CoNIFER uses exome sequencing data to find copy number variants (CNVs) and genotype the copy-number of duplicated genes.
Features
- Can integrate exomes from multiple capture experiments
- SVD normalization eliminates systematic bias and noise
Categories
Bio-InformaticsLicense
GNU General Public License version 3.0 (GPLv3)Follow CoNIFER
Other Useful Business Software
$300 in Free Credit Towards Top Cloud Services
Start your project in minutes. After credits run out, 20+ products include free monthly usage. Only pay when you're ready to scale.
Rate This Project
Login To Rate This Project
User Reviews
Be the first to post a review of CoNIFER!