Comprehensive analysis of RNA-Seq data reveals extensive RNA editing in a human transcriptome

Zhiyu Peng, Yanbing Cheng, Bertrand Chin‐Ming Tan, +12

Nature Biotechnology

Rna ProcessingNatural SciencesGeneticsRna BiologyMolecular Biology +10

Comparison of RNA-seq and microarray-based models for clinical endpoint prediction

Wenqian Zhang, Ying Yu, Falk Hertwig, +71

Genome Biology

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach

Zirui Dong, Jun Zhang, Ping Hu, +16

Genetics in Medicine

An investigation of biomarkers derived from legacy microarray data for their utility in the RNA-seq era

Zhenqiang Su, Hong Fang, Huixiao Hong, +16

Genome biology

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis

Huilin Wang, Zirui Dong, Rui Zhang, +16

Genetics in Medicine

Low-pass GenomeFunctional GenomicsSequencingPrenatal Genetic TestingMedicine +11

A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole-Genome Low-Coverage Sequencing

Zirui Dong, Lupin Jiang, Chuanchun Yang, +17

Human Mutation

Bca EventsBalanced Chromosomal RearrangementsGeneticsWhole-genome Low-coverage SequencingGenetic Epidemiology +23

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage

Zirui Dong, Junhao Yan, Fengping Xu, +36

The American Journal of Human Genetics

ChromatinGenome InstabilityNext-generation SequencingGeneticsRecurrent Miscarriage +8

Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics

Zirui Dong, Huilin Wang, Haixiao Chen, +16

Genetics in Medicine

Structural VariationCytogeneticsMedicineGeneticsGenomes Project +7

Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis

Kwong Wai Choy, Huilin Wang, Mengmeng Shi, +14

Frontiers in Genetics

Low-pass genome sequencing: a validated method in clinical cytogenetics

Matthew Hoi Kin Chau, Huilin Wang, Yunli Lai, +14

Human Genetics

Low-pass Genome SequencingGeneticsNext-generation SequencingGenomicsMedicine +2