(Q34095491)

31 July 2017

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title

Target-enrichment strategies for next-generation sequencing (English)

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Erratum: Target-enrichment strategies for next-generation sequencing

31 July 2017

corrigendum / erratum

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Crossref

DOI

10.1038/NMETH0610-479C

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/NMETH0610-479C

author

Jay Shendure

8

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31 July 2017

Emily H Turner

5

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Lira Mamanova

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object named as

Lira Mamanova

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31 July 2017

2

Alison J Coffey

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31 July 2017

Carol E Scott

3

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31 July 2017

Iwanka Kozarewa

4

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31 July 2017

Akash Kumar

6

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31 July 2017

Eleanor Howard

7

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31 July 2017

Daniel J Turner

9

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31 July 2017

1 February 2010

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31 July 2017

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31 July 2017

7

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31 July 2017

2

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31 July 2017

111-118

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https://scigraph.springernature.com/pub.10.1038/nmeth.1419

31 July 2017

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cites work

The impact of next-generation sequencing technology on genetics

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Crossref

https://api.crossref.org/works/10.1038%2FNMETH.1419

Error Detecting and Error Correcting Codes

21 January 2018

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Crossref

https://api.crossref.org/works/10.1038%2FNMETH.1419

Mutation detection and single-molecule counting using isothermal rolling-circle amplification

21 January 2018

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12 December 2020

cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments

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12 December 2020

Multiplexed genotyping with sequence-tagged molecular inversion probes

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12 December 2020

Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Man-made cell-like compartments for molecular evolution

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12 December 2020

Multiplex sequencing of plant chloroplast genomes using Solexa sequencing-by-synthesis technology

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12 December 2020

A large genome center's improvements to the Illumina sequencing system

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12 December 2020

Direct selection of human genomic loci by microarray hybridization

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12 December 2020

Targeted bisulfite sequencing reveals changes in DNA methylation associated with nuclear reprogramming

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12 December 2020

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

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12 December 2020

Finishing the euchromatic sequence of the human genome

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12 December 2020

Multiplex amplification of large sets of human exons

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12 December 2020

Direct selection: a method for the isolation of cDNAs encoded by large genomic regions

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12 December 2020

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

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12 December 2020

Padlock Probes: Circularizing Oligonucleotides for Localized DNA Detection

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12 December 2020

Genome-wide mapping with biallelic markers in Arabidopsis thaliana

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12 December 2020

MegaPlex PCR: a strategy for multiplex amplification.

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12 December 2020

Identification of genetic variants using bar-coded multiplexed sequencing

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12 December 2020

PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates

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12 December 2020

Microdroplet-based PCR enrichment for large-scale targeted sequencing

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12 December 2020

PCR-generated padlock probes detect single nucleotide variation in genomic DNA.

1 reference

12 December 2020

DNA sequencing with chain-terminating inhibitors

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12 December 2020

Genome-wide identification of human RNA editing sites by parallel DNA capturing and sequencing

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12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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12 December 2020

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

1 reference

12 December 2020

Multigene amplification and massively parallel sequencing for cancer mutation discovery

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12 December 2020

Multiplex amplification of all coding sequences within 10 cancer genes by Gene-Collector

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12 December 2020

High-throughput genotyping of single nucleotide polymorphisms with rolling circle amplification

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12 December 2020

Genome-wide in situ exon capture for selective resequencing

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12 December 2020

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

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12 December 2020

Microarray-based genomic selection for high-throughput resequencing.

1 reference

12 December 2020

Nested Patch PCR enables highly multiplexed mutation discovery in candidate genes

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12 December 2020

Multiplex amplification enabled by selective circularization of large sets of genomic DNA fragments

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12 December 2020

Method for improving sequence coverage uniformity of targeted genomic intervals amplified by LR-PCR using Illumina GA sequencing-by-synthesis technology

1 reference

12 December 2020

Allele-specific PCR amplification due to sequence identity between a PCR primer and an amplicon: is direct sequencing so reliable?

1 reference

12 December 2020

Next-generation DNA sequencing

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12 December 2020

Error-correcting barcoded primers for pyrosequencing hundreds of samples in multiplex

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12 December 2020

Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay

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12 December 2020

Fast and accurate short read alignment with Burrows-Wheeler transform

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12 December 2020

Accurate whole human genome sequencing using reversible terminator chemistry

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12 December 2020

Molecular tools for a molecular medicine: analyzing genes, transcripts and proteins using padlock and proximity probes

1 reference

12 December 2020

Identifiers

DOI

10.1038/NMETH.1419

1 reference

Dimensions Publication ID

31 July 2017

0 references

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