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Science.bina.com: Roche Sequencing Solutions - NGS Bioinformatics Tools Offline

Find powerful bioinformatics tools to precisely call structural variants, indels and SNPs in NGS sequencing..

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Bina | Library

Variant Filtering & Annotation Bina SomaticSeq Data Sheet SomaticSeq NGS Analysis for Pancreatic Neuroendocrine Tumors Watch the seminar presented by Dr. Chamberlain from UCSF on utilizing Bina softwa...
metasv

MetaSV Description Structural variations (SVs) are large genomic rearrangements that are believed to contribute to genomic diversity as well as genomic disorders. Due to their varying lengths, SVs are...

VarSim

VarSim et al. (2015) Bioinformatics. A high fidelity simulation and validation framework for high-throughput genome sequencing with cancer applicationshttp://bioinform.github.io/varsim/ Description Th...