A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
about
The diploid genome sequence of an individual humanFOXM1 upregulation is an early event in human squamous cell carcinoma and it is enhanced by nicotine during malignant transformationVirtual karyotyping with SNP microarrays reduces uncertainty in the diagnosis of renal epithelial tumorsUpregulation of FOXM1 induces genomic instability in human epidermal keratinocytesDisruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar SyndromeIdentification of a 2 Mb human ortholog of Drosophila eyes shut/spacemaker that is mutated in patients with retinitis pigmentosaHomozygously deleted gene DACH1 regulates tumor-initiating activity of glioma cellsOFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilinMicrocephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitorsTMEM165 deficiency causes a congenital disorder of glycosylationPrevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasmsClinical and molecular delineation of the 17q21.31 microdeletion syndromeChromosomal lesions and uniparental disomy detected by SNP arrays in MDS, MDS/MPD, and MDS-derived AMLMolecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarrayImmunologically silent cancer clone transmission from mother to offspringThe application of single nucleotide polymorphism microarrays in cancer researchStructural variation of chromosomes in autism spectrum disorderPax6 3' deletion results in aniridia, autism and mental retardationHighly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarraysAllele-specific amplification in cancer revealed by SNP array analysisCARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Analysis and visualization of chromosomal abnormalities in SNP data with SNPscanIntegrating genetics and epigenetics in breast cancer: biological insights, experimental, computational methods and therapeutic potentialIKZF1 deletions predict relapse in uniformly treated pediatric precursor B-ALL.Integrated molecular analysis of clear-cell renal cell carcinoma.An analytical pipeline for genomic representations used for cytosine methylation studiesGenome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysisGenome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinomaHomozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problemsFast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet CompressionGenomic and molecular characterization of esophageal squamous cell carcinomaExome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvementSNP and gene networks construction and analysis from classification of copy number variations dataA genotype-first approach for the molecular and clinical characterization of uncommon de novo microdeletion of 20q13.33Quantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array dataComparative RNA-Seq and microarray analysis of gene expression changes in B-cell lymphomas of Canis familiaris.Parsimonious higher-order hidden Markov models for improved array-CGH analysis with applications to Arabidopsis thaliana.Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotypeA Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arrays.Mismatch and G-stack modulated probe signals on SNP microarrays.
P2860
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P2860
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
A robust algorithm for copy nu ...... olymorphism genotyping arrays.
@en
type
label
A robust algorithm for copy nu ...... olymorphism genotyping arrays.
@en
prefLabel
A robust algorithm for copy nu ...... olymorphism genotyping arrays.
@en
P2093
P1433
P1476
A robust algorithm for copy nu ...... olymorphism genotyping arrays.
@en
P2093
Akira Hangaishi
Dione K Bailey
Giulia C Kennedy
Kumi Nakazaki
Masashi Sanada
Mineo Kurokawa
Noriko Hosoya
Seishi Ogawa
Shigeru Chiba
P304
P356
10.1158/0008-5472.CAN-05-0465
P407
P577
2005-07-01T00:00:00Z