List of works - Goo Jun

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

scientific article

An integrated map of structural variation in 2,504 human genomes

scientific article

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

scientific article published on 28 November 2012

Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data

scientific article

Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data

scientific article

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

scientific article

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

scientific article

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

scientific article published on 15 September 2013

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

scientific article

In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

scientific article

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

scientific article published on 18 June 2014

Metabolomic profiles associated with subtypes of prediabetes among Mexican Americans in Starr County, Texas, USA

scientific article published on 04 December 2019

Non-crossover gene conversions show strong GC bias and unexpected clustering in humans

scientific article published on 25 March 2015

Optimal sequencing strategies for identifying disease-associated singletons

scientific article

Prosaposin is a regulator of progranulin levels and oligomerization

scientific article published on 30 June 2016

The genetic architecture of type 2 diabetes

scientific article (publication date: 11 July 2016)

Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons

scientific article

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

scientific article

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes

scientific article

List of works by Goo Jun

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

An integrated map of structural variation in 2,504 human genomes

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data

Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

Metabolomic profiles associated with subtypes of prediabetes among Mexican Americans in Starr County, Texas, USA

Non-crossover gene conversions show strong GC bias and unexpected clustering in humans

Optimal sequencing strategies for identifying disease-associated singletons

Prosaposin is a regulator of progranulin levels and oligomerization

The genetic architecture of type 2 diabetes

Whole Exome Sequencing to Identify Genetic Variants Associated with Raised Atherosclerotic Lesions in Young Persons

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

Whole-genome sequencing to understand the genetic architecture of common gene expression and biomarker phenotypes