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DNASTAR - Using VCF Files for SNP Analysis
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See how to use variant call format (VCF) files for filtering SNPs from next-gen sequencing projects in Lasergene Genomics Suite.
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DNASTAR - Using VCF Files for SNP Analysis
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DNASTAR - Variant Analysis Webinar
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DNASTAR - Gene Panels Overview
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DNASTAR - Multiple Genome Assembly and Variant Analysis
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DNASTAR - Mendelian Exome and Gene Panel Assembly and Analysis
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DNASTAR - Microbial Genome Assembly and Analysis Webinar
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DNASTAR - Next-Gen Sequencing Data Management, Assembly, and Analysis Webinar
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DNASTAR - Speed, Accuracy and Capacity for NGS Analysis Webinar
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DNASTAR - Transitioning from SeqMan Pro to SeqMan Ultra
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DNASTAR - Assembling and Analyzing Illumina Data in Lasergene Genomics Suite Webinar
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DNASTAR - Managing Large NGS Data Sets Webinar
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DNASTAR - Gene Panels Webinar
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DNASTAR - Templated Genome Assembly
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DNASTAR - Achieving Highly Accurate NGS Variant Calling Webinar
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DNASTAR - Variant Analysis Workflow
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DNASTAR - Lasergene Genomics overview
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DNASTAR - Optimizing NGS Assemblies Using Illumina and Ion Torrent Data Webinar
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DNASTAR - Lasergene Genomics Suite Overview Webinar
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DNASTAR - Exome Analysis Tutorial
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DNASTAR - Advanced SNP Analysis in Lasergene Genomics Suite Webinar
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DNASTAR - Sanger Validation for NGS Assemblies
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Matthew Keyser - DNASTAR Software for Assembly and Analysis of Microbial Genomes
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DNASTAR - Alingment mehrerer Genome und Variantenanalyse
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Webinar: Get to know SeqMan Ultra
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