Wenwei Zhang

发表

Single tube bead-based DNA co-barcoding for cost effective and accurate sequencing, haplotyping, and assembly

Xun Xu, Fei Fan, Yuliang Dong, 2018 .

stLFRsv: a germline SV analysis pipeline using co-barcoded reads

Xi Chen, Xun Xu, Ou Wang, 2020, bioRxiv.

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

Zhe Lin, Jing Zhao, Yinlong Xie, 2019, bioRxiv.

A portable and cost-effective microfluidic system for massively parallel single-cell transcriptome profiling

Zhifeng Wang, Xun Xu, Tao Wu, 2019, bioRxiv.

Mate-pair Library Construction with Controlled Polymerization Enables Comprehensive Structural Rearrangement Detection

Xun Xu, Kong Xiangdong, Dai Peng, 2018, bioRxiv.

Patch oligodeoxynucleotide synthesis (POS): a novel method for synthesis of long DNA sequences and full-length genes

Wenwei Zhang, Jian Ping, Huilin Wei, 2011, Biotechnology Letters.

Reliable multiplex sequencing with rare index mis-assignment on DNB-based NGS platform

Jian Wang, Xun Xu, Hui Jiang, 2018, BMC Genomics.

Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencing

Wenwei Zhang, Quan Nguyen, Joseph E Powell, 2019, bioRxiv.

3’ Branch Ligation: A Novel Method to Ligate Non-Complementary DNA to Recessed or Internal 3’OH Ends in DNA or RNA

Ou Wang, Ao Chen, Wenwei Zhang, 2018, bioRxiv.

OTG-snpcaller: An Optimized Pipeline Based on TMAP and GATK for SNP Calling from Ion Torrent Data

Wenwei Zhang, Chunyu Geng, Pengyuan Zhu, 2014, PloS one.

Assessment of the cPAS-based BGISEQ-500 platform for metagenomic sequencing

Jian Wang, Xun Xu, Mo Han, 2017, GigaScience.

Comparative performance of the BGI and Illumina sequencing technology for single-cell RNA-sequencing

Wenwei Zhang, Quan Nguyen, Joseph E Powell, 2020, NAR genomics and bioinformatics.

A simple bead-based method for generating cost-effective co-barcoded sequence reads

Xun Xu, Fei Fan, Dan Chen, 2018, Protocol Exchange.

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

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

Caste-specific RNA editomes in the leaf-cutting ant Acromyrmex echinatior

Zhiyu Peng, Wenwei Zhang, Zongji Wang, 2014, Nature Communications.

A Short‐Read Multiplex Sequencing Method for Reliable, Cost‐Effective and High‐Throughput Genotyping in Large‐Scale Studies

Tao Liu, Wei Zhang, Ying Liu, 2013, Human mutation.

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

Weida Tong, Huixiao Hong, Leming Shi, 2014, Genome Biology.

Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly

Jian Wang, Xun Xu, Fei Fan, 2019, Genome research.

A reference human genome dataset of the BGISEQ-500 sequencer

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