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Transcriptomic signatures across human tissues identify functional rare genetic variation

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Transcriptomic signatures across human tissues identify functional rare genetic variation
Systematic characterization of cancer transcriptome at transcript resolution
Transcriptomic signatures across human tissues identify functional rare genetic variation
Cortex-wide transcriptomic regional-identity attenuation in ASD a
Transcriptomic signatures across human tissues identify functional rare genetic variation
Transcriptomic signatures across human tissues identify functional rare genetic variation
Transcriptomic signatures across human tissues identify functional rare genetic variation
Publications — Greenleaf Lab @ Stanford
Transcriptomic signatures across human tissues identify functional rare genetic variation
Into the multiverse: advances in single-cell multiomic profiling: Trends in Genetics
Transcriptomic signatures across human tissues identify functional rare genetic variation
Frontiers Identification of Gene Signature as Diagnostic and Prognostic Blood Biomarker for Early Hepatocellular Carcinoma Using Integrated Cross-Species Transcriptomic and Network Analyses
Transcriptomic signatures across human tissues identify functional rare genetic variation
Epigenomes of Human Hearts Reveal New Genetic Variants Relevant for Cardiac Disease and Phenotype
Transcriptomic signatures across human tissues identify functional rare genetic variation
Frontiers From GWAS to Function: Using Functional Genomics to Identify the Mechanisms Underlying Complex Diseases
Transcriptomic signatures across human tissues identify functional rare genetic variation
Transcriptomic subtyping of malignant peripheral nerve sheath tumours highlights immune signatures, genomic profiles, patient survival and therapeutic targets - eBioMedicine
Transcriptomic signatures across human tissues identify functional rare genetic variation
The functional impact of rare variation across the regulatory cascade - ScienceDirect
Transcriptomic signatures across human tissues identify functional rare genetic variation
Identifying disease-critical cell types and cellular processes by integrating single-cell RNA-sequencing and human genetics
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