Radoje Drmanac

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 .

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

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

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

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

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

Xiaojuan Qi, Xiao Liu, Ou Wang, 2018 .

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

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

Long Fragment Read (LFR) Technology: Cost-Effective, High-Quality Genome-Wide Molecular Haplotyping.

Radoje Drmanac, Brock A Peters, Rebecca Yu Zhang, 2017, Methods in molecular biology.

IterCluster: a barcode clustering algorithm for long fragment read analysis

Xun Xu, Yinlong Xie, Radoje Drmanac, 2020, PeerJ.

Comparison of long-read methods for sequencing and assembly of a plant genome

Wei Tian, Ou Wang, Radoje Drmanac, 2020, bioRxiv.

Pure CTCs, advanced WGS, and precise personalized combination therapies

Radoje Drmanac, Brock A. Peters, John W. Park, 2017, Oncoscience.

A public resource facilitating clinical use of genomes

Euan A Ashley, Jong Bhak, Leonid Peshkin, 2012, Proceedings of the National Academy of Sciences.

Accurate Long-Read Sequencing by Hybridization (SBH) Using the Universal HyChip^ System

Radoje Drmanac, 2000 .

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

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

Multiplexed SNP genotyping using nanobarcode particle technology

Radoje Drmanac, Snezana Drmanac, Chongjun Xu, 2006, Analytical and bioanalytical chemistry.

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.

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

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

Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for “perfect genome” sequencing

Radoje Drmanac, Brock A. Peters, B. Peters, 2015, Front. Genet..

De novo assembly of a haplotype-resolved human genome

Jian Wang, Xun Xu, Lars Bolund, 2015, Nature Biotechnology.

Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations

Yao-Cheng Lin, Jan Tavernier, Radoje Drmanac, 2014, Nature Communications.

Isolation and whole genome sequencing of fetal cells from maternal blood towards the ultimate non‐invasive prenatal testing

Lars Bolund, Wei Wang, Hui Jiang, 2017, Prenatal diagnosis.

Sequencing by hybridization (SBH): advantages, achievements, and opportunities.

Radoje Drmanac, Snezana Drmanac, Chongjun Xu, 2002, Advances in biochemical engineering/biotechnology.

Quantitative Whole Genome Sequencing of Circulating Tumor Cells Enables Personalized Combination Therapy of Metastatic Cancer.

Natali Gulbahce, Radoje Drmanac, Rick Tearle, 2017, Cancer research.

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.

The Ultimate Genetic Test

Radoje Drmanac, R. Drmanac, 2012, Science.

Significant abundance of cis configurations of mutations in diploid human genomes

Ralf Herwig, George M. Church, Radoje Drmanac, 2017, bioRxiv.

Reads on Self-Assembling DNA Nanoarrays Human Genome Sequencing Using Unchained Base

Radoje Drmanac, R. Drmanac, 2010 .

The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes

Alexander Wait Zaranek, Tom Clegg, George M. Church, 2016, GigaScience.