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End-sequence profiling: sequence-based analysis of aberrant genomes

End-sequence profiling: sequence-based analysis of aberrant genomes

http://www.wikidata.org/entity/Q24670275

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Amplification and overexpression of the ID4 gene at 6p22.3 in bladder cancer.A high-resolution map of synteny disruptions in gibbon and human genomes Evaluation of paired-end sequencing strategies for detection of genome rearrangements in cancer Using comparative genomics to reorder the human genome sequence into a virtual sheep genome Mapping and sequencing of structural variation from eight human genomes Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes Complex landscapes of somatic rearrangement in human breast cancer genomes.A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers Statistical aspects of discerning indel-type structural variation via DNA sequence alignment Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.Advances in BAC-based physical mapping and map integration strategies in plants FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data Oncogenomics and the development of new cancer therapies Analysis of next-generation genomic data in cancer: accomplishments and challenges Structural alterations from multiple displacement amplification of a human genome revealed by mate-pair sequencing High resolution detection and analysis of CpG dinucleotides methylation using MBD-Seq technology The cancer genome Circos: an information aesthetic for comparative genomics PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations Paired-end sequencing of long-range DNA fragments for de novo assembly of large, complex Mammalian genomes by direct intra-molecule ligation Contribution of Asian mouse subspecies Mus musculus molossinus to genomic constitution of strain C57BL/6J, as defined by BAC-end sequence-SNP analysis A sequence-based survey of the complex structural organization of tumor genomes.Genomic Comparison of Two O111:H- Enterohemorrhagic Escherichia coli Isolates from a Historic Hemolytic-Uremic Syndrome Outbreak in Australia.Genome evolution in Reptilia: in silico chicken mapping of 12,000 BAC-end sequences from two reptiles and a basal bird.Challenges of sequencing human genomes.Designing deep sequencing experiments: detecting structural variation and estimating transcript abundance GAP-Seq: a method for identification of DNA palindromes.Detection and reconstruction of tandemly organized de novo copy number variations Pooled genomic indexing of rhesus macaque.Detecting common copy number variants in high-throughput sequencing data by using JointSLM algorithm.Sequence-based physical mapping of complex genomes by whole genome profiling Detection and characterization of novel sequence insertions using paired-end next-generation sequencing.Genomic instability in breast cancer: pathogenesis and clinical implications Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines Consistency-based detection of potential tumor-specific deletions in matched normal/tumor genomes Massively parallel sequencing approaches for characterization of structural variation

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End-sequence profiling: sequence-based analysis of aberrant genomes

http://www.wikidata.org/entity/Q24670275

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2003 nî lūn-bûn

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2003 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2003年の論文

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2003年学术文章

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2003年学术文章

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2003年学术文章

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2003年学术文章

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2003年学术文章

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2003年學術文章

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name

End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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type

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End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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End-sequence profiling: sequence-based analysis of aberrant genomes

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Proceedings of the National Academy of Sciences of the United States of America

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End-sequence profiling: sequence-based analysis of aberrant genomes

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Anna Lapuk

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Colin Collins

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David Kowbel

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David R Herndon

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Gregg Magrane

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Guiqing Huang

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Joe W Gray

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John H Brebner

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Koei Chin

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Pieter De Jong

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Initial sequencing and analysis of the human genome

Multicolor Spectral Karyotyping of Human Chromosomes

The Sequence of the Human Genome

Positional cloning of ZNF217 and NABC1: genes amplified at 20q13.2 and overexpressed in breast carcinoma

Comprehensive genome sequence analysis of a breast cancer amplicon

Construction and characterization of a human bacterial artificial chromosome library

Independent amplification and frequent co-amplification of three nonsyntenic regions on the long arm of chromosome 20 in human breast cancer

Genome architecture, rearrangements and genomic disorders

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

High throughput direct end sequencing of BAC clones

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10.1073/PNAS.1232418100

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