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EMC E20-065 : Advanced Analytics Specialist test for Data Scientists Exam

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Test Number : E20-065
Test Name : Advanced Analytics Specialist test for Data Scientists
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E20-065 test Format | E20-065 Course Contents | E20-065 Course Outline | E20-065 test Syllabus | E20-065 test Objectives


Overview
This test is a qualifying test for the Specialist - Data Scientist, Advanced Analytics (DCS-DS) track.
This test focuses on MapReduce, the Hadoop Ecosystem, NoSQL, Natural Language Processing, Social Network Analysis, Data Science Theory and Methods, and Data Visualization.
Dell Technolgies provides free practice questions to assess your knowledge in preparation for the exam. practice questions allow you to become familiar with the topics and question types you will find on the proctored exam. Your results on a practice test offer one indication of how prepared you are for the proctored exam and can highlight syllabus on which you need to study and train further. A passing score on the practice test does not guarantee a passing score on the certification exam.

Topics likely to be covered on this test include:
MapReduce (15%)
MapReduce framework and its implementation in Hadoop
Hadoop Distributed File System (HDFS)
Yet Another Resource Negotiator (YARN)
Hadoop Ecosystem and NoSQL (15%)
Pig
Hive
NoSQL
HBase
Sparkv Natural Language Processing (NLP) (20%)
NLP and the four main categories of ambiguity
Text Preprocessing
Language Modeling
Social Network Analysis (SNA) (23%)
SNA and Graph Theory
Communities
Network Problems and SNA Tools
Data Science Theory and Methods (15%)
Simulation
Random Forests
Multinomial Logistic Regression and Maximum Entropy
Data Visualization (12%)
Perception and Visualization
Visualization of Multivariate Data



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EMC Data Real test Questions

Many Questions surround GRIFFIN examine | E20-065 Cheatsheet and test Cram

The section II GRIFFIN look at, presented at December's American Society of Hematology (ASH) virtual meeting, assessed the efficacy and safeguard of the addition of daratumumab into the lenalidomide, bortezomib, and dexamethasone (RVd) spine in transplant-eligible newly diagnosed sufferers with numerous myeloma.

MedPage today has brought collectively three skilled leaders in the box: moderator Vinay Prasad, MD, is joined by Aaron Goodman, MD, and Al-Ola Abdallah, MD, for a digital roundtable discussion on the GRIFFIN look at during this third of 5 exclusive roundtable episodes.

Episode one: Early Transplant or Delayed? numerous Myeloma consultants Debate

Episode two: Selinexor good enough'd for Myeloma, however Does That Make It a very good Drug?

Following is a transcript of their remarks:

Vinay Prasad, MD: i am back with Aaron Goodman and Dr. Abdallah from Kansas, and they are talking about the GRIFFIN analyze. Now, gents, the GRIFFIN look at simply got here out at ASH and it changed into a most pleasing analyze. It became a randomized part II examine that appeared at the addition of daratumumab, a CD38 antibody, to RVd, which is the commonplace of care in this nation. I do not care what anybody says, RVd remains the real commonplace of care. It has the top of the line records as frontline routine.

The addition of daratumumab was capable of do anything in this randomized part II study. It become capable of deepen responses. There become greater stringent CR. There become a little bit more MRD. however when it comes to its effect on PFS, and its impact on OS in case you reserve Dara for the second-line setting, there are loads of open questions.

We have no conception what it could do in case you just gave Dara later and yet the GRIFFIN examine, to my skills, has impacted the NCCN instructions, and now the NCCN guidelines permit providers to select Dara-RVd as the initial treatment of newly-diagnosed myeloma. i'm wondering if I might get each your opinions on this trial. A small, randomized part II study, surrogate endpoint CR charges, what are your innovations? Aaron Goodman, let's start with you.

Aaron Goodman, MD: Yeah. Why even run randomized phase III stories anymore? You get NCCN world experts to approve. Daratumumab, as anticipated, you add a really effective drug that has actions, a single agent in a refractory myeloma to their regular therapy, then you're going to see an improved CR fee, and that i truly may not be shocked. i'd guess the PFS will likely be more suitable within the randomized analyze.

Prasad: sure.

Goodman: again, I might not be shocked, four medication versus three. they now have considered thousands of trials of three versus two that at all times suggests that. however I feel the most critical point that you brought up is whether daratumumab upfront or even if it can safely be delayed in the beginning or 2nd relapse will have an effect on overall survival. so that you can take a bit bit longer to figure out, but not too a lot longer if you waited and sufferers who have been in the RVd arm of the randomized trial it's accruing presently had entry to daratumumab.

Prasad: They ought to have access to daratumumab. it really is a vital element. They have to have access to Dara on progression. Go on.

Goodman: yes, since you're appropriate. if they will not have entry, then it would not in reality... they recognize daratumumab is a good idea, and if they will not have entry to that drug then, of course, it might reveal an overall survival competencies that basically isn't actual, at the least within the u.s. where they'd have access to daratumumab.

I simply suppose we're jumping the gun. i'm obsessed with these treatment options as tons as my colleagues. I are looking to assist their sufferers just as tons and never be a naysayer to every drug. however we've the examine accruing, going on, the place you're going to reply this query. cannot they wait? we've got been burned too again and again in oncology, as a minimum in my short apply as an attending health care professional, the place they have now jumped the gun on randomized part IIs, or even single-arm phase IIs, the place randomized section IIIs are bad or possibly even detrimental to patient well being, i.e., the BELLINI look at.

