SVLR: Genome Structure Variant Detection Using Long Read Sequencing Data
2020
Genome structural variants have great impacts on human phenotype and diversity, and have been linked to numerous diseases. Long read sequencing technologies arise to make it possible to find structural variants of as long as ten thousand nucleotides. Thus, long read based structural variant detection has been drawing attention of many recent research projects, and many tools have been developed for long reads to detect structural variants recently.
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