Publications
Filters: Author is Zarate, Samantha [Clear All Filters]
A diploid assembly-based benchmark for variants in the major histocompatibility complex. Nat Commun. 2020 ;11(1):4794.
. Parliament2: Accurate structural variant calling at scale. Gigascience. 2020 ;9(12).
. Hidden biases in germline structural variant detection. Genome Biol. 2021 ;22(1):347.
. Benchmarking challenging small variants with linked and long reads. Cell Genom. 2022 ;2(5).
. A complete reference genome improves analysis of human genetic variation. Science. 2022 ;376(6588):eabl3533.
. The complete sequence of a human genome. Science. 2022 ;376(6588):44-53.
. The complete sequence of a human Y chromosome. Nature. 2023 ;621(7978):344-354.
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