Efficient phasing and imputation of low-coverage sequencing data

Simone Rubinacci on X: Really excited to see the GLIMPSE paper

Evaluation of low-pass genome sequencing in polygenic risk score

The size and composition of haplotype reference panels impact the

Boosting variant calling performance using a high-quality

Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies. - Abstract - Europe PMC

Efficient phasing and imputation of low-coverage sequencing data

Functional variant analysis across low-coverage and SNP array call

Frontiers Assessment of Imputation Quality: Comparison of Phasing and Imputation Algorithms in Real Data

Assessment of the performance of different imputation methods for

Imputation strategies for genomic prediction using nanopore

Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an