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For dye-based one-step RT-PCR on the QIAcuity digital PCR instruments
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For the hands-free isolation of DNA from soil and stool using your automation workflow of choice
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NeuMoDx accessories, reagents and consumables are intended for in vitro diagnostic use. Product availability may vary from country to country. Contact your country representative for further details.
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Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
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Comprehensive oncology profiling combining gene fusion detection, gene expression analysis and single nucleotide variant (SNV) calling in just one assay
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S_1084_7_GEN_Boxblue_cmyk_disclaimer
The NeuMoDx system and assays are intended for in vitro diagnostic use. Product availability may vary from country to country. Contact your country representative for further details.
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For rapid rRNA removal for RNA-seq library preparation from Caenorhabditis elegans (worm) samples
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For rapid rRNA removal for RNA-seq library preparation from fish total RNA samples
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For rapid rRNA removal for RNA-seq library preparation from Drosophila melanogaster (fly) samples
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S_1084_7_GEN_Boxblue_cmyk_disclaimer
To support customers developing in-house assays using real-time PCR molecular testing
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In this webinar, we will take a look at a large-scale SNP-based forensic identification panel for DNA analysis with massively parallel sequencing (MPS). The panel was specifically designed for the challenges of identifying missing persons; where DNA is frequently highly degraded, and relationship tests may involve reference samples from across several generations and in a deficient pedigree.
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The FBI CODIS Core Loci Working Group have published the recommendation that the CODIS core loci should be expanded, and a combination of STR markers from the Combined DNA Index System (CODIS), the European Network of Forensic Science Institutes (ENFSI), and the European DNA Profiling Group (EDNAP) should be used to improve the accuaracy of forensic testing. QIAGEN has developed new kits — Investigator 24plex Kits — that coamplify all 23 recommended markers. The kits use novel 6-dye technology to keep the amplicon length of markers short while avoiding overlapping of markers. Kits are available for purified DNA from casework and for reference samples. This webinar will outline the benefits of the Investigator 24plex Kits and highlight the improved workflow, which saves unnecessary re-runs of a sample by use of an internal “Quality Sensor” control. This unique Quality Sensor can distinguish: Successful amplification Degraded DNA Inhibited DNA No DNA Failed PCR amplification Join us to learn how to improve results and streamline your forensic STR analysis with the new Investigator 24plex Kits.
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The core short tandem repeats (STRs) in worldwide use have served the forensic analyst very well for many years. Further, recent expansions of European Standard STR sets plus ongoing discussions to extend CODIS have brought powerful upgrades to the battery of core markers available. However, there are still scenarios when supplementary STRs could enhance the data necessary for interpreting complex forensic patterns: making safer inferences about relatedness across distant relationships in deficient pedigrees, and in the not too distant future, improving the specificity of familial searching or expanding the points of reference to better interpret mixed profiles. The QIAGEN HDplex Kit contains 9 completely novel STRs in addition to ESS or CODIS D12S39, D18S51 and SE33 markers. On an average, these 9 novel STRs provide higher powers of discrimination than kits using the core loci alone. This webinar will outline the completed studies on worldwide patterns of variability in the 12 novel HDplex STRs and their ability to enhance the power of paternity analyses when combined with existing markers. It will also describe the upgraded pop.STR allele frequency browser which provides data for 23 core STRs plus a total of 28 supplementary STRs in 56 global populations. Join us to learn more on: Enhancing data necessary for interpreting complex forensic patterns with supplementary STRs Making safer inferences about relatedness across distant relationships in deficient pedigrees Improving the specificity of familial searching to better interpret mixed profiles
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