Sequence-based characterization of structural variation in the mouse genome. - Wikidata - wikimedia - TriplyDB

Sequence-based characterization of structural variation in the mouse genome.

Sequence-based characterization of structural variation in the mouse genome.

http://www.wikidata.org/entity/Q36193488

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Mouse endogenous retroviruses can trigger premature transcriptional termination at a distance Endogenous retroviruses and the development of cancer Copy number variants and selective sweeps in natural populations of the house mouse (Mus musculus domesticus)Nxf1 natural variant E610G is a semi-dominant suppressor of IAP-induced RNA processing defects Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice Natural genetic variation of integrin alpha L (Itgal) modulates ischemic brain injury in stroke Phenotypic instability between the near isogenic substrains BALB/cJ and BALB/cByJ.Individual differences in recovery from traumatic fear The genetic architecture of the genome-wide transcriptional response to ER stress in the mouse Hnrnph1 Is A Quantitative Trait Gene for Methamphetamine Sensitivity Genome-wide and parental allele-specific analysis of CTCF and cohesin DNA binding in mouse brain reveals a tissue-specific binding pattern and an association with imprinted differentially methylated regions The Mouse Solitary Odorant Receptor Gene Promoters as Models for the Study of Odorant Receptor Gene Choice 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 Mouse genomic variation and its effect on phenotypes and gene regulation Genome-wide association for fear conditioning in an advanced intercross mouse line SMaSH: a benchmarking toolkit for human genome variant calling.Structural evolution of CatSper1 in rodents is influenced by sperm competition, with effects on sperm swimming velocity.fourSig: a method for determining chromosomal interactions in 4C-Seq data Comparative Analysis of CNV Calling Algorithms: Literature Survey and a Case Study Using Bovine High-Density SNP Data High-resolution sex-specific linkage maps of the mouse reveal polarized distribution of crossovers in male germline Identifying genes for neurobehavioural traits in rodents: progress and pitfalls PRC2 represses transcribed genes on the imprinted inactive X chromosome in mice Association study and expression analysis of CYP4A11 gene copy number variation in Chinese cattle Deleted copy number variation of Hanwoo and Holstein using next generation sequencing at the population level.Evidence for local regulatory control of escape from imprinted X chromosome inactivation.Identification of structural variation in mouse genomes.Genomic variability in Mexican chicken population using copy number variants.Genomes of the Mouse Collaborative Cross.Epistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice.Identification of a QTL in Mus musculus for alcohol preference, withdrawal, and Ap3m2 expression using integrative functional genomics and precision genetics.An integrative probabilistic model for identification of structural variation in sequencing data.Modifier genes and the plasticity of genetic networks in mice.Rapid identification of major-effect genes using the collaborative cross.Integrative genetic analysis of allergic inflammation in the murine lung The genomic landscape shaped by selection on transposable elements across 18 mouse strains Genome-wide patterns of standing genetic variation in a marine population of three-spined sticklebacks.Phenotypic impact of genomic structural variation: insights from and for human disease.Genetic regulation of Zfp30, CXCL1, and neutrophilic inflammation in murine lung.Fine mapping of copy number variations on two cattle genome assemblies using high density SNP array.

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Sequence-based characterization of structural variation in the mouse genome.

http://www.wikidata.org/entity/Q36193488

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Sequence-based characterization of structural variation in the mouse genome.

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Sequence-based characterization of structural variation in the mouse genome.

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type

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Sequence-based characterization of structural variation in the mouse genome.

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Sequence-based characterization of structural variation in the mouse genome.

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Sequence-based characterization of structural variation in the mouse genome.

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Sequence-based characterization of structural variation in the mouse genome.

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Sequence-based characterization of structural variation in the mouse genome.

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Amarjit Bhomra

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Avigail Agam

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David J Adams

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Deborah Janowitz

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Helen Whitley

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James Cleak

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Jérôme Nicod

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Kim Wong

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Leo Goodstadt

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Martin Goodson

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Mapping copy number variation by population-scale genome sequencing

Haplotypes at the Tas2r locus on distal chromosome 6 vary with quinine taste sensitivity in inbred mice.

Elusive copy number variation in the mouse genome

LookSeq: A browser-based viewer for deep sequencing data

Skint1, the prototype of a newly identified immunoglobulin superfamily gene cluster, positively selects epidermal gammadelta T cells

Origins and functional impact of copy number variation in the human genome

Genome architecture, rearrangements and genomic disorders

Population genomics of human gene expression

An integrative genomics approach to infer causal associations between gene expression and disease

Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads

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326-329

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10.1038/NATURE10432

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7364

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477

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Binnaz Yalçın

Christoffer Nellåker

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2011-09-14T00:00:00Z

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51646630

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3428933

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