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Amin Ardeshirdavani

Showing results (1-10 of 16) with videos related to

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Nucleic Acids Research|May 6, 2015
Galahad: a web server for drug effect analysis from gene expressionGriet Laenen, Amin Ardeshirdavani, Yves Moreau, et al.
BMC Bioinformatics|December 22, 2018
Towards practical privacy-preserving genome-wide association studyCharlotte Bonte, Eleftheria Makri, Amin Ardeshirdavani, et al.
Nucleic Acids Research|September 20, 2015
Beegle: from literature mining to disease-gene discoverySarah ElShal, Léon-Charles Tranchevent, Alejandro Sifrim, et al.
Plos Computational Biology|December 20, 2021
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samplesPriit Paluoja, Hindrek Teder, Amin Ardeshirdavani, et al.
Genome Medicine|October 21, 2014
NGS-Logistics: federated analysis of NGS sequence variants across multiple locationsAmin Ardeshirdavani, Erika Souche, Luc Dehaspe, et al.
Nucleic Acids Research|May 2, 2016
Candidate gene prioritization with EndeavourLéon-Charles Tranchevent, Amin Ardeshirdavani, Sarah ElShal, et al.
Clinical Case Reports|November 18, 2022
Clinical whole-exome sequencing analysis reveals a novel missense COL11A1 mutation resulting in an 18-week Iranian male aborted fetus with Fibrochondrogenesis 1: A case reportHanifeh Mirtavoos-Mahyari, Sanaz Ajami, Amirhosein Mehrtash, et al.
Bioinformatics (Oxford, England)|February 17, 2018
pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusionAjay Anand Kumar, Lut Van Laer, Maaike Alaerts, et al.
Nature Methods|October 1, 2013
eXtasy: variant prioritization by genomic data fusionAlejandro Sifrim, Dusan Popovic, Leon-Charles Tranchevent, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 25, 2026
Identification of a putative founder effect involving the HACE1:c.1396C>T variant in two Iranian families and review of reported casesMohammad Dehani, Elham Pourbakhtyaran, Nooshin Goudarzi, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|May 6, 2015
Galahad: a web server for drug effect analysis from gene expressionGriet Laenen, Amin Ardeshirdavani, Yves Moreau, et al.
BMC Bioinformatics|December 22, 2018
Towards practical privacy-preserving genome-wide association studyCharlotte Bonte, Eleftheria Makri, Amin Ardeshirdavani, et al.
Nucleic Acids Research|September 20, 2015
Beegle: from literature mining to disease-gene discoverySarah ElShal, Léon-Charles Tranchevent, Alejandro Sifrim, et al.
Plos Computational Biology|December 20, 2021
Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samplesPriit Paluoja, Hindrek Teder, Amin Ardeshirdavani, et al.
Genome Medicine|October 21, 2014
NGS-Logistics: federated analysis of NGS sequence variants across multiple locationsAmin Ardeshirdavani, Erika Souche, Luc Dehaspe, et al.
Nucleic Acids Research|May 2, 2016
Candidate gene prioritization with EndeavourLéon-Charles Tranchevent, Amin Ardeshirdavani, Sarah ElShal, et al.
Clinical Case Reports|November 18, 2022
Clinical whole-exome sequencing analysis reveals a novel missense COL11A1 mutation resulting in an 18-week Iranian male aborted fetus with Fibrochondrogenesis 1: A case reportHanifeh Mirtavoos-Mahyari, Sanaz Ajami, Amirhosein Mehrtash, et al.
Bioinformatics (Oxford, England)|February 17, 2018
pBRIT: gene prioritization by correlating functional and phenotypic annotations through integrative data fusionAjay Anand Kumar, Lut Van Laer, Maaike Alaerts, et al.
Nature Methods|October 1, 2013
eXtasy: variant prioritization by genomic data fusionAlejandro Sifrim, Dusan Popovic, Leon-Charles Tranchevent, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 25, 2026
Identification of a putative founder effect involving the HACE1:c.1396C>T variant in two Iranian families and review of reported casesMohammad Dehani, Elham Pourbakhtyaran, Nooshin Goudarzi, et al.
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