Efficient phasing and imputation of low-coverage sequencing data

By A Mystery Man Writer

PDF) Publisher Correction: Efficient phasing and imputation of low

Imputation of low-coverage sequencing data from 150,119 UK Biobank

Frontiers Comparison of Genotype Imputation for SNP Array and Low-Coverage Whole-Genome Sequencing Data

Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

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

Assessment of the performance of different imputation methods for

Phasing performance. (a,b) Switch error rate (SER, y-axis, log

A comparative analysis of current phasing and imputation software

The data behind increasing adoption of low-pass sequencing in human genomics, by Joe Pickrell, The Gencove Blog

Evaluation of low-pass genome sequencing in polygenic risk score

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

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Schematic of the QUILT model The model for one Gibbs sampling is

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