about
A model selection approach to discover age-dependent gene expression patterns using quantile regression models.PBrowse: a web-based platform for real-time collaborative exploration of genomic data.Impact of sequencing depth in ChIP-seq experiments.Application of a systems approach to study developmental gene regulation.Decoding the complex genetic causes of heart diseases using systems biologyChIP-chip versus ChIP-seq: lessons for experimental design and data analysis.Sequence-specific targeting of dosage compensation in Drosophila favors an active chromatin context.Application of Metamorphic Testing to Supervised ClassifiersTesting and Validating Machine Learning Classifiers by Metamorphic TestingLung stem cell self-renewal relies on BMI1-dependent control of expression at imprinted loci.Verification and validation of bioinformatics software without a gold standard: a case study of BWA and Bowtie.hiHMM: Bayesian non-parametric joint inference of chromatin state mapsBinding of transcription factor GabR to DNA requires recognition of DNA shape at a location distinct from its cognate binding site.iSyTE: integrated Systems Tool for Eye gene discovery.CIDR: Ultrafast and accurate clustering through imputation for single-cell RNA-seq data.Crim1 regulates integrin signaling in murine lens development.An antibody-based leukocyte-capture microarray for the diagnosis of systemic lupus erythematosus.Male-lineage transmission of an acquired metabolic phenotype induced by grand-paternal obesity.Customising an antibody leukocyte capture microarray for systemic lupus erythematosus: beyond biomarker discovery.XGSA: A statistical method for cross-species gene set analysis.Scalability and Validation of Big Data Bioinformatics Software.How to test bioinformatics software?Intercalated discs: multiple proteins perform multiple functions in non-failing and failing human hearts.Integrative analysis identifies co-dependent gene expression regulation of BRG1 and CHD7 at distal regulatory sites in embryonic stem cells.Falco: a quick and flexible single-cell RNA-seq processing framework on the cloud.Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease.Network modelling of gene regulation.Impact of sequencing depth and read length on single cell RNA sequencing data of T cells.Modelling, inference and big data in biophysics.iSyTE 2.0: a database for expression-based gene discovery in the eye.Identification of satellite cells from anole lizard skeletal muscle and demonstration of expanded musculoskeletal potential.An Embryonic and Induced Pluripotent Stem Cell Model for Ovarian Granulosa Cell Development and Steroidogenesis.Light-focusing human micro-lenses generated from pluripotent stem cells model lens development and drug-induced cataract in vitro.NAD Deficiency, Congenital Malformations, and Niacin Supplementation.Biologically active constituents of the secretome of human W8B2+ cardiac stem cells.Maternal obesity heritably perturbs offspring metabolism for three generations without serial programming.Discovery of cell-type specific DNA motif grammar in cis-regulatory elements using random Forest.Verification of phylogenetic inference programs using metamorphic testing.Identification of clinically actionable variants from genome sequencing of families with congenital heart diseaseC3: An R package for cross-species compendium-based cell-type identification
P50
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P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0003-2331-7011
@en
name
Joshua Ho
@ast
Joshua Ho
@en
Joshua Ho
@es
Joshua Ho
@nl
type
label
Joshua Ho
@ast
Joshua Ho
@en
Joshua Ho
@es
Joshua Ho
@nl
altLabel
Joshua W. Ho
@en
Joshua W. K. Ho
@en
Joshua Wing Kei Ho
@en
prefLabel
Joshua Ho
@ast
Joshua Ho
@en
Joshua Ho
@es
Joshua Ho
@nl
P106
P1153
14527168600
P2456
P31
P496
0000-0003-2331-7011