A free SNP genotyping data analysis tool for use with TaqMan® SNP Genotyping Assays.

• State-of-the-art genotype-calling algorithm with an intuitive user interface
• Enhanced multiplate analysis features to meet the requirements of emerging markets and future research

Free software developed specifically for TaqMan® Copy Number Assay data analysis.

• Easy-to-use software with a graphical interface enables quick copy-number calculations
• Assigns confidence values for each copy-number call and includes outlier removal function

Designed for reference-based and nonreference-based analysis such as mutation detection and analysis, SNP discovery, and sequence confirmation.

• Designed for basic and clinical researchers, for genotyping projects and secondary analysis
• Automates variant detection, saving time and money

SOLiD® LifeScope™ Software uses a flexible pipeline architecture to provide maximum flexibility and easy of use for performing high-throughput data analysis for SOLiD® instrument data.

• Streamlined interface—command line and simple web-interface options provide flexibility for user preference
• Efficient infrastructure—designed towork on offline clusters and cloud computing configurations to relieve instrument bottlenecks
• Consolidated analysis—standard base sequence file exports enable the combination of data from multiple sequencing platforms for single project-based analysis
• Versatile application—includes mapping, pairing, SNP finding, structural variations, and whole transcriptome analyses