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Name Authors DOI Group Summary Associated Publications RRIDs used Affiliations External URL Version Publication Date Proper Citation Record Last Update
Clonal virus purification
 
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Mathias Middelboe, Amy M. Chan, and Sif K. Bertelsen DOI:10.17504/protocols.io.dqp5vm VERVE Net For use in "Obtaining pure cyanophage stocks (liquid assay)" Manual of Aquatic Viral Ecology, Manual of Aquatic Viral Ecology, Manual of Aquatic Viral Ecology 1 2016 Mathias Middelboe, Amy M. Chan, and Sif K. Bertelsen 2016. Clonal virus purification. protocols.io https://dx.doi.org/10.17504/protocols.io.dqp5vm 2021-04-15 09:14:51
Isotopic Labeling of Cyanobacteria and DNA Analysis
 
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Bonnie Poulos DOI:10.17504/protocols.io.c9nz5d VERVE Net, Sullivan Lab Protocol for labeling bacteria with N15. The bacterial DNA was made “heavy” so that community viral and host bacterial DNA could be distinguished from each other after sorting by using density gradient centrifugation. Matthew Sullivan Lab 1 2016 Bonnie Poulos 2016. Isotopic Labeling of Cyanobacteria and DNA Analysis. protocols.io https://dx.doi.org/10.17504/protocols.io.c9nz5d 2021-04-15 09:15:20
FVIC (Frequency of Visibly Infected Cells) Protocol
 
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Jennifer Brum DOI:10.17504/protocols.io.dbp2mm VERVE Net, Sullivan Lab Purpose: This protocol describes how to pellet bacterial cells onto grids and stain them so that viruses can be visualized within the cells using transmission electron microscopy. Data obtained from these grids can be used to calculate the frequency of visibly infected cells (FVIC), the frequency of infected cells (FIC), the fraction of mortality due to viral lysis (FMVL), and burst size. Matthew Sullivan Lab, University of Arizona/Ohio State University 1 2016 Jennifer Brum 2016. FVIC (Frequency of Visibly Infected Cells) Protocol. protocols.io https://dx.doi.org/10.17504/protocols.io.dbp2mm 2021-04-15 09:15:20
0.5M EDTA
 
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Ms Alex Aitken DOI:10.17504/protocols.io.c5wy7d VERVE Net, Sullivan Lab This shows how to make 0.5M EDTA http://www.nhm.ac.uk/resources-rx/files/te-buffer_aug12-118648.pdf 1 2016 Ms Alex Aitken 2016. 0.5M EDTA. protocols.io https://dx.doi.org/10.17504/protocols.io.c5wy7d 2021-04-15 09:14:56
The construction and analysis of marker gene libraries
 
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Steven M. Short, Feng Chen, and Steven W. Wilhelm DOI:10.17504/protocols.io.dpi5kd VERVE Net Marker genes for viruses are typically amplified from aquatic samples to determine whether specific viruses are present in the sample, or to examine the diversity of a group of related viruses. In this [protocol], we will provide an overview of common methods used to amplify, clone, sequence, and analyze virus marker genes, and will focus our discussion on viruses infecting algae, bacteria, and heterotrophic flagellates.Short, S. M., F. Chen, and S. W. Wilhelm. 2010. The construction and analysis of marker gene libraries, p. 82–91. In S. W. Wilhelm, M. G. Weinbauer, and C. A. Suttle [eds.], Manual of Aquatic Viral Ecology. ASLO. Manual of Aquatic Viral Ecology, Manual of Aquatic Viral Ecology, Manual of Aquatic Viral Ecology 1 2015 Steven M. Short, Feng Chen, and Steven W. Wilhelm 2015. The construction and analysis of marker gene libraries. protocols.io https://dx.doi.org/10.17504/protocols.io.dpi5kd 2021-04-15 09:15:27
Gradient Recipes
 
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David Dunigan and Irina Agarkova DOI:10.17504/protocols.io.eufbetn VERVE Net The University of Nebraska-Lincoln 1 2016 David Dunigan and Irina Agarkova 2016. Gradient Recipes. protocols.io https://dx.doi.org/10.17504/protocols.io.eufbetn 2021-04-15 09:15:29
Lowry Protein Assay
 
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David Dunigan and Irina Agarkova DOI:10.17504/protocols.io.etxbepn VERVE Net, Fish behavior and physiology, Medicinal Plants Southeastern Pará Research Group University of Nebraska-Lincoln 1 2016 David Dunigan and Irina Agarkova 2016. Lowry Protein Assay. protocols.io https://dx.doi.org/10.17504/protocols.io.etxbepn 2021-04-15 09:14:57
Resuspension Buffer P1
 
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Qiagen DOI:10.17504/protocols.io.hxgb7jw VERVE Net, Sullivan Lab This is a 0.05M Tris-Cl (pH 8.0), 0.01M EDTA resuspension buffer containing RNase A Matthew Sullivan Lab, University of Arizona, The Ohio State University http://people.mbi.ucla.edu/sumchan/qiagenbuffer.html 2 2017 Qiagen 2017. Resuspension Buffer P1. protocols.io https://dx.doi.org/10.17504/protocols.io.hxgb7jw 2021-04-15 09:15:30
Heald Lab Margaritas
 