Prasad: it truly is neatly-put. i like Dara, however I don't love GRIFFIN, and that, that you can have both ideas on your head. Dr. Abdallah, what are your concepts on GRIFFIN?

Al-Ola Abdallah, MD: I might be sincere with you, well, we're going to have to have a debate then, me and Aaron. for instance the progression-free survival is more desirable and the normal survival is a similar. Then why are they no longer doing transplant upfront then? i'd say.

Prasad: [LAUGHTER] you're coming lower back to transplant? Yeah.

Abdallah: Yeah. The americans who are agreeing about that based on the common survival is identical. k, smartly, what if the GRIFFIN trial is going to be standard survival similar? Let me aspect out something. With all my recognize to the colleagues who just like the daratumumab, sure, it deepens... it has an excellent, an extended... depth of the response is deeper.

Prasad: it be deeper. it be deeper. extra MRD negativity.

Abdallah: no one in reality disagrees with that.

Prasad: nobody.

Abdallah: The three questions i will get asked via the sufferers... i am sure they will ask what category of depth of the response and all these things. however they're going to ask is it curable or no longer curable to add the daratumumab? They won't have a solution for that and i wager you they will certainly not have a solution unless eight or 9 years or 10 years from now.

You cannot depend on sustained MRD negativity to inform you that if I even have a sustained MRD negativity for X volume of years, that means that you can reside in remission perpetually. that's no longer the answer for that as a result of there are sufferers who are nevertheless MRD superb in my medical institution, and in fact they have M protein and they've been off the medicine for approximately two decades, and that they're nonetheless following me without any treatment. These are the historic days. They never gave preservation remedy for these patients, so they can't depend just on MRD negativity.

number two, general survival. Is that going to add something moreover the daratumumab? I feel that is additionally a really crucial question. Daratumumab is not a poisonous medication. every person consents with that.

Prasad: sure.

Abdallah: but what's the entire benefit in terms of lasting? it be the progression-free survival. If it be going to add an extra, I have no idea, 6 months or a year, then the debate is going to return lower back once more with why are they even delaying the transplant if that is what they additionally...? the use of an normal survival in this case, using it as an excuse, they have the identical overall survival, no longer to do the transplant early versus late. it really is my biggest subject.

Now if -- and i hope that is now not actual, and i hope i am incorrect -- what if the daratumumab and the RVd, the Dara-RVd, versus RVd ended up with the same progression-free survival? it is a negative. it's a...

Prasad: it truly is a very terrible, a stone-bloodless negative.

Abdallah: Why? inform me, all relapsed myeloma, who's the medical professional that stops basically? All their myeloma physicians accept as true with daratumumab as the backbone to deal with myeloma in the first relapse and 2nd relapse. it be a extremely essential participant as a combination therapy, so not best they lost a player, might be they lost lots of patients that may have benefitted from that. We're definitely hoping that vehicle-T and the BCMA drugs could be a little bit advisable, however they do not know yet. They have no idea.

We recognize that daratumumab as a result of they have been there for a bit bit longer time. i'm hoping i am going to be incorrect, but they would not have... the median development-free survival for RVd and transplant is around 50 months. We're handiest 2 years and we're now not seeing any separation in the development-free survival between the RVd and the Dara-RVd. We're handiest seeing an MRD negativity however how lengthy is that this going to ultimate? it truly is the question we're asking.

Prasad: I accept as true with you. I think that none of us will dispute the incontrovertible fact that Dara is a good and important drug in distinctive myeloma. they all use it, they count on it, and they need Dara. Dara has been referred to as by some the rituximab of diverse myeloma. I don't name it rituximab of myeloma, however I feel it does play an important position. They do use it in the relapsed and refractory settings in the second-line atmosphere and past. The question of GRIFFIN, the query of those frontline studies is, is the pursuits upfront use of Dara in aggregate with the typical spine VRD stronger than saving it on the backend? I think PFS1 won't reply the query as a result of if PFS1 is extended it be a tautology that is real with the aid of definition by myself.

Of direction, if you supply the entire medication that you have in the myeloma device bag right up front, you might be going to have an extended PFS1, but you won't have anything else left to supply the patient. which you could add in some Elo and you'll add in all forms of things, so it is no longer the correct question.

The appropriate query is, VRD then a Dara-containing routine, or Dara-VRD and then a regimen doubtless with or devoid of Dara? It relies upon. that is the query, no matter if or now not you get an extended normal survival.

GRIFFIN, unfortunately, is a small randomized phase II trial. one of the mistakes I see in oncology made too often is individuals will grasp their hat on a survival advantage or a PFS benefit viewed in an underpowered section II analyze.

Now, underpowered section II reviews are infamous for false negatives -- that in other phrases they may discover no improvement when a advantage really exists -- but they're additionally underappreciated for the advantage for false positives, that for those who do find a change in a non-fundamental endpoint, it's possible that that difference is exaggerated or spurious absolutely. They noticed that with Lartruvo, a catastrophic regulatory failure that became on the market and then off the market when a section III trial confirmed no advantage. To Aaron's aspect, they want part III experiences. They deserve to test the sequence approach and that's the reason the open question for daratumumab.

  • Greg Laub joined MedPage today in 2005 as production supervisor and led the launch of the video branch in 2007. he's presently answerable for the web site's video production. comply with


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