Associated Papers
Mapping multimodal phenotypes to perturbations in cells and tissue with CRISPRmap.
Gu J et al.
Nature Biotechnology, 2025
39375448 (PubMed )
Supplement: 41587_2024_2386_MOESM5_ESM.xlsx › Chemo_IR_FDR_LFC_KStest
CRISPRmap: Sequencing-free optical pooled screens mapping multi-omic phenotypes in cells and tissue.
Gu J et al.
Biorxiv : the Preprint Server for Biology, 2023
38234835 (PubMed )
Supplement: media-5.xlsx › ClinVar_update_Dec2023
New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing.
Patiño LC et al.
Human Reproduction (oxford, England), 2017
UV-Associated Mutations Underlie the Etiology of MCV-Negative Merkel Cell Carcinomas.
Wong SQ et al.
Cancer Research, 2015
26627015 (PubMed )
Supplement: 00085472can151877-sup-152397_1_supp_3130424_n439px.xlsx › Supplementary_Table_S7
Novel mutations of the FANCG gene causing alternative splicing in Japanese Fanconi anemia.
Yamada T et al.
Journal of Human Genetics, 2000
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