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Briefings in Bioinformatics
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January 2, 2017
Statistical method evaluation for differentially methylated CpGs in base resolution next-generation DNA sequencing data
Yun Zhang, Saurabh Baheti, Zhifu Sun
Clinical and Translational Gastroenterology
|
September 21, 2020
Whole Exome Sequencing Among 26 Patients With Indeterminate Acute Liver Failure: Response to Letter to the Editor
Jorge Rakela, Mrunal K Dehankar, Saurabh Baheti
The Journal of Allergy and Clinical Immunology. Global
|
October 15, 2025
Idiopathic hypereosinophilic syndrome: Potential pathologic somatic gene variants identified by exome sequencing
Alejandro Ferrer, Mrunal Dehankar, Saurabh Baheti, et al.
American Journal of Rhinology & Allergy
|
August 16, 2023
Genome-wide Epigenetic Study of Chronic Rhinosinusitis Tissues Reveals Dysregulated Inflammatory, Immunologic and Remodeling Pathways
Tripti Brar, Saurabh Baheti, Michael J Marino, et al.
Plos One
|
February 8, 2014
From days to hours: reporting clinically actionable variants from whole genome sequencing
Sumit Middha, Saurabh Baheti, Steven N Hart, et al.
International Forum of Allergy & Rhinology
|
June 10, 2023
Genomewide epigenetic study shows significant DNA hypermethylation in chronic rhinosinusitis versus control ethmoidal tissue
Tripti Brar, Saurabh Baheti, Aditya Vijay Bhagwate, et al.
BMC Genomics
|
February 29, 2016
Targeted alignment and end repair elimination increase alignment and methylation measure accuracy for reduced representation bisulfite sequencing data
Saurabh Baheti, Rahul Kanwar, Meike Goelzenleuchter, et al.
Clinical and Translational Gastroenterology
|
October 15, 2019
Whole Exome Sequencing Among 26 Patients With Indeterminate Acute Liver Failure: A Pilot Study
Jorge Rakela, Jody Rule, Daniel Ganger, et al.
Epigenomics
|
July 21, 2015
DNA methylation profiling: comparison of genome-wide sequencing methods and the Infinium Human Methylation 450 Bead Chip
Denise L Walker, Aditya Vijay Bhagwate, Saurabh Baheti, et al.
Plos One
|
December 21, 2013
SoftSearch: integration of multiple sequence features to identify breakpoints of structural variations
Steven N Hart, Vivekananda Sarangi, Raymond Moore, et al.
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Showing results (1-10 of 55) with videos related to
Sort By:
Page
of 6
Briefings in Bioinformatics
|
January 2, 2017
Statistical method evaluation for differentially methylated CpGs in base resolution next-generation DNA sequencing data
Yun Zhang, Saurabh Baheti, Zhifu Sun
Clinical and Translational Gastroenterology
|
September 21, 2020
Whole Exome Sequencing Among 26 Patients With Indeterminate Acute Liver Failure: Response to Letter to the Editor
Jorge Rakela, Mrunal K Dehankar, Saurabh Baheti
The Journal of Allergy and Clinical Immunology. Global
|
October 15, 2025
Idiopathic hypereosinophilic syndrome: Potential pathologic somatic gene variants identified by exome sequencing
Alejandro Ferrer, Mrunal Dehankar, Saurabh Baheti, et al.
American Journal of Rhinology & Allergy
|
August 16, 2023
Genome-wide Epigenetic Study of Chronic Rhinosinusitis Tissues Reveals Dysregulated Inflammatory, Immunologic and Remodeling Pathways
Tripti Brar, Saurabh Baheti, Michael J Marino, et al.
Plos One
|
February 8, 2014
From days to hours: reporting clinically actionable variants from whole genome sequencing
Sumit Middha, Saurabh Baheti, Steven N Hart, et al.
International Forum of Allergy & Rhinology
|
June 10, 2023
Genomewide epigenetic study shows significant DNA hypermethylation in chronic rhinosinusitis versus control ethmoidal tissue
Tripti Brar, Saurabh Baheti, Aditya Vijay Bhagwate, et al.
BMC Genomics
|
February 29, 2016
Targeted alignment and end repair elimination increase alignment and methylation measure accuracy for reduced representation bisulfite sequencing data
Saurabh Baheti, Rahul Kanwar, Meike Goelzenleuchter, et al.
Clinical and Translational Gastroenterology
|
October 15, 2019
Whole Exome Sequencing Among 26 Patients With Indeterminate Acute Liver Failure: A Pilot Study
Jorge Rakela, Jody Rule, Daniel Ganger, et al.
Epigenomics
|
July 21, 2015
DNA methylation profiling: comparison of genome-wide sequencing methods and the Infinium Human Methylation 450 Bead Chip
Denise L Walker, Aditya Vijay Bhagwate, Saurabh Baheti, et al.
Plos One
|
December 21, 2013
SoftSearch: integration of multiple sequence features to identify breakpoints of structural variations
Steven N Hart, Vivekananda Sarangi, Raymond Moore, et al.
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of 6