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Nancy F Hansen

Showing results (11-20 of 53) with videos related to

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Plos One|January 26, 2022
KLF3 and PAX6 are candidate driver genes in late-stage, MSI-hypermutated endometrioid endometrial carcinomasMeghan L Rudd, Nancy F Hansen, Xiaolu Zhang, et al.
Cancer|September 24, 2017
The FOXA2 transcription factor is frequently somatically mutated in uterine carcinosarcomas and carcinomasMatthieu Le Gallo, Meghan L Rudd, Mary Ellen Urick, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3Nancy F Hansen, Xunde Wang, Mickias B Tegegn, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2017
iPSCs and fibroblast subclones from the same fibroblast population contain comparable levels of sequence variationsErika M Kwon, John P Connelly, Nancy F Hansen, et al.
Scientific Reports|July 30, 2020
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomasAlexander Pemov, Ramita Dewan, Nancy F Hansen, et al.
Pediatrics|May 16, 2012
Incidental medical information in whole-exome sequencingBenjamin D Solomon, Donald W Hadley, Daniel E Pineda-Alvarez, et al.
BMC Cancer|February 15, 2017
First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentationRamita Dewan, Alexander Pemov, Amalia S Dutra, et al.
Cell Stem Cell|March 6, 2012
Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expressionLinzhao Cheng, Nancy F Hansen, Ling Zhao, et al.
Genome Research|September 3, 2010
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencingJamie K Teer, Lori L Bonnycastle, Peter S Chines, et al.
Plos Genetics|March 8, 2014
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African AmericansAmy R Bentley, Guanjie Chen, Daniel Shriner, et al.
Pageof 6

Showing results (11-20 of 53) with videos related to

Sort By:
Pageof 6
Plos One|January 26, 2022
KLF3 and PAX6 are candidate driver genes in late-stage, MSI-hypermutated endometrioid endometrial carcinomasMeghan L Rudd, Nancy F Hansen, Xiaolu Zhang, et al.
Cancer|September 24, 2017
The FOXA2 transcription factor is frequently somatically mutated in uterine carcinosarcomas and carcinomasMatthieu Le Gallo, Meghan L Rudd, Mary Ellen Urick, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3Nancy F Hansen, Xunde Wang, Mickias B Tegegn, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2017
iPSCs and fibroblast subclones from the same fibroblast population contain comparable levels of sequence variationsErika M Kwon, John P Connelly, Nancy F Hansen, et al.
Scientific Reports|July 30, 2020
Comparative clinical and genomic analysis of neurofibromatosis type 2-associated cranial and spinal meningiomasAlexander Pemov, Ramita Dewan, Nancy F Hansen, et al.
Pediatrics|May 16, 2012
Incidental medical information in whole-exome sequencingBenjamin D Solomon, Donald W Hadley, Daniel E Pineda-Alvarez, et al.
BMC Cancer|February 15, 2017
First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentationRamita Dewan, Alexander Pemov, Amalia S Dutra, et al.
Cell Stem Cell|March 6, 2012
Low incidence of DNA sequence variation in human induced pluripotent stem cells generated by nonintegrating plasmid expressionLinzhao Cheng, Nancy F Hansen, Ling Zhao, et al.
Genome Research|September 3, 2010
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencingJamie K Teer, Lori L Bonnycastle, Peter S Chines, et al.
Plos Genetics|March 8, 2014
Gene-based sequencing identifies lipid-influencing variants with ethnicity-specific effects in African AmericansAmy R Bentley, Guanjie Chen, Daniel Shriner, et al.
Pageof 6