New TCR-Seq Service for Analyzing T-Cell Clone Diversity and Clonality
Extracts DNA or RNA and uses Illumina platform for high-throughput sequencing. Utilizes multiple bioinformatics tools, including VDJtools and tcR, to accurately genotype TCR sequences and identify clones. Ideal for R&D of immunotherapy drugs, cancer immunology and viral infection research.
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New Mitochondrial Diseases Panel Sequencing Service Detects Genetic Mutations
Allows researchers to identify mitochondrial DNA and nuclear DNA mutations accurately. Provides high accuracy, sensitivity and specificity, ensuring the reliable results. Contains over 200 genes associated with mitochondrial function and metabolism.
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New RNA-Solutions for Understanding Human Diseases Mechanisms
Provides quality assessment for purified exosomal RNAs utilizing real-time PCR and electrophoresis. Supports exoLR characterization and the development of companion diagnostics and other applications. Ideal for analysis of mRNA, circRNA and lncRNA in exosomes.
Read More »New Cancer Hotspot Panel Sequencing Covers 248 Genes
Accelerate research on disease pathogenesis, disease identification, biomarker discovery and targeted drug development. Provides efficient method for discovering rare somatic mutations. Can detect SNVs, indels and structural rearrangement.
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The ROI of a Full Service Manufacturer
Full service manufacturers incorporate a complete line of production capabilities to facilitate fast, cost-efficient manufacturing of complex products without the need for multiple contractors.
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New Plasmid Identification Service for Microbial Genomics and Bioinformatics Analysis
Provides advanced genomics solutions and genome-based analysis. Available with next-generation sequencing and long-read sequencing platforms. Identifies antibiotic resistance genes, mobile genetic elements and any other genetic information of interest.
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New Long Amplicon Analysis Tool Analyzes Single Molecule Real-Time Sequencing (SMRT) Data
Generates highly accurate, phased and full-length consensus sequences for multiple genes in a single sequencing run. Provides complete, uniform and unbiased coverage across long amplicons. Applications include full-length 16S, 18S and ITS rRNA gene sequencing.
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New RNA-Seq Service Uses Illumina Sequencing Techniques
Designed for input amounts down to 2 pg, applicable for good quality RNA from challenging samples. Offers a powerful tool for analyzing the gene expression in cancer research and studies. Allows to detect splice junctions and significant changes in gene expression for low abundant transcripts.
Read More »Major Industrial Lab to Utilize WaferGen Bio-systems' High-Throughput Genomics Technology
SmartChip MyDesign™ Quantitative PCR System to be Used for- Gene Expression and Other Studies FREMONT, Calif.- – WaferGen Bio-systems, Inc. (Nasdaq:WGBS) announced today an important industrial partnership with Procter Gamble whereby Procter Gamble will utilize WaferGen's SmartChip MyDesign™ quantitative PCR System to conduct various gene expression and other studies. As the amount of...
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Neagle Choice, LLC Announces New Available Services
Neagle Choice has long been known as a quality source for commercial sewing, printing, die cutting, and the manufacturing of a wide range of custom products. Enhancing our service capabilities has been the key to our success, and has driven our growth into many new and exciting markets. Continuing on this trajectory, we now offer precision laser cutting and etching, adding to our long line of manufacturing services. See our video to learn all about it.
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