Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs - Concepedia

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Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs

DOI Full Paper Access

112

Citations

30

References

2014

Year

Giorgio Pistis, Eleonora Porcu, Scott Vrieze, Carlo Sidore, Maristella Steri, Fabrice Danjou, Fabio Busonero, Antonella Mulas, Magdalena Żołędziewska, Andrea Maschio,

European Journal of Human Genetics

Allelic VariantHaplotype DeterminationMedicineGeneticsStudy-specific Whole-genome SequencesStatistical GeneticsBiostatisticsGenetic VariationGenomicsPublic HealthPopulation GeneticsVariant InterpretationCost-effective Study Designs

References

	Year	Citations

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