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Gaia Andreoletti

Showing results (1-10 of 40) with videos related to

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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 27, 2026
Trust, Reproducibility, and Progress: The Roles of Independent Blind Prediction and Assessment and Benchmarking in Computational BiologyGaia Andreoletti, Serghei Mangul, Predrag Radivojac, et al.
Human Mutation|July 24, 2019
Reports from the fifth edition of CAGI: The Critical Assessment of Genome InterpretationGaia Andreoletti, Lipika R Pal, John Moult, et al.
Genome Medicine|May 8, 2015
Erratum to: a SNP profiling panel for sample tracking in whole-exome sequencing studiesReuben J Pengelly, Jane Gibson, Gaia Andreoletti, et al.
Genome Medicine|September 28, 2013
A SNP profiling panel for sample tracking in whole-exome sequencing studiesReuben J Pengelly, Jane Gibson, Gaia Andreoletti, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Familial Ebstein Anomaly: Whole Exome Sequencing Identifies Novel Phenotype Associated With <i>FLNA</i>Catherine L Mercer, Gaia Andreoletti, Aisling Carroll, et al.
JRSM Open|June 14, 2016
Progressive myoclonic epilepsy with Fanconi syndromeEleanor G Seaby, Rodney D Gilbert, Reuben J Pengelly, et al.
Frontiers in Pediatrics|June 8, 2017
Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic ParadigmEleanor G Seaby, Rodney D Gilbert, Gaia Andreoletti, et al.
Journal of Medical Genetics|November 5, 2016
<i>AMMECR1</i>: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosisGaia Andreoletti, Eleanor G Seaby, Jennifer M Dewing, et al.
Human Mutation|July 9, 2019
VIPdb, a genetic Variant Impact Predictor DatabaseZhiqiang Hu, Changhua Yu, Mabel Furutsuki, et al.
Inflammatory Bowel Diseases|August 19, 2016
Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome SequencingJames J Ashton, Gaia Andreoletti, Tracy Coelho, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|February 27, 2026
Trust, Reproducibility, and Progress: The Roles of Independent Blind Prediction and Assessment and Benchmarking in Computational BiologyGaia Andreoletti, Serghei Mangul, Predrag Radivojac, et al.
Human Mutation|July 24, 2019
Reports from the fifth edition of CAGI: The Critical Assessment of Genome InterpretationGaia Andreoletti, Lipika R Pal, John Moult, et al.
Genome Medicine|May 8, 2015
Erratum to: a SNP profiling panel for sample tracking in whole-exome sequencing studiesReuben J Pengelly, Jane Gibson, Gaia Andreoletti, et al.
Genome Medicine|September 28, 2013
A SNP profiling panel for sample tracking in whole-exome sequencing studiesReuben J Pengelly, Jane Gibson, Gaia Andreoletti, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Familial Ebstein Anomaly: Whole Exome Sequencing Identifies Novel Phenotype Associated With <i>FLNA</i>Catherine L Mercer, Gaia Andreoletti, Aisling Carroll, et al.
JRSM Open|June 14, 2016
Progressive myoclonic epilepsy with Fanconi syndromeEleanor G Seaby, Rodney D Gilbert, Reuben J Pengelly, et al.
Frontiers in Pediatrics|June 8, 2017
Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic ParadigmEleanor G Seaby, Rodney D Gilbert, Gaia Andreoletti, et al.
Journal of Medical Genetics|November 5, 2016
<i>AMMECR1</i>: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosisGaia Andreoletti, Eleanor G Seaby, Jennifer M Dewing, et al.
Human Mutation|July 9, 2019
VIPdb, a genetic Variant Impact Predictor DatabaseZhiqiang Hu, Changhua Yu, Mabel Furutsuki, et al.
Inflammatory Bowel Diseases|August 19, 2016
Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome SequencingJames J Ashton, Gaia Andreoletti, Tracy Coelho, et al.
Pageof 4