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Veritas VCS-319 : Administration of Veritas Enterprise Vault 11.x Exam

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Test Number : VCS-319
Test Name : Administration of Veritas Enterprise Vault 11.x
Vendor Name : Veritas
Update : Click Here to Check Latest Update
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VCS-319 test Format | VCS-319 Course Contents | VCS-319 Course Outline | VCS-319 test Syllabus | VCS-319 test Objectives


Exam Title : Veritas Certified Specialist (VCS) - Enterprise Vault
Exam ID : VCS-319
Exam Duration : 105 mins
Questions in test : 75-85
Passing Score : 69%
Exam Center : Pearson VUE
Real Questions : Veritas Enterprise Vault Administration Real Questions
VCE practice test : Veritas VCS-319 Certification VCE Practice Test

Overview, Architecture, and Planning
- Explain the technological benefits of Symantec Enterprise Vault 11 for Exchange.
- Describe the components of Symantec Enterprise Vault 11 for Exchange.
- Identify the difference(s) between Symantec Enterprise Vault 11 for Exchange architectures.

Installation and Configuration
- Identify Symantec Enterprise Vault 11 for Exchange prerequisites.
- Describe the process for installing and configuring Symantec Enterprise Vault 11 for Exchange components.

Administration
- Describe the procedure for managing Symantec Enterprise Vault 11 for Exchange Vault Site components, including, but not limited to, targets, archives, and Vault Storage groups with Enterprise Vault Administration Console (VAC), Enterprise Vault PowerShell, and Enterprise Vault Policy Manager (EVPM).
- Identify and describe how to apply appropriate retention categories.
- Describe the Exchange mailbox archiving process including, but not limited to, provisioning groups, enabling/disabling mailboxes, and archiving tasks.
- Explain the process for managing Indexes.
- Distinguish among Symantec Enterprise Vault 11 for Exchange roles-based administration roles.
- Describe the process for managing Symantec Enterprise Vault 11 for Exchange Policies with Enterprise Vault Administration Console (VAC).
- Describe the process for importing and exporting archives, including PST migration and move archive options.
- Describe Symantec Enterprise Vault 11 for Exchange client functionality (Outlook Add-Ins, OWA, Office Mail App, Vault Cache, and Virtual Vault).
- Describe the creation and maintenance of vault storage in Symantec Enterprise Vault 11 for Exchange with Enterprise Vault Administration Console (VAC) or Enterprise Vault PowerShell.

Monitoring, Reporting, and Troubleshooting
- Describe the Symantec Enterprise Vault 11 for Exchange reporting and monitoring prerequisites.
- Interpret the output from Symantec Enterprise Vault 11 for Exchange Reporting Services.
- Verify Symantec Enterprise Vault 11 for Exchange is installed and functioning (e.g., running services, archiving).
- Identify Symantec Enterprise Vault 11 for Exchange options for monitoring archiving.
- Describe the tools and steps required to troubleshoot Symantec Enterprise Vault 11 for Exchange server and client issues.

Backup, Recovery, and High Availability
- Identify which Symantec Enterprise Vault 11 for Exchange components require backup.
- Describe how to back up and recover Symantec Enterprise Vault 11 for Exchange.
- Describe the Symantec Enterprise Vault 11 for Exchange High Availability options.
- Define the steps to implement and employ Symantec Enterprise Vault 11 for Exchange native High Availability.



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Veritas questions

Genomic sequencing to monitor newborns raises more false alarms than activities blood assessments, look at finds | VCS-319 Study Guide and test Questions

With advanced technology, clinicians can now sequence the genomes of curiously fit newborn infants, in search of to show up hidden inherited illnesses that aren’t caught by way of activities blood checking out. however new research sharpens questions about no matter if these DNA assessments are sufficiently accurate.

in the biggest analyze of its type, posted Monday in the journal Nature drugs, a group led by using researchers at the tuition of California, San Francisco, compared sequencing facts to the effects from typical blood checking out carried out in newborns. They found that entire exome sequencing — a sequencing approach that reads all the chemical letters within the areas of the genome that code for proteins — became up extra false positives and greater false negatives for inherited metabolic problems.

