Seqcess

Your questions are our priority, and our analyses are purposefully designed to provide the insights essential to the success of your projects. At NextGenSeek, we empower scientific breakthroughs by providing state-of-the-art Next-Generation Sequencing (NGS) data analysis solutions. Driven by a passion for discovery, our mission is to accelerate genomics research by delivering thorough NGS data analysis services. We work with various sectors, including healthcare, biotechnology, pharmaceuticals, and academic research, offering tailored solutions to meet the unique challenges of each field. We offer extensive experience in analyzing NGS data across various platforms and experimental designs. Recognizing that each research project is unique, we offer customizable NGS data analysis solutions. Our streamlined workflows and efficient processes are designed to deliver results promptly, without compromising the quality of analysis. Embark on a journey of discovery with NextGenSeek, where cutting-edge technology meets unparalleled expertise in NGS data analysis.

AllSeq is the world’s leading online Sequencing Marketplace. Our online forms help guide you to create an accurate description of your sequencing project, ensuring that you receive accurate, consistent bids. Or you can browse our comprehensive list of service providers, filtering them by platform, application and specialty. AllSeq also provides resources for the sequencing community. The NGS Knowledge Bank contains the latest information on the various sequencing technologies, platforms and applications.

At Intelliseq, we understand that in-depth data analysis and interpretation lies at the very heart of successful genome-wide research. We are focused on the development of novel algorithms and bioinformatic tools devoted to the interpretation of the human DNA sequence. Intelliseq is a team of experienced scientists, geneticists, bioinformaticians and software engineers. We deliver an intuitive cloud-based platform for NGS data analysis and clinical interpretation. We are convinced that the application fulfills its role 100%, enabling very fast and accurate analyses of exome and genome samples, in various areas of interest. Intelliseq has completed a number of orders for OpenExome (currently AnalitykGenetyka) regarding sequencing and bioinformatic analysis of genetic data. Intelliseq performed for us the sequencing of the full transcriptome of RNA samples and bioinformatics analysis of the obtained data. Our products and services are the result of advanced and in-depth research and development activities.

Through innovative clinicaland food safetynext-generation sequencing and software, we deliver clarityin infectious disease genome surveillance that can help protect human lives. Increase lab tech efficiency and productivity with our comprehensive and user-friendly next-generation sequencing platform.

Sequentia Biotech is a bioinformatics company that transforms omics data into knowledge. We offer bioinformatics cloud software, custom software and bioinformatics consulting services for healthcare, pharma, agriculture, industry and environment. The genome and its correct assembly is the starting point for any project that uses omics sciences to achieve a breakthrough in the fields of human health, agriculture and the environment. For this reason, at Sequentia we develop innovative tools that create a new reliable and precise assembly, of both complete genomes and specific parts or groups of genes. The study of the set of genes of a genome is a fundamental step in understanding its biological processes and functions. Our innovative metagenomics pipeline, which complements those of genomics, transcriptomics and epigenomics, is designed to work with both data obtained using shotgun protocols and with selective amplifications (sequencing of 16S, sequencing of 18S, etc.). That is why the study of epigenetics has become a key factor for understanding biological processes.

Next-generation sequencing (NGS) is driving advances in translational and clinical research. Launching the newest addition to Roche’s world-class whole exome sequencing products. From expanding our understanding of cancer, reproductive and developmental biology to unravelling complex microbial populations, NGS is touching all facets of human disease and well­being. Sample prep for next generation sequencing holds the key to unlocking the potential of every sample. From sample collection to library quantification, we offer sample prep solutions for different sample types and sequencing applications that are proven, simple and complete.