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#RAPIDLINK DNA SOFTWARE#
ChimerMarker software is compatible with ABI®PRISM, Applied Biosystems® SeqStudio, and Promega Spectrum Compact CE Systems genetic analyzers, and custom primers or commercially available human identification chemistries for STR genotyping (including Identifiler®, GlobalFiler™ 6-Dye™, PowerPlex®16, PowerPlex®ESI, GenePrint® 24, PowerPlex®Fusion 5 and 6 Dye, Investigator®24Plex). Don Kristt).ĬhimerMarker software also has a linked maternal cell contamination (MCC) application. The chimerism analysis performs repetitive calculations (using published methods. Multi-lineage capabilities for chimerism analysis of T-cells, B-cells, and other cell type populationsĬhimerMarker software includes functions for comparison of samples at different time points to conduct longitudinal studies for monitoring each individual and a comprehensive chimerism analysis report.Easily appends for longitudinal monitoring post-BMT.
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Calculates percent chimerism and quality metrics for single donor or double donor cases.Automatically identifies donor and recipient peaks in post-BMT samples.Accurate, rapid genotyping and chimerism analysis with documented time savings of up to 85%.The software can be used to monitor chimerism level in both an allogeneic stem cells transplant (SCT) or a hematopoietic stem cells transplant (HSCT), bone marrow transplant (BMT, post bone marrow engraftment), and cord and peripheral blood stem cells transplant (PBSCT) samples.Ĭomplete Chimerism Detection, Long-term Monitoring, and Quantification in one program! Information about patients and their donors can be recorded in a specially-designed interface.ĬhimerMarker® automated chimerism analysis software integrates speed and accuracy with a biologist-friendly interface. RapidDNA: Transplant version combines the LIMS function with ChimerMarker® automated chimerism analysis software from SoftGenetics® This can be fully customised to fit your requirements. Our LIMS is specifically designed to automate DNA analysis workflow. Ecology/Agriculture/Wild life (SNPWave®/SNPlex®, AFLP, t-RFLP, Microsatellite (SSR, STR, VNTR), Kinship Analysis of Wild Populations and data base, SBE/ SnapShot®, TILLING® & EcoTilling with slabgel or capillary data, MLVA).
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It creates a centralised DNA database for storing DNA profiles of both known individuals and unknown (e.g., crime scene samples). RapidDNA : Standard version combines LIMS with SQL Database capability.
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