Frontiers | Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
The Competition - Project STARLIGHT
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
Low coverage whole genome sequencing of the RPE-1 cell line reveals a... | Download Scientific Diagram
Comparison of low-coverage and SNP array imputation. (A) Imputation... | Download Scientific Diagram
Genome skimming - Wikipedia
A beginner's guide to low‐coverage whole genome sequencing for population genomics - Lou - 2021 - Molecular Ecology - Wiley Online Library
Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA | Nature Communications
GENEWIZ from Azenta | Low-Pass Whole Genome Sequencing
Low-coverage whole-genome sequencing of cerebrospinal-fluid-derived cell-free DNA in brain tumor patients - ScienceDirect
Is there a bias after DNA fragmentation?
Genome skimming - Wikipedia
Genotyping by low-coverage whole-genome sequencing in intercross pedigrees from outbred founders: a cost-efficient approach | Genetics Selection Evolution | Full Text
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
Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores | Genome Medicine | Full Text
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 sequencing cost-effectively detects known and novel variation in underrepresented populations - ScienceDirect
How to calculate the coverage for a NGS experiment
Sequencing coverage and breadth of coverage
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
Sequencing depth and coverage: key considerations in genomic analyses | Nature Reviews Genetics
GENEWIZ from Azenta | Low-Pass Whole Genome Sequencing
