#cytogenomic

[mplnet]

How Can Cytogenomics Help Solve Women's Health Challenges?

Have you ever asked yourself why a particular health condition occurs more often in women than in men? Why does a specific treatment work for one woman and not another? Perhaps it is in your genes. Cytogenomics is the study of how genes work in cells, and it has opened entirely new doors to women's health care. But just how could this science make a difference in your life?

Understanding Cytogenetic

Cytogenomics is the amalgamation of cytology, the science of cells, and genomics, the study of genes. It examines the way in which genes operate within a cell and how that manner influences health. This field is changing the way doctors observe Women's Health.

The Power of Precision:- This, in turn, allows doctors to have a better understanding of what is occurring inside the body level. That is, they can detect diseases at an earlier stage so that developing proper treatment plans for you can be initiated. It's almost like having a microscope that zooms on the problems at a cellular level.

Personalized Medicine: Every woman is unique in her own way, and so are her healthcare needs. Cytogenomics helps doctors tailor treatments to fit each woman's unique genetic makeup. It often leads to better results and fewer side effects. It's a bit like a custom-made health plan just for you.

Cytogenomics in Action

Let's take a detailed exploration into how cytogenetic is changing the landscape of female health.

Early Detection and Treatment for Breast Cancer:- Through cytogenomic, the time for the detection of breast cancer might be significantly advanced. Which treatment options are suitable for a specific woman? This could mean better care and even an opportunity to win the battle against the disease when done better. Doctors can now diagnose the genetic manifestations of cancer before they appear observable by classical means.

Fertility and Pregnancy:- Cytogenetic may raise questions for infertile women. It can explain why, at times, women cannot get pregnant and why some doctors are often puzzled in trying to help them. In addition, it finds potential problems while pregnant so that both mom and baby have a better chance of staying healthy.

Management of Menopause: Every woman's menopausal experience is unique. Cytogenetic would tell doctors why and could help them develop customized symptom-management plans. That's like having a roadmap for this great change in life.

Making Sure It Works: The Importance of Validation

Of course, any new medical approach needs to be tested thoroughly. That's where Validation comes in. Scientists run many tests to ensure that cytogenetic techniques are accurate and reliable.

This step is crucial. It ensures that the results are trustworthy when your doctor uses cytogenetics to help you. Validation gives both doctors and patients confidence in the science. It's like double-checking your work to make sure everything adds up.

Conclusion

So, what does all this mean for you? It means better health care tailored just for you. It means answers to questions you might have had about your health for years. And it means hope for better treatments for conditions that affect women.

As cytogenetic advances, it's paving the way for a new era in women's health. This field transforms how we approach women's health challenges from more accurate diagnoses to more effective treatments.

Cytogenetics is a groundbreaking science that examines the smallest parts of our bodies, our cells, and genes – helping solve big health problems. Thanks to this, the future of women's health looks brighter than ever. Read More.

[cytgen]

Abstract With this study, we aim to summarize and assess the activity and performance of the Cytogenetic sector of the Laboratory of Medical Genetics—Varna, regarding the conventional cytogenetic analysis of bone marrow samples from patients with (onco)hematological diagnoses. Another purpose is to evaluate the tendencies noticed over a period of eleven years to draw conclusions and share our experience. We have performed the analysis with the G-banding technique on 2653 samples from patients of age 0–93 yr by the current European recommendations and the International System for Human Cytogenomic Nomenclature. The greater part of these samples (90.9%) was with an indication of a hematological malignancy, most commonly Acute myeloid leukemia, Myelodysplastic syndrome, Acute lymphoid leukemia, Chronic myeloid leukemia, and Multiple myeloma. Analysis was successful in 2215 (83.5%)—from those normal karyotypes were found in 1492 (67.4%) and pathology in 723 (32.6%). Regarding the latter, the most common were complex karyotypes (30.6%), Philadelphian chromosome (21.3%), trisomy 8 (5.9%), and deletion in the long arm of chromosome 5 (4.3%). Cytogenetic analysis is a method with great impact on the evaluation of many hematological malignancies and for this reason, it remains an essential part of routine assessment of these diseases. The disadvantages of it mainly in the field of oncohematological diseases, recognized by the scientific society and confirmed in our own experience, suggest a need for an additional genetic method to overcome these limitations.

