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R W W Brouwer

Showing results (1-10 of 7) with videos related to

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Bioinformatics (Oxford, England)|November 11, 2011
NARWHAL, a primary analysis pipeline for NGS dataR W W Brouwer, M C G N van den Hout, F G Grosveld, et al.
Bioinformatics (Oxford, England)|March 15, 2018
Nimbus: a design-driven analyses suite for amplicon-based NGS dataR W W Brouwer, M C G N van den Hout, C E M Kockx, et al.
Virchows Archiv : an International Journal of Pathology|October 5, 2018
Progression of ductal carcinoma in situ to invasive breast cancer: comparative genomic sequencingS C Doebar, N M Krol, R van Marion, et al.
Journal of Biomedical Science|November 4, 2024
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veinsG G Edel, M van Kempen, A Boerema-de Munck, et al.
Molecular Psychiatry|March 22, 2017
A rare missense variant in RCL1 segregates with depression in extended familiesN Amin, F M S de Vrij, M Baghdadi, et al.
Molecular Psychiatry|August 10, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptomsN Amin, O Jovanova, H H H Adams, et al.
Molecular Psychiatry|July 20, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptomsN Amin, O Jovanova, H H H Adams, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|November 11, 2011
NARWHAL, a primary analysis pipeline for NGS dataR W W Brouwer, M C G N van den Hout, F G Grosveld, et al.
Bioinformatics (Oxford, England)|March 15, 2018
Nimbus: a design-driven analyses suite for amplicon-based NGS dataR W W Brouwer, M C G N van den Hout, C E M Kockx, et al.
Virchows Archiv : an International Journal of Pathology|October 5, 2018
Progression of ductal carcinoma in situ to invasive breast cancer: comparative genomic sequencingS C Doebar, N M Krol, R van Marion, et al.
Journal of Biomedical Science|November 4, 2024
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veinsG G Edel, M van Kempen, A Boerema-de Munck, et al.
Molecular Psychiatry|March 22, 2017
A rare missense variant in RCL1 segregates with depression in extended familiesN Amin, F M S de Vrij, M Baghdadi, et al.
Molecular Psychiatry|August 10, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptomsN Amin, O Jovanova, H H H Adams, et al.
Molecular Psychiatry|July 20, 2016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptomsN Amin, O Jovanova, H H H Adams, et al.
Pageof 1