S. Drmanac

发表

This PDF file includes: Materials and Methods

Robert B. Hartlage, W. C. Banyai, Jessica C. Ebert, 2009 .

Processing of cDNA and genomic kilobase-size clones for massive screening, mapping and sequencing by hybridization.

R. Drmanac, S. Drmanac, 1994, BioTechniques.

Gene-representing cDNA clusters defined by hybridization of 57,419 clones from infant brain libraries with short oligonucleotide probes.

R. Drmanac, M. Soares, I. Labat, 1996, Genomics.

Sequencing by hybridization: Towards an automated sequencing of one million M13 clones arrayed on membranes

R. Drmanac, I. Labat, R. Crkvenjakov, 1992, Electrophoresis.

Accurate sequencing by hybridization for DNA diagnostics and individual genomics

R. Drmanac, I. Labat, B. Hauser, 1998, Nature Biotechnology.

cPAS-based sequencing on the BGISEQ-500 to explore small non-coding RNAs

A. Alexeev, R. Drmanac, Yuxiang Li, 2016, Clinical Epigenetics.

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

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

DNA sequence determination by hybridization: a strategy for efficient large-scale sequencing.

L. Hood, R. Drmanac, Z. Strezoska, 1993, Science.

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.

Ou Wang A novel co-barcoding method for whole genome sequencing , haplotyping and scaffolding

Fan, Yang, Han K. Lam, 2018 .

De novo assembly of a haplotype-resolved human genome

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

SBH and the integration of complementary approaches in the mapping, sequencing, and understanding of complex genomes

R. Drmanac, I. Labat, S. Drmanac, 1993 .

Requirements in Screening cDNA Libraries for New Genes and Solutions Offered by SBH Technology

R. Drmanac, I. Labat, S. Drmanac, 1994 .

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

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

CoolMPS: evaluation of antibody labeling based massively parallel non-coding RNA sequencing

R. Drmanac, M. Callow, Hui Jiang, 2020, Nucleic acids research.

Sequencing and Fingerprinting DNA by Hybridization with Oligonucleotide Probes

R. Drmanac, S. Drmanac, D. Little, 2006 .

Sequencing by hybridization arrays.

R. Drmanac, S. Drmanac, 2001, Methods in molecular biology.

CHAPTER FOUR – Sequencing by Hybridization

R. Drmanac, I. Labat, S. Drmanac, 1994 .

Reliable hybridization of oligonucleotides as short as six nucleotides.

R. Drmanac, Z. Strezoska, I. Labat, 1990, DNA and cell biology.

Combinatorial sequencing-by-hybridization: analysis of the NF1 gene.

R. Drmanac, P. Fortina, S. Surrey, 2006, Genetic testing.

Advanced Personal Genome Sequencing as the Ultimate Diagnostic Test

B. Peters, R. Drmanac, S. Drmanac, 2017 .

Clinical and genetic analysis of a rare syndrome associated with neoteny

R. F. Walker, Rebecca Yu Zhang, P. Carnevali, 2017, Genetics in Medicine.

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

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

Multiplexed SNP genotyping using nanobarcode particle technology

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

Identification of APC gene mutations in colorectal cancer using universal microarray‐based combinatorial sequencing‐by‐hybridization

R. Drmanac, P. Fortina, S. Surrey, 2004, Human mutation.

CoolMPS for robust sequencing of single-nuclear RNAs captured by droplet-based method

R. Drmanac, T. Wyss-Coray, Hui Zhang, 2020, Nucleic acids research.

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.

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

Han K. Lam, Rebecca Yu Zhang, B. Peters, 2018, bioRxiv.

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

Xun Xu, Fei Fan, Yuliang Dong, 2018 .

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

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

CoolMPS™: Advanced massively parallel sequencing using antibodies specific to each natural nucleobase

Linsu Chen, R. Drmanac, Jian Wang, 2020, bioRxiv.

cPAS-based sequencing on the BGISEQ-500 to explore small non-coding RNAs

A. Alexeev, R. Drmanac, Yuxiang Li, 2016, Clinical Epigenetics.

DNA sequencing by hybridization with arrays of samples or probes.

R. Drmanac, D. Gietzen, S. Drmanac, 2001, Methods in molecular biology.

Selective DNA amplification from complex genomes using universal double-sided adapters.

R. Drmanac, M. Callow, S. Drmanac, 2004, Nucleic acids research.

cDNA screening by array hybridization.

R. Drmanac, S. Drmanac, R Drmanac, 1999, Methods in enzymology.

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

Yuan Jiang, J. Liu, R. Drmanac, 2018, bioRxiv.

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

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

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

Jessica C. Ebert, B. Peters, B. Kermani, 2010, Science.