[rebeccavoszphlebotomycareers]

Cytogenomics demonstrates that chromosomes are crucial in understanding the human genome and that new high-throughput approaches are central to advancing cytogenetics in the 21st century. After an introduction to (molecular) cytogenetics, being the basic of all cytogenomic research, this book highlights the strengths and newfound advantages of cytogenomic research methods and technologies, enabling researchers to

[ffrepos]

PATH3305 - UWA

Medical Genetics (2018, Sem 1)

Unit coordinator: Dr Clayton Fragall

L1-7 (Mid Sem 1): pp. 4-5 (Organisation of Human Genome) 14 & 17 (Human Genetic Variation) 20-21, 31-32 (Mechanisms of Mutation) 35-36 (Cytogenomics) 37-42** (Population Genetics)

L9-16 (Mid Sem 2): pp. 3-4, 9-10: Interpret thermal curve (Detection of Genetic Variation) 16: No. of exomes sequenced (Overview of NGS) 19-20, 23-25, 27, 29-30 (Phenotypic consequences of genetic variants) 36, 47: Understand all the detection methods & in which situations should each method be used; pros & cons (DNA CNVs: Methods of Detection & Disease)

CNV Detection summary table

48, 50-54: Prevalence of CML & ALL, special cases (Cancer cytogenomics) 55, 57-58 (Pharmacogenetics) 65 (Genetic diagnostic strategies)

L17-22: pp. 1-3: Risk factors (Familial Hypercholesterolaemia) 5-6: Inheritance pattern of hypoalphalipoproteinemia & FHBL (Rare lipid disorders) 11-13, 16: Diseases screened and screening methods (Newborn screening) 17-25: Understand mutational hotspots, causative genes & upregulation treatment (Finding disease genes & Genetic muscle diseases) 26: Introduces many concepts for PATH3308 (Investigating Therapies for NMD)

L23-24: pp. 1-3: Starred items (Mitochondrial Genetics) 4-7: Just appreciate that these are very complicated (Mitochondrial Diseases)

L25-26: See starred items in summary slides (Psychiatric Genetics)

L27: p.1 (Epigenetic Variation)

[oamazonico]

O Amazonico apoia projeto de pesquisa para a conservação da Panthera onca (onça pintada), em seu habitat natural . Esforços têm sido feitos juntando pesquisadores de renome para dar os primeiros passos . #jaguarbiodiversity #pantheraonca #cytogenomics https://www.instagram.com/p/CPVhk9ll-r4/?utm_medium=tumblr

[evoldir]

