Pages that link to "Q21145383"

The following pages link to Evaluation of paired-end sequencing strategies for detection of genome rearrangements in cancer (Q21145383):

Displaying 47 items.

• Next-generation VariationHunter: combinatorial algorithms for transposon insertion discovery (Q24599569) (← links)
• Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding (Q24647100) (← links)
• Statistical aspects of discerning indel-type structural variation via DNA sequence alignment (Q24650301) (← links)
• Diagnostics based on nucleic acid sequence variant profiling: PCR, hybridization, and NGS approaches (Q26752713) (← links)
• FusionSeq: a modular framework for finding gene fusions by analyzing Paired-End RNA-Sequencing data (Q27499410) (← links)
• Marsupial genome sequences: providing insight into evolution and disease (Q28661720) (← links)
• PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data (Q28752684) (← links)
• Yeast genome analysis identifies chromosomal translocation, gene conversion events and several sites of Ty element insertion (Q30438104) (← links)
• THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data (Q30657925) (← links)
• A sequence-based survey of the complex structural organization of tumor genomes (Q33325344) (← links)
• An integrative approach to reveal driver gene fusions from paired-end sequencing data in cancer (Q33514281) (← links)
• Second generation sequencing of the mesothelioma tumor genome (Q33582141) (← links)
• Challenges of sequencing human genomes (Q33592630) (← links)
• Designing deep sequencing experiments: detecting structural variation and estimating transcript abundance (Q33611153) (← links)
• Massively parallel sequencing approaches for characterization of structural variation (Q34121475) (← links)
• Design and validation issues in RNA-seq experiments (Q34178885) (← links)
• Analysis of microsatellite variation in Drosophila melanogaster with population-scale genome sequencing (Q34200344) (← links)
• Expanding the computational toolbox for mining cancer genomes (Q34207474) (← links)
• An integrative probabilistic model for identification of structural variation in sequencing data (Q34209538) (← links)
• Long span DNA paired-end-tag (DNA-PET) sequencing strategy for the interrogation of genomic structural mutations and fusion-point-guided reconstruction of amplicons. (Q34430902) (← links)
• ChopSticks: High-resolution analysis of homozygous deletions by exploiting concordant read pairs (Q34461514) (← links)
• The intra-S phase checkpoint protein Tof1 collaborates with the helicase Rrm3 and the F-box protein Dia2 to maintain genome stability in Saccharomyces cerevisiae (Q34509237) (← links)
• Open adjacencies and k-breaks: detecting simultaneous rearrangements in cancer genomes (Q34552964) (← links)
• Detecting structural variations in the human genome using next generation sequencing (Q34831573) (← links)
• Transcriptional consequences of genomic structural aberrations in breast cancer (Q34867822) (← links)
• Oncogenic gene fusions in epithelial carcinomas (Q34949690) (← links)
• Cancer gene discovery in mouse and man. (Q34962407) (← links)
• Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses (Q34973377) (← links)
• Optimizing PCR assays for DNA-based cancer diagnostics (Q35540946) (← links)
• Inferring the global structure of chromosomes from structural variations (Q35566334) (← links)
• Simultaneous structural variation discovery among multiple paired-end sequenced genomes (Q35581588) (← links)
• Assembly and diploid architecture of an individual human genome via single-molecule technologies (Q35677272) (← links)
• Integrated sequence and expression analysis of ovarian cancer structural variants underscores the importance of gene fusion regulation (Q35692785) (← links)
• nFuse: discovery of complex genomic rearrangements in cancer using high-throughput sequencing (Q36354900) (← links)
• Reprever: resolving low-copy duplicated sequences using template driven assembly (Q36963249) (← links)
• Application of next generation sequencing to human gene fusion detection: computational tools, features and perspectives (Q37020132) (← links)
• A geometric approach for classification and comparison of structural variants (Q37206337) (← links)
• Site-specific Genome Editing in PBMCs With PLGA Nanoparticle-delivered PNAs Confers HIV-1 Resistance in Humanized Mice (Q37467837) (← links)
• Computational methods for discovering structural variation with next-generation sequencing (Q37618538) (← links)
• Application of second-generation sequencing to cancer genomics (Q37739034) (← links)
• Evaluation of next-generation sequencing software in mapping and assembly (Q37869796) (← links)
• Utility of next-generation RNA-sequencing in identifying chimeric transcription involving human endogenous retroviruses (Q38714233) (← links)
• Identification of cancer fusion drivers using network fusion centrality. (Q40035270) (← links)
• Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes (Q41771770) (← links)
• Toolkit for automated and rapid discovery of structural variants (Q47815641) (← links)
• Double insertion of transposable elements provides a substrate for the evolution of satellite DNA. (Q52626819) (← links)
• WITHDRAWN: Evaluation of next-generation sequencing software in mapping and assembly (Q56557212) (← links)