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Haplotype-resolved diverse human genomes and integrated analysis of structural variation
UploadBAMnostic: an OS-agnostic toolkit for genomic sequence analysis
Download from doi.orgResolving Complex Structural Genomic Rearrangements using a Randomized Approach
Download from doi.orgPrimate genome architecture influences structural variation mechanisms and functional consequences
Download from doi.orgCGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome
Download from europepmc.orgCopy number variation prevalence in known asthma genes and their impact on asthma susceptibility
Download from www.ncbi.nlm.nih.govCopy number variation genotyping using family information
Download from dx.doi.orgAn integrated map of genetic variation from 1,092 human genomes
Download from www.nature.comRegulatory element copy number differences shape primate expression profiles
Download from www.pnas.orgNatural genetic variation caused by small insertions and deletions in the human genome
Download from genome.cshlp.orgMapping copy number variation by population scale genome sequencing
Download from www.nature.comA map of human genome variation from population-scale sequencing
Download from www.nature.comSmall insertions and deletions (INDELs) in human genomes
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