Sequencing technologies - the next generation (Q27860568)

Emerging technologies in DNA sequencing

31 March 2020

1 reference

DNA sequencing: bench to bedside and beyond

31 March 2020

1 reference

Sequence census methods for functional genomics

31 March 2020

1 reference

RNA-Seq: a revolutionary tool for transcriptomics

31 March 2020

1 reference

The potential and challenges of nanopore sequencing

31 March 2020

1 reference

Highly parallel genomic assays

31 March 2020

1 reference

Bioinformatics challenges of new sequencing technology

31 March 2020

1 reference

Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations

31 March 2020

1 reference

BTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies.

31 March 2020

1 reference

Accurate multiplex polony sequencing of an evolved bacterial genome

31 March 2020

1 reference

Polony multiplex analysis of gene expression (PMAGE) in mouse hypertrophic cardiomyopathy

31 March 2020

1 reference

A massively parallel PicoTiterPlate™ based platform for discrete picoliter‐scale polymerase chain reactions

31 March 2020

1 reference

Single-molecule DNA sequencing of a viral genome

31 March 2020

1 reference

Real-time DNA sequencing from single polymerase molecules

31 March 2020

1 reference

Alta-Cyclic: a self-optimizing base caller for next-generation sequencing

31 March 2020

1 reference

Termination of DNA synthesis by novel 3'-modified-deoxyribonucleoside 5'-triphosphates.

31 March 2020

1 reference

DNA polymerase fluorescent substrates with reversible 3′-tags

31 March 2020

1 reference

Four-color DNA sequencing by synthesis using cleavable fluorescent nucleotide reversible terminators

31 March 2020

1 reference

Four-color DNA sequencing with 3'-O-modified nucleotide reversible terminators and chemically cleavable fluorescent dideoxynucleotides

31 March 2020

1 reference

Accurate whole human genome sequencing using reversible terminator chemistry

31 March 2020

1 reference

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

31 March 2020

1 reference

Whole-genome sequencing and variant discovery in C. elegans.

31 March 2020

1 reference

Evaluation of next generation sequencing platforms for population targeted sequencing studies

31 March 2020

1 reference

Mapping short DNA sequencing reads and calling variants using mapping quality scores

31 March 2020

1 reference

Human genetic variation and its contribution to complex traits

31 March 2020

1 reference

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

31 March 2020

1 reference

Caenorhabditis elegans mutant allele identification by whole-genome sequencing

31 March 2020

1 reference

Termination of DNA synthesis by N6-alkylated, not 3'-O-alkylated, photocleavable 2'-deoxyadenosine triphosphates

31 March 2020

1 reference

Virtual terminator nucleotides for next-generation DNA sequencing.

31 March 2020

1 reference

Sequence information can be obtained from single DNA molecules

31 March 2020

1 reference

DNA ligases: structure, reaction mechanism, and function

31 March 2020

1 reference

A Ligase-Mediated Gene Detection Technique

31 March 2020

1 reference

A high-resolution, nucleosome position map of C. elegans reveals a lack of universal sequence-dictated positioning

31 March 2020

1 reference

Comparing platforms for C. elegans mutant identification using high-throughput whole-genome sequencing

31 March 2020

1 reference

A sequencing method based on real-time pyrophosphate

31 March 2020

1 reference

Real-time DNA sequencing using detection of pyrophosphate release

31 March 2020

1 reference

Genome sequencing in microfabricated high-density picolitre reactors

31 March 2020

1 reference

31 March 2020

Sequencing in real time

1 reference

Zero-Mode Waveguides for Single-Molecule Analysis at High Concentrations

31 March 2020

1 reference

How to map billions of short reads onto genomes

31 March 2020

1 reference

De novo fragment assembly with short mate-paired reads: Does the read length matter?

31 March 2020

1 reference

Unique features of a highly pathogenic Campylobacter jejuni strain

31 March 2020

1 reference

High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi

31 March 2020

1 reference

High-precision, whole-genome sequencing of laboratory strains facilitates genetic studies

31 March 2020

1 reference

Identification of concomitant infection with Chlamydia trachomatis IncA-negative mutant and wild-type strains by genomic, transcriptional, and biological characterizations

31 March 2020

1 reference

Sensitive, specific polymorphism discovery in bacteria using massively parallel sequencing

31 March 2020

1 reference

The dynamics and time scale of ongoing genomic erosion in symbiotic bacteria

31 March 2020

1 reference

Sequencing of natural strains of Arabidopsis thaliana with short reads

31 March 2020

1 reference

Paired-end mapping reveals extensive structural variation in the human genome

31 March 2020

1 reference

Mapping and sequencing of structural variation from eight human genomes

31 March 2020

1 reference

Assembling millions of short DNA sequences using SSAKE.

