*Partnering in complete Next-Gen Sequencing Solutions From Design to Sequencing to Analysis* We provide expert guidance on experiment design and approach with a diverse set of technologies to advance your project at any stage of development. Our mission is to get you the best genomic data and analysis to help move your research and pre-clinical projects forward. Contact our experienced team to plan solutions for your project and research goals. Our team of Laboratory and Data scientists have been pioneering translational genomics studies since the dawn of NGS. We specialize in working with sample sources that are difficult to sequence such as Low-Yield and FFPE, having optimized these techniques in-house over the past 10 years. Numerous grants have been obtained and supported through our diverse expertise in both research and clinical environments.
TCRb Sequencing is performed on the ThermoFisher platform and can be completed in 14 days or less. We provide raw data files, a detailed clonality report and a free dynamic analysis tool. Our team will assist with sample preparation requirements, experiment planning as well as experimental design. Our Genomics facility also has an integrated data science team if you need deeper analysis in addition to the report provided. Please contact us now with questions.
TCRb Sequencing is performed on the ThermoFisher platform and can be completed in 14 days or less. We provide raw data files, a detailed clonality report and a free dynamic analysis tool. Our team will assist with sample preparation requirements, experiment planning as well as experimental design. Our Genomics facility also has an integrated data science team if you need deeper analysis in addition to the report provided. Please contact us now with questions.
NextGen Sequencing based RNA-Seq services with supporting Bioinformatics and Biostatistics as needed. Illumina and ThermoFisher NGS platforms are available to provide the best matched technology for your needs.
NextGen Sequencing based DNA-Sequencing services with supporting Bioinformatics and Biostatistics as needed. Illumina and ThermoFisher NGS platforms are available to provide the best matched technology for your needs.
10X Genomics Single Cell RNA-Seq and associated expression analysis techniques are supported by our experienced team. We also have a supporting data analysis pipeline with study design support as needed.
Our experienced team can assist in creating targeted gene panels for the best matched Illumina or Ion S5 XL NGS platform to your needs. From custom single gene panels to over 1000+ genes for DNA or RNA sequencing.
CITE-seq uses DNA-barcoded antibodies to convert detection of proteins into a quantitative, sequenceable readout. Antibody-bound oligos act as synthetic transcripts that are captured during most large-scale oligodT-based scRNA-seq library preparation protocols (e.g. 10x Genomics, Drop-seq, ddSeq).
Verify cell lines and potential mutations with our NextGen Sequencing capabilities and platforms. This verification can include targeted panels with optimized detection limits and running times.
National Jewish Health, Center for Genes, Environment and Health (NGS and Data Science) has not received any reviews.
National Jewish Health, Center for Genes, Environment and Health (NGS and Data Science) has not received any endorsements.