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NEW QUESTION: 1
転送要件を満たすには、Azure DevOpsエージェントプールへのアクセスを構成する必要があります。
* ビルドリリースパイプラインを作成するときはプロジェクトエージェントプールを使用してください。
* 組織のエージェントプールとエージェントを表示します。
* 最小特権の原則を使用してください。
Azure 0e％Oos組織とプロジェクトには、どの役割のメンバシップが必要ですか？回答するには、適切な役割のメンバーシップを正しいターゲットにドラッグします。各役割メンバーシップは、1回、複数回、またはまったく使用されない可能性があります。ペイン間の分割バーをドラッグするか、コンテンツまでスクロールする必要がある場合があります。注：それぞれ正しい選択は1ポイントの価値があります。

Answer:
Explanation:

Explanation

Box 1: Reader
Members of the Reader role can view the organization agent pool as well as agents. You typically use this to add operators that are responsible for monitoring the agents and their health.
Box 2: Service account
Members of the Service account role can use the organization agent pool to create a project agent pool in a project. If you follow the guidelines above for creating new project agent pools, you typically do not have to add any members here.

NEW QUESTION: 2
非推奨が計画される前のS3低冗長ストレージの推奨される使用例は何でしたか？
A. 特定の管轄区域外でファイルのコピーを破棄できるようにすることで、ストレージコストを削減するために使用されました。
B. 単一の施設で高レベルの冗長性を備えた再現可能なデータのストレージコストを削減するために使用されました。
C. より低いレベルの冗長性で重要でないデータのストレージコストを削減するために使用されました。
D. 低レベルの冗長性で一般的なディスクドライブの500倍の耐久性を提供することにより、ストレージコストを削減するために使用されました。
Answer: C
Explanation:
Reduced Redundancy Storage (RRS) was introduced In order to reduce storage costs. When first developed, you could use reduced redundancy storage for noncritical, reproducible data at lower levels of redundancy than Amazon S3 provides with standard storage. Now Standard is a more affordable from a cost perspective, because Amazon is deprecating RRS and has changed the pricing structure.
Reference: http://docs.aws.amazon.com/AmazonS3/latest/dev/UsingRRS.html

NEW QUESTION: 3
Conformance to specifications document is one description of _________.
A. Procurement
B. Integration
C. Quality
D. Scope
Answer: C
Explanation:
Quality on a project means that you are conforming to a standard that is set before you start the project.

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 primary function of the fifth paragraph is to
A. Explain effects
B. Evaluate solutions
C. Recommend actions
D. Warn of consequences
E. Identify problems
Answer: E
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.