|Exam Name||:||HP Data Protector software Application(R) Integration-Windows|
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|Updated On||:||April 18, 2019|
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HP0-J35 exam Dumps Source : HP Data Protector software Application(R) Integration-Windows
Test Code : HP0-J35
Test Name : HP Data Protector software Application(R) Integration-Windows
Vendor Name : HP
Q&A : 55 Real Questions
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down load this white paper to discover how HP can assist your firm meet its backup, recuperation and archiving needs with a complete, one-stop backup answer. learn the way the HP information Protector and StoreOnce answer can cut back the quantity of kept records by 95 percent and use incredibly productive deduplication to reduce bandwidth. you will additionally study concerning the facts Protector’s superior facets together with developed-in disaster healing, image integration with other storage arrays, and its means to immediately recover mission-important purposes.
HP Friday announced enhancements to HP statistics Protector application that offers comprehensive insurance policy for virtual environments and flexible facts reduction options, at up to 70 percent under alternatives. This utility lowers the can charge of retaining information by decreasing the volume of information backed-up, using storage skill optimization alternate options akin to virtual full and deduplication.
in keeping with a commissioned look at conducted through Forrester Consulting on behalf of HP, more than half of businesses plan to enhance their center of attention on, and finances regarding, backup and recovery in 2009.
"right now agencies want new how you can find short-term charge savings while laying the groundwork to grow improved," pointed out Jonathan Martin, international vice president & well-known manager, assistance management, software & solutions. "For our 22,000 valued clientele around the globe, HP statistics Protector is the simplest solution that offers CIOs a price-effective enterprise security web for managing information, whereas at the identical time addressing considerations around virtualization, information discount and information protection."
"HP information Protector has been greater to help valued clientele tackle their main priorities in statistics protection, regulatory compliance, consolidation and virtualization. the new developments to HP data Protector, coupled with HP utility's zero p.c financing choice, offers valued clientele a versatile sourcing option to tackle their most essential pain points these days, while making ready for fulfillment upon the return of the economy," observed Avijit Basu, enterprise Head, information management, HP software & solutions India.
HP statistics Protector promises new capabilities to help shoppers' backup and recuperation
HP currently also brought two new storage items - HP StorageWorks business digital Arrays (EVA6400/8400) and the more suitable HP StorageWorks SAN Virtualization features Platform (SVSP) that lengthen the value of HP statistics Protector.
with the aid of offering seamless integration between the brand new HP EVA, HP SVSP and HP facts Protector, consumers advantage from the strengths of each HP hardware and utility for the comprehensive answer for VMware Infrastructure facts protection within the trade. customers advantage from optimized backup of facts replicated on virtual storage, with no have an impact on to their production environments.
Copyright © 2009 IDG Communications, Inc.
HP, Palo Alto, Calif., additionally mentioned its facts insurance plan 7 utility now enables clients to protect facts with the aid of backing it up to the HP Autonomy cloud and offers the skill to effectively do e-discovery on facts kept in the cloud.
the new integration of the Autonomy technology into HP's storage offerings was brought at HP's find convention, held this week in Las Vegas.
[Related: HP's 3PAR Storage Connects To Blades Without SAN, Targeting Cisco, EMC Offerings ]
The flow to combine technology from Autonomy into records Protector 7 become the primary joint engineering assignment performed since HP late remaining 12 months got Autonomy in a large $10.three billion deal, stated Jeff Veis, vice president of advertising and marketing for Autonomy offer protection to solutions at HP
The assignment resulted in HP's facts Protector 7 software being integrated with the Autonomy intelligent statistics working Layer, or IDOL, as a way to satisfy consumer legal discovery and compliance necessities, Veis said.
IDOL is the crown jewel of the Autonomy know-how, Veis referred to.
"IDOL makes use of sophisticated algorithms to analyze sophisticated, unstructured content," he stated. "as an example, if I say 'Apple,' what do I suggest? a pc enterprise? The 'Apple of my eye?' A fruit? but if I say, 'The apple is delicious,' you know what I suggest. IDOL works that way. It is familiar with over 1,000 file codecs, and it is aware data patterns. it be the engine that powers the Autonomy business."
via integrating IDOL to facts Protector, information can circulate in the course of the IDOL engine to create a database in keeping with the that means of the records, making it in a position to be searched now not by using the keywords but through the context, Veis spoke of.
due to this fact, because of the information Protector center of attention on income through channel, solution suppliers will quickly have the potential to offer e-discovery means to purchasers, he observed.
