- Home
- Applications
- genomics
Refine by
Genomics Product Applications
45 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)
Identify new modes of action by investigating a combination of omics types (e.g. genomics, transcriptomics) in target pest, fungi and weed ...
ByGenestack based in Cambridge, UNITED KINGDOM
For Over 40 years the pipetting workstations developed by Tomtec have been used to accelerate numerous genomics work-flows; from sample preparation to amplification (PCR) to template ligation. ...
ByTomtec, Inc. based in Hamden, CONNECTICUT (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)
Modern genomics labs are looking for high-throughput, quality-data workstations to perform PCR reactions at a reduced cost. ...
ByAurora Biomed Inc. based in Vancouver, BRITISH COLUMBIA (CANADA)
Our Environmental Monitoring Systems complement the product testing portfolios of Life Science organisations, including those specialising in GMP, Biopharma, Microbiology, Toxicology, Virology, and Genomic Testing. These advanced systems ensure compliance, accuracy, and efficiency in laboratory ...
ByAutima based in Sydney, AUSTRALIA
Solving challenges in the genomic sequencing industry with Eusoft.Lab: The field of genomic sequencing is continually evolving, with the need to address complex challenges related to data management and laboratory activities. ...
ByEusoft Srl based in Bari, ITALY
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
Single-cell genomics and proteogenomics are rapidly growing. Nature Methods named multimodal omics the method of the year for 2019. ...
ByCuriox Biosystems Pte Ltd based in Singapore, SINGAPORE
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
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)
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
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)
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)