Low-coverage sequencing cost-effectively detects known and novel

Cost-effectively dissecting the genetic architecture of complex

Cost-effectively dissecting the genetic architecture of complex

PDF) Mid-pass whole genome sequencing enables biomedical genetic

Minimizing Reference Bias with an Impute-First Approach

Proportion of single nucleotide variants in saliva genomes (n = 5

Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to

Low-Pass Whole Genome Sequencing

Low-coverage sequencing cost-effectively detects known and novel

Evaluation of low-pass genome sequencing in polygenic risk score

Identification of RP1 as the genetic cause of retinitis pigmentosa

Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to

Best practices for analyzing imputed genotypes from low-pass

Assessment of the performance of different imputation methods for