An Integrated Pipeline for Sequence Variant Identification and Annotation in Next Generation Sequencing Data
A fast and efficient tool for detecting SNPs and Indels in single, paired (case-control) and multiple samples. SeqVItA offers detection of Somatic mutations, rare and common variants across population samples.
Contact: Prashanthi Dharanipragada, Sampreeth Reddy and Dr. Nita Parekh,
Centre for Computational Natural Sciences and Bioinformatics,
International Institute of Information Technology-Hyderabad, India
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