Robert green, a clinical geneticist at Harvard and Brigham and women’s hospital who was now not involved in the analysis, known as the analyze “in reality rigorous.” Its findings, he spoke of, are “a reminder that what they carry to sequencing at this second in time is not as comprehensive as they once in a while think about.”

commercial

for his or her new analyze, the researchers analyzed de-identified data from new child toddlers in California. virtually all the four.4 million children born in the state between 2005 and 2013 have been screened for inherited problems the usage of normal blood-primarily based biomarker trying out through which blood samples drawn from a new child’s heel are analyzed. (The manner doesn't involve DNA testing.) When that know-how, called tandem mass spectrometry, changed into used, a complete of 1,334 of these little ones were sooner or later diagnosed with an inherited metabolic ailment.

the united states researchers and their colleagues performed whole exome sequencing on blood spots kept in a biobank to try to verify the outcomes that method would have yielded had it been used in normal observe.

commercial

They discovered that whole exome sequencing would have neglected 12% of children who certainly have metabolic issues and incorrectly flagged 1.6% as having metabolic disorders that they didn't even have. by comparison, when the tandem mass spectrometry technology became used in movements care, it neglected most effective 1% of little ones who had metabolic issues and incorrectly flagged simplest 0.2%

Had whole exome sequencing been used as a standalone screen in the clinic, the look at suggests, about a hundred and sixty California infants would have gotten false negatives and 8,000 would have gotten false positives.

The findings can also add new fuel to longstanding criticisms of new child sequencing. Critics worry that events sequencing of newborns is just too high priced, may create unnecessary stress for families, and rarely provides cost over commonplace screening.

“even if or no longer you suppose this is a good suggestion from an ethics factor of view, which I consider there are loads of reservations about, it truly is not as helpful as you could believe it’s going to be,” referred to one of the senior authors of the look at, Jennifer Puck, a u.s. health care professional whose analysis makes a speciality of inherited immune issues.

The problem with the sequencing components, Puck pointed out, perceived to lie within the genome’s complexity, a controversy that was exacerbated by means of the diversity of California’s inhabitants. The researchers grew to become up many variations that they didn’t comprehend the way to interpret, including genetic changes that had not ever been said in the literature, and in other situations didn’t discover variants they’d been expecting.

“The genome is much more advanced than individuals provide it credit score for, in an effort to’t just use it as a screening verify,” Puck pointed out.

The analysis didn't absolutely dismiss the utility of genomic sequencing in newborns. The researchers found that it would have been a helpful 2d-line check for newborns whose usual biomarker screens were irregular. “It could unravel many of those circumstances and shorten the diagnostic odysseys of the families and assist obtain a result in these circumstances,” Puck observed.

The examine turned into funded by a national Institutes of health provide and in addition to from Tata Consultancy capabilities, an India-based enterprise that presents genetic sequencing capabilities. a couple of the study authors have affiliations with genetic trying out businesses, together with the paper’s first author, who is an employee of Illumina.

outdoor of research, deep genetic sequencing is well-nigh under no circumstances performed in interestingly match newborns, in large part because of the rate. but some companies and health officials hope as a way to change.

Francis Collins, the director of the NIH, has repeatedly expressed hope that at some point all newborns could have their genomes sequenced at delivery. And within the U.okay., a health minister ultimate fall introduced plans to present sequencing to little ones born in the nation, beginning with a pilot program of 20,000 newborns.

In 2017, the Boston-based enterprise Veritas Genetics launched a $1,500 genome sequencing carrier in China known as myBabyGenome. (Veritas final December ceased its U.S. operations and did not immediately return STAT’s request for comment on Monday morning on the reputation of the myBabyGenome providing in China.)

The chinese language genetics company BGI markets a genetic check for newborns, aimed toward “fogeys who want a comprehensive genetic screen for their baby.” (BGI’s website notes that the check has not been cleared or accredited via the U.S. meals and Drug Administration and is not obtainable in the U.S.)

whereas the brand new analysis suggests that sequencing falls short as a standalone screening formulation, no serious researchers and clinicians are suggesting that it's used that method, mentioned eco-friendly, who has been a cautious proponent of preventive sequencing of apparently match americans.

eco-friendly — the co-chief of a medical trial conventional because the BabySeq mission that sequenced the genomes of greater than 150 infants born in two Boston hospitals — talked about he thinks there might be cases during which sequencing catches inherited ailments neglected by using routine biochemical screening, and vice versa.

“I consider it speaks to the possibility,” eco-friendly stated, “that probably the most finished screening for newborns should be some combination of prevalent newborn screening and a future where we're in a position to quickly, safely, efficiently sequence all newborns.”


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