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C2090-930 | IBM SPSS Modeler Professional v3

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C2090-930 - IBM SPSS Modeler Professional v3 - braindump

Vendor IBM
Exam Number C2090-930
Exam Name IBM SPSS Modeler Professional v3
Questions 60 Q & A
Recent Update March 13, 2019
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C2090-930 exam Dumps Source : IBM SPSS Modeler Professional v3

Test Code : C2090-930
Test Name : IBM SPSS Modeler Professional v3
Vendor Name : IBM
Q&A : 60 Real Questions

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    next Steps

    Why the term unstructured statistics is a misnomer

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    facts scientists, builders and area count number specialists.


    Graphical drag-and-drop and command line.

    Scripting Languages/formats Supported

    helps Anaconda and Apache Spark. The latter offers Scala, Python and R interfaces.

    formats Supported

    Most most important statistics and file codecs are supported through open supply Jupyter Notebooks.


    IBM Watson Studio connects a couple of IBM items, including SPSS Modeler and statistics Science adventure (DSX) together with open source equipment, in an effort to convey a strong Predictive Analytics and laptop learning (PAML) answer.

    The ambiance contains open data units through Jupyter Notebooks, Apache Spark and the Python Pixiedust library. The cloud edition features interactivity with laptop servers and R Studio, together with Python, R., and Scala coder for statistics scientists.

    Reporting and Visualization

    Visualization through SPSS Modeler. powerful logging and reporting capabilities are developed into the product.


    IBM has adopted a pay-as-you-go model. Watson Studio Cloud – regular prices $ninety nine per 30 days with 50 capacity unit hours per 30 days covered. Watson Studio Cloud - commercial enterprise runs $6,000 monthly with 5,000 skill unit hours. Watson Studio laptop prices $199 per 30 days with unlimited modeling. Watson Studio local – for business records science teams N/A.

    IBM Watson Studio Overview and lines at a look:

    vendor and lines

    IBM Watson Studio

    ML focal point

    broad statistics science focal point with cloud and desktop ML platforms.

    Key facets and capabilities

    robust visual cognizance and herbal classification equipment. flexible strategy that comprises open source tools. Connects to IBM SPSS Modeler.

    person comments

    tremendously rated for facets and capabilities. Some complaints revolving round the use of notebooks.

    Pricing and licensing

    Tiered model from $99 per month per user to $6,000 per 30 days per user or greater at commercial enterprise stage.

    IBM Watson Studio is Coming to Your computer | killexams.com Real Questions and Pass4sure dumps

    illustration of a Modeler circulation operating on Watson Studio laptop

    IBM Watson Studio is an incredibly powerful facts science offering. in case you’re now not regularly occurring, Watson Studio is an built-in ambiance designed to make it handy to strengthen, teach, and manage models. It comprises a large choice of tools used for every thing from facts prep and blend to picture consciousness. And now Watson Studio is on its technique to your windows or Mac computer machine.

    Overview of Watson Studio

    Watson Studio comprises a lot of tools all within one built-in environment. probably the most regular equipment of Watson Studio are:

  • SPSS Modeler for information prep, blend, and modeling without coding
  • facts Refinery, a spreadsheet vogue tool, that permits speedy, self-provider information instruction
  • Python, R, and Scala Jupyter Notebooks to create and share documents that include are living code, equations, visualizations, and explanatory text
  • Neural network Modeler for designing TensorFlow, Keras, PyTorch and Caffe structures devoid of coding
  • Interactive Dashboards to convey sharable live studies so the end users can discover their personal insights
  • obtainable Deployment options

    Watson Studio will soon be obtainable as three deployment alternatives:

  • Watson Studio on the IBM Cloud is the easiest method to get started. It presents 3 tiers from a free starter tier with pay-as-you-go compute the entire strategy to an enterprise version.
  • Watson Studio native is our behind-the-firewall solution presenting a comfortable approach so as to add Watson Studio capabilities to your commercial enterprise. includes purchase alternate options for a handful of clients or the entire firm.
  • And coming soon: Watson Studio laptop
  • Introducing Watson Studio desktop

    Watson Studio computing device is our new third deployment option inside the Watson Studio household. It takes the most everyday parts of what is available inside Watson Studio on the cloud and ports it to your home windows or Mac laptop for offline use, for evaluation of facts data you don’t are looking to upload, and for snappy efficiency. All with a quick and simple desktop installing.

