Transcriptomic signatures across human tissues identify functional rare genetic variation
Por um escritor misterioso
Last updated 17 junho 2024
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Cortex-wide transcriptomic regional-identity attenuation in ASD a
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Frontiers From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases
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Detection of aberrant splicing events in RNA-seq data using FRASER
![Transcriptomic signatures across human tissues identify functional rare genetic variation](https://www.frontiersin.org/files/Articles/664379/fgene-12-664379-HTML-r1/image_m/fgene-12-664379-g001.jpg)
Frontiers Putative Causal Variants Are Enriched in Annotated Functional Regions From Six Bovine Tissues
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Enrichment of rare variants underlying aberrant expression, splicing
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Research
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Frontiers Isoform Age - Splice Isoform Profiling Using Long-Read Technologies
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Biomolecules, Free Full-Text
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Genome-wide detection of human variants that disrupt intronic branchpoints
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Single-cell transcriptomic profiling reveals distinct mechanical responses between normal and diseased tendon progenitor cells - ScienceDirect
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Epigenomes, Free Full-Text
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Cells, Free Full-Text
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Network analysis reveals rare disease signatures across multiple levels of biological organization
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