Sequencing depth and coverage: key considerations in genomic analyses | Nature Reviews Genetics
How to calculate the coverage for a NGS experiment
Efficient phasing and imputation of low-coverage sequencing data using large reference panels | Nature Genetics
A beginner's guide to low‐coverage whole genome sequencing for population genomics - Lou - 2021 - Molecular Ecology - Wiley Online Library
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies | Nature Genetics
Genes | Free Full-Text | Ultrahigh-Density Linkage Map Construction Using Low-Coverage Whole-Genome Sequencing of a Doubled Haploid Population: Case Study of Torafugu (Takifugu rubripes)
Low-coverage whole-genome sequencing of extracellular vesicle-associated DNA in patients with metastatic cancer | Scientific Reports
Genome skimming - Wikipedia
Low-coverage whole-genome sequencing of cerebrospinal-fluid-derived cell-free DNA in brain tumor patients - ScienceDirect
Frontiers | Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
Phylogenomics from low‐coverage whole‐genome sequencing - Zhang - 2019 - Methods in Ecology and Evolution - Wiley Online Library
Low coverage whole genome sequencing of the RPE-1 cell line reveals a... | Download Scientific Diagram
Is there a bias after DNA fragmentation?
A beginner's guide to low‐coverage whole genome sequencing for population genomics - Lou - 2021 - Molecular Ecology - Wiley Online Library
Genome skimming - Wikipedia
Accuracy of genotyping by low-coverage sequencing. (A) Concordance... | Download Scientific Diagram
Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA | Nature Communications
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations - ScienceDirect
GENEWIZ from Azenta | Low-Pass Whole Genome Sequencing
Sequencing Coverage for NGS Experiments
Overview of the method. a Sequence data from two extremely low-coverage... | Download Scientific Diagram
Comparison of low-coverage and SNP array imputation. (A) Imputation... | Download Scientific Diagram
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis | Journal of Medical Genetics
GENEWIZ from Azenta | Low-Pass Whole Genome Sequencing
GENEWIZ from Azenta | Low-Pass Whole Genome Sequencing