zCall: a rare variant caller for array-based genotyping: Genetics and population analysis. - Jacqueline I. Goldstein; Andrew Crenshaw; Jason P. Carey; George B. Grant; Jared Maguire; Menachem Fromer; Colm O'Dushlaine; Jennifer L. Moran; Kimberly Chambert; Christine Stevens; Pamela Sklar; Christina M. Hultman; et al. (Bioinform., 2012)

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. - Jie Zheng 006; Mesut A. Erzurumluoglu; Benjamin L. Elsworth; John P. Kemp; Laurence J. Howe; Philip C. Haycock; Gibran Hemani; Katherine Tansey; Charles Laurin; Early Genetics; Lifecourse Epidemiology (EAGLE) Eczema Consortium; Beate St. Pourcain; et al. (Bioinform., 2017)

RICOPILI: Rapid Imputation for COnsortias PIpeLIne. - Max Lam; Swapnil Awasthi; Hunna J. Watson; Jackie Goldstein; Georgia Panagiotaropoulou; Vassily Trubetskoy; Robert Karlsson; Oleksander Frei; Chun-Chieh Fan; Ward De Witte; Nina R. Mota; Niamh Mullins; et al. (Bioinform., 2020)

A structural variation reference for medical and population genetics. - Ryan L. Collins; Harrison Brand; Konrad J. Karczewski; Xuefang Zhao; Jessica Alföldi; Laurent C. Francioli; Amit V. Khera; Chelsea Lowther; Laura D. Gauthier; Harold Wang; Nicholas A. Watts; Matthew Solomonson; et al. (Nat., 2020)

FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. - Hufeng Zhou; Theodore Arapoglou; Xihao Li; Zilin Li; Xiuwen Zheng 001; Jill Moore; Abhijith Asok; Sushant Kumar; Elizabeth E. Blue; Steven Buyske; Nancy J. Cox; Adam Felsenfeld; et al. (Nucleic Acids Res., 2023)