| Cloning |
Product Overviews |
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Gateway MultiSite Cloning (3:59) |
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Lasergene 11 Overview (3:01) |
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Virtual Cloning Overview (1:04) |
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Introducing Lasergene 11 Webinar (44:11) |
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Directional TOPO Cloning (2:59) |
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Using the DNASTAR Cloud (3:57) |
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TA Cloning in 3 Easy Steps (1:44) |
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Lasergene Core Suite Webinar (53:56) |
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Restriction Enzyme Cloning (3:45) |
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Lasergene Genomics Suite Webinar (59:19) |
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Gateway Cloning (3:20) |
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Cloning and Primer Design Webinar (56:58) |
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Creating Custom Cloning Vectors (3:54) |
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De Novo Genome Assembly Webinar (38:30) |
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Alignment and Gene Discovery Webinar (54:36) |
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Gene Discovery Overview (1:05) |
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RNA-Seq Webinar (56:27) |
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Getting Started with GeneQuest (3:12) |
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Protean 3D Overview Webinar (52:06) |
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Aligning Exons to a Reference (2:53) |
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Automated Genome Closure Webinar (56:03) |
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Analyzing Restriction Enyzmes (0:34) |
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Manual Gap Closure Webinar (58:29) |
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Using the Borodovsky Method (0:34) |
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Sanger Sequence Assembly Webinar (50:37) |
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Locating Transcription Factor Binding Sites (2:52) |
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Illumina Assembly and Analysis Webinar (56:09) |
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Gene Expression Analysis |
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Ion Torrent Analysis Webinar (58:24) |
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Protein Analysis |
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Protein Analysis Overview (1:38) |
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Analyzing Gene Expression Patterns (1:17) |
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Protean 3D's Analysis View (1:44) |
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Identifying Co-Regulated Genes (1:15) |
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Using Protean Methods (0:29) |
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Clustering Gene Expression Data (0:40) |
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Finding PROSITE Patterns (3:03) |
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Creating Gene Sets (2:38) |
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Getting Started with Protean 3D (4:39) |
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Using the Gene Table (3:13) |
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Rotating and Moving a Structure (0:33) |
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Using the Gene Ontology View (2:47) |
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Using the Motion Library (0:36) |
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Using the Scatter Plot (0:50) |
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Changing Rendering Styles (3:19) |
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Using Venn Diagrams (4:14) |
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Creating Surfaces and Adjusting Lighting (5:03) |
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Importing Microarray Data (3:19) |
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Predicting Epitopes in Protean 3D (3:38) |
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Importing Annotations in ArrayStar (3:22) |
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Aligning Protein Structures (2:56) |
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Multiple and Pairwise Alignments |
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Viewing Protease Cleavage Sites (1:57) |
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Getting Started with MegAlign Pro (2:49) |
Sequence Analysis and Visualization |
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Sequence Alignment Overview (1:07) |
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Sequence Analysis Overview (11:45) |
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Performing a Pairwise Alignment (2:53) |
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Managing Large Groups of Sequences (2:49) |
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Performing a Dot Plot Pairwise Alignment (3:09) |
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Filtering Enzymes (3:01) |
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Editing an Alignment (2:10) |
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Identifying Enzymes to Excise a Gene (3:09) |
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Performing a Sub-Alignment (3:23) |
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Adding New Restriction Enzymes (2:41) |
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Creating an Agarose Gel Simulation (1:56) |
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Preparing a Map for Presentation (2:43) |
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Customizing Your SeqBuilder Layout (4:43) |
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Performing BLAST and Entrez Searches (4:16) |
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Translation Numbering (1:36) |
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Choosing an Alignment Method (4:09) |
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Batch Translation of Genomic Annotations (2:55) |
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Customizing the Alignment Report (0:40) |
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Modifying the Genetic Code (4:23) |
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Next-Gen Workflows |
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Editing Feature Styles (0:58) |
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Overview: De Novo Genome Assembly (1:35) |
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Importing Vector NTI Data (2:27) |
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Overview: Ref-Guided Genome Assembly (1:30) |
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SeqNinja Overview (4:21) |
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Sequence Assembly and Analysis |
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Assembling Sanger Sequencing Data (3:58) |
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Aligning Sanger Sequences to a Reference (4:12) |
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Annotating the Consensus (2:57) |
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Ion Torrent: De Novo Bacterial Genome (5:03) |
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Assembling into Groups (2:29) |
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Ion Torrent: Ref-Guided Human Amplicon (5:18) |
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Adding Data to an Existing Assembly (2:42) |
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Ion Torrent: Ion AmpliSeq™ Cancer Panel (6:25) |
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Exporting the Consensus (3:12) |
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Ion Torrent: Mate Pair De Novo Assembly (5:16) |
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Visualizing Coverage (2:22) |
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Ion Torrent: Paired-End Assembly (4:34) |
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Analyzing Coverage (0:39) |
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PacBio: Amplicon Resequencing Assembly (5:59) |
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Primer Walking (2:33) |
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PacBio: Templated Genome Assembly (4:29) |
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Performing a Batch BLAST (2:39) |
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454: De Novo Bacterial Assembly (3:49) |
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Recomputing the Consensus (2:28) |
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454 De Novo Transcriptome Assembly (2:47) |
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Searching the Assembly (3:59) |
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Illumina: Ref-Guided Bacterial Genome (2:20) |
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Finding Conflict Splits (4:04) |
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Automated Genome Closure (4:51) |
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Merging Contigs (3:45) |
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Overview: RNA-Seq Workflow (1:20) |
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Changing Assembly and Analysis Settings (3:45) |
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RNA-Seq Alignment and Analysis (5:14) |
SNP Detection and Analysis |
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Overview: ChIP-Seq Workflow (1:31) |
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Setting Up an RNA-Seq Project (0:58) |
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Filtering SNPs (4:05) |
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Setting Up a ChIP-Seq Project (1:17) |
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Finding Coding Change & Splice Site SNPs (2:12) |
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Primers |
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Creating Custom SNP Sets (4:19) |
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Primer Design Overview (2:01) |
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Using the dbSNP Association Feature (1:01) |
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Designing Primers (2:50) |
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Interactive SNP Reports (0:27) |
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Modifying Your Primers (2:53) |
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SNP Discovery Parameters (0:37) |
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Extracting PCR Product for Cloning (2:02) |
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Using the Fisher's Exact Test (4:09) |
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Using Primer Catalogs (2:16) |
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Advanced Multi-Sample SNP Filtering (3:39) |
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Publication-Quality Graphics |
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Using Phenotype Data for SNP Analysis (4:36) |
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Creating a Genomic Map (4:09) |
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Comparing SNP Sets with Venn Diagrams (4:17) |
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Using Data Files to Build a Genome Map (0:55) |
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Using VCF Files for SNP Analysis (3:35) |
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Working with Panels in GenVision (0:27) |
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Integrating Data into a Single Illustration (3:17) |
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Alignment and Phylogenetic Tree Images (4:17) |
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