31 March 2020

1 reference

Short read fragment assembly of bacterial genomes

31 March 2020

1 reference

De novo bacterial genome sequencing: millions of very short reads assembled on a desktop computer

31 March 2020

1 reference

ALLPATHS: de novo assembly of whole-genome shotgun microreads

31 March 2020

1 reference

Velvet: algorithms for de novo short read assembly using de Bruijn graphs

31 March 2020

1 reference

High quality draft sequences for prokaryotic genomes using a mix of new sequencing technologies

31 March 2020

1 reference

De novo assembly using low-coverage short read sequence data from the rice pathogen Pseudomonas syringae pv. oryzae

31 March 2020

1 reference

How to get genomes at one ten-thousandth the cost

31 March 2020

1 reference

Genetic mapping in human disease

31 March 2020

1 reference

Pharmacogenomics: candidate gene identification, functional validation and mechanisms

31 March 2020

1 reference

A-beta-subtype of ketosis-prone diabetes is not predominantly a monogenic diabetic syndrome

31 March 2020

1 reference

Microdroplet-based PCR enrichment for large-scale targeted sequencing

31 March 2020

1 reference

Maskless fabrication of light-directed oligonucleotide microarrays using a digital micromirror array

31 March 2020

1 reference

Direct selection of human genomic loci by microarray hybridization

31 March 2020

1 reference

Genome-wide in situ exon capture for selective resequencing

31 March 2020

1 reference

Microarray-based genomic selection for high-throughput resequencing.

31 March 2020

1 reference

Multiplex amplification of large sets of human exons

31 March 2020

1 reference

A comprehensive assay for targeted multiplex amplification of human DNA sequences

31 March 2020

1 reference

Massively parallel exon capture and library-free resequencing across 16 genomes

31 March 2020

1 reference

Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

31 March 2020

1 reference

Enrichment of super-sized resequencing targets from the human genome

31 March 2020

1 reference

31 March 2020

1 reference

Metagenomic pyrosequencing and microbial identification

31 March 2020

1 reference

Quantification of the yeast transcriptome by single-molecule sequencing

31 March 2020

1 reference

31 March 2020

Direct RNA sequencing

1 reference

ChIP-seq: advantages and challenges of a maturing technology

31 March 2020

1 reference

The diploid genome sequence of an individual human

31 March 2020

1 reference

The complete genome of an individual by massively parallel DNA sequencing

31 March 2020

1 reference

Detection of large-scale variation in the human genome

31 March 2020

1 reference

Large-scale copy number polymorphism in the human genome

31 March 2020

1 reference

Fine-scale structural variation of the human genome

31 March 2020

1 reference

Relative impact of nucleotide and copy number variation on gene expression phenotypes

31 March 2020

1 reference

The diploid genome sequence of an Asian individual

31 March 2020

1 reference

A highly annotated whole-genome sequence of a Korean individual

31 March 2020

1 reference

The first Korean genome sequence and analysis: full genome sequencing for a socio-ethnic group

31 March 2020

1 reference

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

31 March 2020

1 reference

Single-molecule sequencing of an individual human genome

31 March 2020

1 reference

Recurring mutations found by sequencing an acute myeloid leukemia genome

31 March 2020

1 reference

Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

31 March 2020

1 reference

Personal genomes: Standard and pores

31 March 2020

1 reference

Analysis of one million base pairs of Neanderthal DNA

31 March 2020

1 reference

Targeted retrieval and analysis of five Neandertal mtDNA genomes

31 March 2020

1 reference

Evolution and functions of long noncoding RNAs

31 March 2020

1 reference

Origins and Mechanisms of miRNAs and siRNAs

31 March 2020

1 reference

Fluorescent in situ sequencing on polymerase colonies

31 March 2020

1 reference

A new class of cleavable fluorescent nucleotides: synthesis and optimization as reversible terminators for DNA sequencing by synthesis

31 March 2020

1 reference

Terminal phosphate labeled nucleotides: synthesis, applications, and linker effect on incorporation by DNA polymerases

31 March 2020

1 reference

Sequencing by Cyclic Ligation and Cleavage (CycLiC) directly on a microarray captured template

31 March 2020

1 reference

Synthesis and properties of fluorescent nucleotide substrates for DNA-dependent RNA polymerases

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19997069

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mapping the cancer genome. Pinpointing the genes involved in cancer will help chart a new course across the complex landscape of human malignancies.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19997069

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The impact of next-generation sequencing technology on genetics

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19997069