Visualization Clause Samples
Visualization. The parties will [*] via [*], [*], [*] and [*]. The [*] CHM [*] and [*] will be [*] and [*] to [*] for usage at [*] as part of the CHM. [*] will [*] the [*] of this [*] on [*] and [*] at [*] on [*] as part of the CHM. OVERALL CHM PROCESS - [*] In addition, an [*] which [*] the [*], [*] and [*] for [*] and [*] the [*] and to [*] of the [*]) will be [*] and [*] to [*] so that [*] can implement necessary [*] within [*] on [*] a part of the CHM. INFORMATION EXCHANGE DURING THE RESEARCH TERM In the course of the [*], a [*] of [*] will need to be [*]. The [*] of the [*], [*], the [*] and of the [*], the [*] and the [*], will be [*] at [*]. [*] will require [*] to the [*]. [*] will be [*] as [*], [*] and [*] for [*] in [*]. The [*] will be * Certain information on this page has been omitted and filed separately with the Commission. Confidential treatment has been requested with respect to the omitted portions. AZ AND CK CONFIDENTIAL provided for use with [*]. [*] is responsible for acquiring its own [*]. [*] [*] ACCESS TO [*] EMPLOYED DURING THE RESEARCH TERM OF THE COLLABORATION [*] [*] THE CYTOMETRIX(TM) HEPATOTOXICITY MODULE: [*] DELIVERED TO AZ FOR IDENTIFICATION OF HEPATOTOXICITY IN [*] DURING THE [*] [*] of the [*], [*], [*], [*] and [*] for the overall [*] and the [*] will be delivered to [*] during the [*]. [*] will be [*] on the [*] and [*] of the CHM per the [*]. [*] and [*] with [*] for [*], [*] and [*] will be delivered. The [*] will constitute the [*] of the Cytometrix(TM) Hepatotoxicity Module, from [*] to [*] of a [*]. [*] on the [*] and [*] will be provided. [*] [*] [*] [*] [*] * Certain information on this page has been omitted and filed separately with the Commission. Confidential treatment has been requested with respect to the omitted portions. AZ AND CK CONFIDENTIAL [*] THIRD PARTY PRODUCTS INCLUDED IN THE DELIVERABLES [*] INFORMATION EXCHANGE [*] [*] [*] [*] ALGORITHMS USED AS PART OF THE RESEARCH PLAN [*] [*] [*] [*] CYTOMETRIX(TM) HEPATOTOXICITY MODULE Hardware systems: All computers are to be Intel(R) Pentium(R) series, operating systems are to be Microsoft(R) Windows(R) 2000 or above. (Memory, processor requirements TBD) Applications Software: [*] [*] [*] [*] [*] * Certain information on this page has been omitted and filed separately with the Commission. Confidential treatment has been requested with respect to the omitted portions. AZ AND CK CONFIDENTIAL [*] [*] [*] [*] * Certain information on this page has been omitted and filed sepa...
Visualization. Any technique for creating images, diagrams, or animations to communicate information. BIM can be used as a tool to show visual clarity of simple and complex systems and data to help understand Project scope, design options, constructability, coordination and for quality assurance and control.
Visualization. 1. After electrophoresis is complete, open the chamber lid and remove the Chamber Cover. Use the Gel Block Remover to remove the gel blocks. Place one electrode across each end of the gel to prevent curling during drying. Rinse the Chamber Cover before reuse.
2. Close the chamber lid and press the TEST SELECT/CONTINUE button to dry the gel.
3. After the gel has been dried, carefully remove the gel from the electrophoresis chamber.
4. Remove the SPIFE QuickGel Holder from the stainer chamber. While holding the gel agarose side down, slide one side of the gel backing under one of the metal bars. Bend the gel backing so that the gel is bowed, and slip the other side under the other metal bar. The two small notches in the backing must fit over the small pins to secure the gel to the holder.
5. Place the SPIFE QuickGel Holder with the attached gel facing backwards into the stainer chamber.
6. With the appropriate test name on the display, press the START/STOP button. An option to either begin the test or skip the operation will be presented. Press START/STOP to begin. The instrument will stain, destain and dry the gel.
