About - DECIPHER v11.23
Por um escritor misterioso
Last updated 21 fevereiro 2025
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DECIPHER helps the clinical community share and compare human genome variants and phenotypes in a database of tens of thousands of patients worldwide
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About - DECIPHER v11.23
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PhenoSV: interpretable phenotype-aware model for the prioritization of genes affected by structural variants
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Genomics in the long-read sequencing era: Trends in Genetics
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Route Setter Magazine #5 - the trade magazine for the indoor climbing industry - 2022/23 by Vertical-Life - Issuu
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About - DECIPHER v11.23
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Blog - Human Variome Project
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About - DECIPHER v11.23
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Generation of zero-valent sulfur from dissimilatory sulfate reduction in sulfate-reducing microorganisms
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An Atlas of Variant Effects to understand the genome at nucleotide resolution, Genome Biology
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