    Watson Studio on the desktop will scale from someone user all of the manner up to a huge crew, and will be a superb addition to the Watson Studio family unit along with our cloud and native flavors.

    The preliminary main aspects of Watson Studio computer may be a SPSS Modeler canvas along with the data refinery spreadsheet editor. this may encompass backwards compatibility for SPSS Modeler streams.

    merits of Watson Studio computer
  • It’s fast, peculiarly for native info. increase individual productiveness using a in the community put in client.
  • It offers offline use. want to build a model on a plane without WiFi? Watson Studio desktop will work with out a web connection for weeks at a time.
  • Adhere to protection and governance mandates together with your information. Watson Studio laptop permits your whole facts to continue to be on your laptop.
  • unlimited modeling without overages. the use of Watson Studio desktop, that you would be able to enhance models with none incremental cost. This permits you to build models iteratively in your desktop, then move it to Watson Studio on the Cloud to set up.
  • It’s one Watson Studio, so no re-gaining knowledge of required. With the equal designs because the cloud and local models, switching between deployment options is seamless with no exciting working towards.
  • And identical to the rest of Watson Studio, anyone — coders or non-coders — can be able to prepare, blend, discover, and model their records in just minutes.
  • Watson Studio desktop’s potent graphing talentsJoin the Beta

    The Beta for Watson Studio is beginning now with two tools already ported to the desktop: a refreshed edition of SPSS Modeler & facts Refinery. it's going to additionally consist of projects to organize your work, facts property firm, and a handy determine for updates function.

    join the beta to give feedback on how you like these equipment, and recommend which other tools we convey to the computer. The Beta is a part of the IBM SPSS Modeler Subscription Trial, so when you register for that you simply’ll have entry to each downloads.

    After you register, search for the “IBM SPSS Modeler Subscription Trial” card, click down load, then you definately’ll see the Watson Studio computing device Beta downloads on the right hand side of the web page.

    be a part of the discussion on the beta community

    After registering for the beta, be a part of in the discussion on the Watson Studio computer beta group. right here that you may ask questions in regards to the beta, supply thoughts for future features, get forum support, and take part in valuable surveys to have an effect on product direction. be a part of the discussion board right here with the aid of logging in along with your IBMid.

    look forward to future bulletins right here about this interesting addition for the Watson Studio family unit.

    Watson Studio laptop venture organizer

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    IBM SPSS Modeler Professional v3

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    IBM's SPSS predictive analytics tools consist of IBM SPSS Modeler and IBM SPSS Statistics. SPSS Modeler provides data mining and text analysis software, while SPSS Statistics is an integrated family of products. Both tools enable users to build predictive models and execute other analytics tasks.

    The IBM SPSS Modeler targets users who have little or no programming skills. Users are provided with a drag-and-drop user interface, enabling them to build predictive models and perform other data analytics. Modeler can apply different processes and algorithms to help the user discover information hidden in the data. The tool can also assist in integrating and consolidating all types of data sets from dispersed data sources across the organization.

    The IBM SPSS Statistics suite is an integrated set of products geared toward more professional data analysts. SPSS Statistics addresses the complete analytical process, from planning to data collection, analysis, reporting and deployment.