Fwd: Graduate position: UppsalaU.PrimateSpeciationPopGen

Begin forwarded message: > From: evoldir@evol.biology.mcmaster.ca > Subject: Graduate position: UppsalaU.PrimateSpeciationPopGen > Date: 25 January 2020 at 06:52:13 GMT > To: rdmpage@gmail.com > > > A PhD student position in Primate Speciation and Population Genomics > is available in the group of Katerina Guschanski at the Department of > Ecology and Genetics, Uppsala University, Sweden. For more information > about the department see www.ieg.uu.se. > > Project description: > Our group is broadly interested in understanding how long-term > evolutionary and short-term human-mediated processes shape biological > diversity. The advertised project has the goal to study primate evolution > from multiple angles and on different evolutionary time scales.  You will > have the chance to study population and species level processes in a > number of primate taxa using newly generated and publically available > genomic data. Research topics include, but are not limited to: > > i) Speciation genomics and the role of ancient hybridization in driving >   species diversity. You will focus on a group of highly diverse >   African monkeys (guenons) that are renown for their ecological, >   morphological and karyotypic diversity and readily hybridize in >   captivity and the wild. Although the main focus will be on speciation >   genomics, there are possibilities to extend this project to include >   cytogenomics, morphological and ecological analyses, depending on the >   candidate’s interests. > > ii) Population and conservation genomics. Using target DNA capture from >    fecal samples you will study genetic diversity, population >    structure, demography and local adaptation in wild primate >    populations. The generated insights will have direct relevance for >    conservation decision-making. > > The exact project will be developed with the successful candidate and > tailored towards their interests and skills. > > Duties: > The selected candidate will mainly engage in large-scale phylogenomic and > population genomic analyses that require solid bioinformatics skills, but > will also conduct work in the wet lab to produce genomic sequencing data > from non-invasively collected low-quality samples. Duties include active > participation in the research group activities, training of junior group > members in relevant techniques and engagement in collaborative projects. > > Qualifications required: > To be eligible for a PhD-student position the applicant must hold a > master degree (or equivalent) in evolutionary biology, bioinformatics, > or a related field. The technical skills of the candidates will be > evaluated based on the experience with large-scale sequence analysis, > bioinformatics proficiency and experience with phylogenomic and population > genomic studies. The ideal candidate will have a strong interest and > documented knowledge in evolutionary biology, with a drive to understand > processes shaping species diversity. Perseverance and high intrinsic > motivation are required to work on non-model organisms using difficult > samples and data. You will be highly reliable, driven and well-organized, > curious and willing to think outside the box, with the ability to quickly > acquire new skills. Proficiency in spoken and written English is required. > > Qualifications desired: > Previous experience with wet lab molecular techniques, ideally with > low-quality samples, is highly desired. > > Starting date: > As early as possible, ideally by 2020-04-01 or as otherwise agreed. > > Position: > The graduate program covers four years of full-time study. The position > can be combined with teaching or other duties at the department (maximum > 20%), which prolongs the employment with the corresponding time. > > How to apply: > The application should include 1) a cover letter describing your research > interests, your proficiency with molecular laboratory techniques and > programming, experience in handling genomic data, other technical skills > relevant for the project, as well as other qualifications that make you > a suitable candidate, 2) your CV, including any produced publications, > 3) a copy of your master degree, your course grades and a copy of your > master thesis, if available, 4) the names and contact information of > 2-3 reference persons (e-mail address and phone no; you are welcome to > include this information at the end of your cover letter or as attachment > under point 6 of the online application form). As the application form > requires you to upload Description of your education under point 2, you > are welcome to upload your CV here, as long as it provides the relevant > information. You are also not required to fill out other tabs, as long > as your CV covers the relevant points. The application should be written > in English. > > To apply, please follow this link (UFV-PA 2020/247): > https://ift.tt/2NVHjgG > https://ift.tt/37sjdBX > > You are welcome to submit your application no later than 2020-02-24. > > For further information about the position please contact: > Katerina Guschanski: katerina.guschanski@ebc.uu.se, +46 18 471 2673. > > > Katerina Guschanski > Associate professor > Evolutionary Biology Centre > Department of Ecology and Genetics/Animal Ecology > Uppsala University > Norbyvägen 18D > SE-752 36 Uppsala, Sweden > > Lab page: https://ift.tt/2su9mMG > Office: +46 (0)18 471 2673 > Email: katerina.guschanski@ebc.uu.se > > Katerina Guschanski > via IFTTT

[yedita83]

Hoy los seminarios bibliográficos estuvieron aún más interesantes~☆ Artículos de casos clinicos e investigación en laboratorios de Países Asiáticos, en estos dos casos fueron en Japón (Osaka y Tokio) y China (Hong Kong)~♡ lalala~ #geneticdepartment #molecularbiology #dna #cytogenetics #cytogenomic #genomicmedicine #chromosomesrules #qcb #uanl #proudchemist (en Facultad de Medicina. UANL)

[daniels09stuff]

Top CPT Codes And Modifiers For Pathology Medical Billing

Just as any other medical specialty, Pathology too, needs accurate documentation for generating any patient’s medical report. For a pathologist, when taking care of pathology billing and coding, it’s absolutely important to acquire prompt and accurate pathology reports in order to ensure successful reimbursements.

