Genomics Research

The Illumina Library Prep and Array Kit Selector is an interactive online tool designed to help researchers identify the most suitable sequencing library preparation kits and microarrays for their specific projects, including studies in complex disease genomics. By using customizable filters such as research area, application method, species, and system compatibility, users can quickly narrow down options to find kits that match their experimental requirements. This tool streamlines the library selection process, enabling researchers to efficiently compare, share, and order kits tailored to their study needs. Key Features: Customized Filtering: Apply filters by research area, application method, species, and system to find relevant kits. Comprehensive Results: Access a wide range of library prep kits and microarrays suitable for complex disease genomics. User-Friendly Interface: Easily compare, share, and order kits directly through the platform. Research-Focused: Designed specifically for research applications in genomics and molecular biology. Note: The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 84461 74263, +91 98508 70860. Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. Trademarks, service marks, and logos herein are for product identification only. No association with mark owners is claimed unless explicitly specified.Meaning of List Number: R Refurbished | PO Preowned | U Used | T Trading | M Own Manufactured | AD Authorized Dealer of Original Equipment Manufacturer

The 10x Genomics Chromium Controller is a benchtop instrument designed to automate the partitioning of single-cell suspensions into nanoliter-scale Gel Bead-in-Emulsions (GEMs) for high-throughput single-cell analysis. Utilizing microfluidic technology, it enables the generation of millions of individual GEMs, each containing a single cell and its associated reagents. This process is essential for applications such as single-cell RNA sequencing, immune profiling, and chromatin accessibility studies. Note- The price mentioned above is for reference only. Do not consider it for purchase. For the actual price and more product details, please contact us at +91 98508 70860, +91 84461 74263. Key Features High-Throughput Processing Microfluidic Technology Automated Workflow Disclaimer: UNLESS OTHERWISE INDICATED, THE CONTENT OF THIS WEBSITE IS THE PROPRIETARY PROPERTY OF ITS OWNERS. However, trademarks, service marks and/or logos (called "marks") herein associated with the products listed on this website are the property of their respective owners. If they appear with the listed products, it is only used for the purpose of identification of those products. We do not claim any association with the mark owners, unless otherwise so specified. MEANING OF LIST NUMBER: R Refurbished, PO Preowned, U Used, T Trading, M Own Manufactured, AD - Authorized Dealer of Original Equipment Manufacturer.

Note:-The price mentioned above is virtual, do not consider it for purchase. For actual price and more product details, please contact us at +91 97663 07660 and +91 98505 58881 Product Description:The Microbial Genomics Mix is a specialized solution designed for the comprehensive analysis of microbial genomes. By utilizing advanced sequencing technologies, it enables the identification, characterization, and tracking of bacterial, viral, and fungal species at a genomic level. This mix is ideal for applications such as pathogen surveillance, antimicrobial resistance studies, and microbiome research. It offers high sensitivity for detecting genetic variations, mutations, and virulence factors, which are essential for understanding infectious diseases and developing effective treatments. The Microbial Genomics Mix provides valuable insights into microbial diversity, evolution, and epidemiology, contributing to advancements in public health and microbiology research. UNLESS OTHERWISE INDICATED THE CONTENT OF THIS "WEBSITE" IS THE PROPRIETARY PROPERTY OF ITS OWNERS. HOWEVER, TRADEMARKS, SERVICE MARKS AND/OR LOGOS [CALLED "MARKS"] HEREIN ASSOCIATED WITH THE PRODUCTS LISTED ON THIS "WEBSITE" ARE THE PROPERTY OF THEIR RESPECTIVE OWNERS AND IF THEY APPEARS WITH THE LISTED PRODUCTS, IT IS ONLY USED FOR THE PURPOSE OF IDENTIFICATION OF THOSE PRODUCTS. WE DO NOT CLAIM AS ASSOCIATION WITH THE MARK OWNERS, UNLESS OTHERWISE SO SPECIFIED. List No. r MEANING OF MEANS REFURBISHED, "PO" MEANS PREOWNED, "U" MEANS USED, "T" MEANS TRADING, "M" MEANS OWN MANUFACTURED, "AD" MEANS AUTHORISED DEALER OF ORIGINAL EQUIPMENT MANUFACTURER.he Prices.

We are a unique name in the industry to provide our precious clients the best quality Human Genetics Testing Project. The provided service is carried out by our skilled team of professionals in the best possible manner. While performing this service, our experts ensure that the offered service delivers precision results and is within the budget to attain maximum clients satisfaction. Moreover, this service is widely acknowledged by our valuable clients for its flawlessness and hassle free execution.

