Facilitates personal genome annotation and interpretation. SeqsLa is a genomic analysis platform that provides (i) lightning-fast annotation workflow, (ii) comprehensive structural variant annotation, (iii) user-friendly graphical interface, and (iv) others variant filtering utilities. It also includes seven types of filters, which are general property, medical relevance, variant effect, splicing event, genome position, quality control, and tissue specificity, to fulfill different aspects of filtering strategies.
Atgenomix, Taipei, Taiwan; Genome and Systems Biology Degree Program, National Taiwan University and Academia Sinica, Taipei, Taiwan; Graduate Institute of Medical Genomics and Proteomics, National Taiwan University College of Medicine, Taipei, Taiwan; Department of Bio-Industrial Mechatronics Engineering, National Taiwan University, Taipei, Taiwan; Education & Research Center for Bio-Industrial Automation, National Taiwan University, Taipei, Taiwan
SeqsLab funding source(s)
Supported by the MOST 104-2622-E-002-034-CC2 project.