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Veritas VCS-275 : Administration of Veritas NetBackup 7.7 and Appliances 2.7 Exam

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Test Number : VCS-275
Test Name : Administration of Veritas NetBackup 7.7 and Appliances 2.7
Vendor Name : Veritas
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VCS-275 test Format | VCS-275 Course Contents | VCS-275 Course Outline | VCS-275 test Syllabus | VCS-275 test Objectives


Exam Title : Veritas Certified Specialist (VCS) - NetBackup and NetBackup Appliances
Exam ID : VCS-275
Exam Duration : 105 mins
Questions in test : 75-85
Passing Score : 66%
Exam Center : Pearson VUE
Real Questions : Veritas NetBackup and NetBackup Appliances Administration Real Questions
VCE practice test : Veritas VCS-275 Certification VCE Practice Test

Configure NetBackup 7.7 and NetBackup Appliances 2.7
- Describe how to configure various master/media/client settings and host properties using the NetBackup administration console.
- Describe how to configure removable media, volume pools, and volume groups.
- Describe how to configure tape and disk storage, storage units, and storage unit groups.
- Describe how to configure and utilize policy attributes.
- Describe how to configure and utilize policy scheduling.
- Explain how to configure and utilize policy clients and backup selections.
- Explain how to implement specialized backup solutions including synthetic backups, True Image Restore (TIR), multiple data streams, multiplexing, checkpoint restart, and the use of backup duplication solutions such as disk staging, Storage Lifecycle Policies, and Auto Image Replication.
- Describe the function, uses, and administration of the NetBackup deduplication options, such as media server deduplication, client-side deduplication, optimized duplication, storage server and NetBackup Accelerator.
- Describe how to perform catalog backup configuration tasks.
- Describe how to configure Appliances through CLISH and Appliance Web UI.

Monitor and Maintain NetBackup 7.7 and NetBackup Appliances 2.7
- Describe how to obtain and install NetBackup release updates.
- Describe media and image retention concepts and how to use the NetBackup administration console to verify, expire, import, and manually duplicate backup images.
- Describe how to manage NetBackup disk storage, tape devices and tape media.
- Interpret available reports to verify and monitor NetBackup.
- Describe how and when to prioritize, cancel, suspend, resume, restart, retry or manually run backup and duplication jobs.
- Describe how to initiate, prioritize, and monitor NetBackup restore jobs.
- Describe how to interact with NetBackup on Appliances.
- Describe how to manage storage using CLISH and Appliance Web UI.
- Describe how to obtain and install NetBackup Appliance updates using CLISH and Appliance Web UI.
- Monitor NetBackup Appliance hardware.

Tune NetBackup 7.7 and NetBackup Appliances 2.7
- Analyze, optimize, and tune NetBackup.
- Analyze, optimize, and tune NetBackup Appliances using CLISH and Appliance Web UI.

Troubleshoot NetBackup 7.7
- Interpret status codes and job details in order to diagnose and troubleshoot failed jobs.
- Troubleshoot devices and media, including connectivity between master, media, and client.
- Troubleshoot common issues related to NetBackup disaster recovery including recovering the NetBackup catalog.



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Veritas Practice Test

Genomic sequencing to display newborns raises extra false alarms than movements blood tests, study finds | VCS-275 genuine Questions and test dumps

With advanced expertise, clinicians can now sequence the genomes of interestingly in shape newborn little ones, looking for to show up hidden inherited illnesses that aren’t caught by hobbies blood checking out. however new analysis sharpens questions about even if these DNA tests are sufficiently accurate.

in the largest analyze of its kind, published Monday in the journal Nature medicine, a crew led through researchers on the institution of California, San Francisco, compared sequencing information to the effects from usual blood trying out carried out in newborns. They found that whole exome sequencing — a sequencing technique that reads all of the chemical letters within the regions of the genome that code for proteins — became up greater false positives and greater false negatives for inherited metabolic issues.

Robert green, a medical geneticist at Harvard and Brigham and women’s health facility who become now not concerned within the analysis, referred to as the analyze “really rigorous.” Its findings, he pointed out, are “a reminder that what they deliver to sequencing at this moment in time is not as comprehensive as they occasionally think about.”