Going ahead, HP will additionally add facts retention capabilities to statistics Protector in keeping with policies that can also be immediately decided according to the context of the facts, he referred to.
also new with statistics Protector 7 is the skill to returned up records to the HP Autonomy storage cloud.
besides the Autonomy expertise, the HP information Protector software is now also built-in with HP's StoreOnce Catalyst dedupe utility and appliance.
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PALO ALTO, Calif.--(BUSINESS WIRE)--Hewlett-Packard México, S. de R.L. de C.V., today announced Coca-Cola FEMSA, S.A.B. de C.V. (“Coca-Cola FEMSA”), the largest public bottler of Coca Cola products in the world in terms of sales volume, has signed a five-year technology outsourcing services contract to build and manage an HP Converged Infrastructure.
The new services and infrastructure support the company’s Latin American growth while providing better service and lower costs. The agreement adds more than $100 million to HP’s existing Coca-Cola FEMSA relationship, which began in 2000.
HP (NYSE:HPQ) and Coca-Cola FEMSA will consolidate 348 locations to a single data center in Mexico and migrate business-critical SAP applications and server monitoring and management to HP Best Shore locations in Brazil and Argentina. HP Security Services will be provided from HP Best Shore global delivery centers in Costa Rica. HP Best Shore combines HP’s technology portfolio with global delivery expertise to give clients greater flexibility and cost efficiencies while minimizing risk.
HP will continue to manage Coca-Cola FEMSA’s technology infrastructure supporting its Latin American operations in Argentina, Brazil, Colombia, Costa Rica, Guatemala, Mexico, Nicaragua, Panama and Venezuela.
“After experiencing sustained growth across Latin America, these additional efforts to centralize and standardize will give us the support we need to find new opportunities to put beverages in the hands of the Latin American people,” said Hector Calva, chief information officer, Coca-Cola FEMSA. “HP knows our business and industry well. With the team’s extensive experience in data center consolidation, we will have the technology foundation and support critical for our growth plans and future success.”
HP will continue to provide Data Center Services and Storage Services to manage and support Coca-Cola FEMSA’s data center environment. HP provides Server Management to host more than 650 midrange servers and Backup and Restore Services for disaster recovery. The agreement also includes international and regional telecommunications Carrier Management Services in addition to Network Management Services for the company’s LAN/WAN environment. HP also provides Enterprise Application Hosting Services for Coca-Cola FEMSA’s SAP platform and will move to dedicated support.
In addition, HP will continue to deliver Workplace Services for Coca-Cola FEMSA’s 14,500 desktop and notebook PCs, handheld devices, printers and servers as well as moving to dedicated Service Desk Services in Spanish and Portuguese for employees using these devices.
Coca-Cola FEMSA will consolidate its data center on an HP Converged Infrastructure using HP Superdome 2 servers and Integrity BL860c i2 server blades running HP-UX v3, HP StorageWorks Enterprise Virtual Arrays, HP StorageWorks XP24000 and P9500 disk array enterprise class storage systems, and HP Data Protector software for backup and recovery. Each is intended to improve reliability and efficiency in the consolidated data center.
HP Agility Alliance partners, including SAP and Microsoft, will provide additional tools, technologies and resources to HP in support of Coca-Cola FEMSA.
“In a region such as Latin America with its many opportunities for growth, companies that develop an efficient technology infrastructure and business procedures to support an ‘Instant-On’ enterprise will be better able to take advantage of those opportunities,” said Octavio Marquez, managing director, HP Mexico. “Our industry knowledge and decade-long relationship with Coca-Cola FEMSA, as well as our ability to scale when and where the client grows, will continue to help the company achieve its goals.”
In a world of continuous connectivity, the Instant-On Enterprise embeds technology in everything it does to serve customers, employees, partners and citizens with everything they need, instantly.
About Coca-Cola FEMSA
Coca-Cola FEMSA, S.A.B. de C.V. produces and distributes Coca-Cola, Sprite, Fanta, Lift and other trademark beverages of The Coca-Cola Company in Mexico (a substantial part of central Mexico, including Mexico City and southeast Mexico), Guatemala (Guatemala City and surrounding areas), Nicaragua (nationwide), Costa Rica (nationwide), Panama (nationwide), Colombia (most of the country), Venezuela (nationwide), Brazil (greater São Paulo, Campiñas, Santos, the state of Mato Grosso do Sul, part of the state of Goias and part of the state of Minas Gerais) and Argentina (federal capital of Buenos Aires and surrounding areas), along with bottled water, beer and other beverages in some of these territories. The Company has 30 bottling facilities in Latin America and serves over 1,500,000 retailers in the region. The Coca-Cola Company owns a 31.6 percent equity interest in Coca-Cola FEMSA. Visit http://www.coca-colafemsa.com for more information.
