Next Generation Sequencing
Our facilities across Dubai and Bangalore, India provides a range of services including extraction, library preparation, sequencing, and bioinformatics analysis, utilizing cutting-edge Next Generation Sequencing (NGS) technologies in our advanced laboratory. Our team of project managers, offers continuous support throughout your project, from complimentary initial consultations to real-time progress reports and assistance after delivery.
Regardless of whether you are embarking on your first or hundredth NGS project, our committed scientists strive to identify the most suitable NGS service for your research needs. We continuously refine our methodologies to ensure the delivery of top-quality results that adhere to your budget and timeline.
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Whole Genome Sequencing Service
Whole Genome Sequencing (WGS) provides a deep insight into the DNA sequence of humans, animals, plants, and microbial genomes, with data analysis at the individual or population level.
SNP/INDEL/CNV/SV and other variants of the genome can be fully analysed. Our sequencing analysis enables the identification of somatic and germline mutations as well as customized patterns of cancers and other diseases.
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- Why Choose Whole Genome Sequencing?
- Cancer Studies, Personalized Medicine, and Translational Research: Uncover tailored insights for personalized health approaches.
- Discovery of Biomarkers and Pharmacogenetics: Understand how your genetics may impact responses to medications.
- Disease Research: Contribute to advancements in understanding and combating various diseases.
- Plant and Animal Breeding Programs: Optimize breeding strategies for healthier and more resilient crops and livestock.
- Examination of Microorganisms: Gain insights into the fascinating world of microorganisms and their potential applications.
- At Innovate, explore our portfolio of Whole Genome Sequencing products (attach hyperlink here to talk the click below to the product portfolio) to receive the comprehensive genome analysis you need for your research project.
Terms and Conditions: Price automatically adjusted based on package choice during request. Packages are not available for all services, projects, or institutions. Additional charges for nucleic acid extraction, library preparation, and/or data analysis will apply.
Whole Exome Sequencing
Despite constituting only 1% – 2% of the genome, these exons house approximately 89% of all identified disease-causing mutations. Although targeted sequencing of a preselected gene set is an important aspect of the current testing strategy, WES provides an unbiased view of the exome.
Whole exome sequencing operates by employing capture probes, which are synthesized oligonucleotides or baits strategically designed to selectively hybridize with exons—the coding segments of genes. Subsequently, in the library preparation stage, sequencing adapters are introduced to the enriched protein-coding DNA fragments. These fragments are then subjected to high-throughput sequencing, commonly utilizing next-generation sequencing (NGS) technologies.
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- Why Choose Whole Exome Sequencing?
Our Whole Exome Sequencing is versatile and applicable to various research domains, including
- Population genetics studies
- Genetic disorders
- Rare diseases
- Tumor research
Find comprehensive solutions for your diverse research questions with our Whole Exome Sequencing products.”
Our comprehensive exome services encompass clinical and whole exome sequencing, employing various capture methods, based on the requirements.
Our deliverables include variant annotations for clinically relevant mutations, utilizing published variants from literature and databases such as ClinVar, OMIM, GWAS, HGMD, and SwissVar
Furthermore, our services extend to trios analysis, where variants undergo thorough screening to identify de novo mutations within a family trio.
We offer the services across deliverables that maximize your requirement in terms of deadlines and budget.
Value, Standard and Lightning
We offer different services to address a variety of research questions.Would you like to have bioinformatic analyses performed on your data in addition to the included deliverables? Each of our products can be supplemented with further services.
We are happy to advise you
Terms and Conditions: Price automatically adjusted based on package choice during request. Packages are not available for all services, projects, or institutions. Additional charges for nucleic acid extraction, library preparation, and/or data analysis will apply.
Transcriptome Sequencing
RNA sequencing, or RNA-Seq, is used to identify the nucleotide sequence of the RNA strand and detect the quantity of RNA in a sample. Leverage the power of transcriptome sequencing – a robust method for the detection and quantification of RNA molecules.
RNA-Seq provides a deeper insight into the transcriptome of a cell— enabling discovery of novel transcripts and differential gene expression analysis—by generating count data. In analyzing the count data, researchers can quantify RNA fragments and associate RNA sequences to respective genes in the sample.
RNA sequencing (RNA-Seq) services from Innovate Life Sciences provide unparalleled flexibility in the analysis of different RNA species (coding, non-coding, and small transcripts) from a wide range of starting material using short-read sequencing. We offer a variety of RNA-Seq options including total, small, and single-cell RNA-Seq with RNA-Seq data analysis.
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- Our Transcriptome Sequencing services cater to diverse applications and objectives, including:
- Analysis of differential gene expression levels
- Detection of alternative splicing and previously unknown transcripts
- Explore our range of Transcriptome Sequencing products to gain reliable and precise insights into the RNA landscape of a specific cell or tissue at a defined moment in time.
Terms and Conditions: Price automatically adjusted based on package choice during request. Packages are not available for all services, projects, or institutions. Additional charges for nucleic acid extraction, library preparation, and/or data analysis will apply.
Custom Panel Design and Sequencing
Unlock the potential of gene panels – a curated selection of genes enriched and sequenced simultaneously, allowing for high sequencing depth through next-generation sequencing. This method generates manageable data with minimal underrepresented regions. Our partnership with Twist Biosciences enhances our panel design, providing increased depth, detection, and accuracy, alongwith Illumina’s established short-read sequencing, our panels enable the exploration of genes related to drug metabolism, therapeutic responses, or those challenging to sequence with short-read methods.
For short-read panels, leverage our expertise in generating and validating custom designs. Innovate Life Sciences – your gateway to advanced panel sequencing solutions.”
Terms and Conditions: Price automatically adjusted based on package choice during request. Packages are not available for all services, projects, or institutions. Additional charges for nucleic acid extraction, library preparation, and/or data analysis will apply
Metagenomics Analysis
We provide state-of-the-art Full-Length 16S Sequencing and Shotgun Metagenomic Sequencing services, precisely identifying and classifying the diverse microbiome. Unsure which product suits your project best? Our experts are ready to guide you. Beyond sequencing, we offer comprehensive bioinformatic analyses to extract meaningful insights from your data.
Embark on your microbiome analysis journey today, unraveling the rich tapestry of microorganisms and their profound influence on both us and our environment.”
We offer the services across deliverables that maximize your requirement in terms of deadlines and budget.
Value, Standard and Lightning
Terms and Conditions: Price automatically adjusted based on package choice during request. Packages are not available for all services, projects, or institutions. Additional charges for nucleic acid extraction, library preparation, and/or data analysis will apply.
Services Brochure
Terms and Conditions: Price automatically adjusted based on package choice during request. Packages are not available for all services, projects, or institutions. Additional charges for nucleic acid extraction, library preparation, and/or data analysis will apply.
