المؤلفون: Souza, M.G., Vallejo, E.E., Estrada, K.

المصدر: IEEE/ACM Transactions on Computational Biology and Bioinformatics IEEE/ACM Trans. Comput. Biol. and Bioinf. Computational Biology and Bioinformatics, IEEE/ACM Transactions on. 18(3):932-939 Jun, 2021

المؤلفون: Zhonghe Shao, Ting Wang, Jiahao Qiao, Yuchen Zhang, Shuiping Huang, Ping Zeng

المصدر: BMC Bioinformatics, Vol 23, Iss 1, Pp 1-24 (2022)

مصطلحات موضوعية: Genome-wide association study, Multilocus method, SNP-set analysis, Summary statistics, P value combination method, Common and rare variant association study, Computer applications to medicine. Medical informatics, R858-859.7, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2105

URL الوصول: https://doaj.org/article/a7a2f5eeff554070b1f4b14bf6f7c9b5

المؤلفون: Shao, Zhonghe, Wang, Ting, Qiao, Jiahao, Zhang, Yuchen, Huang, Shuiping^{Aff1, Aff2, Aff3, Aff4, Aff5}, Zeng, Ping^{Aff1, Aff2, Aff3, Aff4, Aff5, IDs12859022048973_cor6}

المصدر: BMC Bioinformatics. 23(1)

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المؤلفون: Hongguo Zhang, Wei Li, Yuting Jiang, Jia Li, Mucheng Chen, Ruixue Wang, Jing Zhao, Zhiyu Peng, Hui Huang, Ruizhi Liu

المصدر: Frontiers in Genetics, Vol 13 (2022)

مصطلحات موضوعية: causative genes, linkage analysis, non-obstructive azoospermia, whole exome sequencing, rare variant association study, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.872179/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/6266624c66b14e98839587d993872d42

المؤلفون: Morimoto, Yoshiro^{Aff1, Aff2}, Ono, Shinji, Kurotaki, Naohiro, Imamura, Akira, Ozawa, Hiroki^{Aff1, Aff2}

المصدر: Journal of Neural Transmission: Translational Neuroscience, Neurology and Preclinical Neurological Studies, Psychiatry and Preclinical Psychiatric Studies. 127(11):1517-1526

المؤلفون: Aoife McMahon, Elizabeth Lewis, Annalisa Buniello, Maria Cerezo, Peggy Hall, Elliot Sollis, Helen Parkinson, Lucia A. Hindorff, Laura W. Harris, Jacqueline A.L. MacArthur

المصدر: Cell Genomics, Vol 1, Iss 1, Pp 100005- (2021)

مصطلحات موضوعية: GWAS, genome-wide association study, seqGWAS, sequencing-based GWAS, rare variant association, WGS, Genetics, QH426-470, Internal medicine, RC31-1245

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666979X21000057; https://doaj.org/toc/2666-979X

URL الوصول: https://doaj.org/article/3adcd0fc3e984f08927291aab2224c55

المؤلفون: Techlo, Tanya Ramdal, Rasmussen, Andreas Høiberg, Møller, Peter L., Bøttcher, Morten, Winther, Simon^{Aff3, Aff4}, Davidsson, Olafur B., Olofsson, Isa A., Chalmer, Mona Ameri, Kogelman, Lisette J. A., Nyegaard, Mette, Olesen, Jes, Hansen, Thomas Folkmann^{Aff1, Aff5, Aff6}

المصدر: neurogenetics. 21(3):149-157

المؤلفون: Xinyuan Zhang, Anna O. Basile, Sarah A. Pendergrass, Marylyn D. Ritchie

المصدر: BMC Bioinformatics, Vol 20, Iss 1, Pp 1-10 (2019)

مصطلحات موضوعية: Rare variant association analysis, Sample size imbalance, Power analysis, Simulation study, Computer applications to medicine. Medical informatics, R858-859.7, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12859-018-2591-6; https://doaj.org/toc/1471-2105

URL الوصول: https://doaj.org/article/8fd64d838a46401ca7e6cf4a3d830de4

المؤلفون: Kelly A. Rich, Jennifer Roggenbuck, Stephen J. Kolb

المصدر: Frontiers in Neuroscience, Vol 14 (2021)

مصطلحات موضوعية: amyotrophic lateral sclerosis, genetic testing, gene therapy, genome, genetic variants, rare variant association study (RVAS), Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fnins.2020.603023/full; https://doaj.org/toc/1662-453X

URL الوصول: https://doaj.org/article/b43fcb15e62f4882a2a8c069d2486016