HP creates new possibilities for technology to have a meaningful impact on people, businesses, governments and society. The world’s largest technology company, HP brings together a portfolio that spans printing, personal computing, software, services and IT infrastructure at the convergence of the cloud and connectivity, creating seamless, secure, context-aware experiences for a connected world. More information about HP is available at http://www.hp.com.
This news release contains forward-looking statements that involve risks, uncertainties and assumptions. If such risks or uncertainties materialize or such assumptions prove incorrect, the results of HP and its consolidated subsidiaries could differ materially from those expressed or implied by such forward-looking statements and assumptions. All statements other than statements of historical fact are statements that could be deemed forward-looking statements, including but not limited to statements of the plans, strategies and objectives of management for future operations; any statements concerning expected development, performance or market share relating to products and services; any statements regarding anticipated operational and financial results; any statements of expectation or belief; and any statements of assumptions underlying any of the foregoing. Risks, uncertainties and assumptions include macroeconomic and geopolitical trends and events; the competitive pressures faced by HP’s businesses; the development and transition of new products and services (and the enhancement of existing products and services) to meet customer needs and respond to emerging technological trends; the execution and performance of contracts by HP and its customers, suppliers and partners; the achievement of expected operational and financial results; and other risks that are described in HP’s Quarterly Report on Form 10-Q for the fiscal quarter ended January 31, 2011 and HP’s other filings with the Securities and Exchange Commission, including but not limited to HP’s Annual Report on Form 10-K for the fiscal year ended October 31, 2010. HP assumes no obligation and does not intend to update these forward-looking statements.
© 2011 Hewlett-Packard Development Company, L.P. The information contained herein is subject to change without notice. The only warranties for HP products and services are set forth in the express warranty statements accompanying such products and services. Nothing herein should be construed as constituting an additional warranty. HP shall not be liable for technical or editorial errors or omissions contained herein.
In this meta-analysis, we included data of three European studies: The 5.5 and 8 year follow-up visits of CHOP, the 8 year follow-up visit of the Ulm Birth Cohort Study (UBCS), and the combined 10 year follow-up visits of the “German Infant study on the influence of Nutrition Intervention plus environmental and genetic influences on allergy development” (GINIplus) and the “Influence of Life style factors on the development of the Immune System and Allergies in East and West Germany” (LISA) birth cohort studies. All research was performed in accordance with the Declaration of Helsinki. We included only data and bio-samples from fasted children. Anthropometric measurements were used to calculate the age- and sex-specific z-scores for BMI during childhood using a German reference dataset21.CHOP study
The CHOP study is a double-blind, randomized, multicenter intervention trial conducted in five countries: Germany, Belgium, Italy, Poland, and Spain18. At a mean age of 2 weeks but no later than the age of 8 weeks of life, infants were randomly assigned to a higher or lower protein content infant formula (HP and LP groups, respectively) provided through the first year of life. Additionally, an observational group of breastfed infants was included. This study was approved by the ethics committees of all study centers, and written informed parental consent was obtained for each infant (trial registration: ClinicalTrials.gov; identifier: NCT00338689). Anthropometry data at 5.5 and 8 years were obtained at visits at the study centers. Blood samples were collected during both follow-up visits. Blood samples were collected and centrifuged and the serum samples were frozen at −70 °C. Glucose, HDL cholesterol and LDL cholesterol were analyzed in the respective laboratories of the local study centers with an enzymatic method22. An enzymatic reference method with hexokinase or indirect potentiometry was used for glucose measurement. Serum insulin levels were quantified using immunoradiometric assays (DiaSource, Nivelles, Belgium) at the Children’s Memorial Health Institute Warsaw (Poland). HOMA index was calculated: insulin (mU/l) x glucose (mg/dl)/405 (Matthews 1985). For metabolomics measurements, samples were sent on dry ice to Munich and re-stored at −80 °C until final analysis. We only use data from children who were fasted for at least 6 hours prior to blood withdrawal. In total, 396 children from the 5.5 year follow-up and 355 of the 8 year follow-up visit were included.UBCS
