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Shilpa Nadimpalli

Showing results (1-10 of 15) with videos related to

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Nucleic Acids Research|December 12, 2018
Systematic domain-based aggregation of protein structures highlights DNA-, RNA- and other ligand-binding positionsShilpa Nadimpalli Kobren, Mona Singh
Plos Genetics|March 10, 2015
Pervasive variation of transcription factor orthologs contributes to regulatory network evolutionShilpa Nadimpalli, Anton V Persikov, Mona Singh
Cell Systems|July 27, 2020
PertInInt: An Integrative, Analytical Approach to Rapidly Uncover Cancer Driver Genes with Perturbed Interactions and FunctionalitiesShilpa Nadimpalli Kobren, Bernard Chazelle, Mona Singh
Biodata Mining|January 17, 2025
Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patientsLane Fitzsimmons, , Brett Beaulieu-Jones, et al.
BMC Bioinformatics|October 9, 2012
Formatt: Correcting protein multiple structural alignments by incorporating sequence alignmentNoah M Daniels, Shilpa Nadimpalli, Lenore J Cowen
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Phenotypic overlap between rare disease patients and variant carriers in a large population cohort informs biological mechanismsLane Fitzsimmons, , Brett Beaulieu-Jones, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
VarPPUD: Variant post prioritization developed for undiagnosed genetic disordersRui Yin, Alba Gutierrez, , et al.
Plos Computational Biology|September 22, 2025
VarPPUD: Pinpointing diagnostic variants from sets of prioritized, strong candidate variantsRui Yin, Alba Gutiérrez-Sacristán, , et al.
Genome Biology|January 31, 2024
RExPRT: a machine learning tool to predict pathogenicity of tandem repeat lociSarah Fazal, Matt C Danzi, Isaac Xu, et al.
American Journal of Medical Genetics. Part A|May 29, 2023
The contribution of mosaicism to genetic diseases and de novo pathogenic variantsRory J Tinker, Lisa Bastarache, Kimberly Ezell, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Nucleic Acids Research|December 12, 2018
Systematic domain-based aggregation of protein structures highlights DNA-, RNA- and other ligand-binding positionsShilpa Nadimpalli Kobren, Mona Singh
Plos Genetics|March 10, 2015
Pervasive variation of transcription factor orthologs contributes to regulatory network evolutionShilpa Nadimpalli, Anton V Persikov, Mona Singh
Cell Systems|July 27, 2020
PertInInt: An Integrative, Analytical Approach to Rapidly Uncover Cancer Driver Genes with Perturbed Interactions and FunctionalitiesShilpa Nadimpalli Kobren, Bernard Chazelle, Mona Singh
Biodata Mining|January 17, 2025
Enriched phenotypes in rare variant carriers suggest pathogenic mechanisms in rare disease patientsLane Fitzsimmons, , Brett Beaulieu-Jones, et al.
BMC Bioinformatics|October 9, 2012
Formatt: Correcting protein multiple structural alignments by incorporating sequence alignmentNoah M Daniels, Shilpa Nadimpalli, Lenore J Cowen
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
Phenotypic overlap between rare disease patients and variant carriers in a large population cohort informs biological mechanismsLane Fitzsimmons, , Brett Beaulieu-Jones, et al.
Medrxiv : the Preprint Server for Health Sciences|May 3, 2024
VarPPUD: Variant post prioritization developed for undiagnosed genetic disordersRui Yin, Alba Gutierrez, , et al.
Plos Computational Biology|September 22, 2025
VarPPUD: Pinpointing diagnostic variants from sets of prioritized, strong candidate variantsRui Yin, Alba Gutiérrez-Sacristán, , et al.
Genome Biology|January 31, 2024
RExPRT: a machine learning tool to predict pathogenicity of tandem repeat lociSarah Fazal, Matt C Danzi, Isaac Xu, et al.
American Journal of Medical Genetics. Part A|May 29, 2023
The contribution of mosaicism to genetic diseases and de novo pathogenic variantsRory J Tinker, Lisa Bastarache, Kimberly Ezell, et al.
Pageof 2