Model-based quality assessment and base-calling for second-generation sequencing data
about
BSmooth: from whole genome bisulfite sequencing reads to differentially methylated regionsEstimation of sequencing error rates in short readsSummarizing and correcting the GC content bias in high-throughput sequencingDevelopment of a low bias method for characterizing viral populations using next generation sequencing technologyBM-BC: a Bayesian method of base calling for Solexa sequence dataOligotyping: Differentiating between closely related microbial taxa using 16S rRNA gene data.BlindCall: ultra-fast base-calling of high-throughput sequencing data by blind deconvolution.ViVaMBC: estimating viral sequence variation in complex populations from illumina deep-sequencing data using model-based clusteringVisualization and probability-based scoring of structural variants within repetitive sequences.Statistical Analyses of Next Generation Sequence Data: A Partial Overview.Overcoming bias and systematic errors in next generation sequencing dataBM-map: Bayesian mapping of multireads for next-generation sequencing data.Family-based association tests using genotype data with uncertainty.All Your Base: a fast and accurate probabilistic approach to base callingA platform-independent method for detecting errors in metagenomic sequencing data: DRISEE.MetaMicrobesOnline: phylogenomic analysis of microbial communities.Short-read reading-frame predictors are not created equal: sequence error causes loss of signalImproved base-calling and quality scores for 454 sequencing based on a Hurdle Poisson modelCall for a quality standard for sequence-based assays in clinical microbiology: necessity for quality assessment of sequences used in microbial identification and typing.Robust Detection and Identification of Sparse Segments in Ultra-High Dimensional Data Analysis.Searching for SNPs with cloud computing.Quake: quality-aware detection and correction of sequencing errorspre-miRNA profiles obtained through application of locked nucleic acids and deep sequencing reveals complex 5'/3' arm variation including concomitant cleavage and polyuridylation patternsCharacterization of the Genomic Diversity of Norovirus in Linked Patients Using a Metagenomic Deep Sequencing Approach.Base-calling for next-generation sequencing platformsNext-generation sequencing in the clinic: promises and challenges.Identifying and mitigating bias in next-generation sequencing methods for chromatin biology.Simultaneous mapping of multiple gene loci with pooled segregants.Effective detection of rare variants in pooled DNA samples using Cross-pool tailcurve analysisCLEVER: clique-enumerating variant finder.
P2860
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P2860
Model-based quality assessment and base-calling for second-generation sequencing 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
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Model-based quality assessment and base-calling for second-generation sequencing data
@ast
Model-based quality assessment and base-calling for second-generation sequencing data
@en
type
label
Model-based quality assessment and base-calling for second-generation sequencing data
@ast
Model-based quality assessment and base-calling for second-generation sequencing data
@en
prefLabel
Model-based quality assessment and base-calling for second-generation sequencing data
@ast
Model-based quality assessment and base-calling for second-generation sequencing data
@en
P2860
P1433
P1476
Model-based quality assessment and base-calling for second-generation sequencing data
@en
P2093
Rafael A Irizarry
P2860
P304
P356
10.1111/J.1541-0420.2009.01353.X
P407
P577
2010-09-01T00:00:00Z