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Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores
Immune receptor repertoires in pediatric and adult acute myeloid leukemia
Is ‘likely pathogenic’ really 90% likely? Reclassification data in ClinVar
Neoantigens and genome instability: impact on immunogenomic phenotypes and immunotherapy response
Artificial intelligence in clinical and genomic diagnostics
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