about
Human genetics and genomics a decade after the release of the draft sequence of the human genomeCurrent strategies for mutation detection in phenotype-driven screens utilising next generation sequencingStandardization and quality management in next-generation sequencingPitfalls of establishing DNA barcoding systems in protists: the cryptophyceae as a test caseToward reliable biomarker signatures in the age of liquid biopsies - how to standardize the small RNA-Seq workflowVarBin, a novel method for classifying true and false positive variants in NGS data.Effective filtering strategies to improve data quality from population-based whole exome sequencing studies.Hierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data.A comparison of tools for the simulation of genomic next-generation sequencing data.-Omic and Electronic Health Record Big Data Analytics for Precision Medicine.Analysis of plant microbe interactions in the era of next generation sequencing technologies.ACMG clinical laboratory standards for next-generation sequencing.ChIP-Seq: technical considerations for obtaining high-quality dataGenome-wide characterization of insertion and deletion variation in chicken using next generation sequencing.Human microbiome and HIV/AIDSAll Your Base: a fast and accurate probabilistic approach to base callingTransposable elements are a major cause of somatic polymorphism in Vitis vinifera L.Next-generation sequencing for cancer diagnostics: a practical perspective.A new approach for detecting low-level mutations in next-generation sequence data.ParticleCall: a particle filter for base calling in next-generation sequencing systemsCritical role of bioinformatics in translating huge amounts of next-generation sequencing data into personalized medicine.Base calling for high-throughput short-read sequencing: dynamic programming solutions.Comparing somatic mutation-callers: beyond Venn diagrams.Sequencing error correction without a reference genome.FANSe2: a robust and cost-efficient alignment tool for quantitative next-generation sequencing applications(Post-)genomics approaches in fungal research.Assessing the impact of non-differential genotyping errors on rare variant tests of association.Impacts of degraded DNA on restriction enzyme associated DNA sequencing (RADSeq).Detecting false-positive signals in exome sequencingA somatic reference standard for cancer genome sequencing.OnlineCall: fast online parameter estimation and base calling for illumina's next-generation sequencingRevealing crosstalk of plant and fungi in the symbiotic roots of sewage-cleaning Eichhornia crassipes using direct de novo metatranscriptomic analysis.mTAIL-seq reveals dynamic poly(A) tail regulation in oocyte-to-embryo development.Clinical Interpretation of Genomic Variations.Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.Experience of targeted Usher exome sequencing as a clinical test.Analysis of DNA sequence variants detected by high-throughput sequencingTowards next generation CHO cell biology: Bioinformatics methods for RNA-Seq-based expression profiling.DNA storage under high temperature conditions does not affect performance in human leukocyte antigen genotyping via next-generation sequencing (DNA integrity maintained in extreme conditions).Using state machines to model the Ion Torrent sequencing process and to improve read error rates.
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description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 18 January 2011
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Base-calling for next-generation sequencing platforms
@en
Base-calling for next-generation sequencing platforms.
@nl
type
label
Base-calling for next-generation sequencing platforms
@en
Base-calling for next-generation sequencing platforms.
@nl
prefLabel
Base-calling for next-generation sequencing platforms
@en
Base-calling for next-generation sequencing platforms.
@nl
P2860
P356
P1476
Base-calling for next-generation sequencing platforms
@en
P2093
Christian Ledergerber
P275
P2860
P304
P356
10.1093/BIB/BBQ077
P577
2011-01-18T00:00:00Z
2011-09-01T00:00:00Z