    IBM SPSS Modeler features

    Version 18 provides the following features:

  • More than 30 base machine learning algorithms.
  • Extensions that provide continued improvements for use with open source products, such as R and Python.
  • Enhanced support for several multithreaded analytical algorithms, including Random Trees, Tree-AS, Generalized Linear Engine, Linear-AS, Linear Support Vector Machine and Two-Step-AS clustering.
  • The ability to run a variety of Python and Spark machine learning, as well as other Python analytics libraries natively in Modeler without requiring the use of the Analytic Server, as was required in the previous version.
  • SPSS Modeler bundles are deployed on premises, and SPSS Modeler Gold is available as a cloud offering. The client front end of SPSS Modeler runs under Windows and macOS, while the server component runs on Unix, Linux and Windows.

    IBM SPSS Modeler provides the following editions:

  • SPSS Modeler Personal: A single-user desktop product.
  • SPSS Modeler Professional: A desktop product that works with IBM SPSS Analytic Server, providing improved scalability and performance and enabling applications to be used across an organization.
  • SPSS Modeler Premium: This edition includes advanced algorithms and capabilities, such as text analytics, entity analytics and social network analysis, that increase model accuracy with unstructured data.
  • SPSS Modeler Gold: This edition provides analytical decision management, collaboration and deployment capabilities. SPSS Modeler Gold is also available as a cloud offering.
  • IBM SPSS Statistics features

    SPSS Statistics version 24 includes the following new features:

  • The ability to access more than 100 extensions, enabling users to take advantage of free libraries written in R, Python and SPSS syntax.
  • The IBM SPSS Extension Hub to browse, download, update, remove and generally manage extensions.
  • A major upgrade to the Custom Dialog Builder, enabling users to more easily build and install their own extensions. Enhancements include new controls and new properties for existing controls and several other improvements to the user interface.
  • Improvements that enable users to more easily and quickly import and export data into SPPS Statistics.
  • Improvements to the Custom Tables module, including new statistical functionality and customer-requested features.
  • IBM SPSS Statistics offers the following three editions (each with additional modules):

  • SPSS Statistics Standard tools provide advanced statistical procedures that support linear and nonlinear statistical models, as well as predictive simulation modeling, which accounts for uncertain inputs, geospatial analytics and customized tables.
  • SPSS Statistics Professional tools support data preparation, missing values and data validity, decision trees, and forecasting.
  • SPSS Statistics Premium adds advanced analytical techniques, including structural equation modeling, in-depth sampling assessment and testing. This bundle also includes procedures that target direct marketing and high-end charts and graphs.
  • Pricing for the SPSS Modeler and SPSS Statistics predictive analytics tools vary depending on the bundle options, the number of users and the license period. SPSS Statistics is now available as a subscription option or a perpetual license. IBM offers free trials of both IBM SPSS Modeler and IBM SPSS Statistics.

    Next Steps

    Why the term unstructured data is a misnomer

    How big data is changing data modeling techniques

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    Cancer associated fibroblasts sculpt tumour microenvironment by recruiting monocytes and inducing immunosuppressive PD-1 + TAMs | killexams.com real questions and Pass4sure dumps

    Isolation of fibroblasts from normal and cancerous breast tissue

    Normal breast tissues were obtained from 3 patients undergoing reduction mammoplasty and breast cancer tissues were obtained from 4 patients undergoing therapeutic mastectomy. All fibroblasts were isolated using a previously described protocol41,53 that utilizes Collagenase I (1 mg/mL) and Hyaluronidase (125 U/mL) enzymes followed by differential sedimentation and plating. Enzymatically digested tissues were then cultured in high serum media conditions which select for fibroblast growth (Dulbecco’s Modified Eagle’s medium [DMEM] supplemented with 10% foetal bovine serum at 37 C, 5% CO2). All human breast tissues for all of the experiments were obtained in accordance with the laws and institutional guidelines, as approved by the institutional review board of Hacettepe University (Approval numbers: GO 16/64 - 20 and GO 17/380 - 31). Informed consent was obtained from all participants.

