Multigene amplification and massively parallel sequencing for cancer mutation discovery. - Wikidata - awgldk - TriplyDB

Multigene amplification and massively parallel sequencing for cancer mutation discovery.

Multigene amplification and massively parallel sequencing for cancer mutation discovery.

http://www.wikidata.org/entity/Q35799619

about

Connector inversion probe technology: a powerful one-primer multiplex DNA amplification system for numerous scientific applications DNA sequencing by denaturation: experimental proof of concept with an integrated fluidic device Targeted enrichment of genomic DNA regions for next-generation sequencing Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy.A comprehensive assay for targeted multiplex amplification of human DNA sequences Keeping up with the next generation: massively parallel sequencing in clinical diagnostics The impact of next-generation sequencing technology on genetics Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders Direct multiplex sequencing (DMPS)--a novel method for targeted high-throughput sequencing of ancient and highly degraded DNA Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing Next generation sequencing for clinical diagnostics-principles and application to targeted resequencing for hypertrophic cardiomyopathy: a paper from the 2009 William Beaumont Hospital Symposium on Molecular Pathology.Evaluation of human gene variant detection in amplicon pools by the GS-FLX parallel Pyrosequencer.Preparing a re-sequencing DNA library of 2 cancer candidate genes using the ligation-by-amplification protocol by two PCR reactions.Microarray-based multicycle-enrichment of genomic subsets for targeted next-generation sequencing.Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process.Pharmacogenetics and personal genomes.Targeted resequencing of candidate genes using selector probes.Performance of microarray and liquid based capture methods for target enrichment for massively parallel sequencing and SNP discovery.Targeted deep resequencing of the human cancer genome using next-generation technologies.Rapid identification of heterozygous mutations in Drosophila melanogaster using genomic capture sequencing.A flexible approach for highly multiplexed candidate gene targeted resequencing.A cross-sample statistical model for SNP detection in short-read sequencing data.Targeted sequencing library preparation by genomic DNA circularization.A rapid, cost-effective method of assembly and purification of synthetic DNA probes >100 bp.Next-generation sequencing for cancer diagnostics: a practical perspective.Enrichment of genomic DNA for polymorphism detection in a non-model highly polyploid crop plant.Targeted DNA sequencing and in situ mutation analysis using mobile phone microscopy Experiences with array-based sequence capture; toward clinical applications.Microarray oligonucleotide probe designer (MOPeD): A web service Multiplex target capture with double-stranded DNA probes High-quality DNA sequence capture of 524 disease candidate genes Automated serial extraction of DNA and RNA from biobanked tissue specimens Accurate detection of subclonal single nucleotide variants in whole genome amplified and pooled cancer samples using HaloPlex target enrichment.Review of massively parallel DNA sequencing technologies.The Human OligoGenome Resource: a database of oligonucleotide capture probes for resequencing target regions across the human genome.Mutation-induced protein interaction kinetics changes affect apoptotic network dynamic properties and facilitate oncogenesis.CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing.What Next? The Next Transit from Biology to Diagnostics: Next Generation Sequencing for Immunogenetics.Sensitive and inexpensive digital DNA analysis by microfluidic enrichment of rolling circle amplified single-molecules

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

http://www.wikidata.org/entity/Q35799619

description

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name

Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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Proceedings of the National Academy of Sciences of the United States of America

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Multigene amplification and massively parallel sequencing for cancer mutation discovery.

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David Bicknell

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Fredrik Dahl

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Hanlee Ji

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Johan Stenberg

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Katrina Welch

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Mats Nilsson

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

Michael Zhang

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Ronald W Davis

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Simon Fredriksson

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

Genome sequencing in microfabricated high-density picolitre reactors

NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

dbSNP: the NCBI database of genetic variation

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

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

Sequence information can be obtained from single DNA molecules

PieceMaker: selection of DNA fragments for selector-guided multiplex amplification

Multiplex PCR: use of heat-stable Thermus thermophilus RecA protein to minimize non-specific PCR products.

PupasView: a visual tool for selecting suitable SNPs, with putative pathological effect in genes, for genotyping purposes

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