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The Hidden Costs of Integrating Free Data
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Identification of Putative Functional Variants in Claudin-Low...
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Connect the Dots: Deriving Insights from Thousands of 'Omics...
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Methods and Challenges of Variant Annotation in Hereditary...
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Simultaneous, High-yield Extraction and Purification of DNA...
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NGS Variant Annotation, Filtering and Triage Using QCI...
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Differentiate DNA from RNA using NanoDrop Spectrophotometers
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Protein quantification and qualification
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Nucleic Acid Contamination Application Ebook
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Utilization and Implementation of Molecular Markers in a...
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The Human Gene Mutation Database: Empowering a Generation of...
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Trends in Variant Interpretation Workflows: Expert Insights...
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Utilizing Targeted SNP-Based Genotyping to Rapidly Introgress...
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Viral Pathogenesis Research: Molecular Detection with RNAscope
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Genome-wide Study Reveals a Pseudogene-Associated Recurrent...
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Targeted Genotyping by Sequencing in Routine Breeding: A...
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Rapid Assessment of Novel Alleles and QTL Through Background...
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Closing the precision medicine gap in community practice...
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Spatial Expression Analyses Elucidate Mechanisms of circRNAs...
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Spatial Profiling of Lung Tissue from SARS-CoV-2-Positive...
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RNAscope 2.5 LS or BaseScope RED Assay Combined with...
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RNAscope or BaseScope RED Assay Combined with...
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RNAscope LS Multiplex Fluorescent Assay Combined with...
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Prevalence of Hereditary Cancer and Benefits of Multi-Gene...
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Combining the RNAscope ISH Technology with IHC to Spatially...
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Extracellular Matrix Gene Expression and Cytotoxic T...
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RNAscope for COVID-19 Research
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RNAscope in COVID-19 Research
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RNAscope Multiplex Fluorescent v2 Assay Combined with...
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Discern Highly Homologous Sequences in Intact Tissue with...
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Automated BRCA Variant Assessment Shows 99.6% Concordance...
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The RNAscope Multiplex In Situ Hybridization Technology...
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Molecularly Guided Highly Multiplexed Spatial Profiling
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Genome-wide Study Reveals a Pseudogene Associated Recurrent...
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Visualize KRAS Point Mutations Using BaseScope ISH
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Sime Darby Plantation Solves the Trade-Off Between Trait...
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Detect Small Regulatory RNAs with Spatial & Morphological...
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Overcoming Agricultural and Human Health Challenges With KASP...
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Publications Utilizing the RNAscope Assay to Validate and...
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Visualization of in Vivo Gene Editing Heterogeneity at the...
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Single-cell DNA Analysis of a Novel Acute Erythroid Leukemia...
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Variant Interpretation in Oncology: Results From an End-User...
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Simultaneous Visualization of RNA and Protein Targets Using...
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miRNAscope: A Novel In Situ Hybridization Technology for the...
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Highly Multiplexed Spatial Mapping Using the RNAscope...
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Preclinical CAR-T Cell Target Safety, Biodistribution, and...
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Spatial RNA Profiling in the Nervous System with the RNAscope...
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Visualize Gene Expression and Splice Junctions at the...
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Tissue Biodistribution of AAV-based Gene Therapy with the...
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Using QuPath to analyze RNAscope, BaseScope and miRNAscope...
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Introducing the Novel miRNAscope in situ Hybridization Assay...
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Dissecting the Cellular and Subcellular Localization of...
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Electroporation Made Easy for Hard-to-Transfect Cells
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Single-cell Sequencing 101: DNA & Multiomics for Precision...
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Expand Bulk Sequencing Analysis with BioLegend and Illumina
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New Technology to Generate Commutable and Comprehensive...
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Experience with SARS-CoV-2 (COVID-19) Assay Validation
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Multi-Center Evaluation of Circulating Tumor DNA Assays
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Expert Advice Establishing a SARS-CoV-2 Assay for COVID-19
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Consistent Performance of Highly Multiplexed RNA Fusion...
