Scholarly Works - Preprints
Preprint
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July 7, 2026
We present FRACTEL, a statistical framework for region-level analysis of CRISPR perturbation screens. FRACTEL aggregates gRNA p-values using a bounded minimum across order statistics, preserving scale and enabling adaptive sensitivity to sparse or diffuse ...
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Preprint
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March 31, 2026
Identifying genetic variants in noncoding DNA that impact gene expression and thereby contribute to disease risk remains a difficult but important challenge in genomic medicine. Modern reporter assays such as STARR-seq and MPRA provide an efficient and eff ...
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Preprint
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March 31, 2026
Interpreting the effects of novel mutations on phenotypic traits remains challenging, particularly for cis -regulatory variants. For rare variants, individuals typically possess at most one affected copy of the causal allele, leading to allelic imbalance, ...
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Preprint
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May 17, 2025
Delayed diagnosis of Mendelian disease substantially prevents early therapeutic intervention that could improve symptoms and prognosis. One major contributing challenge is the functional interpretation of non-coding variants that cause disease by altering ...
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