Sensitive and accurate detection of copy number variants using read depth of coverage. - Wikidata - awgldk - TriplyDB

Sensitive and accurate detection of copy number variants using read depth of coverage.

Sensitive and accurate detection of copy number variants using read depth of coverage.

http://www.wikidata.org/entity/Q42566509

about

Drug-resistant genotypes and multi-clonality in Plasmodium falciparum analysed by direct genome sequencing from peripheral blood of malaria patients GROM-RD: resolving genomic biases to improve read depth detection of copy number variants COPS: a sensitive and accurate tool for detecting somatic Copy Number Alterations using short-read sequence data from paired samples Host-Pathogen Coevolution: The Selective Advantage of Bacillus thuringiensis Virulence and Its Cry Toxin Genes Human genetics and genomics a decade after the release of the draft sequence of the human genome Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives Personal genome sequencing: current approaches and challenges Using ERDS to infer copy-number variants in high-coverage genomes forestSV: structural variant discovery through statistical learning TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology Mapping copy number variation by population-scale genome sequencing VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing Practical aspects of NGS-based pathways analysis for personalized cancer science and medicine Somatic mosaicism in the human genome Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns A genetic model for neurodevelopmental disease Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges Computational characterisation of cancer molecular profiles derived using next generation sequencing Detection of Genomic Structural Variants from Next-Generation Sequencing Data Analysis of next-generation genomic data in cancer: accomplishments and challenges CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data A genome-wide approach for detecting novel insertion-deletion variants of mid-range size Detectable clonal mosaicism in the human genome Phylogenetic quantification of intra-tumour heterogeneity The Arabidopsis thaliana mobilome and its impact at the species level Tumour evolution inferred by single-cell sequencing The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation Summarizing and correcting the GC content bias in high-throughput sequencing Chromosomal structural variations during progression of a prostate epithelial cell line to a malignant metastatic state inactivate the NF2, NIPSNAP1, UGT2B17, and LPIN2 genes PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations Copy number variation detection and genotyping from exome sequence data.Combined examination of sequence and copy number variations in human deafness genes improves diagnosis for cases of genetic deafness.Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome Joint mouse-human phenome-wide association to test gene function and disease risk.Validation of rearrangement break points identified by paired-end sequencing in natural populations of Drosophila melanogaster.A survey of copy-number variation detection tools based on high-throughput sequencing data.Modeling read counts for CNV detection in exome sequencing data.Copy Number Variation detection from 1000 Genomes Project exon capture sequencing data.A Poisson hierarchical modelling approach to detecting copy number variation in sequence coverage data.

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P2860

Sensitive and accurate detection of copy number variants using read depth of coverage.

http://www.wikidata.org/entity/Q42566509

description

2009 nî lūn-bûn

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2009年の論文

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2009年論文

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2009年論文

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2009年论文

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2009年论文

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2009年论文

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name

Sensitive and accurate detection of copy number variants using read depth of coverage.

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Sensitive and accurate detection of copy number variants using read depth of coverage.

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type

label

Sensitive and accurate detection of copy number variants using read depth of coverage.

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Sensitive and accurate detection of copy number variants using read depth of coverage.

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prefLabel

Sensitive and accurate detection of copy number variants using read depth of coverage.

@en

Sensitive and accurate detection of copy number variants using read depth of coverage.

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Genome Research

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Sensitive and accurate detection of copy number variants using read depth of coverage.

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Kenny Ye

http://www.w3.org/2001/XMLSchema#string

Seungtai Yoon

http://www.w3.org/2001/XMLSchema#string

Vladimir Makarov

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Zhenyu Xuan

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P2860

The diploid genome sequence of an Asian individual

Structural variation in the human genome

Fine-scale structural variation of the human genome

Mapping and sequencing of structural variation from eight human genomes

Strong association of de novo copy number mutations with autism

Accurate whole human genome sequencing using reversible terminator chemistry

Mapping short DNA sequencing reads and calling variants using mapping quality scores

Disruption of the neurexin 1 gene is associated with schizophrenia

Paired-end mapping reveals extensive structural variation in the human genome

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

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1586-1592

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scholarly article

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10.1101/GR.092981.109

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9

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19

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