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Chapter and Conference Paper
SVEM: A Structural Variant Estimation Method Using Multi-mapped Reads on Breakpoints
Recent development of next generation sequencing (NGS) technologies has led to the identification of structural variants (SVs) of genomic DNA existing in the human population. Several SV detection methods util...
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Chapter and Conference Paper
HapMonster: A Statistically Unified Approach for Variant Calling and Haploty** Based on Phase-Informative Reads
Haplotype phasing is essential for identifying disease-causing variants with phase-dependent interactions as well as for the coalescent-based inference of demographic history. One of approaches for estimating ...