    Characterization of fibroblasts with immunocytochemistry

    Characterizations of fibroblasts were performed by immunocytochemistry stainings with vimentin, pan-cytokeratin and α-SMA according to the manufacturer’s instructions. Cells (7 × 104 cells/300 µL in each well) were cultured in eight well chamber slides and immunocytochemical / morphological analyses were performed when the cells reached a surface confluency of >80%. A biotin/streptavidin/horseradish peroxidase detection system was utilized and binding of the antibody was demonstrated with diaminobenzidine (DAB) substrate. The images were captured by Olympus BX50 microscope.

    Preparation of conditioned medium (CM)

    CMs were obtained from CAFs, NFs and MDA-MB-231 breast cancer cells. When the aforementioned cells reached to a confluency of >80%, they were serum starved. After 48 h, CMs were collected from cell supernatants and clarified by centrifugation.

    Isolation and culture of peripheral CD14+ monocytes

    PBMCs were isolated from healthy volunteers’ peripheral blood using density gradient separation with Histopaque-1077. Separation of CD14+ monocytes from PBMCs was accomplished by using a magnetic bead based positive selection protocol with a purity of >95%. CD14+ monocytes were cultured alone as control monocytes or with CMs from CAFs, NFs or MDA-MB-231 breast cancer cells (CM:RPMI, 1:1) for 7-days.

    Phenotypical analyses with flow cytometry

    CD14+ PBMCs isolated from healthy donors were cultured with CMs from NFs, CAFs, MDA-MB-231 breast cancer cells as well as in standard medium for 7 days, then analysed using flow cytometry. M1 macrophages were cultured with CMs from CAFs or MDA-MB-231 cells for 48 hours, then analysed by flow cytometry.

    Cultured monocytes or macrophages were detached using Accutase cell detachment solution, according to the manufacturer’s instructions. Cells were stained with antibodies against CD206, CD163, HLA-DR, CD14, and PD-1. All antibodies were conjugated to Phycoerythrin (PE) or Fluorescein isothiocyanate (FITC). Respective isotype-matched antibody controls were used as negative controls.

    Isolation of peripheral blood CD4+ T-cells

    PBMCs were isolated from healthy volunteers’ peripheral blood using density gradient separation with Histopaque-1077. Separation of CD4+ T-cells from PBMCs was accomplished by using a magnetic bead based negative selection protocol with a purity of >95%. CD4+ T-cells were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10% foetal calf serum, 2.1 mM L-glutamine, 100 U/mL penicillin and 100 mg/mL streptomycin at 37 °C, 5% CO2.

    CFSE proliferation assays

    In order to assess the effects of CAF-, NF- and MDA-MB-231-educated monocytes on CD4+ T lymphocytes, we performed functional analyses with flow cytometry. Carboxyfluorescein succinimidyl ester (CFSE) labelled CD4+ T-cells were activated by CD3/CD28 magnetic beads (except the negative control group). Activated T-cells were cultured with either control monocytes or with monocytes that had been cultured with CMs from CAFs, NFs or MDA-MB-231 cells for 7 days. After 96 hours, proliferation of CFSE labelled CD4+ T cells was evaluated by flow cytometry.

    Evaluation of cell migration

    In order to evaluate the effects of CAFs, NFs, or MDA-MB-231 cells on monocyte recruitment, we performed in vitro migration assays. Monocyte cells were seeded into the upper compartment in serum-free medium (5 × 104 cells in 200 µl). The 5 µm Transwell chambers were placed into 24-well culture wells containing CMs from CAFs, NFs, or MDA-MB-231 cells. After 5 h incubation, non-migrated cells were removed by cotton swab. Migrated cells were fixed by methanol and stained with Crystal violet. Migrated cells were counted in five different fields of polycarbonate filter under a microscope (magnification x100).

