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Dmitri Parkhomchuk

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Nucleic Acids Research|July 22, 2009
Transcriptome analysis by strand-specific sequencing of complementary DNADmitri Parkhomchuk, Tatiana Borodina, Vyacheslav Amstislavskiy, et al.
Gene|June 5, 2016
Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening toolJulia Hentschel, Dana Tatun, Dmitri Parkhomchuk, et al.
Genome Medicine|August 2, 2013
Estimating exome genotyping accuracy by comparing to data from large scale sequencing projectsVerena Heinrich, Tom Kamphans, Jens Stange, et al.
Plos One|May 15, 2009
Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysisMichal R Schweiger, Martin Kerick, Bernd Timmermann, et al.
Plos One|August 14, 2013
Filtering for compound heterozygous sequence variants in non-consanguineous pedigreesTom Kamphans, Peggy Sabri, Na Zhu, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndromePeter M Krawitz, Daniela Schiska, Ulrike Krüger, et al.
Blood|June 5, 2013
A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGTPeter M Krawitz, Britta Höchsmann, Yoshiko Murakami, et al.
Science (New York, N.Y.)|July 5, 2008
A global view of gene activity and alternative splicing by deep sequencing of the human transcriptomeMarc Sultan, Marcel H Schulz, Hugues Richard, et al.
Nature Genetics|May 12, 2015
PDE3A mutations cause autosomal dominant hypertension with brachydactylyPhilipp G Maass, Atakan Aydin, Friedrich C Luft, et al.
Cancer Cell|February 16, 2013
Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancerJoachim Weischenfeldt, Ronald Simon, Lars Feuerbach, et al.
Pageof 1

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

Sort By:
Pageof 1
Nucleic Acids Research|July 22, 2009
Transcriptome analysis by strand-specific sequencing of complementary DNADmitri Parkhomchuk, Tatiana Borodina, Vyacheslav Amstislavskiy, et al.
Gene|June 5, 2016
Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening toolJulia Hentschel, Dana Tatun, Dmitri Parkhomchuk, et al.
Genome Medicine|August 2, 2013
Estimating exome genotyping accuracy by comparing to data from large scale sequencing projectsVerena Heinrich, Tom Kamphans, Jens Stange, et al.
Plos One|May 15, 2009
Genome-wide massively parallel sequencing of formaldehyde fixed-paraffin embedded (FFPE) tumor tissues for copy-number- and mutation-analysisMichal R Schweiger, Martin Kerick, Bernd Timmermann, et al.
Plos One|August 14, 2013
Filtering for compound heterozygous sequence variants in non-consanguineous pedigreesTom Kamphans, Peggy Sabri, Na Zhu, et al.
Molecular Genetics & Genomic Medicine|October 22, 2014
Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndromePeter M Krawitz, Daniela Schiska, Ulrike Krüger, et al.
Blood|June 5, 2013
A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGTPeter M Krawitz, Britta Höchsmann, Yoshiko Murakami, et al.
Science (New York, N.Y.)|July 5, 2008
A global view of gene activity and alternative splicing by deep sequencing of the human transcriptomeMarc Sultan, Marcel H Schulz, Hugues Richard, et al.
Nature Genetics|May 12, 2015
PDE3A mutations cause autosomal dominant hypertension with brachydactylyPhilipp G Maass, Atakan Aydin, Friedrich C Luft, et al.
Cancer Cell|February 16, 2013
Integrative genomic analyses reveal an androgen-driven somatic alteration landscape in early-onset prostate cancerJoachim Weischenfeldt, Ronald Simon, Lars Feuerbach, et al.
Pageof 1