Associated Papers
ClinVAP: a reporting strategy from variants to therapeutic options.
Sürün B et al.
Bioinformatics (oxford, England), 2020
31830259 (PubMed )
Supplement: btz924_supplementary_data.zip › btz924-suppl_data › SupplementaryMaterialB_ExampleReport.pdf
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
Fragoza R et al.
Nature Communications, 2019
31515488 (PubMed )
Supplement: 41467_2019_11959_MOESM7_ESM.xlsx › SD3_-_COSMIC_Mutations
A somatic reference standard for cancer genome sequencing.
Craig DW et al.
Scientific Reports, 2016
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