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Human Genomics|September 1, 2019
Novel analytical methods to interpret large sequencing data from small sample sizesFlorence Lichou, Sébastien Orazio, Stéphanie Dulucq, et al.Human Genomics|August 21, 2019
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genesMolly Went, Ben Kinnersley, Amit Sud, et al.Human Genomics|February 21, 2019
Update on the human and mouse lipocalin (LCN) gene family, including evidence the mouse Mup cluster is result of an "evolutionary bloom"Georgia Charkoftaki, Yewei Wang, Monica McAndrews, et al.Human Genomics|December 15, 2021
Driving mosaicism: somatic variants in reference population databases and effect on variant interpretation in rare genetic diseaseVladimir Avramović, Simona Denise Frederiksen, Marjana Brkić, et al.Human Genomics|December 21, 2021
Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing datasetDaniel D Domogala, Tomasz Gambin, Roni Zemet, et al.Human Genomics|November 22, 2021
Single-cell transcriptome identifies molecular subtype of autism spectrum disorder impacted by de novo loss-of-function variants regulating glial cellsNasna Nassir, Asma Bankapur, Bisan Samara, et al.Human Genomics|October 31, 2018
Link between short tandem repeats and translation initiation site selectionMasoud Arabfard, Kaveh Kavousi, Ahmad Delbari, et al.Human Genomics|December 21, 2004
The extent and importance of intragenic recombinationEric de Silva, Lawrence A Kelley, Michael P H StumpfHuman Genomics|December 21, 2004
Comparison of regional gene expression differences in the brains of the domestic dog and humanErin Kennerly, Susanne Thomson, Natasha Olby, et al.Human Genomics|December 21, 2004
Analysis of the glutathione S-transferase (GST) gene familyDaniel W Nebert, Vasilis VasiliouPageof 112