About - DECIPHER v11.23
Por um escritor misterioso
Last updated 20 outubro 2024
DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide
About - DECIPHER v11.23
PhenoSV: interpretable phenotype-aware model for the prioritization of genes affected by structural variants
Genomics in the long-read sequencing era: Trends in Genetics
Route Setter Magazine #5 - the trade magazine for the indoor climbing industry - 2022/23 by Vertical-Life - Issuu
About - DECIPHER v11.23
Blog - Human Variome Project
About - DECIPHER v11.23
Generation of zero-valent sulfur from dissimilatory sulfate reduction in sulfate-reducing microorganisms
An Atlas of Variant Effects to understand the genome at nucleotide resolution, Genome Biology
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