Author

Wenlan Tian

Complete Genomics (United States)

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

Genomics· 2

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:deconvolution· 1 Approach:experimental assay· 1 Research Focus:genome assembly· 1 Organism:human· 1 Approach:machine learning (classical)· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Andrei Alexeev· 2 shared Ao CheniD· 2 shared Chongjun XuiD· 2 shared Nina Barua· 2 shared Radoje Drmanac· 2 shared Snezana Drmanac· 2 shared Yinlong Xie· 2 shared Brock A. PetersiD· 1 shared

Activity by Year

2019-2019 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 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

2 shared papersGenomics

Andrei Alexeev

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

GenomicsbioRxivPreprintDec 20, 2019

Advanced Whole Genome Sequencing Using an Entirely PCR-free Massively Parallel Sequencing Workflow

Hanjie Shen, Pengjuan Liu, Zhanqing Li…·Radoje Drmanac

This paper demonstrates that PCR-free whole genome sequencing using the DNBSEQ platform and machine learning variant calling significantly reduces InDel errors and improves variant calling performance.

4 citations

whole-genome sequencingmachine learning (classical)

𝕏 PostBluesky

GenomicsGenome ResearchPeer-reviewedMay 1, 2019

Efficient long single molecule sequencing for cost effective and accurate sequencing, haplotyping, and de novo assembly

Ou Wang, Robert G. Chin, Xiaofang Cheng…·Brock A. Peters

This paper introduces stLFR, a low-cost method for long DNA sequencing that enables accurate variant calling, haplotyping, and de novo assembly.

232 citations

humanwhole-genome sequencing

𝕏 PostBluesky