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Giulia C Kennedy

Showing results (11-20 of 69) with videos related to

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Journal of Personalized Medicine|January 21, 2023
Maximizing Small Biopsy Patient Samples: Unified RNA-Seq Platform Assessment of over 120,000 Patient BiopsiesP Sean Walsh, Yangyang Hao, Jie Ding, et al.
BMC Pulmonary Medicine|January 7, 2022
Percepta Genomic Sequencing Classifier and decision-making in patients with high-risk lung nodules: a decision impact studySonali Sethi, Scott Oh, Alexander Chen, et al.
Human Genomics|December 14, 2004
The genomic distribution of population substructure in four populations using 8,525 autosomal SNPsMark D Shriver, Giulia C Kennedy, Esteban J Parra, et al.
American Journal of Human Genetics|October 28, 2005
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPsHoward R Slater, Dione K Bailey, Hua Ren, et al.
Genomics|February 6, 2002
Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotypingJian-Bing Fan, Urvashi Surti, Patricia Taillon-Miller, et al.
American Journal of Human Genetics|March 15, 2006
Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic VariationsHoward R Slater, Dione K Bailey, Hua Ren, et al.
BMC Genomics|October 22, 2010
Use of consensus sequences for the design of high density resequencing microarrays: the influenza virus paradigmIndia Leclercq, Nicolas Berthet, Christophe Batéjat, et al.
Cancer Research|July 19, 2005
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arraysYasuhito Nannya, Masashi Sanada, Kumi Nakazaki, et al.
Arthritis and Rheumatism|January 1, 2009
Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysisAnne Hinks, Anne Barton, Neil Shephard, et al.
BMC Cancer|April 1, 2025
Analytical validation of the Percepta Nasal Swab classifier; an RNA next-generation sequencing assay for the assessment of lung cancer risk in pulmonary nodulesShuyang Wu, Ruochen Jiang, Grazyna Fedorowicz, et al.
Pageof 7

Showing results (11-20 of 69) with videos related to

Sort By:
Pageof 7
Journal of Personalized Medicine|January 21, 2023
Maximizing Small Biopsy Patient Samples: Unified RNA-Seq Platform Assessment of over 120,000 Patient BiopsiesP Sean Walsh, Yangyang Hao, Jie Ding, et al.
BMC Pulmonary Medicine|January 7, 2022
Percepta Genomic Sequencing Classifier and decision-making in patients with high-risk lung nodules: a decision impact studySonali Sethi, Scott Oh, Alexander Chen, et al.
Human Genomics|December 14, 2004
The genomic distribution of population substructure in four populations using 8,525 autosomal SNPsMark D Shriver, Giulia C Kennedy, Esteban J Parra, et al.
American Journal of Human Genetics|October 28, 2005
High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPsHoward R Slater, Dione K Bailey, Hua Ren, et al.
Genomics|February 6, 2002
Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotypingJian-Bing Fan, Urvashi Surti, Patricia Taillon-Miller, et al.
American Journal of Human Genetics|March 15, 2006
Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic VariationsHoward R Slater, Dione K Bailey, Hua Ren, et al.
BMC Genomics|October 22, 2010
Use of consensus sequences for the design of high density resequencing microarrays: the influenza virus paradigmIndia Leclercq, Nicolas Berthet, Christophe Batéjat, et al.
Cancer Research|July 19, 2005
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arraysYasuhito Nannya, Masashi Sanada, Kumi Nakazaki, et al.
Arthritis and Rheumatism|January 1, 2009
Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysisAnne Hinks, Anne Barton, Neil Shephard, et al.
BMC Cancer|April 1, 2025
Analytical validation of the Percepta Nasal Swab classifier; an RNA next-generation sequencing assay for the assessment of lung cancer risk in pulmonary nodulesShuyang Wu, Ruochen Jiang, Grazyna Fedorowicz, et al.
Pageof 7