The UBCS is a longitudinal prospective birth cohort study. Women that gave birth at the Department of Gynaecology and Obstetrics at the University of Ulm between November 2000 and November 2001 were recruited23. Participation was voluntary and written informed consent was obtained in each case. The study was approved by the ethics committees of the Universities of Ulm and Heidelberg and of the physicians’ boards of the states of Baden-Wuerttemberg and Bavaria. There have been regular follow-up examinations up to 8 years, when anthropometry data was obtained by trained staff at the Ulm University hospital and blood samples from 413 children were withdrawn between 8 and 9 a.m. after an overnight fast of at least 10 h. Samples were processed immediately and plasma aliquots were frozen at −80 °C19. For metabolomics measurements, samples were sent on dry ice to Munich and re-stored at −80 °C until final analysis. Fasting plasma concentrations of insulin were measured as a batch using a commercially available ELISA (Mercodia). Concentrations of fasting plasma glucose were measured by using HemoCue B-Glucose Analyzer (Quest Diagnostics, Spain). HOMA was calculated accordingly. Fasting lipoproteins ApoAI, ApoB were determined by immunonephelometric methods, using the Health Care Diagnostic Product (Siemens GmbH, Germany) on a Dade Behring nephelometer BNII System.GINIplus/LISA study
The study population consists of a subsample of children living in Munich, Leipzig and Bad Honnef who participated in the 10-year follow-up. GINIplus is a prospective birth cohort of 5,991 children born at full-term and normal weight recruited between 1995 and 1998. Children with at least one atopic parent or sibling were allocated to an intervention study arm which investigated the effect of different hydrolyzed formulas consumed during the first year of life on allergy development (N = 2,252)24. All children whose parents did not give consent for the randomized clinical trial or who did not have a family history of allergic diseases were allocated to the observation study arm (N = 3,739). LISAplus is a population-based prospective birth cohort of 3,097 children born at full-term and normal weight recruited between 1997 and 1999. Detailed descriptions of the recruitment and follow-up strategy for both cohorts are available24,25. Both studies were approved by the local Ethics Committees (the Bavarian Board of Physicians (reference numbers: 01212 and 07098), University of Leipzig (reference number: 345/2007), and Board of Physicians of North-Rhine-Westphalia (reference numbers: 2003355 and 2008153)) and written consent was obtained from all parents of the participants.
There have been regular follow-up examinations up to 15 years in study centers with anthropometric measurements and blood withdrawal. After blood withdrawal, the samples were processed immediately and plasma aliquots were frozen at −80 °C. For metabolomics measurements at Ludwigs-Maximilians-Universität (LMU), samples were sent on dry ice to Munich and re-stored at −80 °C until final analysis. Overnight fasted samples were available for 252 children. Glucose measurements in blood were performed by standard laboratory methods by the individual hospitals. Fasting insulin in serum was measured centrally by the fully mechanized system, LIAISON (DiaSorin). HOMA-IR was calculated accordingly. The measurement of serum lipoproteins was performed using homogenous enzymatic colorimetric methods according to the manufactures instructions on a Modular Analytics System from Roche Diagnostics GmbH Mannheim.Metabolomics analyses
Metabolomics analyses were performed at LMU Munich. Amino acids (AA), non-esterified fatty acids (NEFA), carboxylic acids (CA), acylcarnitines (acyl-Carn) and phospholipids (PL) were measured. We report all metabolite concentrations in µmol/L. As a point to note, the analytical technique applied here is not capable of determining the position of the double bonds and the distribution of carbon atoms between fatty acid (FA) side chains. The acyl-Carn, PL and NEFA are mentioned as X:Y. In this nomenclature, X is the length of the carbon chain, Y is the number of double bonds.
50 µL of plasma were thawed and diluted with 450 µl methanol, containing internal standards representing different groups of metabolites (AA- Labeled amino acid standards set A (NSK-A-1, Cambridge Isotope Laboratories – CIL, USA), 15N2-L-Asparagine (NLM-3286-0.25, CIL, USA) and Indole-D5-L-Tryptophan (DLM-1092-0.5, CIL, USA); NEFA- 13C16-palmitic acid (CLM-409-MPT-PK, CIL, USA); acyl-CARN D3-acetyl-carnitine (DLM-754-PK, CIL, USA), D3-octanoyl-carnitine (DLM-755-0.01, CIL, USA) and D3-palmitoyl-carnitine (DLM-1263-0.01, CIL, USA); PL- Tridecanoyl-2-hydroxy-sn-glycero-3-phosphocholine (855476, Avanti Polar Lipids, USA) and 1,2-dimyristoyl-sn-glycero-3-phosphocholine (850345, Avanti Polar Lipids, USA)); TCA D3-Methylmalonic Acid (DLM-387-PK, CIL, USA).
