SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data.
about
Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesinGAP-sv: a novel scheme to identify and visualize structural variation from paired end mapping dataMutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencingStructural variation discovery in the cancer genome using next generation sequencing: computational solutions and perspectivesAdvances in the Molecular Analysis of Soft Tissue Tumors and Clinical ImplicationsInherited Mutations in Women With Ovarian CarcinomaShort read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.Hybrid capture and next-generation sequencing identify viral integration sites from formalin-fixed, paraffin-embedded tissue.A survey of copy-number variation detection tools based on high-throughput sequencing data.Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.G-CNV: A GPU-Based Tool for Preparing Data to Detect CNVs with Read-Depth Methods.PSE-HMM: genome-wide CNV detection from NGS data using an HMM with Position-Specific Emission probabilities.Repair of DNA double-strand breaks by templated nucleotide sequence insertions derived from distant regions of the genome.Accurate and exact CNV identification from targeted high-throughput sequence data.Detection of genomic variations and DNA polymorphisms and impact on analysis of meiotic recombination and genetic mapping.ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping informationAn integrative probabilistic model for identification of structural variation in sequencing data.VERSE: a novel approach to detect virus integration in host genomes through reference genome customizationCurrent status and future perspectives for sequencing livestock genomesCREST maps somatic structural variation in cancer genomes with base-pair resolution.Deep sequencing with intronic capture enables identification of an APC exon 10 inversion in a patient with polyposis.Investigation of Mendelian forms of obesity holds out the prospect of personalized medicine.Characterising chromosome rearrangements: recent technical advances in molecular cytogeneticsSystems genetics in "-omics" era: current and future development.Making the difference: integrating structural variation detection tools.Hi-C as a tool for precise detection and characterisation of chromosomal rearrangements and copy number variation in human tumoursTargeted next generation sequencing of clinically significant gene mutations and translocations in leukemia.Discovery of an expanded set of avian leukosis subroup E proviruses in chickens using Vermillion, a novel sequence capture and analysis pipeline.Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: an NRG Oncology/Gynecologic Oncology Group Study.Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53.Detection of induced mutations in CaFAD2 genes by next-generation sequencing leading to the production of improved oil composition in Crambe abyssinica.MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples.
P2860
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P2860
SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data.
description
2010 nî lūn-bûn
@nan
2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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2010年学术文章
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name
SLOPE: a quick and accurate me ...... next-generation sequence data.
@ast
SLOPE: a quick and accurate me ...... next-generation sequence data.
@en
type
label
SLOPE: a quick and accurate me ...... next-generation sequence data.
@ast
SLOPE: a quick and accurate me ...... next-generation sequence data.
@en
prefLabel
SLOPE: a quick and accurate me ...... next-generation sequence data.
@ast
SLOPE: a quick and accurate me ...... next-generation sequence data.
@en
P2093
P2860
P356
P1433
P1476
SLOPE: a quick and accurate me ...... next-generation sequence data.
@en
P2093
Eric J Duncavage
Haley J Abel
John D Pfeifer
Jon R Armstrong
Vincent J Magrini
P2860
P304
P356
10.1093/BIOINFORMATICS/BTQ528
P407
P50
P577
2010-09-27T00:00:00Z