Product DemonstrationsLife Sciences

DNASTAR: Using VCF Files for SNP Analysis

6 Jul 2013

DNASTAR: Using VCF Files for SNP Analysis

In this video see how to use variant call format (VCF) files for filtering SNPs from next-gen sequencing projects in Lasergene Genomics Suite.

Other videos from DNASTAR Inc.

Learn How to Use SeqMan Pro for All Your Sequence Editing Needs
12 Feb 2014
Proteomics with DNASTAR’s Lasergene Protean 3D
26 Aug 2013
Aligning Protein Structures with DNASTAR’s Lasergene Protean 3D
18 Aug 2013
DNASTAR: Primer Design Software
11 Aug 2013
Metagenomic Assembly with Host Removal Using DNASTAR’s SeqMan NGen
4 Aug 2013
Getting Started with DNASTAR’s Lasergene® MegAlign Pro™
28 Jul 2013
Illumina-Reference Guided Genome Assembly with DNASTAR’s SeqMan NGen
21 Jul 2013
SeqNinja: 3 Useful Functions for Large Data Sets
16 Jul 2013
Detecting Viral Integration Sites Using DNASTAR's SeqMan NGen
14 Jul 2013
Using the DNASTAR Cloud
11 Jul 2013
Identifying Protease Cleavage Sites Using Protean 3D
8 Jul 2013
DNASTAR Sanger Sequence Assembly
30 Jun 2013
Agarose Gel Simulation with DNASTAR’s GeneQuest Software
27 Jun 2013
Exploring Copy Number Variation (CNV) with DNASTAR’s ArrayStar SeqMan NGen Software
24 Jun 2013
Analyzing SNPs in Coding Sequences and Splice Sites using DNASTAR’s SeqMan Software
20 Jun 2013
Introducing DNASTAR’s Lasergene 11
9 Jun 2013
DNASTAR Lasergene 10.1 - A New Generation in Sequence Assembly and Analysis
10 Oct 2012
Genome Assembly Software Demo
10 May 2012
Ion Torrent Amplicon Assembly
10 May 2012

Links

DNASTAR Inc.Company website

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