Annotated Reference Genomes available for use with NextGENe Software

In order to efficiently align large genomes and to locate Indels found in 2nd generation sequencing data NextGENe utilizes a modified BWA methodology. The following annotated pre-indexed reference genomes are complimentary to NextGENe software users. Additional annotated genomes are available upon request.

To Request annotated reference genome please email info@softgenetics.com indicated reference of interest and from which platform the data has been generated.

Review additional NextGENe software applications:

• SNP/INDEL & Structural Variant Analysis
• Prediction and Rare Disease Discovery
• Whole Genome Alignment
• Transcriptome/RNA-SEQ: Expression and Alternative Splicing Analysis
• miRNA, ChipSeq, Serial Analysis of Gene Expression (SAGE) & Digital Gene Expression (DGE) Analysis
• de novo assembly
• Targeted Re-Sequencing
• Forensic Profiling
• Automation Pipeline

Pricing & Trial Version:
Request 30-day trial/Price Quote

Reference Material:
Download/View NextGENe® Brochure
NextGENe User Manual
Annotated Reference Genomes

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