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26 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. ...
ByAccuGenomics, Inc. based in Wilmington, NORTH CAROLINA (USA)
Because the BacVax method is based on genomic and structural vaccinology, any bacteria can be analyzed for targets. ...
ByBacVax, Inc. based in Phoenix, ARIZONA (USA)
Metagenomics is the study of all microbial genomes present in an environment, from the bottom of the sea to inside our own bodies. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (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)
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)
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 RNA-seq library prep, Single-Cell sorting on PCR plate, Whole-genome sequencing ...
ByNanoCellect Biomedical, Inc. based in San Diego, CALIFORNIA (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. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Unlike conventional vaccination strategies, cancer vaccines are designed to mount responses against tumor-specific antigens, arising from somatic mutations specific to the cancer genome. They promise a highly tailored approach by targeting patient-specific ...
ByEnpicom B.V. based in s-Hertogenbosch, NETHERLANDS
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)
Overcome CRISPR delivery limitations with FluidFM: for multiplex genome editing and fast cell line development. The discovery of CRISPR-Cas9 for targeted gene engineering has revolutionized life sciences. ...
ByCytosurge AG based in Glattbrugg, SWITZERLAND
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 ...
ByNanoCellect Biomedical, Inc. based in San Diego, CALIFORNIA (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
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. ...
ByPluton Biosciences, Inc. based in St. Louis, MISSOURI (USA)
Whole genome, exome, or targeted panel DNA sequencing (DNA-Seq) studies can identify genetic variants that contribute to disease and phenotypes. ...
ByPartek Incorporated based in Chesterfield, MISSOURI (USA)
Cancer is one of the leading causes of deaths in India and a major public health concern. It is estimated that there are around 1 million new cancer cases every year and as many as 5 lakh deaths occur annually. Around 71% of all cancer deaths in India occur in people 30 to 69 years of age, when adults are very productive. The burden of cancer is expected to further increase due to increase in life expectancy, heavy use of tobacco and other risk factors such as radiation, viruses, ...
ByinDNA Research Labs based in , INDIA
The particles contain no viral genome and are replicative defective and non-pathogenic. The particle capsid surface has repetitive, immunogenic sites, where peptides of interest can be inserted and allows us to generate monovalent or bivalent vaccines as required. ...
By2A Pharma ApS based in Aalborg Øst, DENMARK
The modular fashion with which Affilin® ligands can be fused together makes creating multi-specific binders an easy task. Combined with varying linker lengths, composition, and orientation, plus the optional addition of further accessory modules, our Navigo experts build the designed molecules as previously planned on the drawing ...
ByNavigo Proteins GmbH based in Halle, GERMANY
Solid tumor-specific Affilin molecules are currently being evaluated as CAR-T ligands. Specifically, they were confirmed to be functionally expressed on the effector cell surface, mediate target cell-binding and effective target cell-killing in a dose-dependent fashion. Importantly they were just as effective as commonly used antibody ...
ByNavigo Proteins GmbH based in Halle, GERMANY
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)