    Evaluation of EMT-related protein expressions by Western Blot

    MDA-MB-231 breast cancer cells were cultured for 24 hours prior to CM treatments. The cells were then treated with CMs from NF-, CAF-, MDA-MB-231- educated monocytes or from control monocytes for 48 hours. At the end of this period, cells were lysed in RIPA (Thermo Fisher Scientific, Waltham, MA, USA) lysis buffer supplemented with protease and phosphatase inhibitor cocktail (Thermo Fisher Scientific, Waltham, MA, USA). E-cadherin (primary antibody: Cell Signaling Technology, Danvers, MA, USA; #3195) and vimentin (primary antibody: Cell Signaling Technology, Danvers, MA, USA; 5741) protein expressions in samples were examined by the Western blot method. GAPDH (primay antibody: Cell Signaling Technology, Danvers, MA, USA, #5174) was used as the Western blot loading control. The membranes were visualized by chemiluminescence (ECL) and densitometry analyses of the protein bands were performed.

    Evaluation of EMT-related gene expressions by quantitative real-time PCR

    MDA-MB-231 breast cancer cells were cultured for 24 hours prior to CM treatments. The cells were then treated with CMs from NF-, CAF-, MDA-MB-231- educated monocytes or from control monocytes for 48 hours. At the end of this period, RNA isolation from the cells was performed according to the Zymo Quick-RNA Miniprep Kit protocol. Complementary DNA was synthesized with Thermo Scientific RevertAid First Strand cDNA Kit according to the manufacturer’s instructions. Real-time qPCR was performed using LightCycler FastStart DNA Master SYBR Green (Roche, Basel, Switzerland). The qPCR data were analysed using the Livak model (2−ΔΔCt). Snail (Snail_reverse 5′-CTGCTGGAAGGTAAACTCTGGA-3′, Snail_forward 5′-CGAGTGGTTCTTCTGCGCTA-3′), Slug (Slug_reverse 5′-TTCTCCCCCGTGTGAGTTCTAA-3′, Slug_forward 5′-CACTGCGATGCCCAGTCTA-3′), and Twist (Twist_reverse 5′-CCCACGCCCTGTTTCTTTGA-3′, Twist_forward 5′-GCCGGAGACCTAGATGTCATT-3′) gene expressions were evaluated. β -actin was used as the reference gene.

    Evaluation of cell invasion

    MDA-MB-231 breast cancer cell invasion was evaluated by using Transwell inserts in vitro. Monocytes were differentiated for 7 days using CMs from NF, CAF or MDA-MB-231 cells as well as in standard medium. All the differentiated monocytes were then serum starved for 48 h and corresponding supernatants were then collected. MDA-MB-231 cells in serum-free medium were seeded into upper compartments of Transwell inserts which were pre-coated with Matrigel (5 × 104 cells in 200 µl). The lower compartment contained the aforementioned supernatants, which were obtained from monocytes. After 24 hours, non-migrated cells were removed by cotton swab. Migrated cells were fixed by methanol and stained with Crystal violet. Migrated cells were counted in five different fields of polycarbonate filter under a microscope (magnification x200).

    Induction of M1/M2 polarization of macrophages

    CD14+ monocytes were cultured in medium containing macrophage colony-stimulating factor (M-CSF) (50 ng/ml) for 7 days to obtain M0 macrophages. In order to acquire M1 macrophages, M0 macrophages were further cultured in medium containing interferon gamma (IFNγ) (100 ng/ml) and lipopolysaccharides (LPS) (10 ng/ml) for 2 more days. On the other hand, M0 macrophages were further cultured in medium containing IL-4 (20 ng/ml) for 2 more days in order to obtain M2 macrophages.

    Assessment of soluble factors by ELISA

    In order to evaluate the levels of IL-12 and IL-10 cytokines in the culture supernatants of M1 and M2 macrophages, we performed enzyme-linked immunosorbent assays (ELISA). We cultured M1 or M2 macrophages alone (as negative control) or with CMs from CAFs, or MDA-MB-231 breast cancer cells for 2 days. After this period, the cells were further cultured for additional 2 days in serum-free medium. Culture supernatants were stored at −80 °C until the assays were performed.

