Goo Jun

发表

A novel deep learning model using dosimetric and clinical information for grade 4 radiotherapy-induced lymphopenia prediction

Yang Xiang, Radhe Mohan, Xiaoqian Jiang, 2019, Physics in medicine and biology.

Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19

David C. Glahn, Thomas D. Dyer, Jennifer E. Below, 2016, BMC Proceedings.

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

David M Herrington, Chunhong Mao, Timothy D Howard, 2017, Scientific Reports.

Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees

Christian Fuchsberger, John Blangero, Ravindranath Duggirala, 2014, BMC Proceedings.

Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data.

Hyun Min Kang, Michael Boehnke, Gonçalo R Abecasis, 2015, American journal of human genetics.

Mapping and characterization of structural variation in 17,795 human genomes

Eric S. Lander, Haley J. Abel, Yeting Zhang, 2020, Nature.

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

Richard M Myers, Hyun Min Kang, Shawn Levy, 2014, Psychophysiology.

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

Giulio Genovese, John Blangero, David Reich, 2015, eLife.

Multi-platform discovery of haplotype-resolved structural variation in human genomes

Li Ding, Amina Noor, Ali Bashir, 2018, Nature Communications.

Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration

Margaret A. Pericak-Vance, David E. Larson, Elaine R. Mardis, 2013, Nature Genetics.

Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus

Nicola L. Beer, Pablo Cingolani, Mark I. McCarthy, 2015, PLoS genetics.

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

He Zhang, Thomas Meitinger, Raimund Erbel, 2014, The New England journal of medicine.

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Taesung Park, Christian Gieger, Tien Yin Wong, 2017, Scientific Data.