The GENDULF algorithm: mining transcriptomics to uncover modifier genes for monogenic diseases

Modifier genes are believed to account for the clinical variability observed in many Mendelian disorders, but their identification remains challenging due to the limited availability of genomics data from large patient cohorts. Here, we present GENDULF (GENetic moDULators identiFication), one of the...

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Bibliografiske detaljer
Udgivet i:Mol Syst Biol
Main Authors: Auslander, Noam, Ramos, Daniel M, Zelaya, Ivette, Karathia, Hiren, Crawford, Thomas O., Schäffer, Alejandro A, Sumner, Charlotte J, Ruppin, Eytan
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2020
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Methods
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7754056/
https://ncbi.nlm.nih.gov/pubmed/33438800
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/msb.20209701
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