Transcriptomic signatures across human tissues identify functional rare genetic variation
Por um escritor misterioso
Last updated 30 maio 2024
Clinical implementation of RNA sequencing for Mendelian disease diagnostics, Genome Medicine
Transcriptomic taxonomy and neurogenic trajectories of adult human, macaque, and pig hippocampal and entorhinal cells - ScienceDirect
Clinical implementation of RNA sequencing for Mendelian disease diagnostics, Genome Medicine
Integrated analysis of genomic and transcriptomic data for the discovery of splice-associated variants in cancer
Spatial Transcriptomics: Emerging Technologies in Tissue Gene Expression Profiling
The functional impact of rare variation across the regulatory cascade
Functional characterization of regionally variable transcriptomic
Frontiers Rare diseases of epigenetic origin: Challenges and opportunities
The functional impact of rare variation across the regulatory cascade - ScienceDirect
Single-cell RNA sequencing highlights the functional role of human endogenous retroviruses in gallbladder cancer - eBioMedicine
Transcriptomic signatures across human tissues identify functional rare genetic variation
A guide for the diagnosis of rare and undiagnosed disease: beyond the exome, Genome Medicine
Learning interpretable cellular and gene signature embeddings from single-cell transcriptomic data
The functional impact of rare variation across the regulatory cascade
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