Whether it’s a clinical lab, a physician office lab or even an independent lab, each of these will have different needs and ways to deal with issues related to patient documentation, payer types, or set of procedures. Also, billing for pathology involves a huge variety of different code types and it’s essential for pathologists to be fluent in it while staying updated with the periodic updates.

What Is CPT®?

Pathologists will need to accurately use CPT® which is the medical code set for physicians and health care professionals. Current Procedural Terminology, commonly known as CPT® acts as a uniform language for coding billing medical services and procedures for reimbursements in order to streamline reporting, increase accuracy and efficiency. Each CPT® code represents a written description of a service or procedure that eliminates the need to write a detailed interpretation of what was rendered to a patient. CPT® codes were created by the American Medical Association (AMA) in 1996 to standardize the reporting of medical, surgical, and diagnostic offerings and procedures.

Considering the various services and procedures, the AMA has organized CPT® codes into three types:

CPT® Category I

CPT® Category II

CPT® Category III

Codes used in Pathology Billing and Coding:

CPT codes (dermatologists)- 88300 to 88332

Level III surgical pathology (abscess, anus, hematoma, etc.)- 88304

Level IV surgical pathology or microscopic examination (lip, skin tongue, etc)- 88305

CPT New Codes:

Obstetric panel (including HIV testing) – 80081

Molecular Pathology Procedures – Gene Specific and Genome procedures- 81170, 81162, 81218, 81219, 81272, 81273, 81276, 81311, 81314.

Cytogenomic microarray analyses- 81228, 81229, 81405, 81406

Long QT syndrome gene analyses- 81280, 81282

Genomic Sequencing Procedures and other Molecular Multianalyte Assays- 81412, 81432, 81433, 81434, 81437, 81438, 81442

Multianalyte Assays with MAAAs- 81490, 81493, 81525, 81528, 81535, +81536, 81538, 81540, 81545, 81595, 0009M, 0010M

Immunofluorescence Stains- +88350

CPT Revised Codes:

Molecular Pathology- 81210, 81275, 81355, 81401, 81402, 81403, 81404, 81405, 81406

Genomic Sequencing Procedures and other Molecular Multianalyte Assays- 81435, 81436, 81445, 81450, 81455

Chemistry– 82542, 83789

Immunology– 86708, 86709

Microbiology– 87301, 87305, 87320, 87324, 87327, 87328, 87329, 87332, 87335, 87336, 87337, 87338, 87339, 87340, 87341, 87350, 87380, 87385, 87389, 87390, 87391, 87400, 87420, 87425, 87427, 87430, 87449, 87450, 87451, 87502, +87503

Surgical Pathology- 88346

What is a Modifier?

Modifiers help alter a service, method, or item for compensation purposes in specific instances. To provide greater specificity for the treatment or process given, modifiers may add information or amend the description in accordance with physician documentation. The use of an appropriate modifier to respond to reimbursement can prove to be a success.

