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Exam Number : ISO20KF
Exam Name : IT Service Management Foundation Bridge based on ISO/IEC 20000:2018
Vendor Name : Exin
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Title: IT Service Management Foundation Bridge based on ISO/IEC 20000:2018

Test Detail:
The IT Service Management Foundation Bridge based on ISO/IEC 20000:2018 certification is offered by EXIN. It is designed for IT professionals who have already obtained an ITIL Foundation certification and want to expand their knowledge and skills in IT service management aligned with the ISO/IEC 20000 standard. The certification provides an understanding of the key concepts and principles of ISO/IEC 20000 and its relationship with ITIL.

Course Outline:
The IT Service Management Foundation Bridge course covers the essential aspects of ISO/IEC 20000:2018 and its alignment with ITIL. The course aims to bridge the knowledge gap between ITIL Foundation and ISO/IEC 20000. The following is a general outline of the key areas covered in the certification program:

1. Introduction to ISO/IEC 20000:
- Overview of IT service management and its importance
- Introduction to ISO/IEC 20000 and its purpose
- Key terms and definitions in ISO/IEC 20000
- Relationship between ISO/IEC 20000 and ITIL

2. ISO/IEC 20000 Requirements and Processes:
- Understanding the structure of ISO/IEC 20000:2018
- Requirements of the ISO/IEC 20000 standard
- Service management processes and their alignment with ITIL
- Documentation and records management in ISO/IEC 20000

3. ISO/IEC 20000 Certification and Audits:
- Certification process and requirements for ISO/IEC 20000
- Roles and responsibilities in the certification process
- Conducting internal audits and management reviews
- Continual improvement and the PDCA (Plan-Do-Check-Act) cycle

4. Relationship between ITIL and ISO/IEC 20000:
- Alignment of ITIL with ISO/IEC 20000 processes
- ITIL best practices and their applicability to ISO/IEC 20000
- Benefits of integrating ITIL and ISO/IEC 20000 frameworks
- Achieving service excellence through combined approaches

Exam Objectives:
The IT Service Management Foundation Bridge certification exam assesses candidates' understanding of ISO/IEC 20000:2018 and its relationship with ITIL. The exam objectives include, but are not limited to:

1. Demonstrating knowledge of ISO/IEC 20000 key concepts and principles.
2. Understanding the requirements and processes of ISO/IEC 20000:2018.
3. Recognizing the certification process and roles in ISO/IEC 20000.
4. Identifying the relationship between ITIL and ISO/IEC 20000.

Syllabus:
The IT Service Management Foundation Bridge certification program typically includes self-study materials or instructor-led training provided by EXIN or authorized training providers. The syllabus provides a breakdown of the syllabus covered throughout the course, including specific learning objectives and milestones. The syllabus may include the following components:

- Introduction to ISO/IEC 20000
- ISO/IEC 20000 Requirements and Processes
- ISO/IEC 20000 Certification and Audits
- Relationship between ITIL and ISO/IEC 20000
- exam Preparation and Practice Tests
- Final IT Service Management Foundation Bridge Certification Exam



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New Prenatal Genetic testing may Predict Your baby | Killexams.com Resources

I actually have two toddlers. for the time being, all i do know about their genes is that they each have forty six chromosomes, and one is XY and one is XX.

I are trying to deal with them equally, to assume equal talents. but what if I knew my daughter carried a “smart” gene and my son didn't? When he came domestic from college with a B, would I anticipate it changed into simply his genes, and never push him to are attempting more durable? And what if I may have commonly used this earlier than he have been born, at a time when he become just a bit blip on an ultrasound? Frankly, I’m now not bound i might have confidence myself with this suggestions.

Such expertise isn’t, of path, feasible yet. For one factor, they haven’t yet found many genes that may reliably predict intelligence. And in the mean time, even if they did comprehend what genes they had been hunting for, they wouldn’t be able to find them very early in pregnancy. but thanks to a brand new variety of fetal genetic trying out this may well be starting to exchange.

once upon a time, every little thing about your baby changed into a surprise except the moment of start. Is it a boy or a woman? Does he (or she!) have all 10 fingers and 10 toes? And, most crucial: is the baby fit? Genetic problems—Down Syndrome, Trisomy 18 and others—had been often a surprise within the birth room.

