A protocol for applying low-coverage whole-genome sequencing data

STAR Protocols is an open access, peer-reviewed journal from Cell Press. We offer structured, transparent, accessible, and repeatable step-by-step experimental and computational protocols from all areas of life, health, earth and physical sciences.

Best practices for variant calling in clinical sequencing, Genome Medicine

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Copy number profiling using nanopore low-pass whole genome sequencing.

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A) In this study we performed paired-end high coverage whole genome

Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory

Bo XIE, Chinese Academy of Sciences, Beijing, CAS, Shanghai Institutes for Biological Sciences