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Genome Biology
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October 10, 2025
Evaluating the potential and limitations of nanopore adaptive sampling for targeted transcriptome sequencing
Nicole DeBruyne, Feng Wang, Yang Xu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 20, 2024
Long-read RNA sequencing: A transformative technology for exploring transcriptome complexity in human diseases
Isabelle Heifetz Ament, Nicole DeBruyne, Feng Wang, et al.
Journal of Veterinary Internal Medicine
|
July 11, 2022
A novel mutation of the CLCN1 gene in a cat with myotonia congenita: Diagnosis and treatment
Christian Woelfel, Kathryn Meurs, Steven Friedenberg, et al.
Biorxiv : the Preprint Server for Biology
|
September 4, 2023
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of <i>FAIM2</i>
Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Cell Genomics
|
May 2, 2024
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2
Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Science Advances
|
April 15, 2026
Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretation
Robert Wang, Feng Wang, Nicole DeBruyne, et al.
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Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Genome Biology
|
October 10, 2025
Evaluating the potential and limitations of nanopore adaptive sampling for targeted transcriptome sequencing
Nicole DeBruyne, Feng Wang, Yang Xu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
November 20, 2024
Long-read RNA sequencing: A transformative technology for exploring transcriptome complexity in human diseases
Isabelle Heifetz Ament, Nicole DeBruyne, Feng Wang, et al.
Journal of Veterinary Internal Medicine
|
July 11, 2022
A novel mutation of the CLCN1 gene in a cat with myotonia congenita: Diagnosis and treatment
Christian Woelfel, Kathryn Meurs, Steven Friedenberg, et al.
Biorxiv : the Preprint Server for Biology
|
September 4, 2023
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of <i>FAIM2</i>
Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Cell Genomics
|
May 2, 2024
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2
Sheridan H Littleton, Khanh B Trang, Christina M Volpe, et al.
Science Advances
|
April 15, 2026
Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretation
Robert Wang, Feng Wang, Nicole DeBruyne, et al.
Page
of 1