Amplification of complex gene libraries by emulsion PCR. - Test2 - elhamkhani - TriplyDB

Amplification of complex gene libraries by emulsion PCR.

Amplification of complex gene libraries by emulsion PCR.

http://www.wikidata.org/entity/Q33247540

about

High-fidelity gene synthesis by retrieval of sequence-verified DNA identified using high-throughput pyrosequencing Targeted enrichment of genomic DNA regions for next-generation sequencing Exposing malaria in-host diversity and estimating population diversity by capture-recapture using massively parallel pyrosequencing.Selection platforms for directed evolution in synthetic biology Oligonucleotide Functionalised Microbeads: Indispensable Tools for High-Throughput Aptamer Selection From design to screening: a new antimicrobial peptide discovery pipeline A method for multiplex gene synthesis employing error correction based on expression Model-Free RNA Sequence and Structure Alignment Informed by SHAPE Probing Reveals a Conserved Alternate Secondary Structure for 16S rRNA Single-Tube Reaction Using Perfluorocarbons: A Prerequisite Step Leading to the Whole-Slide In Situ Technique on Histopathological Slides An efficient multistrategy DNA decontamination procedure of PCR reagents for hypersensitive PCR applications Identification of ancient remains through genomic sequencing Chimeric 16S rRNA sequence formation and detection in Sanger and 454-pyrosequenced PCR amplicons Lab-on-a-chip technologies for single-molecule studies Creating biocompatible oil-water interfaces without synthesis: direct interactions between primary amines and carboxylated perfluorocarbon surfactants.Improving precision of proximity ligation assay by amplified single molecule detection.Selection of restriction endonucleases using artificial cells Metagenomic analysis of a permafrost microbial community reveals a rapid response to thaw.Petri dish PCR: laser-heated reactions in nanoliter droplet arrays Isolation of putative FOXO1 genomic elements using an improved in vitro technique to isolate genomic regulatory sequences Microdroplets in microfluidics: an evolving platform for discoveries in chemistry and biology.Extensive libraries of gene truncation variants generated by in vitro transposition.Variation in the circumsporozoite protein of Plasmodium falciparum: vaccine development implications.Pulsation of electrified jet in capillary microfluidics Rational protein sequence diversification by multi-codon scanning mutagenesis.Metagenomics: Facts and Artifacts, and Computational Challenges*Emulsion PCR: a high efficient way of PCR amplification of random DNA libraries in aptamer selection.Development of methods for quantitative comparison of pooled shRNAs by mass sequencing.Detection of rare point mutation via allele-specific amplification in emulsion PCR.Massively parallel haplotyping on microscopic beads for the high-throughput phase analysis of single molecules.The same self-peptide selects conventional and regulatory CD4⁺ T cells with identical antigen receptors.Seasonal diversity of planktonic protists in Southwestern Alberta rivers over a 1-year period as revealed by terminal restriction fragment length polymorphism and 18S rRNA gene library analyses.Filtering duplicate reads from 454 pyrosequencing data.Solid-phase PCR in a picowell array for immobilizing and arraying 100,000 PCR products to a microscope slide.In vitro selection of fab fragments by mRNA display and gene-linking emulsion PCR.Particles and microfluidics merged: perspectives of highly sensitive diagnostic detection.Selection of a T7 promoter mutant with enhanced in vitro activity by a novel multi-copy bead display approach for in vitro evolution Amplification and re-generation of LNA-modified libraries.Versatile design and synthesis platform for visualizing genomes with Oligopaint FISH probes Enrichment of mutations in multiple DNA sequences using COLD-PCR in emulsion.Next generation sequencing analysis reveals a relationship between rDNA unit diversity and locus number in Nicotiana diploids.

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P2860

Amplification of complex gene libraries by emulsion PCR.

http://www.wikidata.org/entity/Q33247540

description

2006 nî lūn-bûn

@nan

2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հուլիսին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

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name

Amplification of complex gene libraries by emulsion PCR.

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Amplification of complex gene libraries by emulsion PCR.

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type

label

Amplification of complex gene libraries by emulsion PCR.

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Amplification of complex gene libraries by emulsion PCR.

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prefLabel

Amplification of complex gene libraries by emulsion PCR.

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Amplification of complex gene libraries by emulsion PCR.

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Amplification of complex gene libraries by emulsion PCR.

@en

P2093

Andrew D Griffiths

http://www.w3.org/2001/XMLSchema#string

Dan S Tawfik

http://www.w3.org/2001/XMLSchema#string

Oliver J Miller

http://www.w3.org/2001/XMLSchema#string

Sergio G Peisajovich

http://www.w3.org/2001/XMLSchema#string

Shlomo Magdassi

http://www.w3.org/2001/XMLSchema#string

P2860

Genome sequencing in microfabricated high-density picolitre reactors

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

Molecular haplotyping by linking emulsion PCR: analysis of paraoxonase 1 haplotypes and phenotypes.

PCR amplification from single DNA molecules on magnetic beads in emulsion: application for high-throughput screening of transcription factor targets

Accurate multiplex polony sequencing of an evolved bacterial genome

Evaluation of PCR-generated chimeras, mutations, and heteroduplexes with 16S rRNA gene-based cloning

Directed evolution of polymerase function by compartmentalized self-replication

Generic expansion of the substrate spectrum of a DNA polymerase by directed evolution.

Single-molecule reverse transcription polymerase chain reaction using water-in-oil emulsion.

P2888

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545-550

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scholarly article

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10.1038/NMETH896

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7

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3

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Richard Williams

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2006-07-01T00:00:00Z

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6993642

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1046539255

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16791213

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