7. When the process is completed, the instrument will beep. Carefully remove the SPIFE QuickGel Holder from the stainer because the metal piece on the holder will be hot. Take the gel off of the holder and replace the holder. Refer to Evaluation of the Hemoglobin Bands. The following instructions are for using the QuickGel Chamber (Cat. No. 1284) for electrophoresis.
Visualization. Visualization features in blockchain analytics tools enable investigators to visualize the flow of funds across different cryptocurrencies and blockchains. By creating visual representations of transaction networks and relationships, investiga- tors can gain insights into the complexity of chain hopping activities and identify key nodes or entities involved. It is crucial to choose the right tool for the investigation, depending on the circumstanc- es and taking into account the blockchains involved. • The tool should support a wide range of cryptocurrencies and blockchains from the most popular like Bitcoin and Ethereum to the ones most used by criminals like Tron; • Must be able to provide robust analytics, including transaction tracing, address clustering, and wallet identification. Features like graph visualizations are es- sential and can help illustrate complex relationships, • A user-friendly interface is crucial, especially for investigators who may not be blockchain experts. The tool should offer intuitive navigation and clear visuali- zations; • Real-time monitoring and alerts for suspicious activities can be vital for timely investigations; • Evaluate the pricing model to ensure it fits within budget constraints while offer- ing the necessary features; • Research the tool’s reputation within the industry, including user reviews and case studies, to assess its reliability and effectiveness. So-called “layer 2 solutions” in the context of blockchain refer to technologies or pro- tocols that are built on top of an existing blockchain network (which constitute Layer 1, such as Bitcoin or Ethereum). The primary goal of Layer 2 solutions is to enhance the scalability, efficiency, and speed of the blockchain without compromising its security or decentralization. These solutions handle transactions off the main blockchain, reducing the load and congestion on Layer 1 while still benefiting from its security features. This also means that often transactions performed on Layer 2 are not visible, or not entirely, on Layer 1. Key Characteristics of Layer 2 Solutions • Off-Chain Processing: Transactions or computations are moved off the main chain (Layer 1) to a secondary layer. This off-chain processing reduces the data burden on the main blockchain, increasing its overall speed and efficiency. • Enhanced Scalability: By processing many transactions outside the main chain, Layer 2 solutions can significantly increase the number of transactions per second tha...
Visualization. 1. After the gel has been dried, open the chamber lid and carefully remove the gel from the electrophoresis chamber.
2. Remove the Gel Holder from the stainer unit. Attach the gel to the holder by placing the round hole in the gel backing over the left pin on the holder and the obround hole over the right pin on the holder.
3. Place the Gel Holder with the attached gel facing backwards into the stainer unit.
4. With the appropriate test name on the display, press the START/STOP button. An option to either begin the test or skip the operation will be presented. Press START/STOP to begin. The instrument will stain, destain and dry the gel.
5. When the gel has completed the process, the instrument will beep. Remove the Gel Holder from the stainer.
Visualization. 1. After the gel has been dried, carefully remove the gel from the electrophoresis chamber.
2. Remove the Gel Holder from the stainer chamber. Attach the gel to the holder by placing the round hole in the gel backing over the left pin on the holder and the obround hole over the right pin on the holder.
Visualization. Visualization allows to estimate resource consumption for remote visualization. Depending on screen resolution, refresh rate and achievable level of image compression, remote visualization will consume CPU time on the remote visualization host and network bandwidth.
1. Light, for typical 2D application with low refresh rate
2. Medium, for 2D and lightweight 3D applications
3. High, for intensive 3D application The algorithms will try to find Instances that fits the remote visualization needs and will compute the associated costs of the Instance and the Data transfers associated with the streaming of the “remote screen” (based on assumptions about the size of screen and the average bandwidth need in each strategy for an h264 interactive video stream).
Visualization. 1. After electrophoresis is complete, open the chamber lid and use the Gel Block Remover to remove the gel blocks. Dispose of blades and cups as biohazardous waste. Replace the electrodes on each end of the gel to prevent curling during drying.