Read More : 

[thecryptoreport]

Weekly Stock Market Update: Deliveroo Value Rises to More Than $7 Billion Ahead of Future IPO

Weekly Stock Market Update: Deliveroo Value Rises to More Than $7 Billion Ahead of Future IPO

Last Week’s Top Five Market Winners Nasdaq Stock Market (NASDAQ) The past seven days welcomed positive results for BioNano Genomics Inc. (BNGO), Tilray Inc. (TLRY), Globalstar (GSAT), Gevo Inc. (GEVO) and Tellurian Inc. (TELL) on the Nasdaq Stock Market. BioNano Genomics Inc. (BNGO) stocks had another strong week, up +79.36% following the company’s Next-Generation Cytogenomics Symposium.…

[1librarynet]

Abstracts of the 12th European Cytogenomics Conference 2019 https://bit.ly/3gY3w9N

[marketnewssize]

The launch of technologically advanced products of flow cytometry and a higher adoption rate of these products in various research and diagnostic applications are some factors which boost the market growth. The advent of flow cytometry technology in novel research applications, such as cytogenomics, proteomics, and marine cell biology is a factor which further intensifies the progress of the flow cytometry market in the forecast period of 2020-2027. On the other hand, factors such as high cost associated with instruments and reagents, lack of awareness among potential end users, and the limited availability of technical expertise are likely to impede the flow cytometry market growth.

[leedsomics]

New Tools for Hop Cytogenomics: Identification of Tandem Repeat Families from Long-Read Sequences of Humulus lupulus

Hop (Humulus lupulus L.) is known for its use as a bittering agent in beer and has a rich history of cultivation, beginning in Europe and now spanning the globe. There are five wild varieties worldwide, which may have been introgressed with cultivated varieties. As a dioecious species, its obligate outcrossing, non-Mendelian inheritance, and genomic structural variability have confounded directed breeding efforts. Consequently, understanding genome evolution in Humulus represents a considerable challenge, requiring additional resources, including integrated genome maps. In order to facilitate cytogenetic investigations into the transmission genetics of hop, we report here the identification and characterization of 17 new and distinct tandem repeat sequence families. A tandem repeat discovery pipeline was developed using k-mer filtering and dot plot analysis of PacBio long-read sequences from the hop cultivar Apollo. We produced oligonucleotide FISH probes from conserved regions of HuluTR120 and HulTR225 and demonstrated their utility to stain meiotic chromosomes from wild hop, var. neomexicanus. The HuluTR225 FISH probe hybridized to several loci per nucleus and exhibited irregular, non-Mendelian transmission in male meiocytes of wild hop. Collectively, these tandem repeat sequence families not only represent unique and valuable new cytogenetic reagents but also have the capacity to inform genome assembly efforts and support comparative genomic analyses. http://dlvr.it/RPLjtB

[expertofmarketinsights-blog]

Global Flow Cytometry Market analysis 2026

Increasing novel application of flow cytometer, such as cytogenomics, proteomics, and marine cell biology, is expected to drive the flow cytometry market in near future. Whereas, increasing demand for flow cytometry in hospitals and diagnostic centers for the effective diagnosis as well as monitoring of diseases supports the growth of market. Moreover, limited availability of technical expertise hampers the growth of flow cytometry market.

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Market Dynamics

Flow cytometry is quite an unexplored field, which is rapidly advancing due to technological advancements in the recent past. The increasing FDA approval for various clinical test favors the growth of flow cytometry market in near future. For instance, in 2017 the use of flow cytometer in detection of leukemia & lymphoma cancers was approved by FDA. Therefore, rising prevalence of HIV and cancer favors the growth of flow cytometer market.

Whereas, number of advantages of flow cytometer over traditional analytical methods such  as, ELISA that include the ability of flow cytometer to deliver precise and accurate results in less time, with same price.

Furthermore, in 2017 there were number of product launches, which supports the growth of flow cytometry market in near future. For instance, Beckman Coulter Life Sciences received FDA approval for product named the Navios EX flow cytometer in August 2107.

