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NEW QUESTION: 1
Your company has 10 offices. Each office has a local network that contains several Hyper-V hosts that run Windows Server 2016. All of the offices are connected by high speed, low latency WAN links.
You need to ensure that you can use QoS policies for Live Migration traffic between the offices.
Which component should you install?
A. the Network Controller server role
B. the Multipath I/O feature
C. the Data Center Bridging feature
D. the Routing role service
E. the Canary Network Diagnostics feature
Answer: C
Explanation:
Explanation/Reference:
Explanation:
NICs with a standard NIC team and two RDMA NICs
This configuration emphasizes the use of RDMA. To converge other workloads such as Live Migration, Cluster and Management on the same RDMA NICs, the NICs must also support Data Center Bridging (DCB). To provide high availability to Storage, you can enable Microsoft Multipath I/O (MPIO).
With this configuration, you can apply all QoS features, including Bandwidth Management, Classification and Tagging, and PFC in the management operating system.
References: https://technet.microsoft.com/en-us/library/jj735302(v=ws.11).aspx

NEW QUESTION: 2
Which term describes a software application that seeks connectivity to the network via a network access device?
A. server
B. authenticator
C. WLC
D. supplicant
Answer: D

NEW QUESTION: 3
What happens if the Candidate Profile background element is mapped to the Employee Profile background element?
There are 2 correct answers to this question.
Response:
A. The employee data is pre-populated to the candidate profile
B. Only external work experience data is pre-populated to the candidate profile
C. The candidate profile data is populated to the employee profile.
D. The background sections display in the candidate profile in exactly the same order they are configured in the Employee Profile
Answer: A,C

NEW QUESTION: 4
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 author's attitude toward the gene therapy as a future cure for cancer, peripheral vascular disease, arthritis, Neurodegenerative disorders and other acquired diseases is
A. Amusement
B. Cautious optimism
C. Censure
D. Indifference
E. Disapproval
Answer: B
Explanation:
Explanation/Reference:
Explanation:
The best answer is D.
In the opening sentence, the author optimistically states that gene therapy offers a new treatment paradigm for curing human disease. However, in the fifth paragraph the author mentions some of the problems.