A protocol for applying low-coverage whole-genome sequencing data in structural variation studies
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A protocol for applying low-coverage whole-genome sequencing data
Detection of trait-associated structural variations using short
Overview of Structural Variation
Home - HumPOG
An exploration of machine-learning based variant callers for SNV
Long-read sequencing settings for efficient structural variation
Detecting structural variations with precise breakpoints using low
陆艳
Comprehensive Structural Variant Detection: From Mosaic to
Comprehensive evaluation of structural variation detection
Genome Sequencing - ClearIAS