DNA sequencing technologies: 2006-2016. (Q38774619)

6 September 2017

title

DNA sequencing technologies: 2006-2016. (English)

1 reference

6 September 2017

1 reference

1

Elaine R Mardis

1 reference

6 September 2017

publication date

5 January 2017

1 reference

6 September 2017

1 reference

6 September 2017

volume

12

1 reference

6 September 2017

issue

2

1 reference

6 September 2017

page(s)

213-218

1 reference

Next-generation sequencing platforms

6 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Tn5 transposase and tagmentation procedures for massively scaled sequencing projects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Sequencing technologies - the next generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Coming of age: ten years of next-generation sequencing technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Fast and accurate short read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Whole exome capture in solution with 3 Gbp of data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

An SNP map of the human genome generated by reduced representation shotgun sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Utility of different gene enrichment approaches toward identifying and sequencing the maize gene space

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Microfluidic amplification as a tool for massive parallel sequencing of the familial hypercholesterolemia genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Finishing the euchromatic sequence of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Sequencing the AML genome, transcriptome, and epigenome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Enhanced structural variant and breakpoint detection using SVMerge by integration of multiple detection methods and local assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Limitations of next-generation genome sequence assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

An Incomplete Understanding of Human Genetic Variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

An integrated map of structural variation in 2,504 human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Reconstructing complex regions of genomes using long-read sequencing technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Genetic variation and the de novo assembly of human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Assembling large genomes with single-molecule sequencing and locality-sensitive hashing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Oxford Nanopore sequencing, hybrid error correction, and de novo assembly of a eukaryotic genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

HapCol: accurate and memory-efficient haplotype assembly from long reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Assembly and diploid architecture of an individual human genome via single-molecule technologies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Genome assembly using Nanopore-guided long and error-free DNA reads

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

A global reference for human genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Resolving the complexity of the human genome using single-molecule sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Microsecond time-scale discrimination among polycytidylic acid, polyadenylic acid, and polyuridylic acid as homopolymers or as segments within single RNA molecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Genome-wide identification of polycomb-associated RNAs by RIP-seq

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Exome Sequencing and the Management of Neurometabolic Disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Personalized medicine in a phase I clinical trials program: the MD Anderson Cancer Center initiative

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Cancer immunology. Mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Cancer immunotherapy. A dendritic cell vaccine increases the breadth and diversity of melanoma neoantigen-specific T cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Personal neoantigen cancer vaccines: The momentum builds

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Reliable Detection of Mismatch Repair Deficiency in Colorectal Cancers Using Mutational Load in Next-Generation Sequencing Panels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

Library construction for next-generation sequencing: overviews and challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2016.182

31 March 2020

Identifiers

DOI

10.1038/NPROT.2016.182

1 reference

Dimensions Publication ID

6 September 2017

1052207071

0 references

ORKG ID

R9295

0 references

1 reference