about
Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) methodaffy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism callingThe genetic effect of copy number variations on the risk of type 2 diabetes in a Korean populationGenome-wide profiling of structural genomic variations in Korean HapMap individualsOver-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceExploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.Inference of chromosome-specific copy numbers using population haplotypesInheritance model introduces differential bias in CNV calls between parents and offspringA genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate riskIdentification of copy number variations and common deletion polymorphisms in cattle.Genomic characteristics of cattle copy number variations.Reconstructing CNV genotypes using segregation analysis: combining pedigree information with CNV assayAnalysis of genome-wide copy number variations in Chinese indigenous and western pig breeds by 60 K SNP genotyping arraysA genome-wide detection of copy number variations using SNP genotyping arrays in swine.Reconstructing DNA copy number by joint segmentation of multiple sequencesInherited MST1 deficiency underlies susceptibility to EV-HPV infectionsFast detection of de novo copy number variants from SNP arrays for case-parent trios.Molecular characterization of an intact p53 pathway subtype in high-grade serous ovarian cancer.Copy number variation genotyping using family information.Observations on Copy Number Variations in a Kidney-yang Deficiency Syndrome Family.A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts.Haplotype phasing and inheritance of copy number variants in nuclear families.Analysis of copy number variation using whole genome exon-focused array CGH in Korean patients with primary congenital glaucomaThe impact of genomics on pediatric research and medicine.CNV analysis in the Lithuanian population.Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism.Joint detection of copy number variations in parent-offspring trios.A stochastic inference of de novo CNV detection and association test in multiplex schizophrenia families.qKAT: a high-throughput qPCR method for KIR gene copy number and haplotype determinationNew technologies for delineating and characterizing the lipid exome: prospects for understanding familial combined hyperlipidemia.Genome-wide comparisons of variation in linkage disequilibrium.Comparing CNV detection methods for SNP arrays.ParseCNV integrative copy number variation association software with quality tracking.A bayesian integrative model for genetical genomics with spatially informed variable selection.Chromosome dynamic changes in two cultured Chinese human embryonic stem cell lines: single nucleotide polymorphism, copy number variation and loss of heterozygosity.A HIERARCHICAL BAYESIAN MODEL FOR INFERENCE OF COPY NUMBER VARIANTS AND THEIR ASSOCIATION TO GENE EXPRESSION.An integrative segmentation method for detecting germline copy number variations in SNP arrays.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Modeling genetic inheritance of copy number variations.
@en
type
label
Modeling genetic inheritance of copy number variations.
@en
prefLabel
Modeling genetic inheritance of copy number variations.
@en
P2093
P2860
P50
P356
P1476
Modeling genetic inheritance of copy number variations
@en
P2093
Hakon Hakonarson
Mahlet G Tadesse
Maja Bucan
Mingyao Li
P2860
P356
10.1093/NAR/GKN641
P407
P577
2008-10-02T00:00:00Z