    Measurement of cell proliferation by MTT assay

    MDA-MB-231 breast cancer cell proliferation was evaluated via MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) assay. MDA-MB-231 cells were seeded in 96-well plates. After about a day of incubation, CMs obtained from CAF- or NF-educated-monocytes were added to the wells and MDA-MB-231 cell proliferations were analysed after an additional 48 hours (72 hours in total) by adding 25 μl MTT reagent (final concentration: 1 mg/ml) in each well. 4 hours after adding the MTT reagent, the precipitate was solubilized by 80 μl detergent reagent. The plates were then left overnight in the dark and the absorbances were recorded at 570 nm.

    Real-time and label-free analysis of MDA-MB-231 cells with the xCELLigence system

    In order to assess the real-time effects of CAF- and NF-educated monocytes on MDA-MB-231 breast cancer cell proliferation, we performed functional analyses with the RTCA xCELLigence System (ACEA, San Diego, CA, USA). This system utilizes gold biosensor microelectrodes to measure electrical impedance. The background impedance of the microelectrodes were first measured with cell culture medium. Then, MDA-MB-231 breast cancer cells were added to each well of the E-plate. After about a day of incubation, CMs obtained from CAF- or NF-educated-monocytes were added to the wells and the cell indices were measured by electrical impedance over an additional period of 48 hours (72 hours in total).

    Tissue samples and immunohistochemical stainings

    A total of 50 human invasive breast cancer tissue samples were investigated. Patients who had received preoperative/adjuvant chemotherapy or radiotherapy were excluded. Clinical and pathological variables including age, tumour grade and size, lymph node involvement, Ki-67 staining as well as ER, PR and HER2 status were evaluated.

    Formalin-fixed paraffin-embedded tumour samples were used for tissue microarrays (TMAs). Blocks were made utilizing a 4.0 mm tissue cylinder through a histologically representative area of each donor tumour block. From each donor block, 1–2 cores were cut and 8 TMA blocks were prepared. Immunohistochemical stainings for CD163 (Biocare, Clone 10D6, 10 min EDTA, 1:100), CD206 (Abcam, ab64693, 20 min EDTA, 1:200) and α-SMA (Neomarkers, Clone 1A4, 1:1000) as well as Haematoxylin and Eosin (H&E) were performed on the 4-μm thick sections taken from the tissue microarrays using Leica Bond Max III Autostainer, following manufacturer’s instructions. Concentrations and antigen retrieval methods were optimized for each antibody using appropriate positive and negative controls.

    TAM and CAF grade evaluations

    All tissue microarray slides stained with anti-CD163 or anti-CD206 were analysed to identify areas with the highest levels of TAM infiltration. For each case, three hot spots in the tumour stroma (40x objective) were selected for counting TAMs. The median values of CD163+ or CD206+ macrophage numbers in stroma within the areas were used to categorize the patients into high and low grade groups. The intensity of CAFs (α-SMA positive spindle-shaped fibroblasts) was classified into 2 grades, using a modification of a method previously described54: negative to scanty (low grade) or abundant (high grade) in a blinded analysis performed by 2 of the authors (K.K., and B.G.Y.).

    Statistical analyses

    The Mann-Whitney U test, Student’s t-test, chi-squared test, and Fisher’s exact test were used to examine differences in continuous and categorical variables. A 5% type-I error level was used to infer statistical significance. All statistical analyses were carried out using IBM SPSS Statistics for Windows Software version 23.

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    Wordpress : http://wp.me/p7SJ6L-fE
    weSRCH : https://www.wesrch.com/business/prpdfBU1HWO000RIBO
    Scribd : https://www.scribd.com/document/356766425/Pass4sure-C2090-930-Practice-Tests-with-Real-Questions
    Dropmark-Text : http://killexams.dropmark.com/367904/12024133
    Youtube : https://youtu.be/7rsNeRb4gUs
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    Box.net : https://app.box.com/s/00onvbvs3w19kq68on93egtduo0lw1nh
    zoho.com : https://docs.zoho.com/file/2q0x218a94fd5e2e445daa7f6994b36d7f2d8

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