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Key features of the study:

This report provides an in-depth analysis of global flow cytometry market provides market size (US$ Million) and Cumulative Annual Growth Rate (CAGR %) for the forecast period (2017 – 2025), considering 2016 as the base year

It elucidates potential revenue opportunities across different segments and explains attractive investment proposition matrix for this market

This study also provides key insights about market drivers, restraints, opportunities, new product launches or approval, regional outlook, and competitive strategy adopted by the leading players

It profiles leading players in the global flow cytometry market based on the following parameters – company overview, financial performance, product portfolio, geographical presence, distribution strategies, key developments and strategies, and future plans

Key companies covered as a part of this study include Becton Dickinson and Company, General Electric Company, Luminex Corporation, Thermo Fisher Scientific, Inc., Bio-Rad Laboratories, Inc., Miltenyi Biotec GmbH, Merck & Co Inc., Sysmex Corporation, Agilent Technologies, Inc. and Danaher Corporation.

Insights from this report would allow marketers and the management authorities of the companies to make informed decisions regarding their future product launch, technology up-gradation, market expansion, and marketing tactics

The global flow cytometry market report caters to various stakeholders in this industry including investors, suppliers, flow cytometry manufacturers, distributors, new entrants, and financial analysts

Stakeholders would have ease in decision-making through the various strategy matrices used in analyzing the flow cytometry market

Detailed Segmentation:

Global Flow Cytometry Market, By Technology:

Cell Based

Bead Based

Global Flow Cytometry Market, By Product:

Analyzer

Sorter

Reagents & Consumables

Global Flow Cytometry Market, By End User:

Hospitals

Clinical Testing Labs

Research Laboratories

Global Flow Cytometry Market, By Geography:

North America

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Coherent Market Insights is a prominent market research and consulting firm offering action-ready syndicated research reports, custom market analysis, consulting services, and competitive analysis through various recommendations related to emerging market trends, technologies, and potential absolute dollar opportunity.

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[wenitinblog-blog]

Microarray Analysis expected to grow with a healthy CAGR BY 2027

Microarray Analysis Market Reports contains broad essential research alongside the point by point examination of subjective and additionally quantitative viewpoints by different industry specialists, key feeling pioneers to pick up the more profound understanding of the market and industry execution.

Life science relates to the study of living organisms which includes plants, humans, and microorganisms among others.

With unparalleled network, advancing socioeconomics, noteworthy development in patent applications in developing markets and pharmaceutical request changes around the world, the pattern of Life science is likewise changing and moving forward.

The center rule behind microarrays is hybridization between two DNA strands, the property of corresponding nucleic corrosive successions to explicitly combine with each other by framing hydrogen bonds between correlative nucleotide base sets.

Get Sample Report @ https://www.marketresearchfuture.com/sample_request/777 .

Global Microarray Analysis Market is driven by factors which include increasing government expenditure, growth in research and development activities need for early cancer detection, increasing healthcare expenditure, and diagnosis and large-scale DNA/gene chip initiatives. Microarray helps to reduce criticality occurred during the understanding of the cell and its associated diseases. It is utilized for the investigation of natural materials, for example, DNA, RNA, little tissues, or protein, by immobilizing them on silicon-thin film. It is assessed that 2 million building and life science occupations will wind up noticeably open amid estimated period because of proceed with ascend in maturing populace. Microarray, the blend of mechanical robotics, chemistry, computer science, and biology are utilized to think about many focuses inside a genome which is made out of thousands of qualities at one time.

Global Microarray Analysis Market Report: Application

The components, for example, worldwide development, increment tax assessment by government, mindfulness about training in Life science field, enhanced R&D use driving worldwide interest for hereditary examination which incorporates Microarray, populace genomics, and atomic science among other life science contemplate zones.

Microarrays are useful for processing thousands of samples cost-effectively to identify transformations and structural variations in gene expression and methylation. Microarray analysis is been used in various industries such as healthcare, life science, medical among others. For instance, cancer germline mutation analysis is used to study cancer predisposition, cytogenomics is useful in detection of low-level mosaics, CNV’s, LOH, across the genome, Agrigenomics genotyping is used for the study about plants and animals, and many more.

