Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome
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Diversity of human copy number variation and multicopy genesUsing mtDNA sequences to estimate SNP parameters in ESTs.A simple route to single-nucleotide polymorphisms in a nonmodel species: identification and characterization of SNPs in the Artic ringed seal (Pusa hispida hispida).Resolving genomic disorder-associated breakpoints within segmental DNA duplications using massively parallel sequencing.Single molecule linear analysis of DNA in nano-channel labeled with sequence specific fluorescent probes.Primate segmental duplications: crucibles of evolution, diversity and disease.No effect of genome-wide copy number variation on measures of intelligence in a New Zealand birth cohort.Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversityAn assessment of the sequence gaps: unfinished business in a finished human genome.Genetic architecture of colorectal cancer.How homologous recombination generates a mutable genome.Human SNPs resulting in premature stop codons and protein truncation.Strategies for the detection of copy number and other structural variants in the human genome.Multiallelic Positions in the Human Genome: Challenges for Genetic Analyses.FOXO3 gene variants and human aging: coding variants may not be key players.Genetic structures of copy number variants revealed by genotyping single sperm.Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genesAneuploidy: from a physiological mechanism of variance to Down syndrome.SNP Mining in Functional Genes from Nonmodel Species by Next-Generation Sequencing: A Case of Flowering, Pre-Harvest Sprouting, and Dehydration Resistant Genes in Wheat.Population transcriptomics reveals a potentially positive role of expression diversity in adaptation.Complex SNP-related sequence variation in segmental genome duplications.Comment on "A Database of Human Immune Receptor Alleles Recovered from Population Sequencing Data".Confirmation of association of FCGR3B but not FCGR3A copy number with susceptibility to autoantibody positive rheumatoid arthritis.Strategies for excluding false Y-chromosomal SNP entries from human genome databases.Duplicating SNPs.
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P2860
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome
description
im August 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 August 2002
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2002
@uk
name
Chromosomal regions containing ...... plications in the human genome
@en
Chromosomal regions containing ...... ingle nucleotide polymorphisms
@nl
type
label
Chromosomal regions containing ...... plications in the human genome
@en
Chromosomal regions containing ...... ingle nucleotide polymorphisms
@nl
prefLabel
Chromosomal regions containing ...... plications in the human genome
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Chromosomal regions containing ...... ingle nucleotide polymorphisms
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P2093
P356
P1476
Chromosomal regions containing ...... plications in the human genome
@en
P2093
Joseph Cheung
Kazuhiko Nakabayashi
Lap-Chee Tsui
Miguel Angel Pujana
P304
P356
10.1093/HMG/11.17.1987
P577
2002-08-01T00:00:00Z