about
Detection of Genomic Structural Variants from Next-Generation Sequencing DataViral quasispecies assembly via maximal clique enumerationMATE-CLEVER: Mendelian-inheritance-aware discovery and genotyping of midsize and long indelsSV-AUTOPILOT: optimized, automated construction of structural variation discovery and benchmarking pipelines.Identification of copy number variants in whole-genome data using Reference Coverage Profiles.ChopSticks: High-resolution analysis of homozygous deletions by exploiting concordant read pairs.A survey of tools for variant analysis of next-generation genome sequencing data.Unraveling overlapping deletions by agglomerative clustering.Ulysses: accurate detection of low-frequency structural variations in large insert-size sequencing libraries.Pilon: an integrated tool for comprehensive microbial variant detection and genome assembly improvement.Wham: Identifying Structural Variants of Biological ConsequenceDiscovery of large genomic inversions using long range informationSocrates: identification of genomic rearrangements in tumour genomes by re-aligning soft clipped reads.Making the difference: integrating structural variation detection tools.Genotyping inversions and tandem duplications.Detecting horizontal gene transfer by mapping sequencing reads across species boundaries.Robust and exact structural variation detection with paired-end and soft-clipped alignments: SoftSV compared with eight algorithms.Repeat- and error-aware comparison of deletions.PopIns: population-scale detection of novel sequence insertions.Whole genome sequence of a Turkish individual.A deterministic analysis of genome integrity during neoplastic growth in Drosophila.Jointly aligning a group of DNA reads improves accuracy of identifying large deletions.Gustaf: Detecting and correctly classifying SVs in the NGS twilight zone.RSVSim: an R/Bioconductor package for the simulation of structural variations.iCopyDAV: Integrated platform for copy number variations-Detection, annotation and visualization.
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
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2012年论文
@zh-cn
name
CLEVER: clique-enumerating variant finder.
@en
CLEVER: clique-enumerating variant finder.
@nl
type
label
CLEVER: clique-enumerating variant finder.
@en
CLEVER: clique-enumerating variant finder.
@nl
prefLabel
CLEVER: clique-enumerating variant finder.
@en
CLEVER: clique-enumerating variant finder.
@nl
P2093
P2860
P50
P356
P1433
P1476
CLEVER: clique-enumerating variant finder.
@en
P2093
Alexander Schönhuth
Ivan G Costa
Markus Bauer
Stefan Canzar
P2860
P304
P356
10.1093/BIOINFORMATICS/BTS566
P407
P577
2012-10-11T00:00:00Z