Low-coverage sequencing cost-effectively detects known and novel

Minimizing Reference Bias with an Impute-First Approach

Identification of RP1 as the genetic cause of retinitis pigmentosa

Pre-imputation non-reference variant concordance.​ We computed

Low-coverage sequencing cost-effectively detects known and novel

Constructing germline research cohorts from the discarded reads of

PGC: Incorporating Diverse Populations in Psychiatric Genetics

Low-coverage sequencing cost-effectively detects known and novel

PDF) Simulation of African and non-African low and high coverage

Cost-effectively dissecting the genetic architecture of complex

PDF) Mid-pass whole genome sequencing enables biomedical genetic

Constructing germline research cohorts from the discarded reads of

The data behind increasing adoption of low-pass sequencing in

Best practices for analyzing imputed genotypes from low-pass

Best practices for analyzing imputed genotypes from low-pass

Best practices for analyzing imputed genotypes from low-pass