SoftGenetics Resources

NextGENeLR

What Is Variant Calling?

Learn the fundamentals of variant calling, key workflows, and tools to confidently identify genetic differences in sequencing analysis with SoftGenetics.

NextGENeLR

How to Analyze Mixed DNA Samples: Tools and Best Practices

Discover tools and best practices for analyzing mixed DNA samples in forensics, oncology, and contamination studies with SoftGenetics.

NextGENeLR

Types of DNA Sequencing: When Should You Use Each?

Discover the relevance of fragment analysis in genetic research, its applications, and how SoftGenetics software enhances variant detection & analysis.

GeneMarker

What Is Fragment Analysis and Why Is It Still Essential?

Discover the relevance of fragment analysis in genetic research, its applications, and how SoftGenetics software enhances variant detection & analysis.

GeneMarker

STR Analysis vs. SNP Genotyping: When to Use Each

Compare STR analysis and SNP genotyping to determine the best approach for your research goals. Learn about their unique advantages and hybrid approaches.

How to Analyze Microsatellites Using Capillary Electrophoresis

Analyze microsatellites using capillary electrophoresis for accurate, high-resolution genetic data in breeding, biodiversity, and conservation studies.

Accurate Variant Detection from Long-Read Sequencing

Discover how NextGENeLR enhances long-read sequencing analysis, tackling higher error rates and complex variants for accurate genetic insights

What’s New in NextGENeLR?

Discover NextGENeLR: Enhanced precision, effortless workflows, and accessible long-read sequencing analysis for all researchers. Start your free trial.