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Leroy Bondhus

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

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BMC Bioinformatics|September 5, 2022
DMRscaler: a scale-aware method to identify regions of differential DNA methylation spanning basepair to multi-megabase featuresLeroy Bondhus, Angela Wei, Valerie A Arboleda
Briefings in Bioinformatics|May 9, 2022
Balancing the transcriptome: leveraging sample similarity to improve measures of gene specificityLeroy Bondhus, Roshni Varma, Yenifer Hernandez, et al.
Epigenetics & Chromatin|February 1, 2025
Epigene functional diversity: isoform usage, disordered domain content, and variable binding partnersLeroy Bondhus, Aileen A Nava, Isabelle S Liu, et al.
HGG Advances|May 23, 2022
Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart diseaseSarah J Spendlove, Leroy Bondhus, Gentian Lluri, et al.
BMC Medical Genomics|November 29, 2024
ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3Isabella Lin, Zain Awamleh, Mili Sinvhal, et al.
Biorxiv : the Preprint Server for Biology|August 14, 2023
<i>KAT6A</i> mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior <i>HOXC</i> clusterMeghna Singh, Sarah Spendlove, Angela Wei, et al.
Science Translational Medicine|May 1, 2024
Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency diseaseRuth Johnson, Alexis V Stephens, Rachel Mester, et al.
Pageof 1

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

Sort By:
Pageof 1
BMC Bioinformatics|September 5, 2022
DMRscaler: a scale-aware method to identify regions of differential DNA methylation spanning basepair to multi-megabase featuresLeroy Bondhus, Angela Wei, Valerie A Arboleda
Briefings in Bioinformatics|May 9, 2022
Balancing the transcriptome: leveraging sample similarity to improve measures of gene specificityLeroy Bondhus, Roshni Varma, Yenifer Hernandez, et al.
Epigenetics & Chromatin|February 1, 2025
Epigene functional diversity: isoform usage, disordered domain content, and variable binding partnersLeroy Bondhus, Aileen A Nava, Isabelle S Liu, et al.
HGG Advances|May 23, 2022
Polygenic risk scores of endo-phenotypes identify the effect of genetic background in congenital heart diseaseSarah J Spendlove, Leroy Bondhus, Gentian Lluri, et al.
BMC Medical Genomics|November 29, 2024
ASXL1 truncating variants in BOS and myeloid leukemia drive shared disruption of Wnt-signaling pathways but have differential isoform usage of RUNX3Isabella Lin, Zain Awamleh, Mili Sinvhal, et al.
Biorxiv : the Preprint Server for Biology|August 14, 2023
<i>KAT6A</i> mutations in Arboleda-Tham syndrome drive epigenetic regulation of posterior <i>HOXC</i> clusterMeghna Singh, Sarah Spendlove, Angela Wei, et al.
Science Translational Medicine|May 1, 2024
Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency diseaseRuth Johnson, Alexis V Stephens, Rachel Mester, et al.
Pageof 1