After centrifugation (4000 rpm, 10 min, room temperature), supernatants were divided according to the following methods:Amino acids
100 µL of the supernatant were prepared using derivatization as previously reported26. The supernatant was evaporated with nitrogen to dryness and the free amino acids were derivatized with 50 µl butanolic HCl for 15 min at 600 rpm at 60 °C. After evaporation, the residue was dissolved in 50 ml flow solution. AA butylesters were determined by ion-pair liquid chromatography coupled to mass spectrometry detection (LC-MS/MS). 10 µL of the prepared sample were injected into the HPLC system (HPLC 1100, Agilent, Waldbronn, Germany) and chromatographic separation was performed with a XBridge C18 column (Waters GmbH, Eschborn, Germany). MS detection was performed with an API 2000 triple quadrupole instrument (Sciex, Darmstadt, Germany) with an APCI source operating in positive ion ionization mode. Data acquisition on the mass spectrometer was controlled by Analyst 1.6.2 software (AB Sciex, Darmstadt, Germany). Data handling and quantification were also performed with Analyst 1.6.2 software.Nonesterified fatty acids
100 µL of the supernatant were analyzed as previously reported27. The supernatant was mixed for 20 min at 600 rpm at room temperature and transferred for LC-MS/MS analysis. An UPLC diphenyl column (Pursuit UPS Diphenyl, Varian, Darmstadt, Germany) was used for chromatographic separation with an Agilent 1200 SL series HPLC system (Waldbronn, Germany). The injection volume was set to 10 µL with an eluent flow rate of 700 mL/min. A hybrid triple quadrupole mass spectrometer (QTRAP4000, Sciex, Darmstadt, Germany) operating in negative ESI mode was coupled to the HPLC system for identification of NEFA.Carboxylic acids
Carboxylic acids (CA) were measured by a modified LC-MS/MS method based on previously published methods28. 100 μL of the supernatant were evaporated to dryness and re-suspended in 50 μL water. Five μL of the extracted samples were injected to an Agilent 1200 HPLC and molecular species were separated on a Kinetex F5 core-shell HPLC column, 150 × 2.1 mm, 2.6 μm particle size (Phenomenex, Aschaffenburg, Germany). The mobile phase A was water with 1% formic acid and mobile phase B was composed of methanol/isopropanol (50:50) with 1% formic acid. The gradient elution at a flow rate of 200 μL/min was from 1% B to 85% B within 9 minutes and turned back to initial conditions of 1% B within 1 minute. Re-equilibration was held for 5 minutes at 1% B. The triple quadrupole mass spectrometer (QTRAP4000) was operated in negative scheduled multiple reaction monitoring mode using electrospray ionization (ESI).Phospholipids
Flow-injection mass spectrometry (FIA-MS/MS) was used to analyze PL. 30 μL of the centrifuged supernatant was mixed with 500 µL methanol (containing 1 µM ammonium acetate) for 20 min at 600 rpm and then used for FIA-MS/MS analysis. Samples were analyzed with a triple quadrupole mass spectrometer (QTRAP4000) with an electrospray ionization (ESI) source which was used in both positive and negative mode. The MS was coupled to an Agilent 1200 SL series HPLC system. MS/MS analysis was run in Multiple Reaction Monitoring (MRM) mode with 184 Da (choline head group) as product ion for the PL. Analyst 1.6.2 software and the statistical program R (R Project for Statistical Computing, http://www.r-project.org/) were used to post-process the entire analytical process.
The analysis comprised diacyl-phosphatidylcholines (PCaa), acyl-alkyl-phosphatidylcholines (plasmalogens, PCae), sphingomyelins (SM), lyso-phosphatidylcholines (lysoPC), and sum of hexoses. “a” indicates that the acyl chain is bound via an ester bond to the backbone, while “e” means binding by an ether bond.
