New Publication: Identifying embryo aneuploidy risk genes using whole-exome sequencing data
Our study on identifying embryo aneuploidy risk genes using whole-exome sequencing data is published in PNAS. Congrats to all co-authors!
Our study on identifying embryo aneuploidy risk genes using whole-exome sequencing data is published in PNAS. Congrats to all co-authors!
Our study on identifying novel genes involved in meiosis and fertility in Drosophila melanogaster is published in Scientific Reports. Congratulations to Siqi and all co-authors!
Our study on identifying novel proteins from mass-spec data using a proteogenomic approach is published in Molecular & Cellular Proteomics. Congratulations to Xiaolong and Siqi!
Our study on identifying embryo aneuploidy risk genes using ultra-low coverage whole-genome sequencing from preimplantation genetic testing (PGT-A) is published in American Journal of Human Genetics. Congratulations to Siqi and all … Read More
Our study on determining the expression of LINEs in human tissues and cell lines using long-read sequencing transcriptome data is published in Genes. Congratulations to all co-authors!
Our study on determining the contribution of structure variations to the risk of ASD and language impairments in the NJLAGS cohort is published in International Journal of Molecular Sciences. Congratulations … Read More
Our study on the distribution and propties of transposable elements in ten Noctuidae (moth) genomes is published in the special issue of Mobile-Element-Related Genetic Variation in Genes.