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Optimizing TMB Use in Cancer Research and Care: The Friends...
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New Tools and Strategies for High Quality TMB Analysis by NGS
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Turn Your Sequencing Lab Into a COVID-19 Research and...
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Accurate and Efficient Interpretation With QCI Precision...
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Analyzing Complex Genomic Variants in Somatic Cancer
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Power Up Your Variant Knowledge Using the Human Gene Mutation...
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SARS-CoV-2 Sequencing and High-Throughput Detection
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The Human Gene Mutation Database: Empowering a Generation of...
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Deep Understanding of Cell and Gene Therapy Genome Editing...
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Single-cell Multiomics Reveals Novel Correlations Between...
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In-depth Quantification of Cell and Gene Therapy DNA...
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Non-invasive Preimplantation Genetic Testing
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Positioning Your Diagnostics Lab for Success
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Shortened Hybridization Times with KAPA HyperCap v3 Using...
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Rapid Implementation of SARS-CoV-2 Testing: A GenomeWeb eCase...
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Next-Generation Sequencing Assay Validation: A Practical...
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Development of NTRK Reference Materials for Global Assay...
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Amplified ccfDNA for Assay Development, Validation, and...
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Germline Insights from NGS Somatic Testing: Clinical...
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A Multi-Laboratory Investigation of 18 Oncogenic RNA Fusions...
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Improving and Standardizing TMB Assay Performance
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Expert Advice Establishing a SARS-CoV-2 Assay for COVID-19: A...
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How to Develop a Clinical NGS Assay Without Losing Your Mind...
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Development and Validation of Blood Tumor Mutational Burden...
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Next-Generation Sequencing Assay Validation A Practical Guide...
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Characterization of Tumor Normal Cell Line Pairs for TMB...
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Development of SNP Matched NIPT Reference Materials for...
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Experience with SARS-CoV-2 (COVID-19) Assay Validation: A...
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Genomics Clinical Implementation Success Stories: Development...
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2 Tools for Overcoming Your Clinical Lab's Toughest Quality...
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Development of Matched Maternal-Fetal Noninvasive Prenatal...
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Variant Interpretation Then and Now: Moving Toward Rigorous,...
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NSCLC Sample Report for North America
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From Somatic Variants Towards Precision Oncology
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Incidental Findings in Clinical Genomics: How to Handle...
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Genetic Testing Lab Sees 25-Fold Scale-Up with New...
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Lab Performing Expanded Carrier Screening Boosts Efficiency...
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The Importance of Expert Curation in Clinical NGS Testing
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HGMD and ClinVar: Avoiding the Knowledge Blind Spot
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Deliver Oncologist-Ready Reports in Minutes With Clinically...
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Reference Materials for Measurable Residual Disease (MRD)...
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Development of Reference Material for Blood Tumor Mutational...
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Keeping up With the Genomes: Scaling Clinical Variant...
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Development and performance of a formalin-damaged multiplexed...
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Use of HGMD Mutation Data Within Popular Variant Annotation...
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NGS-based Reference Materials for Fusion and Somatic Variant...
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Bigger, Faster, Cheaper: Breaking the Bottleneck in Clinical...
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Finding a Diagnosis in a Race Against Time
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High Quality Products + Lower Lifetime Costs = Eppendorf OEM
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Isotachophoresis Improves Nucleic Acid Extraction and...
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Case Study: Eppendorf OEM for Lab Automation
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Increased DNA Yield and Reduced PCR Duplicates Using the...
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Case Study: Eppendorf OEM for a Clinical Analyzer
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Accurate Detection and Whole Genome Characterization of...
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CAS-CLOVER The clean alternative to CRISPR/Cas9 for gene...
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A Real-Time-Assay for the fast and gel-free detection of...
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Fast Real-Time PCR Detection of HLA-B*27 Directly from Blood...
