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For analyzing “Next Generation” Sequencing data, generated by platforms like the Genome Sequencer FLX System from Roche Applied Science (454 Life Sciences) and short read systems such as the Illumina® Genome Analyzer (Solexa sequencing technology). Designed with speed and simplicity of use in mind, NextGENe is capable of completing much of the analysis on a standard PC, and soon the analysis will be fully compatible with Linux platform. By statistically polishing the large sets of data into manageable fragments, NextGENe can quickly generate accurate results. NextGENe can be used to identify Single Nucleotide Polymorphisms (SNPs) and small Insertions and Deletions (Indels) for large scale resequencing projects and transcriptome analyses.

De novo assembly of both long and short sequences will be available shortly, as well as analysis of data from the Applied Biosystem SOLiD™ System.

The software is designed to handle the unique hurdles presented by each platform, such as the homopolymers for pyrosequencing and short reads generated by both the bridge amplification sequencing by synthesis method and the sequencing by ligation method, while utilizing the system’s advantages.

• Compatible with all Next Generation Sequencing systems
• Performs Assembly, SNP/Indel detection, Transcriptome Analysis
• “Low-end” Hardware Requirements
• Easy & Intuitive User Interface
• Exclusive SoftGenetics technical support


For more information, please click the link below:
NextGENe Product information

More SoftGenetics products are available:
SoftGenetics Product information

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