Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis. - Wikidata - awgldk - TriplyDB

Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.

Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.

http://www.wikidata.org/entity/Q34714895

about

Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing Dissecting immunity by germline mutagenesis High throughput sequencing approaches to mutation discovery in the mouse A nonsense mutation in TMEM95 encoding a nondescript transmembrane protein causes idiopathic male subfertility in cattle Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations Applications of comparative evolution to human disease genetics Mutation of the gastric hydrogen-potassium ATPase alpha subunit causes iron-deficiency anemia in mice Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing.Second-generation high-throughput forward genetic screen in mice to isolate subtle behavioral mutants.The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data ESCRT-II/Vps25 constrains digit number by endosome-mediated selective modulation of FGF-SHH signaling.A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers.A strategy to identify dominant point mutant modifiers of a quantitative trait.Fast homozygosity mapping and identification of a zebrafish ENU-induced mutation by whole-genome sequencing.Modifier genes and the plasticity of genetic networks in mice.Discovery Genetics - The History and Future of Spontaneous Mutation Research.ENU-induced phenovariance in mice: inferences from 587 mutations.Exon capture and bulk segregant analysis: rapid discovery of causative mutations using high-throughput sequencing.MutMap+: genetic mapping and mutant identification without crossing in rice.Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis.Real-time resolution of point mutations that cause phenovariance in mice.Identification of mutations in zebrafish using next-generation sequencing.Increased susceptibility to DNA virus infection in mice with a GCN2 mutation Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.Variant mapping and mutation discovery in inbred mice using next-generation sequencing Mutation discovery in mice by whole exome sequencing.Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.Mutation mapping and identification by whole-genome sequencing.A forward genetic screen reveals roles for Nfkbid, Zeb1, and Ruvbl2 in humoral immunity Cell Receptor-Basement Membrane Interactions in Health and Disease: A Kidney-Centric View The functional diversity of essential genes required for mammalian cardiac development.Using next-generation sequencing to isolate mutant genes from forward genetic screens.Getting started in mapping-by-sequencing.Genetic Modifier Screens in Mice.Innate immunity and the new forward genetics.MMAPPR: mutation mapping analysis pipeline for pooled RNA-seq.A Comparison of the Chicken and Turkey Proteomes and Phosphoproteomes in the Development of Poultry-Specific Immuno-Metabolism Kinome Peptide Arrays.HCFC2 is needed for IRF1- and IRF2-dependent Tlr3 transcription and for survival during viral infections.The 50th Midwinter Conference of Immunologists at Asilomar.

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Rapid identification of a disease allele in mouse through whole genome sequencing and bulk segregation analysis.

http://www.wikidata.org/entity/Q34714895

description

2010 nî lūn-bûn

@nan

2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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type

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Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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Rapid identification of a dise ...... and bulk segregation analysis.

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GENETICS.110.124586

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Rapid identification of a dise ...... and bulk segregation analysis.

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Carrie N Arnold

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Charles Ross

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Martin Schwander

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Nora G Smart

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Pei Lin

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Ulrich Müller

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Yu Xia

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P2860

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV

Targeted capture and massively parallel sequencing of 12 human exomes

A map of human genome variation from population-scale sequencing

Sequencing technologies - the next generation

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

The impact of next-generation sequencing technology on genetics

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function

Identification of Lps2 as a key transducer of MyD88-independent TIR signalling

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10.1534/GENETICS.110.124586

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