Public articles linked to the same research event.
发表出处待核验 This work builds a frozen, content-hashed data asset and a uniform scoring harness that maps seven MaveDB saturation genome editing (SGE) score sets to GRCh38, harmonises orientation and freezes them into immutable matrices, then evaluates nineteen variant effect predictors across sixteen strata using per-gene Spearman rho pooled by DerSimonian-Laird random-effects meta-analysis with per-stratum measurement-reliability estimates, attenuation correction, paired dependent-correlation tests and leave-one-gene-out validation, covering 64,178 variants and seven cancer susceptibility genes.
This work builds a frozen, content-hashed data asset and a uniform scoring harness that maps seven MaveDB saturation genome editing (SGE) score sets to GRCh38, harmonises orientation and freezes them into immutable matrices, then evaluates nineteen variant effect predictors across sixteen strata using per-gene Spearman rho pooled by DerSimonian-Laird random-effects meta-analysis with per-stratum measurement-reliability estimates, attenuation correction, paired dependent-correlation tests and leave-one-gene-out validation, covering 64,178 variants and seven cancer susceptibility genes.
This work builds a frozen, content-hashed data asset and a uniform scoring harness that maps seven MaveDB saturation genome editing (SGE) score sets to GRCh38, harmonises orientation and freezes them into immutable matrices, then evaluates nineteen variant effect predictors across sixteen strata using per-gene Spearman rho pooled by DerSimonian-Laird random-effects meta-analysis with per-stratum measurement-reliability estimates, attenuation correction, paired dependent-correlation tests and leave-one-gene-out validation, covering 64,178 variants and seven cancer susceptibility genes.
This work builds a frozen, content-hashed data asset and a uniform scoring harness that maps seven MaveDB saturation genome editing (SGE) score sets to GRCh38, harmonises orientation and freezes them into immutable matrices, then evaluates nineteen variant effect predictors across sixteen strata using per-gene Spearman rho pooled by DerSimonian-Laird random-effects meta-analysis with per-stratum measurement-reliability estimates, attenuation correction, paired dependent-correlation tests and leave-one-gene-out validation, covering 64,178 variants and seven cancer susceptibility genes.