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

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PDF] A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar

Yang GAO, PhD, Fudan University, Shanghai

Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue, Genome Medicine

Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient approach, Genetics Selection Evolution

248228 PDFs Review articles in BIOINFORMATICS

Yan Lu's research works Sichuan University, Chengdu (SCU) and other places

PDF) Analysis of population structure and genetic diversity in low-variance Saimaa ringed seals using low-coverage whole-genome sequence data

Low-coverage whole-genome sequencing of cerebrospinal-fluid-derived cell-free DNA in brain tumor patients - ScienceDirect