Author

Hao Tran

San Diego Biomedical Research Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:experimental assay· 2 Research Focus:database / resource· 1 Research Focus:genome assembly· 1 Assay:long-read sequencing· 1 Assay:multiome· 1 Assay:scATAC-seq· 1 Assay:scRNA-seq· 1 Research Focus:software / tool· 1

Frequent Co-Authors

An Nguyen· 1 shared Cecilie Boysen· 1 shared Dat Tran· 1 shared Devin K. Porter· 1 shared Greg C. Humphrey· 1 shared Guoya Mo· 1 shared Ha An Nguyen· 1 shared Huu Che· 1 shared

Activity by Year

2020-2020 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperBioinformatics

An Nguyen

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

BBrowser: Making single-cell data easily accessible

Tri Le, Tan Phan, Minh Pham, Dat Tran, Loc Lam, Ngoc Tung Nguyen, Thao Truong, Hy Vuong, Tam Luu, Nam Phung, Ngan Pham, Trang Thi Thu Nguyen, Oanh Minh Pham, An Nguyen, Huy Tan Nguyen, , Son Truong Pham

A downloadable application pairs a curated single-cell database with a big-data analytics layer and a visualisation module for exploring single-cell omics data.

bioRxiv · Dec 11, 2020 · PreprintBioinformatics

Ultra-low input single tube linked-read library method enables short-read NGS systems to generate highly accurate and economical long-range sequencing information for de novo genome assembly and haplotype phasing

Zhoutao Chen, Long Pham, Tsai-Chin Wu, Guoya Mo, Yu Xia, Peter L. Chang, Devin K. Porter, Tấn Đức Phan, Huu Che, Hao Tran, Vikas Bansal, Justin P. Shaffer, Pedro Belda‐Ferre, Greg C. Humphrey, Rob D. Knight, , Ming Lei

The paper introduces a low-cost, high-accuracy method for generating long-range sequencing data using short-read NGS systems, enabling de novo genome assembly and haplotype phasing with minimal DNA input.

Genome Research · Jun 1, 2020Peer-reviewedGenomics