If you use SNPnexus in your work and/or publication(s), please cite:
- [1] Jorge Oscanoa, Lavanya Sivapalan, Emanuela Gadaleta, Abu Z Dayem Ullah, Nicholas R Lemoine, Claude Chelala, SNPnexus: a web server for functional annotation of human genome sequence variation (2020 update), Nucleic Acids Research, 2020, 48(W1):W185-W192.
- [2] Abu Z Dayem Ullah, Jorge Oscanoa, Jun Wang, Ai Nagano, Nicholas Lemoine, Claude Chelala, SNPnexus: assessing the functional relevance of genetic variation to facilitate the promise of precision medicine, Nucleic Acids Research, 2018, 46(W1):W109-W113.
- [3] Abu Z Dayem Ullah, Nicholas R Lemoine and Claude Chelala, A practical guide for the functional annotation of genetic variations using SNPnexus, Briefings in Bioinformatics, 2013, 14(4):437-47.
- [4] Abu Z Dayem Ullah, Nicholas R Lemoine and Claude Chelala, SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update), Nucleic Acids Research, 2012, 40(W1):W65-W70.
- [5] Claude Chelala, Arshad Khan and Nicholas R Lemoine, SNPnexus: A web database for functional annotation of newly discovered and public domain Single Nucleotide Polymorphisms, Bioinformatics, 2009, 25(5):655-61.