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Rebecca Heald Lab DOI:10.17504/protocols.io.ea8bahw VERVE Net This protocol is part of the VERVE holiday drive to collect exotic off-the-shelf laboratory recipes. More details here. protocols.io https://mcb.berkeley.edu/labs/heald/Protocols/Preparation%20of%20Heald%20Lab%20Margaritas.pdf 1 2015 Rebecca Heald Lab 2015. Heald Lab Margaritas. protocols.io https://dx.doi.org/10.17504/protocols.io.ea8bahw 2021-04-15 09:15:32
VBRC Base By Base: Export a sequence selection to a different file
 
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Nick Tang DOI:10.17504/protocols.io.eckbauw VERVE Net, Upton-Lab Viral Bioinformatic Resource CentreProvide databases of viral genomic information. Please check the Organisms menu to see which viruses we support: we’re now focusing on large DNA viruses The VOCs (Virus Orthologous Clusters) database is at the heart of our system. The database links directly to integrated tools for comparative analyses. VOCs sorts genes into ortholog clusters (e.g. RNA polymerase) to simplify data retrieval. Provide easy access to the genes, gene families, and genomes of the different virus families. via a unique series of powerful Java tools that support multiple computer platforms (see VBRC Tools menu). design and build software to tackle specific bioinformatics/virology problems, often in collaboration with virologists. Rally the research community to provide expert curation of these viral genomes by: Adding value to GenBank sequences through enhancing and updating genome annotations Linking to research reviews/papers for the research community. Collaborate with researchers to help on specific bioinformatics problems, e.g. Custom searches of the databases Building new features into our tools Help with genome annotation University of Victoria: Department of Biochemistry and Microbiology http://athena.bioc.uvic.ca/ 1 2016 Nick Tang 2016. VBRC Base By Base: Export a sequence selection to a different file. protocols.io https://dx.doi.org/10.17504/protocols.io.eckbauw 2021-04-15 09:15:30
Obtaining pure cyanophage stocks (plaque purification)
 
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Mathias Middelboe, Amy M. Chan, and Sif K. Bertelsen DOI:10.17504/protocols.io.dqq5vv VERVE Net, Suttle Laboratory of Marine Molecular Microbiology and Virology Manual of Aquatic Viral Ecology, Manual of Aquatic Viral Ecology, Manual of Aquatic Viral Ecology http://www.aslo.org/books/mave/MAVE_118.pdf 1 2016 Mathias Middelboe, Amy M. Chan, and Sif K. Bertelsen 2016. Obtaining pure cyanophage stocks (plaque purification). protocols.io https://dx.doi.org/10.17504/protocols.io.dqq5vv 2021-04-15 09:15:35
Exotic Lab Methods
 
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Numerous scientists DOI:10.17504/protocols.io.ebhbaj6 VERVE Net This collection is part of the VERVE holiday drive to collect exotic off-the-shelf laboratory recipes. More details here.If you know creative/unusual protocols like these, please tweet them to #ExoticMethods, e-mail to "[email protected]", or share directly as a protocol here, tagging with "ExoticMethods". University of Arizona 1 2016 Numerous scientists 2016. Exotic Lab Methods. protocols.io https://dx.doi.org/10.17504/protocols.io.ebhbaj6 2021-04-15 09:15:05
16S PCR Universal
 
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Natalie Solonenko DOI:10.17504/protocols.io.c5my45 VERVE Net, Sullivan Lab Matthew Sullivan Lab, University of Arizona/Ohio State University 1 2016 Natalie Solonenko 2016. 16S PCR Universal. protocols.io https://dx.doi.org/10.17504/protocols.io.c5my45 2021-04-15 09:15:35
VBRC Base By Base: View gene annotations
 
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Nick Tang DOI:10.17504/protocols.io.ecqbavw VERVE Net, Upton-Lab Viral Bioinformatic Resource CentreProvide databases of viral genomic information. Please check the Organisms menu to see which viruses we support: we’re now focusing on large DNA viruses The VOCs (Virus Orthologous Clusters) database is at the heart of our system. The database links directly to integrated tools for comparative analyses. VOCs sorts genes into ortholog clusters (e.g. RNA polymerase) to simplify data retrieval. Provide easy access to the genes, gene families, and genomes of the different virus families. via a unique series of powerful Java tools that support multiple computer platforms (see VBRC Tools menu). design and build software to tackle specific bioinformatics/virology problems, often in collaboration with virologists. Rally the research community to provide expert curation of these viral genomes by: Adding value to GenBank sequences through enhancing and updating genome annotations Linking to research reviews/papers for the research community. Collaborate with researchers to help on specific bioinformatics problems, e.g. Custom searches of the databases Building new features into our tools Help with genome annotation University of Victoria: Department of Biochemistry and Microbiology http://athena.bioc.uvic.ca/ 1 2016 Nick Tang 2016. VBRC Base By Base: View gene annotations. protocols.io https://dx.doi.org/10.17504/protocols.io.ecqbavw 2021-04-15 09:15:06
One-Step Growth Curves for Cyanophages
 
