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The landscape of genomic structural variation in Indigenous Australians

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Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of...

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RNA sequencing and target long-read sequencing reveal an intronic transposon...

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Whole-genome sequencing reveals the molecular implications of the stepwise...

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Bacteroides is increased in an autism cohort and induces autism-relevant...

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Randomized phase II study of preoperative afatinib in untreated head and neck...

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Exploring the hemicellulolytic properties and safety of Bacillus...

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ACIDES: on-line monitoring of forward genetic screens for protein engineering

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Deep screening of antibody–antigen affinities

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Ultrafast bisulfite sequencing detection of 5-methylcytosine in DNA and RNA

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Terminal modifications independent cell-free RNA sequencing enables sensitive...

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Koban culture genome-wide and archeological data open the bridge between...

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Publisher Correction: A 39 kb structural variant causing Lynch syndrome...

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Author Correction: A chromosome-level reference genome of the Antarctic...

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Alternative splicing of latrophilin-3 controls synapse formation

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Enhancing the quality of panel-based tumor mutation burden assessment: a...

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Human whole-exome genotype data for Alzheimer’s disease

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A recurrent synonymous L1CAM variant in a fetus with hydrocephalus

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Author Correction: Trimodal single-cell profiling reveals a novel pediatric...

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Illumina reads correction: evaluation and improvements

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