Identification of genomic indels and structural variations using split reads
about
Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectivesHigh-throughput sequencing for biology and medicineTechnological considerations for genome-guided diagnosis and management of cancerHigh-throughput sequencing technologiesAnalysis of variable retroduplications in human populations suggests coupling of retrotransposition to cell divisionA 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.Identification of copy number variants in whole-genome data using Reference Coverage Profiles.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.Identification of structural variation in mouse genomes.An improved approach for accurate and efficient calling of structural variations with low-coverage sequence data.High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?Identification of medium-sized genomic deletions with low coverage, mate-paired restricted tagsOn the power and the systematic biases of the detection of chromosomal inversions by paired-end genome sequencing.Ulysses: accurate detection of low-frequency structural variations in large insert-size sequencing libraries.Detection and characterization of small insertion and deletion genetic variants in modern layer chicken genomes.The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection.Next-generation sequencing of experimental mouse strainsBatAlign: an incremental method for accurate alignment of sequencing readsStructural Variant Detection by Large-scale Sequencing Reveals New Evolutionary Evidence on Breed Divergence between Chinese and European Pigs.Current analysis platforms and methods for detecting copy number variationWhole-genome sequencing identifies recurrent mutations in hepatocellular carcinomaNext-generation sequencing-based method shows increased mutation detection sensitivity in an Indian retinoblastoma cohort.Child development and structural variation in the human genome.Whole-genome CNV analysis: advances in computational approachesAccurate indel prediction using paired-end short reads.Quantitative detection of low-abundance somatic structural variants in normal cells by high-throughput sequencing.MSeq-CNV: accurate detection of Copy Number Variation from Sequencing of Multiple samples.Detecting Copy Number Variation via Next Generation Technology
P2860
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P2860
Identification of genomic indels and structural variations using split reads
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Identification of genomic indels and structural variations using split reads
@ast
Identification of genomic indels and structural variations using split reads
@en
type
label
Identification of genomic indels and structural variations using split reads
@ast
Identification of genomic indels and structural variations using split reads
@en
prefLabel
Identification of genomic indels and structural variations using split reads
@ast
Identification of genomic indels and structural variations using split reads
@en
P2093
P2860
P356
P1433
P1476
Identification of genomic indels and structural variations using split reads
@en
P2093
Alex Abyzov
Alexander E Urban
Michael Snyder
Zhengdong D Zhang
P2860
P2888
P356
10.1186/1471-2164-12-375
P407
P577
2011-07-25T00:00:00Z
P5875
P6179
1023980772