We might also still have interaction within the ritual counting of fingers and toes on their new child, however it’s focused on demonstrate: basically, they checked for these months in the past in an ultrasound. And for many girls, genetic trying out right through pregnancy has ruled out—or all however ruled out—the probability that their child has a genetic abnormality.

lately, the introduction of “mobile-free fetal DNA checking out” has altered the landscape of prenatal genetic trying out further. You might also have heard of those tests by means of their company names: harmony or MaterniT21, amongst others. The technology for every is largely the same: they depend on a sample of maternal blood with no risk to the fetus, and they have accuracy quotes coming near those of fetal diagnostic verify like amniocentesis or Chorionic Villus Sampling (CVS), however with none possibility to the fetus. In different phrases, these new tests give the best of each worlds—and a recipe for moral fission.

The Evolution of Fetal Screening

Prenatal genetic trying out, imperfect even though it has been, isn't new. beginning within the Seventies, amniocentesis allowed docs to establish genetic disorders in utero, usually mid-pregnancy. within here decade, CVS provided an alternative choice to amniocentesis that can be carried out previous in pregnancy—within the first trimester in place of the second—and provide identical assistance. These two techniques give finished genetic guidance on the fetus—labs can actually sequence its whole genome.

This skill that besides the fact that children these are most widely used to notice the most ordinary genetic disorders—Down Syndrome, for instance—they might, in precept, be used to discover extra minor genetic abnormalities, or even to establish typical genomic diversifications, equivalent to a predisposition for having crimson hair. (Such makes use of are rare, mind you, on the grounds that each tactics are invasive and raise some small chance to the fetus.) traditionally, the choice has been prenatal screening that relied basically on an ultrasound, which isn’t harmful to the fetus however additionally can not concretely diagnose an issue, hence, they must be followed up by way of one of the vital invasive methods if a problem is suspected.

→ enlarge Chart

The incontrovertible fact that they are able to check features of a child in utero, mixed with the availability of abortion, has all the time made some people nervous. It suggests eugenics, or a way forward for “clothier infants.” this is no longer all fanciful challenge: in some international locations prenatal sex decision and sex-selective abortion have altered the common sex ratios within the population (for instance, in latest years in China, one hundred twenty boys are born for every a hundred girls). but the reality is that, in customary, and in the U.S. in selected, prenatal screening has been comfortably confined to critical genetic issues—the possibility of harming the fetus has outweighed the value of the assistance for other makes use of.

however the new prenatal screening exams are a game changer. They signify a major technological step forward because the key to deciding on issues or genetic dangers is being in a position to see the baby’s DNA. Amniocentesis and CVS accomplish this with amniotic fluid or placental fabric, each of which comprise fetal cells and, therefore, fetal DNA. but that capacity going inner the womb—with a needle, usually—and really taking some cells. And that’s what incorporates the risk.

Some fetal cells also circulate in the maternal bloodstream right through pregnancy—that’s no longer information—it’s simply that the volume of fetal cells in maternal blood is very low, making them elaborate to make use of in a practical method. The technological step forward turned into the cognizance of “cellphone-free fetal DNA”—it truly is, fetal DNA backyard of cells.

When phone-free DNA is remoted in maternal plasma, 10% to 20% of it's fetal in origin. In lay phrases, this means that researchers can be confident that a huge share of what they're extracting comes from the fetus. In precept, if one could conveniently separate the maternal and fetal DNA, it will be possible to sequence the whole fetal DNA the usage of this technique.

technology continues to be no longer fairly there yet, but this manner presently works by means of hunting for issues in the cell-free DNA which wouldn’t be there if the DNA it have been simply the mom’s.

consider about it in terms of gender: women have two X chromosomes; guys have one X and one Y. think about you appear in mom’s mobile-free DNA and also you find a bunch of Y chromosomes. The baby could be a boy, correct? in case you don’t see any Y chromosomes, a lady.

similarly, a fetus with Down Syndrome has three copies of chromosome 21, instead of two, but two copies of the entire other chromosomes. So if you study a mixture of fetal and maternal DNA together, from a genetically average mom, and spot enormously extra copies of chromosome 21, you could possibly suspect the baby has Down Syndrome. If any chromosomal imbalance is incredible sufficient, the verify consequences will flag a possible problem.

in the mean time, these exams fall brief of what's possible with amniocentesis or CVS checking out. a method wherein they fall brief is they center of attention on best the three most commonplace trisomies: Down syndrome (trisomy 21), Trisomy 18 and Trisomy 13. Invasive testing will become aware of other trisomies, and may notice other sorts of chromosomal issues as neatly. an extra shortcoming: both false negatives and false positives are viable.

