High-throughput variation detection and genotyping using microarrays - Test2 - elhamkhani - TriplyDB

High-throughput variation detection and genotyping using microarrays

High-throughput variation detection and genotyping using microarrays

http://www.wikidata.org/entity/Q24617968

about

Sequencing by hybridization of long targets A novel custom resequencing array for dilated cardiomyopathy Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays Diagnosis of HNF-1alpha mutations on a PNA zip-code microarray by single base extension Microarray-based resequencing of multiple Bacillus anthracis isolates Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan Optimal Probe Length Varies for Targets with High Sequence Variation: Implications for Probe Library Design for Resequencing Highly Variable Genes Phi29 polymerase based random amplification of viral RNA as an alternative to random RT-PCR Advantages of Array-Based Technologies for Pre-Emptive Pharmacogenomics Testing Identification of novel sequence variations in microRNAs in chronic lymphocytic leukemia Single assay for simultaneous detection and differential identification of human and avian influenza virus types, subtypes, and emergent variants Reconstructed ancestral sequences improve pathogen identification using resequencing DNA microarrays Family-based genome-wide association scan of attention-deficit/hyperactivity disorder Smallpox virus resequencing GeneChips can also rapidly ascertain species status for some zoonotic non-variola orthopoxviruses GeneChip resequencing of the smallpox virus genome can identify novel strains: a biodefense application.Identifying influenza viruses with resequencing microarrays.Use of consensus sequences for the design of high density resequencing microarrays: the influenza virus paradigm.Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays.Large-scale evolutionary surveillance of the 2009 H1N1 influenza A virus using resequencing arrays Haplotype and missing data inference in nuclear families.AccuTyping: new algorithms for automated analysis of data from high-throughput genotyping with oligonucleotide microarrays.A wing expressed sequence tag resource for Bicyclus anynana butterflies, an evo-devo model.A molecular scheme for improved characterization of human embryonic stem cell lines An evaluation of Comparative Genome Sequencing (CGS) by comparing two previously-sequenced bacterial genomes.Persistent infection and promiscuous recombination of multiple genotypes of an RNA virus within a single host generate extensive diversity High throughput genetic analysis of congenital myasthenic syndromes using resequencing microarrays Interspecies hybridization on DNA resequencing microarrays: efficiency of sequence recovery and accuracy of SNP detection in human, ape, and codfish mitochondrial DNA genomes sequenced on a human-specific MitoChip.Genotyping of Bacillus cereus strains by microarray-based resequencing Performance of mitochondrial DNA mutations detecting early stage cancer.Mitochondrial DNA variants of respiratory complex I that uniquely characterize haplogroup T2 are associated with increased risk of age-related macular degeneration.Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regions.ReseqChip: automated integration of multiple local context probe data from the MitoChip array in mitochondrial DNA sequence assembly.Mitochondrial mutations in adenoid cystic carcinoma of the salivary glands.High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype.Empirical evaluation of oligonucleotide probe selection for DNA microarrays Polymorphisms in the mitochondrial DNA control region and frailty in older adults Genome-wide association scan of attention deficit hyperactivity disorder Mechanisms of surface-mediated DNA hybridization.Characterization of sal(A), a novel gene responsible for lincosamide and streptogramin A resistance in Staphylococcus sciuri

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High-throughput variation detection and genotyping using microarrays

http://www.wikidata.org/entity/Q24617968

description

2001 nî lūn-bûn

@nan

2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2001年の論文

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2001年論文

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2001年論文

@zh-hant

2001年論文

@zh-hk

2001年論文

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2001年論文

@zh-tw

2001年论文

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name

High-throughput variation detection and genotyping using microarrays

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High-throughput variation detection and genotyping using microarrays

@en

High-throughput variation detection and genotyping using microarrays

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type

label

High-throughput variation detection and genotyping using microarrays

@ast

High-throughput variation detection and genotyping using microarrays

@en

High-throughput variation detection and genotyping using microarrays

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prefLabel

High-throughput variation detection and genotyping using microarrays

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High-throughput variation detection and genotyping using microarrays

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High-throughput variation detection and genotyping using microarrays

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Genome Research

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High-throughput variation detection and genotyping using microarrays

@en

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A Chakravarti

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

C Kashuk

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C T Yohn

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D J Cutler

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D J Mathews

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E E Eichler

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J A Warrington

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K P Tobin

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M E Zwick

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M M Carrasquillo

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Initial sequencing and analysis of the human genome

The Sequence of the Human Genome

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

Base-calling of automated sequencer traces using phred. II. Error probabilities

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

Consed: a graphical tool for sequence finishing

Identification of common molecular subsequences

Characterization of single-nucleotide polymorphisms in coding regions of human genes

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1913-25

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scholarly article

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10.1101/GR.197201

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P433

11

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11

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2001-11-01T00:00:00Z

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11662062

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11691856

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311146

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