Using FIA-MS/MS, it is not possible to determine which single FA is bound to the SM backbone and of which configuration this backbone is. To identify the exact configuration of SM 32:2, a chromatographic separation was used which was previously described for individual glycerophospholipid species29, combined with mass spectrometric fragmentation of lithium adducts30. Identification was achieved by retention time and fatty acid specific fragmentation and quantification of SM 32:2 was achieved by comparison to commercially available standard SM (d18:1/18:0). A calibration curve from 0.1 µM to 5.0 µM standards were prepared equal to 6 quality control samples, 9 plasma samples containing low levels of SM 32:2 and 10 plasma samples containing high levels of SM 32:2. 20 µL of samples were prepared by adding 200 µL methanol including SM (d18:1/6:0) as internal standard. After mixing, freezing at −20 °C for 20 minutes, and centrifugation (4000 U/Min for 10 min), the supernatant was used for the analyses of SM by LC-MS/MS analyses with 1200 SL HPLC system coupled to a 4000QTRAP tandem mass spectrometer. Chromatographic separation was achieved with Kinetex C18, 2.6 µm, 100 × 2.1 mm HPLC column (Phenomenex, Aschaffenburg, Germany) and gradient elution29. Mass spectrometric detection was conducted in positive MRM with 184 Da as fragment as well as fragments of lithium induced fragmentation30. The two potential combinations of SM 32:2 shared the same precursor ion mass (679.5 Da), but had different lithium-induced fragments (SM (d18:1/14:1): 250.2, 264.2; SM (d18:2/14:0): 252.2, 262.2). For the MRM transition, we focused on 679.5/250.2 and 679.5/252.2.Acylcarnitines
FIA-MS/MS was used to analyze acyl-CARN. 100 μL of the centrifuged supernatant was used for FIA-MS/MS analysis. Samples were analyzed with a QTRAP4000 mass spectrometer with an electrospray ionization (ESI) source which was used in positive ionization mode. The MS was coupled to an Agilent 1200 SL series HPLC system. MS/MS analysis was run in MRM mode. Analyst 1.6.2 software and the statistical program R (R Project for Statistical Computing, http://www.r-project.org/) were used to post-process the entire analytical process.Quality Control
The quality control (QC) procedure was applied to the measurement of each follow-up visit separately.
For the CHOP study and GINIplus/LISA study, we assessed the measurement quality using 6 QC samples per batch. A batch was included in the analysis if the intra-batch coefficient of variation after outlier elimination (exclusion of the most extreme measurement lying more than 1.5 IQR apart from the nearest measurement) was < 0.2. If less than five QC sample measurements were available in a batch, the batch was not included either. A metabolite was included if it passed quality control in at least 50% of the batches. Inter-batch variation was removed by calculating the median ratios of the quality controls and using these to align the medians of the samples.
To quantify measurement accuracy of the UBCS, six plasma quality control (QC) samples were consistently measured twice along with the samples per batch. We calculated the coefficient of variation (CV) for each QC sample across the batches and excluded metabolites whose CV was > 35%.Statistical analyses
Statistical analyses were performed using the statistical program R (version 3.3.3). Initially, we screened the data for extreme and potentially influential observations in BMI, HOMA levels or concentrations of metabolites and removed the measurement if it was >1.5 times the SD away from the second highest value. The batch effect was removed by dividing each measurement of a batch with the corresponding ratio of the batch QC median to the overall QC median. In doing so, the correction necessary to align all batch medians of the QC samples was applied to the samples in the respective batch. The procedure was performed for each study and follow-up separately.
To assess the associations of outcomes and metabolites, we firstly analyzed each study separately using linear models regressing the outcomes BMI z-score, weight, height, LDL, HDL, and HOMA levels on the metabolites. We ran bivariate linear models and, with exception of BMI z-score, multiple linear models adjusted for child age and sex. In a second step, we compiled the data from the three studies to perform an individual participant data meta-analysis, without the data of the CHOP 5.5 year follow-up. The association between outcome and metabolite was assumed to be the same across all studies (fixed effects model). LDL and HDL were not included in the meta-analysis due to the heterogeneity in the analytical methods to determine the lipoproteins. We furthermore included sex as a potential confounder. Additionally, the meta-analysis models for the HOMA level and metabolites were adjusted for BMI z-score. To quantify the variance explanation capacity of the metabolite in the respective outcome, we calculated the partial R2. Heterogeneity of the effect sizes was assessed using Cochran’s Q31. We furthermore repeated all analyses stratifying according to the child’s sex. We used the same models as described above without adjustment for sex.
Predictive analyses were based on the 5.5 and 8 years data from the CHOP study. For prediction, z-BMI and HOMA levels at 8 years were regressed on the metabolite concentrations of the 5.5 year follow-up in bivariate linear regression models and adjusted for either BMI z-score or HOMA at 5.5 years.
All p-values were adjusted for multiple testing by using the Bonferroni method. A Bonferroni corrected p-value < 0.05 was considered statistically significant.
BARCELONA, SPAIN, Oct 14, 2014 (Marketwired via COMTEX) -- HP HPQ, +2.26% and VMware today announced they are expanding their longstanding partnership to deliver HP ConvergedSystem 200-HC EVO: RAIL(TM), a hyper-converged infrastructure appliance powered by VMware EVO: RAIL. The HP ConvergedSystem 200-HC EVO: RAIL will provide midmarket and enterprises a radically simplified approach to purchasing, deploying, scaling and securing support for their software-defined IT infrastructure.