Length in bp Turn Around Time in Days 100-1000 8 1000-1500 10 1500-2000 12 2000-3000 15 Deliverables: 2 - 5 ug of lyophilized Gene fragment / cloned gene Sequence trace data with alignment Sanger sequencing electropherogram The genes will be cloned into our default pUC57-Amp or pUC57-Kan vectors with multiple cloning sites. We can also clone the genes into customers supplied vectors upon request Competitive Advantages Affordable price, plus free subcloning to most commercial vectors. Free codon optimization to deliver maximal functional protein expression. Simple or complex genes, all at same prices. Stringent quality control with 100% Sanger sequencing accuracy. Consultation personal support throughout the entire project.

Next Generation Sequencing based genomics reaserch services using Illumina, PacBio, ONT (oxford nanopore) platform and comprehensive bioinformatics service

Metabolic analysis denotes the current health status of an individual. This information helps the physician in choosing treatment methods that are most appropriate for the individual. The goal of treatment is optimal management as well as prevention of diseases. Metabolic analysis is done by assessing the nutritional, biological, biochemical and hormonal status of the individual. Based on metabolic analysis, different health management modules are being recommended, the modules being: Gene therapy - This is a futuristic technique of treating diseases by using genes instead of drugs or surgery. This technique may allow a health practitioner to treat a health disorder by inserting a gene into the patient's cells instead of administering drugs or performing surgery.Nutrigenomics - Nutrigenomics, as discussed, is the study of the effect of food on gene expression. Understanding the diet-genome interactions in an individual will help the physician in choosing the right nutrition to ensure proper disease management which can eventually prevent disease, thus gradually reducing the necessity for drugs.Pharmacogenomics - Parmacogenomics, as discussed, studies how variation in the genes of an individual effects variation in his or her response to drugs. Based on the information on a person's genetic makeup, the physician is able to choose the appropriate drug and the appropriate dosage that would ensure optimal health for the patient. Metabolic analysis helps doctors follow a holistic approach to health. Focus is not only on treatment and management of diseases but also on prevention of the diseases that the individual is vulnerable to. The goal of treatment is to ensure maximum life span with maximum quality of life.

GENOMICS Genus ABS is on the cutting edge of technology, with ABS first implementing DNA marker selection in 1996. Our sister company PIC has more

Next generation sequencing technologies have increased data output volumes and lowered the cost of DNA sequencing beyond what is possible with standard dye-terminator methods. This has lead to a significant advancement of understanding of several epigenetic mechanisms, namely genome-wide DNA methylation and protein-DNA interaction. We offers many inexpensive solutions for next-generation sequencing including full package kits to conveniently construct high quality DNA libraries from low quantity or difficult samples.

Resequencing genomes where a reference genome is available. The genome is randomly sheared and libraries constructed for sequencing and aligned against the reference genome.

A wide range of Genomics services to assist your scientific research.

Microsatellite Instability Testing Products

The general whole-genome sequencing workflow starts with the generation of sequencer-ready DNA fragment libraries from genomic DNA. For whole-genome sequencing, the combination of short inserts and longer reads allow characterization of any genome. For de novo WGS, the unparalleled raw read accuracy of Illumina next-generation sequencing (NGS) technology provides high quality, long contig assemblies.

Eurofins Genomics represents the genomic division within the Eurofins Scientific Group. With facilities in Europe, the United States and Asia, Eurofins Genomics is an internationally leading provider of DNA sequencing services, genotyping services, DNA synthesis products and bioinformatics services for pharma, diagnostics, food, agriculture, biotechnological and research markets.

Genomics

Eurofins Genomics represents the genomic division within the Eurofins Scientific Group.With facilities in Europe, the United States and Asia, Eurofins Genomics is an internationally leading provider of DNA sequencing services, genotyping services, DNA synthesis products and bioinformatics services for pharma, diagnostics, food, agriculture, biotechnological and research markets.

