Publications
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Filters: Author is Sahraeian, Sayed Mohammad Ebrahim [Clear All Filters]
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions. Cell Genom. 2022 ;2(5).
. Hidden biases in germline structural variant detection. Genome Biol. 2021 ;22(1):347.
. Curated variation benchmarks for challenging medically relevant autosomal genes. Nat Biotechnol. 2022 ;40(5):672-680.
. Assessing reproducibility of inherited variants detected with short-read whole genome sequencing. Genome Biol. 2022 ;23(1):2.
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