As organizations migrate from inefficient legacy systems, the complexities associated with building virtual infrastructure is fueling a 33 percent compound annual growth rate (CAGR) in the integrated systems market, which IDC estimates will grow from $5.4 billion in 2013 to $14.3 billion by 2017.(1) Hyper-converged systems are the next phase of the converged infrastructure evolution, aimed to help midsize businesses that require flexible, open architecture to simplify IT operations and transform the speed and efficiency of application service delivery.
"This collaboration between HP and VMware to deliver EVO: RAIL(TM) will provide organizations with an innovative approach to driving better business outcomes through a software-defined data center architecture," said Raghu Raghuram, executive vice president, Software-Defined Data Center Division, VMware. "Together, HP and VMware are helping customers dramatically simplify and accelerate the delivery of software-defined infrastructure services while lowering operating expenses."
Hyper-convergence introduces a new IT infrastructure delivery and consumption model with a software-centric architecture that tightly integrates compute, network, storage and management resources seamlessly. HP ConvergedSystem 200-HC EVO: RAIL promises to provide businesses a cost-effective solution to improve service deployment and new workload efficiencies. Customers will be able to quickly deploy a single appliance, enabling faster response times to business demands, simplified infrastructure administration and reduced operating costs.
"Today businesses are looking for more efficient ways to speed time to application and service delivery that reduce the strain on existing infrastructure, said Nariman Teymourian, senior vice president and general manager, Converged Systems, HP. "Our collaboration with VMware to deliver hyper-converged infrastructure reinforces our commitment to provide customers superior technology choices as they migrate from inefficient legacy systems to modern integrated infrastructure."
The HP ConvergedSystem 200-HC EVO: RAIL features a pre-integrated, pre-tested 100 percent VMware software stack, to provide high availability at both the compute and storage layers, with VMware vSphere(R), VMware Virtual SAN(TM), VMware vRealize(TM) Log Insight(TM) (formerly vCenter(TM) Log Insight(TM)), and the EVO: RAIL engine. VMware EVO: RAIL integrates these technologies to greatly simplify by consolidating IT resources into a single appliance, eliminating the need for complex integration and enabling new applications to come online quickly.
The EVO: RAIL engine radically simplifies appliance scale-out, management and operations. Customers benefit from time to value to first virtual machine in minutes, as well as non-disruptive patching and upgrades of the appliance. Software-defined infrastructure services can be deployed rapidly and in a repeatable reliable fashion starting with one appliance of four nodes and growing to four appliances of 16 nodes.
In addition, HP and VMware are jointly collaborating to extend HP OneView, an innovative management platform for convergence, to EVO: RAIL to offer customers greater efficiencies and an integrated experience. Architected for simplicity and convergence, in future releases HP OneView will be able to directly manage the EVO: RAIL appliance to help unify the management of the hyper-converged and traditional infrastructure deployments.
HP's new ConvergedSystem 200 line of hyper-converged solutions will feature two new solutions -- an HP EVO: RAIL version and an HP StoreVirtual version, offering customers greater choice and flexibility.
Pricing and Availability HP ConvergedSystem 200-HC EVO: RAIL is expected to ship in the first quarter of 2015. Pricing will be announced at general availability. Contact an HP channel partner to learn more about HP ConvergedSystem 200-HC EVO: RAIL.
Customers can purchase HP ConvergedSystem 200-HC EVO: RAIL as a single SKU covering hardware, software and support and services costs directly from HP's channel. HP will provide customers with single point-of-contact support for this hyper-converged infrastructure appliance.
VMware at VMworld(R) 2014 Europe VMware will feature its products and services in Hall 8.1 at VMworld Europe, held Oct. 14-16 at Fira Gran Via in Barcelona. VMware EVO: RAIL appliances will be featured at VMworld Europe in the EVO: ZONE.
View VMworld 2014 Europe keynotes live (and on-demand) on Oct. 14 and 15 at VMware Now.
About HP HP creates new possibilities for technology to have a meaningful impact on people, businesses, governments and society. With the broadest technology portfolio spanning printing, personal systems, software, services and IT infrastructure, HP delivers solutions for customers' most complex challenges in every region of the world. More information about HP is available at www.hp.com.
About VMware VMware VMW, +1.41% is the leader in virtualization and cloud infrastructure solutions that enable businesses to thrive in the Cloud Era. Customers rely on VMware to help them transform the way they build, deliver and consume Information Technology resources in a manner that is evolutionary and based on their specific needs. With 2013 revenues of $5.21 billion, VMware has more than 500,000 customers and 75,000 partners. The company is headquartered in Silicon Valley with offices throughout the world and can be found online at www.vmware.com.
