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Efficient phasing and imputation of low-coverage sequencing data

Efficient phasing and imputation of low-coverage sequencing data

Imputation strategies for genomic prediction using nanopore

Functional variant analysis across low-coverage and SNP array call

Simone Rubinacci on X: Our paper describing a new method

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PDF] GeneImp: Fast Imputation to Large Reference Panels Using

The construction of a haplotype reference panel using extremely

A cautionary tale of low-pass sequencing and imputation with

Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank - Abstract - Europe PMC

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Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

Running time per individual of different imputation methods for

A cautionary tale of low-pass sequencing and imputation with respect to haplotype accuracy, Genetics Selection Evolution

Imputation strategies for genomic prediction using nanopore

E07.1 - Efficient phasing and imputation of low coverage