Fine-scale structural variation of the human genome - sprookjes - yvandenbroek - TriplyDB

Fine-scale structural variation of the human genome

Fine-scale structural variation of the human genome

http://www.wikidata.org/entity/Q22122044

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Bacteria-human somatic cell lateral gene transfer is enriched in cancer samples Drug-resistant genotypes and multi-clonality in Plasmodium falciparum analysed by direct genome sequencing from peripheral blood of malaria patients Evaluation of paired-end sequencing strategies for detection of genome rearrangements in cancer Towards a comprehensive structural variation map of an individual human genome Human genetics and genomics a decade after the release of the draft sequence of the human genome Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration Population stratification of a common APOBEC gene deletion polymorphism The DNA sequence and biological annotation of human chromosome 1 Mapping and sequencing of structural variation from eight human genomes Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes The UCSC Genome Browser Database: update 2006 High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery inGAP-sv: a novel scheme to identify and visualize structural variation from paired end mapping data Mapping copy number variation by population-scale genome sequencing Genomic drift and copy number variation of chemosensory receptor genes in humans and mice Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library Accurate whole human genome sequencing using reversible terminator chemistry Advances in translational bioinformatics: computational approaches for the hunting of disease genes Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding Statistical aspects of discerning indel-type structural variation via DNA sequence alignment Paired-end mapping reveals extensive structural variation in the human genome Global variation in copy number in the human genome Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies.Duplication and positive selection among hominin-specific PRAME genes.CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Bias of selection on human copy-number variants.BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive Associations between activation-induced cytidine deaminase/apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like cytidine deaminase expression, hepatitis B virus (HBV) replication and HBV-associated liver disease (Review)Advances in BAC-based physical mapping and map integration strategies in plants Current concepts on primary open-angle glaucoma genetics: a contribution to disease pathophysiology and future treatment A high-resolution map of segmental DNA copy number variation in the mouse genome Sensitive Tumorigenic Potential Evaluation of Adult Human Multipotent Neural Cells Immortalized by hTERT Gene Transduction Genome-Wide Detection of CNVs and Their Association with Meat Tenderness in Nelore Cattle FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data Computational characterisation of cancer molecular profiles derived using next generation sequencing Segmental duplications and copy-number variation in the human genome.A copy number variation map of the human genome

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P2860

Fine-scale structural variation of the human genome

http://www.wikidata.org/entity/Q22122044

description

2005 nî lūn-bûn

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2005 թվականի մայիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Fine-scale structural variation of the human genome

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Nature Genetics

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Fine-scale structural variation of the human genome

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Andrew J Sharp

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Daniel Pinkel

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Donna Albertson

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Hillary Hayden

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Jeffrey A Bailey

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Lisa M Pertz

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Maynard V Olson

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Rajinder Kaul

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V Anne Morrison

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Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster

Detection of large-scale variation in the human genome

Large-scale copy number polymorphism in the human genome

The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

A common inversion under selection in Europeans

Recent segmental duplications in the human genome

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

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727-732

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183906

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10.1038/NG1562

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7

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37

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Evan E. Eichler

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2005-05-15T00:00:00Z

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7846499

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1014017119

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15895083

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