Junhua Rao

发表

Sequencing and de novo assembly of 150 genomes from Denmark as a population reference

Lars Bolund, Bent Petersen, Christian N. S. Pedersen, 2017, Nature.

Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a population scale

A. Krogh, Jun Wang, Siyang Liu, 2015, GigaScience.

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios

Jakob Grove, Anders D. Børglum, Xun Xu, 2015, Nature Communications.

Detection and characterization of copy number variants based on whole-genome sequencing by MGI platforms

Hui Jiang, Junhua Rao, F. Mu, 2019 .

A reference human genome dataset of the BGISEQ-500 sequencer

Hui Jiang, Wenwei Zhang, Xinming Liang, 2017, GigaScience.

Germline and somatic variant identification using BGISEQ-500 and HiSeq X Ten whole genome sequencing

Hui Jiang, Wenwei Zhang, Xinming Liang, 2018, PloS one.

Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios

Bent Petersen, Patrick F. Sullivan, Christian N. S. Pedersen, 2018, BMC Bioinformatics.

Characterization of RNA editome in primary and metastatic lung adenocarcinomas

Leo J. Lee, Kui Wu, Junhua Rao, 2016, Oncotarget.

Performance of copy number variants detection based on whole-genome sequencing by DNBSEQ platforms

Xin Liu, Hui Jiang, Fang Chen, 2020, BMC Bioinform..

An integrated Asian human SNV and indel benchmark established using multiple sequencing methods

Jie Huang, Ting Yu, Yangyi Chen, 2020, Scientific Reports.

Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios

John van Beusekom, Anders E. Halager, P. Sullivan, 2018, BMC Bioinform..

An integrated Asian human SNV and indel benchmark combining multiple sequencing methods

Xinming Liang, Guangyi Fan, Jiezhong Zhang, 2019, bioRxiv.

Geospatial immune heterogeneity reflects the diverse tumor-immune interactions in intrahepatic cholangiocarcinoma.

Junhua Rao, Haorong Lu, Kui Wu, 2022, Cancer discovery.

Erratum to: A reference human genome dataset of the BGISEQ-500 sequencer

Wenwei Zhang, Hui Jiang, Yuxiang Li, 2018, GigaScience.

An integrated Asian human SNV and indel benchmark established using multiple sequencing methods

Guangyi Fan, Junhua Rao, Xinming Liang, 2020, Scientific Reports.

Discovery, genotyping and characterization of structural variation and novel sequence at single nucleotide resolution from de novo genome assemblies on a population scale

A. Krogh, Jun Wang, Siyang Liu, 2015, GigaScience.

Sequencing and de novo assembly of 150 genomes from Denmark as a population reference

Anders E. Halager, P. Sullivan, A. Krogh, 2017, Nature.

Benchmarking the HLA typing performance of Polysolver and Optitype in 50 Danish parental trios

Anders E. Halager, P. Sullivan, A. Krogh, 2018, BMC Bioinformatics.