Working with Variant Call Format Files in Lasergene Genomics
DNASTAR’s Variant Annotation workflow provides functional annotation and enriched information for analyzing human samples in variant call format (VCF).
Is Open Source NGS Software for You?
An interview with Eric Cabot Ph.D. Dr. Eric Cabot received his MS from the University...
Q&A: NGS Sequence Assembly on the Cloud
Get your 5 FREE Cloud Assemblies! What is "Cloud Assemblies"? It’s a new service you...
Free NGS Assembly and Alignment for Genomic Sequencing Data
We know that for many researchers, performing large scale next-generation sequence alignments or de novo sequence assemblies on their computers can be a problem due to insufficient hard disk space or memory.
Tips for Successful Transcriptome Sequence Assembly
By Matthew Keyser De novo assembly of whole transcriptome sequencing data from non-model organisms can...
Rapid, Large-Scale Prioritizing of Human Variants with Lasergene Genomics Suite
Lasergene Genomics Suite now includes access to the Variant Annotation Database (VAD) for human sequencing...
DNASTAR LabViews: Dr. Robab Katani of Penn State
In our latest DNASTAR LabViews interview, we talk with Dr. Robab Katani of Penn State about her...
DNASTAR LabViews: Dr. Xiao-Ning Zhang of St. Bonaventure University
We are excited to announce our newest video series, DNASTAR LabViews, a collection of short...
Decreased Memory Requirements for De Novo Genome Assembly in Lasergene 13
Users often ask how much RAM is required for a de novo genome assembly in...
How much disk space do I need for my templated genome assembly?
Previously, we've described the RAM dependencies for de novo genome assemblies, which show a linear...
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