The VA Module can automatically retrieve reference sequences from the genomic database, report variants with genomic coordinates, and report genomic annotations for SNPs. The Variant Analysis (VA) Module provides fast analysis of Sanger sequencing data. The robust algorithms will call SNPs, mutations, insertions, deletions, and heterozygous insertions⁄deletions for data generated using Applied Biosystems genetic analyzers. Variant Reporter Software is designed for reference-based and non-reference-based analysis such as mutation detection and analysis, SNP discovery and validation, and sequence confirmation.
#DNA SEQUENCE CHROMATOGRAM VIEWER SOFTWARE DOWNLOAD#
Variant Reporter Software Download trial version › It provides library functions for comparison to a known group of sequences, as well as features to assist with 21 CFR Part 11 compliance (Security, Audit and electronic signature features), which can be important in clinical research labs. SeqScape Software is a resequencing package designed for mutation detection and analysis, SNP discovery and validation, pathogen sub-typing, allele identification, and sequence confirmation. Windows™ 7 SP1, 32-bit or 64-bit or Windows™ 10 The improved sensitivity makes Sanger sequencing a fast, cost effective, and accurate way to call low-frequency somatic variants where the number of relevant targets is limited. Minor Variant Finder Software enables 5% somatic variant detection using Sanger sequencing.