<style face="normal" font="default" size="100%">Association of structural variation with cardiometabolic traits in Finns.</style>

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<style face="normal" font="default" size="100%">Association of structural variation with cardiometabolic traits in Finns.</style>

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<style face="normal" font="default" size="100%">Chromosome-scale, haplotype-resolved assembly of human genomes.</style>

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<style face="normal" font="default" size="100%">Efficient phasing and imputation of low-coverage sequencing data using large reference panels.</style>

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<style face="normal" font="default" size="100%">Haplotype-resolved diverse human genomes and integrated analysis of structural variation.</style>

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<style face="normal" font="default" size="100%">Towards population-scale long-read sequencing.</style>

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<style face="normal" font="default" size="100%">Inherited causes of clonal haematopoiesis in 97,691 whole genomes.</style>

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<style face="normal" font="default" size="100%">Mapping and characterization of structural variation in 17,795 human genomes.</style>

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<style face="normal" font="default" size="100%">Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions.</style>

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<style face="normal" font="default" size="100%">Rapid, Paralog-Sensitive CNV Analysis of 2457 Human Genomes Using QuicK-mer2.</style>

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<style face="normal" font="default" size="100%">A structural variation reference for medical and population genetics.</style>

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<style face="normal" font="default" size="100%">Transcriptomic signatures across human tissues identify functional rare genetic variation.</style>

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<style face="normal" font="default" size="100%">A multi-task convolutional deep neural network for variant calling in single molecule sequencing.</style>

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<style face="normal" font="default" size="100%">Accurate detection of complex structural variations using single-molecule sequencing.</style>

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<style face="normal" font="default" size="100%">Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms.</style>

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<style face="normal" font="default" size="100%">Characterizing reduced coverage regions through comparison of exome and genome sequencing data across 10 centers.</style>

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<style face="normal" font="default" size="100%">Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line.</style>

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<style face="normal" font="default" size="100%">Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.</style>

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<style face="normal" font="default" size="100%">Genetic effects on gene expression across human tissues.</style>

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<style face="normal" font="default" size="100%">Genome-wide profiling of heritable and de novo STR variations.</style>

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<style face="normal" font="default" size="100%">The impact of structural variation on human gene expression.</style>

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<style face="normal" font="default" size="100%">Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.</style>

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<style face="normal" font="default" size="100%">Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA.</style>