2. Close the chamber lid and press the CONTINUE button to dry the gel.
3. After the gel has been dried, open the chamber lid and carefully remove the gel from the electrophoresis chamber.
4. Remove the SPIFE QuickGel Holder from the stainer chamber. While holding the gel agarose side down, slide one side of the gel backing under one of the metal bars. Bend the gel backing so that the gel is bowed, and slip the other side under the other metal bar. The two small notches in the backing must fit over the small pins to secure the gel to the holder.
5. Place the SPIFE QuickGel Holder with the attached gel facing backwards into the stainer chamber.
6. Use the arrows under STAINER UNIT to select the appropriate test. Press START and choose an operation to proceed. The instrument will stain, destain and dry the gel.
7. When the process is completed, the instrument will beep. Carefully remove the SPIFE QuickGel Holder from the stainer because the metal piece on the holder will be hot. Scan the bands in a densitometer or the QuickScan Touch/2000. Qualitative Evaluation: The urine and CSF samples run on the QuickGel SPE Gel can only be visually inspected for the presence of the bands. Quantitative Evaluation: Scan the samples on the QuickGel SPE Gel in the QuickScan Touch/2000, agarose side up, on the acid blue setting. A slit size of 5 is recommended. Stability of End Product: The completed, dried, QuickGel SPE Gel is stable for an indefinite period of time.
Visualization. As is described in the introduction, we wanted to keep the model viewer as “dumb” as possible, in order to illustrate the way in which XML trans- formations can be used for creating several visualizations for a single XML document. For this purpose, we have made a specific XML schema which can be interpreted by the model viewer without having to know anything about the ArchiMate language. The following XML fragment illustrates this language. <container height="80" id="014" type="interaction" width="100" > <box color="khaki1" height="80" type="round" width="100" x="0" y="0" z="0" /> <label fieldname="name" halign="center" text="register policy" x="50" y="40" z="1" /> <icon height="15" type="splitcircle" width="15" x="75" y="10" z="1" /> </container> <container height="80" id="013" type="interaction" width="100" > <box color="khaki1" height="80" type="round" width="100" x="0" y="0" z="0" /> <label fieldname="name" halign="center" text="sign contract" x="50" y="40" z="1" /> <icon height="15" type="splitcircle" width="15" x="75" y="10" z="1" /> </container> <arrow from="013" id="020" to="014" type="triggering" > <line type="solid" width="1" z="0" /> <headarrowtip size="10" type="filledarrow" z="1" /> </arrow> The intermediate visualization language has two main constructs: con- tainers and arrows. Containers are rectangular areas in which several visual elements can be placed. The exact location of those visual elements can be defined relative to the size and position of the container. Each container has a unique iden- tifier which can be used to refer to the original elements in the architectural description. Arrows are linear directed elements. They have a head and a tail, which both have to be connected to containers (via their identifiers). They also have unique identifiers themselves. In the example above, two containers and one arrow are defined. In Figure 10.6 the output of the interpretation of this XML fragment by the model viewer is shown. As can be seen in the XML fragment, some visual elements, like “split circle”, are built into the model viewer. This has mainly been done for reasons of efficiency. Sign contract Register policy For the transformation of the original XML model to the visualization information, we have created scripts that transform each concept into its corresponding visualization. An example is given below. <div class="rule"> <div class="antecedent"> <interaction id="rml-id" name="rml-name" color="rml-color"/> </div> This example ...
Visualization. 1. After the gel has been dried, open the chamber lid and carefully remove the gel from the electrophoresis chamber.
2. Remove the Gel Holder from the stainer chamber. Attach the gel to the holder by placing the round hole over the left pin and the obround hole over the right pin.
3. Place the Gel Holder with the attached gel facing backwards into the stainer chamber.
4. Use the arrows under STAINER UNIT to select the appropriate test. Press START and choose an operation to proceed. The instrument will stain, destain and dry the gel.
5. When the process is completed, the instrument will beep. Remove the Gel Holder from the stainer and scan the bands in a densitometer.