The allelic landscape of human blood cell trait variation and links to common complex disease
Many common variants have been associated with hematological traits, but identification of causal genes and pathways has proven challenging. We performed a genome-wide association analysis in the UK Biobank and INTERVAL studies, testing 29.5 million genetic variants for association with 36 red cell,...
Slični predmeti
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Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
od: Chen, L, i dr.
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Phasing for medical sequencing using rare variants and large haplotype reference panels
od: Sharp, K, i dr.
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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.
od: Delaneau, O, i dr.
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