About - DECIPHER v11.23
Por um escritor misterioso
Last updated 24 setembro 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
Identification of a Disease-Defining Gene Fusion in Epithelioid Hemangioendothelioma
The utility of multiple genomic technologies for interpretation of modern next generation sequencing: A novel case of three FANCA gene variants resulting in autosomal recessive Fanconi anaemia - ScienceDirect
X‐linked ichthyosis: New insights into a multi‐system disorder - Wren - 2022 - Skin Health and Disease - Wiley Online Library
Full article: Decoding the therapeutic landscape of alpha-linolenic acid: a network pharmacology and bioinformatics investigation against cancer-related epigenetic modifiers
GENA-LM: A Family of Open-Source Foundational DNA Language Models for Long Sequences
Route Setter Magazine #5 - the trade magazine for the indoor climbing industry - 2022/23 by Vertical-Life - Issuu
Cells December-1 2022 - Browse Articles
X‐linked ichthyosis: New insights into a multi‐system disorder - Wren - 2022 - Skin Health and Disease - Wiley Online Library
News – Cardiovascular Genetics & Genomics Group
Deciphering the phylogeny of violets based on multiplexed genetic and metabolomic approaches - ScienceDirect
Deciphering the possible reciprocal loop between hepatic stellate cells and cancer cells in the tumor microenvironment of the liver - ScienceDirect
DECIPHER – Mapping the Clinical Genome
SIGNET: transcriptome-wide causal inference for gene regulatory networks
Pancreatic fat in type 2 diabetes: Causal or coincidental?
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