera. protocols.io https://dx.doi.org/10.17504/protocols.io.hh6b39e | 2021-04-15 09:14:48 | |||
|
Plaque Assay for the Aureococcus anophagefferens Virus (AaV) Resource Report Resource Website |
Eric Gann | DOI:10.17504/protocols.io.g2nbyde | Protist Research to Optimize Tools in Genetics (PROT-G), The Aquatic Microbial Ecology Research Group - AMERG (The Buchan, Zinser and Wilhelm labs) | We have developed a plaque assay for AaV with a modified protocol from Schroeder et. al 2002. Protocol modified from:Schroeder, D.C., et al., Coccolithovirus (Phycodnaviridae): Characterisation of a new large dsDNAalgal virus that infects Emiliania huxleyi. Archives of Virology, 2002.147(9): p. 1685-1698. | http://rdcu.be/oJCt | 1 | 2017 | Eric Gann 2017. Plaque Assay for the Aureococcus anophagefferens Virus (AaV). protocols.io https://dx.doi.org/10.17504/protocols.io.g2nbyde | 2021-04-15 09:15:12 | |||
|
Single-cell RNA extraction and cDNA library preparation from challenging marine protists (e.g. Acantharea) Resource Report Resource Website |
Margaret Brisbin, Lisa Mesrop | DOI:10.17504/protocols.io.mvhc636 | Protist Research to Optimize Tools in Genetics (PROT-G) | Marine protists are important in all marine ecosystems, but many are not culturable and therefore difficult to study. The increasing development of single-cell techniques is allowing for more marine protists to be studied, but many single-cell protocols are only optimized for model organisms and do not perform well with marine plankton. The SMART-seq v4 manual specifically states that cells entering the pipeline should be washed and resuspended in cell culture-grade PBS, but most marine protists do not tolerate PBS. Additionally, many marine protists have mineral skeletons, the components of which may interfere with the chemistry of the SMART-seq kit. Calcium and Strontium both dissolve to form divalent cations which could saturate the kit's RNase inhibitor. When we synthesized cDNA directly from acantharians (SrSO4 skeletons) without first extracting RNA, the cDNA was highly degraded with a 300 bp average fragment length. Therefore, it is desirable to perform RNA extractions from single marine protists before cDNA synthesis and amplification, but the amount of RNA in single marine protists is too low to be extracted with column-based kits (even the MN Nucleospin RNA XS kit suggested in the SMART-seq manual). To overcome these problems, we developed a column-free method for extracting RNA from single marine protists by making use of Agencourt RNAClean XP magnetic beads. When this protocol is followed, the synthesized cDNA is higher quality with a 2,000 bp average fragment length. | Okinawa Institute of Science and Technology, University of Southern California | 1 | 2018 | Margaret Brisbin, Lisa Mesrop 2018. Single-cell RNA extraction and cDNA library preparation from challenging marine protists (e.g. Acantharea). protocols.io https://dx.doi.org/10.17504/protocols.io.mvhc636 | 2021-04-15 09:14:52 | |||
|
Cryopreservation of thraustochytrids Resource Report Resource Website |
Mariana Rius | DOI:10.17504/protocols.io.h9fb93n | Protist Research to Optimize Tools in Genetics (PROT-G) | Stony B | 1 | 2017 | Mariana Rius 2017. Cryopreservation of thraustochytrids. protocols.io https://dx.doi.org/10.17504/protocols.io.h9fb93n | 2021-04-15 09:14:52 | ||||
|
Euplotes crassus transformation using FuGene HD Transfection Reagent as vehicle Resource Report Resource Website |
RACHELE CESARONI | DOI:10.17504/protocols.io.g5bby2n | Protist Research to Optimize Tools in Genetics (PROT-G) | University of Bern, Institute of Biology | 6 | 2017 | RACHELE CESARONI 2017. Euplotes crassus transformation using FuGene HD Transfection Reagent as vehicle. protocols.io https://dx.doi.org/10.17504/protocols.io.g5bby2n | 2021-04-15 09:15:29 | ||||
|
Transfection of Micromonas commoda CCMP2709 Resource Report Resource Website |
Lisa Sudek, Alexandra Worden, Manny Ares | DOI:10.17504/protocols.io.57kg9kw | Protist Research to Optimize Tools in Genetics (PROT-G), Worden Lab | This protocol describes the transformation of the picoprasinophyte alga Micromonas commoda, a green alga that is found in tropical to temperate oceans. The strain used was genome-sequenced in (1). The original strain name was NOUM17, housed as RCC299. The latter was rendered axenic, genome-sequenced, and deposited at the CCMP (now NCMA) as CCMP2709 and also maintained in the Worden lab. The below protocol is an adaptation of transformation methods used for the choanoflagellate Salpingoeca rosetta. We are grateful to N. King and D. Booth for their invaluable support in initial stages of experiments, as well as help from C. Poirier, M. Hamilton, K. Hoadley, C. Eckmann and especially C. Yung throughout the entire development. | Monterey Bay Aquarium Research Institute, Moss Landing, USA, Monterey Bay Aquarium Research Institute, Moss Landing, USA; Ocean EcoSystems Biology Unit, Marine Ecology Division, Helmholtz Centre for Ocean Research, Kiel, Germany, University of California, Santa Cruz | 1 | 2019 | Lisa Sudek, Alexandra Worden, Manny Ares 2019. Transfection of Micromonas commoda CCMP2709. protocols.io https://dx.doi.org/10.17504/protocols.io.57kg9kw | 2021-04-15 09:14:59 | |||
|
Glass bead transformation of Heterosigma akashiwo Resource Report Resource Website |