This system relies on a statistical threshold look at various: Sufficiently imbalanced, and the look at various pings “high quality.” no longer sufficiently imbalanced, it comes up poor. although, once in a while the imbalance in the chromosome counts isn’t dazzling adequate to flag as a positive check, even when the child does have a chromosomal abnormality. this is what is known as a “false negative.” And on the different facet, now and again the chromosomes seem to be imbalanced within the sample but the baby is great. this is what is referred to as a “false superb.”

False negatives are pretty rare in these new blood tests—for a girl in her early 30s with a terrible result on this screening, the chance of a baby with a chromosomal abnormality is set 1 in 90,000. False positives on this look at various are additionally constrained, however they matter greater. For that equal lady in her early 30s with a good examine outcome, the opportunity of having a baby with a chromosomal issue is set sixty six%. In different phrases, one out of three girls who get hold of consequences indicating abnormalities will actually have a baby who's genetically normal.

Answering—and elevating—greater Questions

consultants agree that consequential selections a couple of being pregnant may still now not be made without an invasive look at various as a comply with-up. however this is prone to be a brief challenge. easily, the problem is considered one of genetic sequencing capability and statistics. Already these exams are near best on detection of gender. And the precision with which genetic predictions can also be made will also improve. It appears unlikely they are greater than just a few years away from the potential to make use of these exams as diagnostic.

As these checks improve, so too will the latitude of conditions they can observe. Researchers closing year pronounced on a case wherein they used a edition of this check to detect a small genetic situation called a microdeletion. The affect of this microdeletion, which become passed on from the mom, is an expanded risk for nearsightedness and gentle hearing loss. The mother within the study discovered that she changed into passing on her poor eyesight and bad listening to to her child.

In principle, this expertise may well be used to detect the rest for which they have a widely used genetic link. Researchers engaged in Gene-vast affiliation experiences (GWAS) have, in the past few years, made progress on selecting a couple of genes which code for intelligence. think about you’ve confirmed your self and also you recognize you lift one of those intelligence genes but, alas, your better half doesn't. Now think about which you could comfortably gain knowledge of in case your fetus got your smart genes, or your spouse’s now not-so-sensible ones. Or your genes for height, your possibility for weight problems, and your better half’s gene for stubbornness (okay, they haven’t discovered this one yet).

Now take it a step extra. Fetal DNA starts off to flow into within the mother’s blood at the very beginning of being pregnant. in the intervening time, these checks wait until 10 or eleven weeks of pregnancy so the awareness of fetal DNA is excessive sufficient to make use of for accurate detection. but as the sequencing and statistics enhance, they can also locate that it is viable to do the identical checking out at eight weeks. Or six.

What if you may know, at six weeks of pregnancy, even if your newborn would inherit your height, or hair color, or IQ? As i discussed earlier, early gender trying out is already used for gender-selective abortion, generally backyard the U.S. This changed into genuine even when gender detection become no longer feasible except 18 or 20 weeks.

These technologies will lift questions a ways past gender. Many people terminate a pregnancy after they be taught the fetus has Down Syndrome. What about learning that the infant will have autism? Or without problems that their IQ is probably going to be beneath general? they are conserving Pandora’s box. as soon as they open it and let the counsel out, they lose handle over what it's used for.

i might argue there are extra implications. Let’s say I discover my fetus has an multiplied genetic chance for weight problems, and i subsequently have that baby. How will I treat her? Will I obsess about everything she eats, every ounce of child fats that doesn’t automatically soften away? Will she develop up to be overweight, or have an ingesting disease i was birthday celebration to with my be concerned? could this definitely make things worse in place of enhanced? The concept that more guidance is more advantageous relies on their capability to disregard it. but is this something that, as a parent, you could ever truly ignore?

I’m knowledgeable as an economist, and one in every of their widespread ideas is that more advice is superior. counsel helps us make stronger—extra most appropriate—choices. And, crucially, greater suggestions cannot make you worse off, when you consider that you could always simply ignore it. under this conception, these advances in genetic testing should still be welcomed without reservation.

in lots of dimensions, the improvements in testing bring most effective decent. The potential to greater accurately discover critical genetic circumstances earlier in pregnancy permits girls and their companions to make difficult decisions about pregnancy termination prior within the pregnancy when the clinical issues are less enormous.

EXPECTING-BETTER_book

The steadiness between the values of counsel and the chance of mis-use is a tricky one. it would be a shame to fail to pursue applied sciences which are prone to carry terrific good points. at the same time, it is naïve to pursue them without brooding about their penalties. And they should still start considering these now.

ready or no longer, the long run is coming.

Emily Oster is a professor of economics at Brown tuition and the author of anticipating more suitable


 

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