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NEW QUESTION: 1
cr1.8xlargeインスタンスタイプはどのくらいのメモリを提供しますか？
A. 124 GB
B. 184 GB
C. 224 GB
D. 244 GB
Answer: D
Explanation:
説明
CR1インスタンスは、メモリ最適化インスタンスの一部です。すべてのAWSインスタンスファミリーの中で、GB RAMあたりの最低コストを提供します。 CR1インスタンスは、同じファミリーのM2インスタンスと比較して、最大244 GBのRAMを提供し、より高速なCPU（NUMAをサポートするIntel Xeon E5-2670）で実行できるメモリ最適化インスタンスの新世代の一部です。帯域幅を集中的に使用するアプリケーションのクラスターネットワーキングをサポートしています。 cr1.8xlargeは、CR1ファミリの最大のインスタンスタイプの1つであり、244 GBのRAMを提供できます。
http://aws.amazon.com/ec2/instance-types/
NEW QUESTION: 2
What is the benefit of the RESOURCEUTILIZATION option on the client during a restore?
A. to increase the memory usage on the client
B. to increase the number of concurrent restore sessions
C. to decrease the memory usage on the client
D. to increase the communication buffer from the client to the server
Answer: B
Explanation:
Use the resourceutilization option in your option file to regulate the level of resources the IBM Spectrum Protec server and client can use during processing.
When you request a restore, the default is to use a maximum of one session.
Additional restore sessions are based on:
resourceutilization value
Etc.
References: https://www.ibm.com/support/knowledgecenter/en/SSEQVQ_8.1.0/client/c_opt_resourceutilization_sessres.html
NEW QUESTION: 3
Based on your knowledge of genetic inheritance, which of these statements is true for autosomal recessive genetic disorders?
A. Only females are affected.
B. The disorder is always carried on the X chromosome.
C. Heterozygotes are affected.
D. Two affected parents always have affected children.
Answer: D
Explanation:
Explanation/Reference:
Explanation:
(A) The term heterozygote refers to an individual with one normal and one mutant allele at a given locus on a pair of homologous chromosomes. An individual who is heterozygous for the abnormal gene does not manifest obvious symptoms. (B) Disorders carried on either the X or Y sex chromosome are referred to as sex-linked recessive. (C) Either sex may be affected by autosomal recessive genetic disorders because the responsible allele can be on any one of the 46 chromosomes. (D) If both parents are affected by the disorder and are not just carriers, then all their children would manifest the same disorder.
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