(Q38774619)

6 September 2017

title

DNA sequencing technologies: 2006-2016. (English)

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6 September 2017

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1

Elaine R Mardis

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6 September 2017

publication date

5 January 2017

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6 September 2017

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6 September 2017

volume

12

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6 September 2017

issue

2

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6 September 2017

page(s)

213-218

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Next-generation sequencing platforms

6 September 2017

cites work

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

Tn5 transposase and tagmentation procedures for massively scaled sequencing projects

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

Sequencing technologies - the next generation

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

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Fast and accurate short read alignment with Burrows-Wheeler transform

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Whole exome capture in solution with 3 Gbp of data

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

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

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

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

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

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

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Finishing the euchromatic sequence of the human genome

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Sequencing the AML genome, transcriptome, and epigenome

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

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Limitations of next-generation genome sequence assembly

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An Incomplete Understanding of Human Genetic Variation

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

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Reconstructing complex regions of genomes using long-read sequencing technology

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Genetic variation and the de novo assembly of human genomes

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

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

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

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

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A global reference for human genetic variation

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

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

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

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

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

21 January 2018

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

21 January 2018

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Exome Sequencing and the Management of Neurometabolic Disorders.

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

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

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

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PD-1 Blockade in Tumors with Mismatch-Repair Deficiency

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

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

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Personal neoantigen cancer vaccines: The momentum builds

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

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Library construction for next-generation sequencing: overviews and challenges

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31 March 2020

Identifiers

DOI

10.1038/NPROT.2016.182

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Dimensions Publication ID

6 September 2017

1052207071

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ORKG ID

R9295

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