Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations - ScienceDirect

Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations - ScienceDirect

Interferon pathway lupus risk alleles modulate risk of death from

Assessment of the performance of different imputation methods for

PDF) Genome-wide CNV analysis uncovers novel pathogenic regions in

AI applications in functional genomics - Computational and

Assessment of the performance of different imputation methods for

NyuWa Genome resource: A deep whole-genome sequencing-based

Chapter 5: Demand, services and social aspects of mitigation

Identification of RP1 as the genetic cause of retinitis pigmentosa

Understanding and increasing coverage : Knowledge Base

Enabling low-pass whole genome sequencing

Detecting selection in low-coverage high-throughput sequencing data using principal component analysis, BMC Bioinformatics

JLPEA, Free Full-Text

Low-coverage sequencing cost-effectively detects known and novel