Low-coverage sequencing cost-effectively detects known and novel
By A Mystery Man Writer
Description
A cost-effective sequencing method for genetic studies combining
Cost-effectively dissecting the genetic architecture of complex
Boosting variant calling performance using a high-quality
Identification of RP1 as the genetic cause of retinitis pigmentosa
Minimizing Reference Bias with an Impute-First Approach
Mid-pass whole genome sequencing enables biomedical genetic
Constructing germline research cohorts from the discarded reads of
Assessment of the performance of different imputation methods for
Mid-pass whole genome sequencing enables biomedical genetic
Low-Pass Whole Genome Sequencing
from
per adult (price varies by group size)