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Matthew Sullivan DOI:10.17504/protocols.io.dan2dd VERVE Net, Sullivan Lab Sullivan Lab 1 2016 Matthew Sullivan 2016. One-Step Growth Curves for Cyanophages. protocols.io https://dx.doi.org/10.17504/protocols.io.dan2dd 2021-04-15 09:15:36
Isolation and Purification of Plasmid DNA from E. coli
 
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David Dunigan and Irina Agarkova DOI:10.17504/protocols.io.ertbd6n VERVE Net University of Nebraska-Lincoln 1 2016 David Dunigan and Irina Agarkova 2016. Isolation and Purification of Plasmid DNA from E. coli. protocols.io https://dx.doi.org/10.17504/protocols.io.ertbd6n 2021-04-15 09:15:09
MetaVelvet : An extension of Velvet assembler to de novo metagenome assembly from short sequence reads
 
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Afiahayati, Sato K, Namiki T, Hachiya T, Tanaka H, Sakakibara Y. DOI:10.17504/protocols.io.d7q9mv VERVE Net, Hurwitz Lab Motivation: An important step of "metagenomics" analysis is the assembly of multiple genomes from mixed sequence reads of multiple species in a microbial community. Most conventional pipelines employ a single-genome assembler with carefully optimized parameters and post-process the resulting scaffolds to correct assembly errors. Limitations of the use of a single-genome assembler for de novo metagenome assembly are that highly conserved sequences shared between different species often causes chimera contigs, and sequences of highly abundant species are likely mis-identified as repeats in a single genome.Methods:We modified and extended a single-genome and de Bruijn-graph based assembler, Velvet, for de novo metagenome assembly. Our fundamental ideas are first decomposing de Bruijn graph constructed from mixed short reads into individual sub-graphs and second building scaffolds based on every decomposed de Bruijn sub-graph as isolate species genome. Hurwitz Lab, Hurwitz Lab, Hurwitz Lab, Hurwitz Lab, Hurwitz Lab, Hurwitz Lab 1 2016 Afiahayati, Sato K, Namiki T, Hachiya T, Tanaka H, Sakakibara Y. 2016. MetaVelvet : An extension of Velvet assembler to de novo metagenome assembly from short sequence reads. protocols.io https://dx.doi.org/10.17504/protocols.io.d7q9mv 2021-04-15 09:15:36
Running "16sblaster" at iPlant
 
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Ken Youens-Clark DOI:10.17504/protocols.io.egmbbu6 VERVE Net, Hurwitz Lab See upcoming paper by Watts, Hurwitz, Youens-Clark.Code is freely available at Github. University of Arizona 1 2016 Ken Youens-Clark 2016. Running "16sblaster" at iPlant. protocols.io https://dx.doi.org/10.17504/protocols.io.egmbbu6 2021-04-15 09:15:36
Script R7: Intra and Inter Personal Dissimilarity
 
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HANNIGAN GD, GRICE EA, ET AL. DOI:10.17504/protocols.io.eipbcdn VERVE Net, Club Grice This protocol outlines the analysis used for intra and interpersonal diversity of the virome and whole metagenome using the Bray Curtis dissimilarity metric. We visualize the differences as bar plots and calculate the statistical significance of the differences using a t-test. Based on the methods from the following publication:Hannigan, Geoffrey D., et al. "The Human Skin Double-Stranded DNA Virome: Topographical and Temporal Diversity, Genetic Enrichment, and Dynamic Associations with the Host Microbiome." mBio 6.5 (2015): e01578-15. Kindler L, Stoliartchouk A, Teytelman L, Hurwitz BL, Method-centered digital communities on protocols.io for fast-paced scientific innovation. F1000Research doi: 10.12688/f1000research.9453.2 DEPARTMENT OF DERMATOLOGY UNIVERSITY OF PENNSYLVANIA, DEPARTMENT OF DERMATOLOGY UNIVERSITY OF PENNSYLVANIA, DEPARTMENT OF DERMATOLOGY UNIVERSITY OF PENNSYLVANIA http://mbio.asm.org/content/6/5/e01578-15.full 1 2016 HANNIGAN GD, GRICE EA, ET AL. 2016. Script R7: Intra and Inter Personal Dissimilarity. protocols.io https://dx.doi.org/10.17504/protocols.io.eipbcdn 2021-04-15 09:15:09
Preparation of PBCV-1 Lysin
 
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David Dunigan and Irina Agarkova DOI:10.17504/protocols.io.etdbei6 VERVE Net University of Nebraska-Lincoln 1 2016 David Dunigan and Irina Agarkova 2016. Preparation of PBCV-1 Lysin. protocols.io https://dx.doi.org/10.17504/protocols.io.etdbei6 2021-04-15 09:15:11

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