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Genomics Offers Advanced Solutions For Genomic Product Applications In North America
19 applications found
Copy Number Variants (CNV) are a clinically important variant type to identify in both somatic and germline genomes. NGS workflows and analytics are increasingly able to resolve duplications, deletions, and other CNVs, alongside SNVs and Indels in a streamlined workflow. These detection algorithms rely on consistent coverage and reads across the genome to accurately identify copy number changes within the genome. However, GC rich regions, suboptimal capture and sequencing primers can impact resolution of CNVs ...
ByAccuGenomics, Inc. based in Wilmington, NORTH CAROLINA (USA)
Oligonucleotide refers to a very short single or double-stranded fragment of nucleic acid that can be joined together to form a single-stranded biopolymers. Oligo Pools are customizable genomic research products polymerized from various oligonucleotide fragments, playing an important role in gene synthesis, next-generation sequencing, library preparation, and so ...
ByCD Biosciences - htDNA-chip® based in Shirley, NEW YORK (USA)
Metagenomics is the study of all microbial genomes present in an environment, from the bottom of the sea to inside our own bodies. If you have shotgun NGS sequencing data, Partek provides powerful, easy-to-use analysis tools to characterize microbial ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Because the BacVax method is based on genomic and structural vaccinology, any bacteria can be analyzed for targets. Our vaccines will be able to address bacterial infections that currently have no vaccine options available, and we are ready to fill that ...
ByBacVax, Inc. based in Phoenix, ARIZONA (USA)
DNA sequencing refers to the analysis of the base sequence of specific DNA fragments, namely the arrangement of adenine (A), thymine (T), cytosine (C) and guanine (G). The emergence of rapid DNA sequencing methods can greatly promote the research and discovery of biology and medicine. At present, the lowest-cost and high-throughput next-generation sequencing is the most widely used. Next-generation sequencing technology, also known as high-throughput sequencing technology, solves the problem that first-generation ...
ByCD Biosciences - htDNA-chip® based in Shirley, NEW YORK (USA)
Meeting regulatory requirements and maintaining quality doesn’t have to take up a lot of valuable time. With the PCS, MVS, and Artel’s Services, clinical labs can streamline regulatory compliance, maximizing productivity. ...
ByArtel, Inc. by Advanced Instruments based in Westbrook, MAINE (USA)
Copy number variation (CNV) is a type of structural variation and it encompasses duplication or deletion events that affect a considerable section of the genome. Those events may be mirrored by changes in gene expression levels and are consequently involved in pathogenesis. Partek tools enable you to start with raw data, detect amplified or deleted regions, and interpret or integrate the data with other assays such as gene expression. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Helping providers make insightful decision based on analysis of disparate data sources such as medical records, lab data, genomic data, literature etc. Enhanced by a massive 2million QA KnowledgeBase for making clinical co-relations generating novel insights and meaningful associations. ...
ByOptrahealth Inc based in San Jose, CALIFORNIA (USA)
In the era of global information, traditional storage technologies have been slightly tested. DNA must realize reliable information encoding. Only when DNA becomes a viable competitor of traditional storage technology is the first step for DNA to realize information storage. The most important thing is to produce nucleotide strings cheaply and quickly. For DNA, it is composed of four different monomers, consisting of a deoxyribonucleic acid having a skeleton with phosphoric acid. First, DNA is a polymer biological ...
ByCD Biosciences - htDNA-chip® based in Shirley, NEW YORK (USA)
Single cell RNA-Seq is revolutionizing the study of complex tissues and diseases. The powerful and easy-to-use tools in Partek® Flow® empower researchers to analyze their own single cell RNA-Seq ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
At the end of 2019, a novel coronavirus was identified as the cause of a cluster of pneumonia cases in Wuhan, a city in the Hubei Province of China. The severity and rapid spread of COVID-19 (caused by SARS-CoV-2), resulted in a global pandemic declared by the World Health Organization in March 2020. The virus has spread to more than 100 countries, including the United ...
ByNovavax based in Gaithersburg, MARYLAND (USA)
Gene expression is the most fundamental level at which the genotype gives rise to a phenotype. Whether you have RNA-Seq, qPCR or microarray data, Partek provides easy-to-use tools that guide you through the analysis process from start to finish within a point-and-click interface. With over 8,000 citations, see why our gene expression analysis tools are the most trusted in the genomics ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Locus has built an automated, generalizable platform that is systematically unlocking the power of bacteriophage and CRISPR-Cas3 across multiple therapeutic ...
ByLocus Biosciences, Inc. based in Morrisville, NORTH CAROLINA (USA)
High Performance Across the Breadth of Biotech. The NX One is a perfect fit for a wide variety of sectors and application areas spanning fundamental biological research to industrial and clinical workflows. Access your cells faster and at a fraction of the ...
ByNodexus Inc. based in Hayward, CALIFORNIA (USA)
Whole genome, exome, or targeted panel DNA sequencing (DNA-Seq) studies can identify genetic variants that contribute to disease and phenotypes. Partek offers powerful and easy-to-use tools for processing and analyzing your DNA sequencing data. With the latest databases and bioinformatics tools available in a point-and-click interface, variant analysis is simple. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Realize the value of global clinical and genomic data with us. We help reduce your risk, enhance your pipeline value and advance your enterprise data strategy by solving the barriers of data access and enabling rapid insight ...
ByBC Platforms based in Zürich, SWITZERLAND
Sample preparation is a significant yet underappreciated step that allows for high quality sequencing and analysis, critical to achieving breakthroughs in medicine, agriculture, and other industries. NanoCellect’s microfluidic cell sorter, the WOLF, allow the cell’s integrity to be maintained for numerous sequencing and multi-omics techniques. The WOLF’s ability to flexibly fit into any genomic researcher’s lab, make it a key step to any cell sequencing analysis workflow. 10x Genomics ...
ByNanoCellect Biomedical, Inc. based in San Diego, CALIFORNIA (USA)
Isolating edited-pluripotent stem cells with traditional sorting techniques can subject the cells to rough conditions in which gene expression, genomic stability and overall cell-health can become compromised. Microfluidic cell sorting with the WOLF, along with single cell deposition using the N1 single cell dispenser, eliminates the challenges that pluripotent stem cells face by sorting at gentle pressures without decompression shock and shear stress, and allow for efficient single cell deposition for high ...
ByNanoCellect Biomedical, Inc. based in San Diego, CALIFORNIA (USA)
Microbe Inotech Laboratories, Inc. provides a microbial genomics platform through licensed database agreements focused on the characterization of microorganisms, pathogens and anti-microbial resistance for pathogen detection, food safety inspections and issues, pharmaceutical discovery, public health surveillance, water and wastewater analysis, agriculture and microbiome analysis and comparisons. From a post-sequencingmetagenomic sample (i.e. DNA extracted from your sample) the MiL Inc. provides identification ...
ByPluton Biosciences, Inc. based in St. Louis, MISSOURI (USA)