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for his or her new look at, the researchers analyzed de-recognized facts from new child little ones in California. practically all of the 4.4 million babies born within the state between 2005 and 2013 had been screened for inherited disorders using typical blood-based mostly biomarker checking out during which blood samples drawn from a new child’s heel are analyzed. (The procedure does not contain DNA checking out.) When that technology, known as tandem mass spectrometry, turned into used, a complete of 1,334 of these children were subsequently clinically determined with an inherited metabolic ailment.

the us researchers and their colleagues carried out total exome sequencing on blood spots kept in a biobank to are trying to check the outcomes that method would have yielded had it been used in standard practice.

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They discovered that whole exome sequencing would have ignored 12% of infants who indeed have metabolic problems and incorrectly flagged 1.6% as having metabolic problems that they didn't even have. through comparison, when the tandem mass spectrometry know-how become used in events care, it missed handiest 1% of little ones who had metabolic disorders and incorrectly flagged only 0.2%

Had whole exome sequencing been used as a standalone reveal in the medical institution, the study suggests, about 160 California infants would have gotten false negatives and eight,000 would have gotten false positives.

The findings may additionally add new gas to longstanding criticisms of new child sequencing. Critics worry that hobbies sequencing of newborns is simply too expensive, may additionally create needless stress for families, and infrequently adds value over general screening.

“no matter if or not you believe here's a good suggestion from an ethics point of view, which I believe there are a lot of reservations about, it definitely is not as constructive as you may think it’s going to be,” spoke of some of the senior authors of the look at, Jennifer Puck, a america health care provider whose analysis focuses on inherited immune disorders.

The difficulty with the sequencing method, Puck observed, gave the impression to lie in the genome’s complexity, an argument that become exacerbated by way of the range of California’s population. The researchers became up many editions that they didn’t know the way to interpret, together with genetic adjustments that had by no means been stated within the literature, and in different circumstances didn’t discover variants they’d been expecting.

“The genome is a lot more complicated than americans provide it credit score for, so that they can’t simply use it as a screening verify,” Puck spoke of.

The research did not absolutely brush aside the utility of genomic sequencing in newborns. The researchers found that it would had been a valuable 2nd-line test for newborns whose average biomarker monitors were irregular. “It may resolve many of these cases and shorten the diagnostic odysseys of the households and help achieve a outcomes in those instances,” Puck talked about.

The look at turned into funded through a national Institutes of fitness grant and in addition to from Tata Consultancy functions, an India-primarily based enterprise that presents genetic sequencing features. a number of the analyze authors have affiliations with genetic trying out groups, together with the paper’s first author, who is an employee of Illumina.

backyard of research, deep genetic sequencing is just about in no way carried out in curiously match newborns, in colossal half as a result of the cost. however some businesses and fitness officials hope that allows you to alternate.

Francis Collins, the director of the NIH, has repeatedly expressed hope that in the future all newborns can have their genomes sequenced at beginning. And within the U.okay., a health minister remaining fall introduced plans to present sequencing to children born in the country, beginning with a pilot application of 20,000 newborns.

In 2017, the Boston-based company Veritas Genetics launched a $1,500 genome sequencing provider in China referred to as myBabyGenome. (Veritas ultimate December ceased its U.S. operations and didn't automatically return STAT’s request for comment on Monday morning on the popularity of the myBabyGenome providing in China.)

The chinese language genetics business BGI markets a genetic look at various for newborns, aimed toward “folks who need a comprehensive genetic screen for their child.” (BGI’s web page notes that the verify has no longer been cleared or accepted by way of the U.S. food and Drug Administration and isn't obtainable in the U.S.)

whereas the brand new research suggests that sequencing falls short as a standalone screening method, no critical researchers and clinicians are suggesting that or not it's used that means, talked about green, who has been a cautious proponent of preventive sequencing of apparently in shape americans.

eco-friendly — the co-chief of a clinical trial generic as the BabySeq task that sequenced the genomes of more than a hundred and fifty children born in two Boston hospitals — said he thinks there could be situations in which sequencing catches inherited illnesses neglected by using routine biochemical screening, and vice versa.

“I consider it speaks to the opportunity,” green stated, “that essentially the most finished screening for newborns may be some aggregate of generic newborn screening and a future where they are capable of straight away, safely, efficiently sequence all newborns.”


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