Han S, Camp SY, Chu H, et al. Integrative Analysis of Germline Rare Variants in Clear and Non-Clear Cell Renal Cell Carcinoma. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.01.18.23284664
Publications
Sahgal P, Patil DT, Sztupinszki ZM, et al. Replicative stress in gastroesophageal adenocarcinoma is associated with chromosomal instability and sensitivity to DNA damage response inhibitors. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.27.534412
Anvar NE, Lin C, Ma X, et al. Efficient gene knockout and genetic interactions: the IN4MER CRISPR/Cas12a multiplex knockout platform. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.01.03.522655
Guo MH, Francioli LC, Stenton SL, et al. Inferring compound heterozygosity from large-scale exome sequencing data. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.03.19.533370
Harada T, Perez MW, Kalfon J, et al. Rapid-kinetics degron benchmarking reveals off-target activities and mixed agonism-antagonism of MYB inhibitors. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.04.07.536032
Zhou T, Zhang R, Jia D, et al. Concurrent profiling of multiscale 3D genome organization and gene expression in single mammalian cells. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.07.20.549578
Zhou T, Zhang R, Jia D, et al. Concurrent profiling of multiscale 3D genome organization and gene expression in single mammalian cells. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.07.20.549578
Moyakhe LB, Dalvie S, Mufford MS, Stein DJ, Koen N. Polygenic risk associations with developmental and mental health outcomes in childhood and adolescence: A systematic review. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.03.31.23287877
Koenig Z, Yohannes MT, Nkambule LL, et al. A harmonized public resource of deeply sequenced diverse human genomes. bioRxiv : the preprint server for biology. 2023. doi:10.1101/2023.01.23.525248
Roberts AM, DiStefano MT, Riggs ER, et al. Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.03.30.23287948