| Cloning |
Product Overviews |
 |
Gateway MultiSite Cloning (3:59) |
|
Lasergene 11 Overview (3:02) |
|
Virtual Cloning Overview (1:04) |
|
Introducing Lasergene 11 Webinar (44:11) |
|
Directional TOPO Cloning (2:59) |
|
Using the DNASTAR Cloud (3:57) |
|
TA Cloning in 3 Easy Steps (1:44) |
|
Lasergene Core Suite Webinar (53:56) |
|
Restriction Enzyme Cloning (3:45) |
|
Lasergene Genomics Suite Webinar (59:19) |
|
Gateway Cloning (3:20) |
|
Cloning and Primer Design Webinar (56:58) |
|
Creating Custom Cloning Vectors (3:54) |
|
De Novo Genome Assembly Webinar (38:30) |
|
Gene Detection |
|
Alignment and Gene Discovery Webinar (54:36) |
|
Gene Discovery Overview (1:05) |
|
RNA-Seq Webinar (56:27) |
|
Getting Started with GeneQuest (3:12) |
|
Protean 3D Overview Webinar (52:06) |
|
Aligning Exons to a Reference (2:53) |
|
Automated Genome Closure Webinar (56:03) |
|
Analyzing Restriction Enyzmes (0:34) |
|
Manual Gap Closure Webinar (58:29) |
|
Using the Borodovsky Method (0:34) |
|
Sanger Sequence Assembly Webinar (50:37) |
|
Locating Transcription Factor Binding Sites (2:52) |
|
Illumina Assembly and Analysis Webinar (56:09) |
|
Gene Expression Analysis |
|
Ion Torrent Analysis Webinar (58:24) |
|
|
|
Protein Analysis |
|
|
|
|
Protein Analysis Overview (1:38) |
|
Analyzing Gene Expression Patterns (1:17) |
|
Protean 3D's Analysis View (1:44) |
|
Identifying Co-Regulated Genes (1:15) |
|
Using Protean Methods (0:29) |
|
Clustering Gene Expression Data (0:40) |
|
Finding PROSITE Patterns (3:03) |
|
Creating Gene Sets (2:38) |
|
Getting Started with Protean 3D (4:39) |
|
Using the Gene Table (3:13) |
|
Rotating and Moving a Structure (0:33) |
|
Using the Gene Ontology View (2:47) |
|
Using the Motion Library (0:36) |
|
Using the Scatter Plot (0:50) |
|
Changing Rendering Styles (3:19) |
|
Using Venn Diagrams (4:14) |
|
Creating Surfaces and Adjusting Lighting (5:03) |
|
Importing Microarray Data (3:19) |
|
Predicting Epitopes in Protean 3D (3:38) |
|
Importing Annotations in ArrayStar (3:22) |
|
Aligning Protein Structures (2:56) |
|
Multiple and Pairwise Alignments |
|
Viewing Protease Cleavage Sites (1:57) |
|
|
Getting Started with MegAlign Pro (2:49) |
Sequence Analysis and Visualization |
|
|
Sequence Alignment Overview (1:07) |
|
Sequence Analysis Overview (11:45) |
|
Performing a Pairwise Alignment (2:53) |
|
Managing Large Groups of Sequences (2:49) |
|
Performing a Dot Plot Pairwise Alignment (3:09) |
|
Filtering Enzymes (3:01) |
|
|
Editing an Alignment (2:10) |
|
Identifying Enzymes to Excise a Gene (3:09) |
|
Performing a Sub-Alignment (3:23) |
|
Adding New Restriction Enzymes (2:41) |
|
|
|
Creating an Agarose Gel Simulation (1:56) |
|
|
|
Preparing a Map for Presentation (2:43) |
|
|
|
Customizing Your SeqBuilder Layout (4:43) |
|
|
|
Performing BLAST and Entrez Searches (4:16) |
|
|
|
Translation Numbering (1:36) |
|
Choosing an Alignment Method (4:09) |
|
Batch Translation of Genomic Annotations (2:56) |
|
Customizing the Alignment Report (0:40) |
|
Modifying the Genetic Code (4:23) |
|
Next-Gen Workflows |
|
Editing Feature Styles (0:58) |
|
|
Overview: De Novo Genome Assembly (1:36) |
|
Importing Vector NTI Data (2:27) |
|
|
Overview: Ref-Guided Genome Assembly (1:31) |
|
SeqNinja Overview (4:21) |
|
|
|
Sequence Assembly and Analysis |
|
|
|
|
Assembling Sanger Sequencing Data (3:58) |
|
Metagenomic Assembly and Analysis (3:46) |
|
Aligning Sanger Sequences to a Reference (4:12) |
|
|
|
Annotating the Consensus (2:57) |
|
|
Ion Torrent: De Novo Bacterial Genome (5:03) |
|
Assembling into Groups (2:29) |
|
Ion Torrent: Ref-Guided Human Amplicon (5:18) |
|
Adding Data to an Existing Assembly (2:42) |
|
Ion Torrent: Ion AmpliSeq™ Cancer Panel (6:25) |
|
Exporting the Consensus (3:12) |
|
Ion Torrent: Mate Pair De Novo Assembly (5:16) |
|
Visualizing Coverage (2:22) |
|
Ion Torrent: Paired-End Assembly (4:34) |
|
Analyzing Coverage (0:39) |
|
PacBio: Amplicon Resequencing Assembly (5:59) |
|
Primer Walking (2:33) |
|
PacBio: Templated Genome Assembly (4:29) |
|
Performing a Batch BLAST (2:39) |
|
|
454: De Novo Bacterial Assembly (3:49) |
|
Recomputing the Consensus (2:28) |
|
|
454 De Novo Transcriptome Assembly (2:47) |
|
Searching the Assembly (3:59) |
|
Illumina: Ref-Guided Bacterial Genome (2:21) |
|
Finding Conflict Splits (4:04) |
|
Automated Genome Closure (4:51) |
|
Merging Contigs (3:46) |
|
Overview: RNA-Seq Workflow (1:20) |
|
Changing Assembly and Analysis Settings (3:45) |
|
RNA-Seq Alignment and Analysis (5:14) |
SNP Detection and Analysis |
|
Overview: ChIP-Seq Workflow (1:31) |
|
|
|
|
Setting Up an RNA-Seq Project (0:58) |
|
Filtering SNPs (4:05) |
|
Setting Up a ChIP-Seq Project (1:17) |
|
|
|
Primers |
|
Creating Custom SNP Sets (4:19) |
|
Primer Design Overview (2:01) |
|
Using the dbSNP Association Feature (1:01) |
|
Designing Primers in SeqBuilder (2:50) |
|
Interactive SNP Reports (0:27) |
|
Modifying Your Primers (2:53) |
|
SNP Discovery Parameters (0:37) |
|
Extracting PCR Product for Cloning (2:02) |
|
Using the Fisher's Exact Test (4:09) |
|
Using Primer Catalogs (2:16) |
|
Advanced Multi-Sample SNP Filtering (3:39) |
|
Publication-Quality Graphics |
|
Using Phenotype Data for SNP Analysis (4:36) |
|
Creating a Genomic Map (4:09) |
|
Comparing SNP Sets with Venn Diagrams (4:17) |
|
Using Data Files to Build a Genome Map (0:55) |
|
Using VCF Files for SNP Analysis (3:35) |
|
Working with Panels in GenVision (0:27) |
|
|
|
Integrating Data into a Single Illustration (3:17) |
|
|
|
Alignment and Phylogenetic Tree Images (4:17) |
|
|
