Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias. - Wikidata - awgldk - TriplyDB

Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias.

Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias.

http://www.wikidata.org/entity/Q34133415

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Modeling host genetic regulation of influenza pathogenesis in the collaborative cross Mapping the genomic architecture of adaptive traits with interspecific introgressive origin: a coalescent-based approach A multi-megabase copy number gain causes maternal transmission ratio distortion on mouse chromosome 2 Deconstructing Mus gemischus: advances in understanding ancestry, structure, and variation in the genome of the laboratory mouse Re-evaluating data quality of dog mitochondrial, Y chromosomal, and autosomal SNPs genotyped by SNP array.High-resolution sex-specific linkage maps of the mouse reveal polarized distribution of crossovers in male germline An HMM-based comparative genomic framework for detecting introgression in eukaryotes.Immunocompetent mouse allograft models for development of therapies to target breast cancer metastasis.Quantitative trait locus mapping methods for diversity outbred mice.Comparative analysis and visualization of multiple collinear genomes.A powerful tool for genome analysis in maize: development and evaluation of the high density 600 k SNP genotyping array.SNP array profiling of mouse cell lines identifies their strains of origin and reveals cross-contamination and widespread aneuploidy.A novel intronic single nucleotide polymorphism in the myosin heavy polypeptide 4 gene is responsible for the mini-muscle phenotype characterized by major reduction in hind-limb muscle mass in mice Maximum likelihood inference of reticulate evolutionary histories.Genetic architecture of skewed X inactivation in the laboratory mouse.Vitis phylogenomics: hybridization intensities from a SNP array outperform genotype calls Development of the catfish 250K SNP array for genome-wide association studies.Genetic Analysis of Substrain Divergence in Non-Obese Diabetic (NOD) Mice Genomic copy number variation in Mus musculus Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping.Informatics resources for the Collaborative Cross and related mouse populations Adaptive evolution and effective population size in wild house mice DNA methylation at the Igf2/H19 imprinting control region is associated with cerebellum mass in outbred mice Chromosome transplantation as a novel approach for correcting complex genomic disorders The Mouse Universal Genotyping Array: From Substrains to Subspecies Genome-Wide Detection of Gene Coexpression Domains Showing Linkage to Regions Enriched with Polymorphic Retrotransposons in Recombinant Inbred Mouse Strains.Rapid genotype imputation from sequence without reference panels Whole Genome Sequence of Two Wild-Derived Mus musculus domesticus Inbred Strains, LEWES/EiJ and ZALENDE/EiJ, with Different Diploid Numbers Development of a 690 K SNP array in catfish and its application for genetic mapping and validation of the reference genome sequence.High-Resolution Maps of Mouse Reference Populations Striking Immune Phenotypes in Gene-Targeted Mice Are Driven by a Copy-Number Variant Originating from a Commercially Available C57BL/6 Strain Male Infertility Is Responsible for Nearly Half of the Extinction Observed in the Mouse Collaborative Cross.High throughput SNP discovery and genotyping in hexaploid wheat.Conversion of array-based single nucleotide polymorphic markers for use in targeted genotyping by sequencing in hexaploid wheat (Triticum aestivum).Tools for Genetic Studies in Experimental Populations of Polyploids.

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Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias.

http://www.wikidata.org/entity/Q34133415

description

2012 nî lūn-bûn

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2012 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2012年の論文

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Discovery of novel variants in ...... nd reduces ascertainment bias.

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Discovery of novel variants in ...... nd reduces ascertainment bias.

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Discovery of novel variants in ...... nd reduces ascertainment bias.

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Chen-Ping Fu

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Fernando Pardo-Manuel de Villena

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Gary A Churchill

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Hyuna Yang

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Keith Sheppard

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Leonard McMillan

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P2860

Lineage-specific biology revealed by a finished genome assembly of the mouse

A map of human genome variation from population-scale sequencing

Genome-wide survey of SNP variation uncovers the genetic structure of cattle breeds

Fast and accurate short read alignment with Burrows-Wheeler transform

Silhouette scores for assessment of SNP genotype clusters

Elusive copy number variation in the mouse genome

MRBAYES: Bayesian inference of phylogenetic trees

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

A simple genetic architecture underlies morphological variation in dogs

Integrating common and rare genetic variation in diverse human populations

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