Lista de obras - Weichen Zhou - Dominio Público Uruguay

A robust benchmark for detection of germline large deletions and insertions

artículo científico publicado en 2020

A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models

artículo científico publicado en 2018

Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks

artículo científico publicado en 2011

Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population

artículo científico publicado en 2011

Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.

artículo científico publicado en 2010

Author Correction: A robust benchmark for detection of germline large deletions and insertions

artículo científico publicado en 2020

CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis

artículo científico publicado en 2014

Cas9 targeted enrichment of mobile elements using nanopore sequencing

artículo científico publicado en 2021

Characterization of nuclear mitochondrial insertions in the whole genomes of primates

artículo científico publicado en 2020

Comprehensive identification of somatic nucleotide variants in human brain tissue

artículo científico publicado en 2021

Comprehensive identification of somatic nucleotide variants in human brain tissue

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome

artículo científico publicado en 2014

Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders

artículo científico publicado en 2017

Genome architecture and its roles in human copy number variation.

artículo científico publicado en 2014

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

scientific article published on 28 January 2014

Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

artículo científico publicado en 2020

Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms

artículo científico publicado en 2013

Predictive model for inflammation grades of chronic hepatitis B: Large-scale analysis of clinical parameters and gene expressions.

artículo científico publicado en 2017

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

artículo científico publicado en 2015

knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable

artículo científico publicado en 2018

Lista de obras de Weichen Zhou

A robust benchmark for detection of germline large deletions and insertions

A standardized fold change method for microarray differential expression analysis used to reveal genes involved in acute rejection in murine allograft models

Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks

Association of heme oxygenase-1 gene polymorphisms with essential hypertension and blood pressure in the Chinese Han population

Association of polymorphisms in the solute carrier organic anion transporter family member 1B1 gene with essential hypertension in the Uyghur population.

Author Correction: A robust benchmark for detection of germline large deletions and insertions

CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis

Cas9 targeted enrichment of mobile elements using nanopore sequencing

Characterization of nuclear mitochondrial insertions in the whole genomes of primates

Comprehensive identification of somatic nucleotide variants in human brain tissue

Comprehensive identification of somatic nucleotide variants in human brain tissue

Correlation between frequency of non-allelic homologous recombination and homology properties: evidence from homology-mediated CNV mutations in the human genome

Efficient CNV breakpoint analysis reveals unexpected structural complexity and correlation of dosage-sensitive genes with clinical severity in genomic disorders

Genome architecture and its roles in human copy number variation.

Genome-wide CNV analysis in mouse induced pluripotent stem cells reveals dosage effect of pluripotent factors on genome integrity

Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

Increased genome instability in human DNA segments with self-chains: homology-induced structural variations via replicative mechanisms

Predictive model for inflammation grades of chronic hepatitis B: Large-scale analysis of clinical parameters and gene expressions.

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

knnAUC: an open-source R package for detecting nonlinear dependence between one continuous variable and one binary variable