Lista de obras - Warren A. Cheung - Dominio Público Uruguay

Compensating for literature annotation bias when predicting novel drug-disease relationships through Medical Subject Heading Over-representation Profile (MeSHOP) similarity ⬇️

artículo científico publicado el 7 de mayo de 2013

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

artículo científico publicado en 2019

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

scientific article published on 14 March 2019

Epigenome data release: a participant-centered approach to privacy protection

artículo científico publicado en 2015

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

artículo científico publicado en 2017

Gene characterization index: assessing the depth of gene annotation

artículo científico publicado en 2008

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

artículo científico publicado en 2016

H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

artículo científico publicado en 2019

Identification of novel antibacterial peptides by chemoinformatics and machine learning

artículo científico publicado en 2009

Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator

artículo científico publicado en 2016

Increased DNA methylation variability in type 1 diabetes across three immune effector cell types.

artículo científico publicado en 2016

Inferring novel gene-disease associations using Medical Subject Heading Over-representation Profiles

artículo científico publicado en 2012

Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

artículo científico publicado en 2017

Optimization of antibacterial peptides by genetic algorithms and cheminformatics

artículo científico publicado en 2010

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

artículo científico publicado en 2015

Pursuit-Evasion Voronoi Diagrams in \ell_1

article

Quantitative biomedical annotation using medical subject heading over-representation profiles (MeSHOPs)

artículo científico publicado en 2012

Risk of re-identification of epigenetic methylation data: a more nuanced response is needed

artículo científico publicado en 2015

Single-cell analysis of human adipose tissue identifies depot and disease specific cell types

scientific article published on 23 December 2019

The transcription factor encyclopedia

artículo científico publicado en 2012

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

artículo científico publicado en 2015

n-SIFT: n-dimensional scale invariant feature transform

artículo científico publicado en 2009

Lista de obras de Warren A. Cheung

Compensating for literature annotation bias when predicting novel drug-disease relationships through Medical Subject Heading Over-representation Profile (MeSHOP) similarity ⬇️

Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements

Epigenome data release: a participant-centered approach to privacy protection

Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome

Gene characterization index: assessing the depth of gene annotation

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

H3K27M induces defective chromatin spread of PRC2-mediated repressive H3K27me2/me3 and is essential for glioma tumorigenesis

Identification of novel antibacterial peptides by chemoinformatics and machine learning

Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator

Increased DNA methylation variability in type 1 diabetes across three immune effector cell types.

Inferring novel gene-disease associations using Medical Subject Heading Over-representation Profiles

Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

Optimization of antibacterial peptides by genetic algorithms and cheminformatics

Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation

Pursuit-Evasion Voronoi Diagrams in \ell_1

Quantitative biomedical annotation using medical subject heading over-representation profiles (MeSHOPs)

Risk of re-identification of epigenetic methylation data: a more nuanced response is needed

Single-cell analysis of human adipose tissue identifies depot and disease specific cell types

The transcription factor encyclopedia

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

n-SIFT: n-dimensional scale invariant feature transform