Low-coverage sequencing cost-effectively detects known and novel

Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

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

Mid-pass whole genome sequencing enables biomedical genetic

Influence of (A) minimum r 2 threshold and (B) lower MAF threshold

Low-coverage sequencing cost-effectively detects known and novel

PDF) Two-stage family-based designs for sequencing studies

Low-Pass Whole Genome Sequencing

Imputation of low-coverage sequencing data from 150,119 UK Biobank

PDF) Cost-effectively dissecting the genetic architecture of