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Szabolcs Szelinger

Showing results (1-10 of 53) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 5, 2011
Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome AnalyzerSzabolcs Szelinger, Ahmet Kurdoglu, David W Craig
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2011
Microarray-based genome-wide association studies using pooled DNASzabolcs Szelinger, John V Pearson, David W Craig
Journal of Biomedical Informatics|November 21, 2009
BING: biomedical informatics pipeline for Next Generation SequencingJeffrey Kriseman, Christopher Busick, Szabolcs Szelinger, et al.
Journal of Clinical Medicine|June 24, 2022
A Case Report of Immunotherapy-Resistant MSI-H Gastric Cancer with Significant Intrapatient Tumoral Heterogeneity Characterized by Histologic DedifferentiationNikhila Kethireddy, Leonidas Arvanitis, Janine LoBello, et al.
F1000Research|November 5, 2015
Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensitiesMohan Narayanan, Keri Ramsey, Theresa Grebe, et al.
Bioinformatics (Oxford, England)|July 12, 2008
Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studiesNils Homer, Waibhav D Tembe, Szabolcs Szelinger, et al.
Gynecologic Oncology Reports|October 25, 2023
Underreporting <i>of SMARCB1</i> alteration by clinical sequencing: Integrative patho-genomic analysis captured <i>SMARCB1</i>/INI-1 deficiency in a vulvar yolk sac tumorChristina H Wei, Edward Wang, Evita Sadimin, et al.
Neuroscience Letters|August 16, 2011
Induction of pluripotent stem cells from autopsy donor-derived somatic cellsBrooke E Hjelm, Jon B Rosenberg, Szabolcs Szelinger, et al.
Translational Psychiatry|November 25, 2020
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in miceKazuo Nakajima, Alannah Miranda, David W Craig, et al.
Plos Genetics|September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysNils Homer, Szabolcs Szelinger, Margot Redman, et al.
Pageof 6

Showing results (1-10 of 53) with videos related to

Sort By:
Pageof 6
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2011
Bar-coded, multiplexed sequencing of targeted DNA regions using the Illumina Genome AnalyzerSzabolcs Szelinger, Ahmet Kurdoglu, David W Craig
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2011
Microarray-based genome-wide association studies using pooled DNASzabolcs Szelinger, John V Pearson, David W Craig
Journal of Biomedical Informatics|November 21, 2009
BING: biomedical informatics pipeline for Next Generation SequencingJeffrey Kriseman, Christopher Busick, Szabolcs Szelinger, et al.
Journal of Clinical Medicine|June 24, 2022
A Case Report of Immunotherapy-Resistant MSI-H Gastric Cancer with Significant Intrapatient Tumoral Heterogeneity Characterized by Histologic DedifferentiationNikhila Kethireddy, Leonidas Arvanitis, Janine LoBello, et al.
F1000Research|November 5, 2015
Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensitiesMohan Narayanan, Keri Ramsey, Theresa Grebe, et al.
Bioinformatics (Oxford, England)|July 12, 2008
Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studiesNils Homer, Waibhav D Tembe, Szabolcs Szelinger, et al.
Gynecologic Oncology Reports|October 25, 2023
Underreporting <i>of SMARCB1</i> alteration by clinical sequencing: Integrative patho-genomic analysis captured <i>SMARCB1</i>/INI-1 deficiency in a vulvar yolk sac tumorChristina H Wei, Edward Wang, Evita Sadimin, et al.
Neuroscience Letters|August 16, 2011
Induction of pluripotent stem cells from autopsy donor-derived somatic cellsBrooke E Hjelm, Jon B Rosenberg, Szabolcs Szelinger, et al.
Translational Psychiatry|November 25, 2020
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in miceKazuo Nakajima, Alannah Miranda, David W Craig, et al.
Plos Genetics|September 5, 2008
Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarraysNils Homer, Szabolcs Szelinger, Margot Redman, et al.
Pageof 6