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NEW QUESTION: 1
HOTSPOT
You deploy a new version of a cloud-service application to a staging slot. The application consists of one web role. You prepare to swap the new version of the application into the production slot.
Your Azure account has access to multiple Azure subscriptions. You load the Azure
PowerShell cmdlets into the Windows PowerShell command shell. The command shell is
NOT configured for certificate-based authentication.
You must use the Windows PowerShell command window to configure the application. You need to create five instances of the web role. How should you configure the relevant
Windows PowerShell script?

Answer:
Explanation:

Explanation:

Step1: Add-AzureAccount
Create a new account
Step 2: Select-AzureSubscription
Change the name of the subscription
Step 3: Set-AzureRole -ServiceName -slot Staging
The Set-AzureRole cmdlet sets the number of instances of a specified role to run in an
Azure deployment.
-Slot specifies the deployment environment of the deployment to modify. The acceptable values for this parameter are: Production Staging
References:
https://cann0nf0dder.wordpress.com/2015/03/07/handling-azure-powershell-with-multiple- azure-subscriptions/
https://docs.microsoft.com/en-us/powershell/module/azure/set-azurerole?view=azuresmps-
4.0.0

NEW QUESTION: 2
Gene therapy offers a new treatment paradigm for curing human disease. Rather than altering the disease phenotype by using agents that interact with gene products, or are themselves gene products, gene therapy can theoretically modify specific genes resulting in disease cure following a single administration.
Initially gene therapy was envisioned for the treatment of genetic disorders, but is currently being studied for use with a wide range of diseases, including cancer, peripheral vascular disease, arthritis, Neurodegenerative disorders and other acquired diseases.
Certain key elements are required for a successful gene therapy strategy. The most elementary of these is that the relevant gene be identified and cloned. Upon completion of the Human Genome Project, gene availability will be unlimited. Once identified and cloned, the next consideration must be expression of the gene. Questions pertaining to the efficiency of gene transfer and gene expression remain at the forefront of gene therapy research, with current debates revolving around the transfer of desired genes to appropriate cells, and then to obtaining sufficient levels of expression for disease treatment. With luck, future research on gene transfer and tissue-specific gene expression will resolve these issues for the majority of gene therapy protocols.
Other important considerations for a gene therapy strategy include a sufficient understanding of the pathogenesis of the targeted disorder, potential side effects of the gene therapy treatment, and a more in depth understanding of the target cells which are to receive gene therapy.
Gene transfer vector is the mechanism by which the gene is transferred into a cell. Currently there are at least 150 clinical gene therapy protocols worldwide. Since the approval process for these protocols is not as public outside the U.S., it is difficult to ascertain the exact number of worldwide protocols. As of December 1995, 1024 patients had been treated with either a gene transfer or gene therapy protocol.
Much controversy exists regarding how many of these patients have benefited from their gene therapy, and no one has yet been cured.
Public controversy in the field of human gene therapy is driven by several factors. Ordinary citizens as well as scientists easily understand the enormous potential of gene therapy, but the former may not appreciate all the pitfalls and uncertainly that lie in the immediate future. The financial interests of biotechnology firms and, some have asserted the career interests of some gene therapists have encouraged extravagant, or at least verily optimistic public statements about contemporary gene therapy. In spite of the proliferation of protocols, the actual number of patients treated remains small, and only one genuinely controlled study of human gene therapy has been published as of this date The primary function of the fifth paragraph is to
A. Warn of consequences
B. Identify problems
C. Explain effects
D. Evaluate solutions
E. Recommend actions
Answer: B
Explanation:
Explanation/Reference:
Explanation:
The best answer is C.
The fifth paragraph is devoted to identifying various problems in the field today, such as the exaggerated claims made by biotechnological firms with vested financial interests.

NEW QUESTION: 3
Examine this query:

What information does this query provide?
A. total memory used by the first 10 threads
B. total memory used by the first 10 connections
C. total memory used across all connections associated with the user on thread number 10
D. total memory used across all connections associated with the user on connection number 10
E. total memory used by thread number 10
F. total memory used by connection number 10
Answer: F

NEW QUESTION: 4
Examine the following output:
[oracIe@gr5153 ~]$ sudo crsctl config crs CRS-4622: Oracle High Availability Services autostart is enabled. [oracIe@gr5153 ~]$ srvctl config database -d RACDB -a Database unique name: RACDB Database name: RACDB Oracle home : /u01/app/oracle/product/l11.2.0/dbhome_1 Oracle user: oracle Spfile: +DATA/ RACDB /spfileRACDB.ora Domain: Start options: open Stop options: immediate Database role: PRIMARY Management policy: AUTOMATIC Server pools: POOL1 Database instances: Disk Groups: DATA, FRA Services: Database is enabled Database is policy managed
Oracle Clusterware is started automatically after the system boot. Which two statements are true regarding the attributes of RACDB?
A. Oracle Clusterware automatically starts RACDB.
B. Database resource Is not managed by crsd for high availability and needs to be restarted manually if it fails.
C. Database resource is managed by crsd for high availability and may be automatically restarted in place if it fails.
D. You must manually start RACD
Answer: A,C
Explanation:
Switch Between the Automatic and Manual Policies By default, Oracle Clusterware is configured to start the VIP, listener, instance, ASM, database services, and other resources during system boot. It is possible to modify some resources to have their profile parameter AUTO_START set to the value 2. This means that after node reboot, or when Oracle Clusterware is started, resources with AUTO_START=2 need to be started manually via srvctl. This is designed to assist in troubleshooting and system maintenance. When changing resource profiles through srvctl, the command tool automatically modifies the profile attributes of other dependent resources given the current prebuilt dependencies. The command to accomplish this is: srvctl modify database -d <dbname> -y AUTOMATIC|MANUAL
D60488GC11 Oracle 11g: RAC and Grid Infrastructure Administration Accelerated 15 - 3
3.4.1 Benefits of Using Oracle Clusterware Oracle Clusterware provides the following benefits: Tolerates and quickly recovers from computer and instance failures. Simplifies management and support by means of using Oracle Clusterware together with Oracle Database. By using fewer vendors and an all Oracle stack you gain better integration compared to using third-party clusterware. Performs rolling upgrades for system and hardware changes. For example, you can apply Oracle Clusterware upgrades, patch sets, and interim patches in a rolling fashion, as follows: Upgrade Oracle Clusterware from Oracle Database 10g to Oracle Database 11g Upgrade Oracle Clusterware from Oracle Database release 11.1 to release 11.2 Patch Oracle Clusterware from Oracle Database 11.1.0.6 to 11.1.0.7 Patch Oracle Clusterware from Oracle Database 10.2.0.2 Bundle 1 to Oracle Database 10.2.0.2 Bundle 2 Automatically restarts failed Oracle processes. Automatically manages the virtual IP (VIP) address so when a node fails then the node's VIP address fails over to another node on which the VIP address can accept connections. Automatically restarts resources from failed nodes on surviving nodes. Controls Oracle processes as follows: For Oracle RAC databases, Oracle Clusterware controls all Oracle processes by default. For Oracle single-instance databases, Oracle Clusterware allows you to configure the Oracle processes into a resource group that is under the control of Oracle Clusterware. Provides an application programming interface (API) for Oracle and non-Oracle applications that enables you to control other Oracle processes with Oracle Clusterware, such as restart or react to
failures and certain rules.
Manages node membership and prevents split-brain syndrome in which two or more instances
attempt to control the database.
Provides the ability to perform rolling release upgrades of Oracle Clusterware, with no downtime
for applications.
Oracle@ Database High Availability Overview
11g Release 2 (11.2)

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