VMware, VMware vSphere, vRealize Log Insight, vCloud, VMware EVO: RAIL, VMware Virtual SAN, VMware vCenter Log Insight and VMworldare registered trademarks or trademarks of VMware, Inc. in the United States and other jurisdictions. All other marks and names mentioned herein may be trademarks of their respective companies.
(1) IDC's Worldwide Integrated Systems 2014-2017 Forecast, March, 2014 IDC #246938.
This news advisory contains forward-looking statements that involve risks, uncertainties and assumptions. If such risks or uncertainties materialize or such assumptions prove incorrect, the results of HP and its consolidated subsidiaries could differ materially from those expressed or implied by such forward-looking statements and assumptions. All statements other than statements of historical fact are statements that could be deemed forward-looking statements, including but not limited to statements of the plans, strategies and objectives of management for future operations; any statements concerning expected development, performance, market share or competitive performance relating to products and services; any statements regarding anticipated operational and financial results; any statements of expectation or belief; and any statements of assumptions underlying any of the foregoing. Risks, uncertainties and assumptions include the need to address the many challenges facing HP's businesses; the competitive pressures faced by HP's businesses; risks associated with executing HP's strategy; the impact of macroeconomic and geopolitical trends and events; the need to manage third party suppliers and the distribution of HP's products and services effectively; the protection of HP's intellectual property assets, including intellectual property licensed from third parties; risks associated with HP's international operations; the development and transition of new products and services and the enhancement of existing products and services to meet customer needs and respond to emerging technological trends; the execution and performance of contracts by HP and its suppliers, customers and partners; the hiring and retention of key employees; integration and other risks associated with business combination and investment transactions; the execution, timing and results of restructuring plans, including estimates and assumptions related to the cost and the anticipated benefits of implementing those plans; the resolution of pending investigations, claims and disputes; and other risks that are described in HP's Quarterly Report on Form 10-Q for the fiscal quarter ended April 30, 2013 and HP's other filings with the Securities and Exchange Commission, including HP's Annual Report on Form 10-K for the fiscal year ended October 31, 2013. HP assumes no obligation and does not intend to update these forward-looking statements.
Copyright 2014 Hewlett-Packard Development Company, L.P. The information contained herein is subject to change without notice. The only warranties for HP products and services are set forth in the express warranty statements accompanying such products and services. Nothing herein should be construed as constituting an additional warranty. HP shall not be liable for technical or editorial errors or omissions contained herein. Intel and Xeon are registered trademarks of Intel Corporation in the United States and other countries.
VMware Forward-Looking Statements This press release contains forward-looking statements including, among other things, statements regarding the HP ConvergedSystem 200-HC EVO: RAIL, its expected features and benefits to customers and expectations for the CAGR of the integrated systems market through 2017. These forward-looking statements are subject to the safe harbor provisions created by the Private Securities Litigation Reform Act of 1995. Actual results could differ materially from those projected in the forward-looking statements as a result of certain risk factors, including but not limited to (i) changes to business information technology strategies; (ii) adverse changes in general economic or market conditions; (iii) delays or reductions in information technology spending; (iv) competitive factors, including but not limited to pricing pressures, industry consolidation, entry of new competitors into enterprise, cloud and end user computing markets, and new product and marketing initiatives by our competitors; (v) our customers' ability to develop, and to transition to, new products and computing strategies such as software-defined data centers and hybrid cloud computing; (vi) the uncertainty of customer acceptance of emerging technology; (vii) rapid technological and market changes in virtualization software and platforms for cloud and enterprise computing; (viii) changes to product development timelines; (ix) VMware's ability to protect its proprietary technology; (x) changes and new developments to regulatory requirements; and (xi VMware's ability to attract and retain highly qualified employees. These forward looking statements are based on current expectations and are subject to uncertainties and changes in condition, significance, value and effect as well as other risks detailed in documents filed with the Securities and Exchange Commission, including our most recent reports on Form 10-K and Form 10-Q and current reports on Form 8-K that we may file from time to time, which could cause actual results to vary from expectations. VMware assumes no obligation to, and does not currently intend to, update any such forward-looking statements after the date of this release.Editorial contacts Stefanie Cannon HP +1 650 236-4001 firstname.lastname@example.org Ken Lotich VMware +1 916 740 4335 KLotich@vmware.com www.hp.com/go/newsroom
(C) 2014 Marketwire L.P. All rights reserved.
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