Global Key Players:

Applied Microarrays, biome rieux SA, Discerna, Gyros AB, Luminex Corporation, NextGen Sciences, PLC. and ProteoGenix, Affymetrix, Inc., Agilent Technologies, Inc., Sequenom, Inc., Roche NimbleGen, Illumnia, Inc.

Browse Report @ https://www.marketresearchfuture.com/reports/global-microarray-analysis-market .

The advantages of Microarray analysis includes:

Reproducible, high-quality data at a low cost

Support fast, high throughput, multiplex processing

Available in expert and custom formats

Global Microarray Analysis Market Report: Market Segmentation

Global Microarray Analysis Market can be segmented into types, methods, applications, and end-users.

Global Microarray Analysis Market by Applications:

SNP detection, Genotyping, Forensic analysis, Research, Diagnostics, Others

Global Microarray Analysis Market by End-users:

Pharmaceuticals, Medical, Healthcare, Laboratories, Others

Global Microarray Analysis Market by Types:

DNA Microarray, LOC (Lab-on a-Chip), Protein Microarray, Tissue Microarray, Others

Global Microarray Analysis Market by Methods:

Human genotyping, Non-human genotyping, Gene expression analysis, Methylation analysis, Mutation analysis, others

Global Microarray Analysis Market Report: Regional Analysis

The regional analysis includes North America, Europe, Asia Pacific, Middle East and rest of the world.

Increasing clinical trials and drug discovery activities, upgrading technological advancements such as Chip-on-chip, CGH, splice variants and microRNAs, wider application area of microarray and government initiatives and support are expected to develop new market opportunities for the Global Microarray Market. Moreover, increasing mergers and acquisition, growing collaborations and partnerships, and product launches are some of the latest trends in the Global Microarray Market.

North America:

North America is dominating the Global Microarray Analysis Market followed by Europe. Increasing technological advancement, improved healthcare industries, growing research & development activities, increased usage of personalized medicines, increasing cancer incidences and growing government support are the major growth driven factors of Microarray market in North America region.

Asia-pacific:

Asia-pacific is the emerging market in Global Microarray Analysis Market during the forecasted period. The improving healthcare infrastructure, growing prevalence of chronic diseases, increasing government expenditure, growing drug discovery and development activities are the major growth drivers of Microarray Market in Asia-Pacific region. The China, Russia and India are the emerging economies due to improved lifestyle, growing awareness about biological terms and its benefits and government support in Asia-Pacific region. In India, top Indian pharma companies are now partly foreign-owned and are already generating more than half of their sales outside the country. Besides this, economic growth has increased the buying power of India’s middle class for healthcare services in general, particularly medicines. Emergence of lifestyle diseases such as diabetes, cardiovascular disease and cancer has increased the demand for medicines.

Global Microarray Analysis Market Report: Latest News

Molecular Devices Launches High-Content Imaging System with New 3D Analysis Software, announced on 19th April 2016.

The Agilent Cary 8454 UV-Visible spectrophotometer builds on 30 years of experience in photodiode array (PDA) technology and delivers an updated instrument that is easy to use, is ideal for routine applications, and meets the compliance needs of global pharmaceutical companies.

Microarray Analysis Market Report: Global Market Influencer

Adoption of personalized medicines, wide range of application areas, and technological advancements are other factors which are driving the Microarray market.

However, standardization in microarray data and lack of skilled professionals are some of the major factors hindering the growth of the Global Microarray Analysis Market.

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[oamazonico]

O Amazonico apoia projeto de pesquisa para a conservação da Panthera onca (onça pintada), em seu habitat natural . Esforços têm sido feitos juntando pesquisadores de renome para dar os primeiros passos. A onça em questão , só foi sedada pelos melhores veterinários , aliás gostaria de parabenizar o grupo, pelo excelente trabalho . #jaguarbiodiversity #pantheraonca #cytogenomics (at Curitiba, Brazil) https://www.instagram.com/p/CPVaAo6FYCw/?utm_medium=tumblr