Deepak Nanjappa and Kathryn Coyne | DOI:10.17504/protocols.io.hjkb4kw | Protist Research to Optimize Tools in Genetics (PROT-G) | This protocol was developed for the glass bead-mediated transformation of Heterosigma akashiwo. This species does not grow on solid medium, so transformants are grown "in bulk" and should not be considered clonal. We have repeated this protocol with success and have been able to maintain transformants on selection medium for several months. | University of Delaware | 2 | 2017 | Deepak Nanjappa and Kathryn Coyne 2017. Glass bead transformation of Heterosigma akashiwo. protocols.io https://dx.doi.org/10.17504/protocols.io.hjkb4kw | 2021-04-15 09:15:01 | |||
|
MBBM Media Resource Report Resource Website |
Alyssa Alsante | DOI:10.17504/protocols.io.gdrbs56 | Protist Research to Optimize Tools in Genetics (PROT-G), The Aquatic Microbial Ecology Research Group - AMERG (The Buchan, Zinser and Wilhelm labs) | Van Etten, J. (n.d.). Formulation of Modified Bold's Basal Medium (MBBM). Retrieved from http://ncv.unl.edu/vanettenlab/ | http://ncv.unl.edu/vanettenlab/MBBM.pdf | 2 | 2016 | Alyssa Alsante 2016. MBBM Media. protocols.io https://dx.doi.org/10.17504/protocols.io.gdrbs56 | 2021-04-15 09:15:35 | |||
|
Establishment of clonal algal cultures by flow cytometry sorting Resource Report Resource Website |
Marie D., Le Gall F., Edern R., Gourvil P., Vaulot, D. | DOI:10.17504/protocols.io.mn4c5gw | Ecology of Marine Plankton (ECOMAP) team - Roscoff, Protist Research to Optimize Tools in Genetics (PROT-G), Roscoff Culture Collection | This protocol can be used :to isolate novel cultures from natural samplesto isolate novel cultures from enriched samplesto purify existing cultures and remove contaminantsto obtain clonal cultures from a unialgal strainReference : Marie, D., Le Gall, F., Edern, R., Gourvil, P. & Vaulot, D. 2017. Improvement of phytoplankton culture isolation using single cell sorting by flow cytometry. J. Phycol. in press. | CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff, CNRS et UPMC, Station Biologique de Roscoff | http://doi.wiley.com/10.1111/jpy.12495 | 2 | 2018 | Marie D., Le Gall F., Edern R., Gourvil P., Vaulot, D. 2018. Establishment of clonal algal cultures by flow cytometry sorting. protocols.io https://dx.doi.org/10.17504/protocols.io.mn4c5gw | 2021-04-15 09:15:08 | ||
|
Transient transformation of Ostreococcus species (OTTH595, RCC809 and RCC802) and Bathycoccus Resource Report Resource Website |
François-Yves Bouget, Valérie Vergé and Jean-Claude Lozano | DOI:10.17504/protocols.io.g86bzze | Protist Research to Optimize Tools in Genetics (PROT-G) | This protocol describes the preparation of cells and introduction of DNA into the cells by electroporation. For selection of stable transformants or measure of transient gene expression see related protocols. | 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 | Laboratoire d'Oceanographie Microbienne. Banyuls sur Mer, Laboratoire d'Oceanographie Microbienne. Banyuls sur Mer | https://doi.org/10.1038/s41592-020-0796-x | 1 | 2017 | François-Yves Bouget, Valérie Vergé and Jean-Claude Lozano 2017. Transient transformation of Ostreococcus species (OTTH595, RCC809 and RCC802) and Bathycoccus. protocols.io https://dx.doi.org/10.17504/protocols.io.g86bzze | 2021-04-15 09:15:35 | |
|
Fluorescence activated cell sorting (FACS) of Perkinsus marinus transformants Resource Report Resource Website |
Imen Lassadi | DOI:10.17504/protocols.io.hh2b38e | 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 | https://doi.org/10.1038/s41592-020-0796-x | 1 | 2017 | Imen Lassadi 2017. Fluorescence activated cell sorting (FACS) of Perkinsus marinus transformants. protocols.io https://dx.doi.org/10.17504/protocols.io.hh2b38e | 2021-04-15 09:15:05 |
Can't find your Protocol?
We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. If you want to find a specific protocol and you know the DOI of the protocol already, it's easier to enter a DOI to search. You can refine the search results using Facets on the left side of the search results page. If you are on the table view, you can also search in a specific column by clicking the column title and enter the keywords.
If you still could not find your protocol in the search results, please help us by adding it into the system — it's easy. Create and publish your protocols at Protocols.io.
Welcome to the dkNET Resources search. From here you can search through a compilation of resources used by dkNET and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that dkNET has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.
If you have an account on dkNET then you can log in from here to get additional features in dkNET such as Collections, Saved Searches, and managing Resources.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
If you are logged into dkNET you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the facets that you can filter the data by.
If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.
The NIDDK Information Network (dkNET) serves the needs of basic and clinical investigators by providing seamless access to large pools of data and research resources relevant to the mission of The National Institute of Diabetes Digestive and Kidney Diseases (NIDDK). dkNET is hosted at University of California San Diego, and is supported by NIH NIDDK grant U24DK097771.
Email: info_at_ dknet.org