Genotyping Services

CCR5 32 Detection by Molecular Method | Transplant Genomics Awesome Genetics offers CCR5 32 Detection by Molecular Method, an advanced Transplant Genomics test designed to identify the CCR5 32 (32-base pair deletion) mutation in the CCR5 gene. This genetic variant is clinically significant in transplant medicine, immunogenetics, infectious disease research, and precision medicine, as it influences immune function and susceptibility to certain diseases. Using advanced molecular diagnostic technology, the test accurately detects the presence or absence of the CCR5 32 mutation, providing reliable genetic information for clinical evaluation, research applications, and transplant-related assessments. CCR5 32 detection may support donor evaluation in specialized transplant settings, genetic risk assessment, and research involving immune system function and HIV resistance. The test is recommended for transplant centres, immunology laboratories, research institutions, infectious disease specialists, and clinicians requiring accurate CCR5 genotyping for diagnostic or research purposes. At Awesome Genetics, all transplant genomics tests are performed using advanced molecular laboratory platforms, validated protocols, and stringent quality assurance standards to ensure highly accurate, reliable, and timely diagnostic reports. Applications: CCR5 32 Mutation Detection Transplant Genomics Donor Genetic Evaluation Immunogenetic Assessment Infectious Disease Research HIV Resistance Genetic Studies Precision Medicine Clinical and Research Applications Key Features: Accurate detection of the CCR5 32 mutation Advanced molecular diagnostic technology High analytical sensitivity and specificity Supports transplant and immunogenetic evaluation Reliable and confidential reporting Advanced laboratory infrastructure Fast turnaround time Suitable for transplant centres, hospitals, immunology laboratories, diagnostic laboratories, and research institutions At Awesome Genetics, we are committed to delivering high-quality transplant genomics services that provide accurate genetic insights to support clinical decision-making, research, and personalized healthcare.

Aviagen includes genomics information in the routine selection of its elite lines. Genomics information will complement existing selection techniques, adding to the continuous improvement of Aviagen products year-on-year. Aviagen s genomics project is concerned with identifying naturally occurring markers within the genome of elite birds and using those markers to help breed stronger and more productive birds through the current selective breeding program, a completely natural process. In line with Aviagen s tradition of innovation and dedication to R D, this major achievement comes as a result of long-term commitment to cutting-edge research and bringing together the expertise of top scientists in the field of genomics and the internal knowledge gained from more than 50 years at the forefront of breeding. Aviagen commenced using genomics in its commercial selection program in June 2012 and became the first company to include genomic information as a critical additional source of information in the R D breeding program.

At the turn of Human Genome project era, Scientific world has evolved to understands molecular biology in its holistic form and called it Genome. Further newer chapter of trascriptome, proteome and metabolome were added to research terms. But along with this new arenas need for infrastructure and expertise to execute and data interpretation is on need. Our young and indulgent team of scientist continuously update and keep ourselves prepared for diverse scientific task given to us. With help of microarray and NGS, we upscale scientist projects to international standards. With a dedicated bioinformatics team, gigantic data produced from these technologies is analyzed and complex hypothesis is put at check with simple interpretation. At completion of more than 20 successful projects, now we are confident with complex assignments.

BENCOS Genomics Data Analysis is a bioinformatics driven initiative specializing in Next Generation Sequencing (NGS) Data Analysis Interpretation. Our area of focus is in Human Genome Interpretation, especially for clinical and research use. We use advances in the area of Computer Science, Information Science, Data Management, Statistics and Systems Biology to solve complex problems in Genomics. We envision using cutting edge big data approaches along with machine learning algorithms to delve deeper into the understanding of the human genome and develop novel solutions to drug discovery. Research in genomics has taken a new turn with the advent of Next Generation Sequencing Technology. Understanding genes on a deep level may help to unlock many of the mysteries surrounding our most intractable diseases, including cancer, heart disease and degenerative conditions such as Alzheimer s. One of the main advantages of modern sequencing technologies is that the researchers can actually detect many different types of genetic alterations at once. For researchers in academia and pharmaceutical/ biotechnology industries, utilizing the advancement in the Next Generation Sequencing technology, can lead to early target identification, new genetic lesions associated with disease can be found, and overall development times associated with therapeutics and diagnostics to newly identified targets can be significantly shortened. The cost of sequencing has come down drastically which has led to data deluge. It is important therefore to properly analyze the data to get meaningful results. Researchers from academia and pharmaceutical and biotechnology industries are utilizing this wealth of information to delve deeper into the biology of normal life and disease. We at BENCOS understand the complexity of the NGS data analysis and would offer our proprietary data analysis platforms to researchers so as to enable discovering and deciphering of the genomic data in a simple, efficient and effective manner. Our Data Analysis services include: Variant Calling (Only Tertiary Analysis) Exome Sequence Analysis Whole Genome Sequence Analysis Transcriptome Sequence Analysis (1-3 Pairs) Small RNA Sequence Standard Small RNA Sequence Custom Microarray Data Analysis

Genomics Research Service

Next Generation Genomics

Genomics (NGS)

Genomics Research Service

EUROFINS GENOMICS PRIMERS

Genomics Research

Genome Research