about
Abundance and functional diversity of riboswitches in microbial communitiesAncient DNA studies: new perspectives on old samplesRapid and accurate pyrosequencing of angiosperm plastid genomesMultiplex amplification enabled by selective circularization of large sets of genomic DNA fragmentsOptical recognition of converted DNA nucleotides for single-molecule DNA sequencing using nanopore arraysSingle-molecule mechanical identification and sequencingGenetic design and statistical power of nested association mapping in maizeKeeping up with the next generation: massively parallel sequencing in clinical diagnosticsDe novo assembly of human genomes with massively parallel short read sequencingMultiplex amplification of all coding sequences within 10 cancer genes by Gene-CollectorPieceMaker: selection of DNA fragments for selector-guided multiplex amplificationShotgun haplotyping: a novel method for surveying allelic sequence variation.Specificity and overlap in gene segment-defined antibody repertoires.An analysis of the feasibility of short read sequencingBTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies.miRNA profiling for biomarker discovery in multiple sclerosis: from microarray to deep sequencingOptimal Probe Length Varies for Targets with High Sequence Variation: Implications for Probe Library Design for Resequencing Highly Variable GenesA technological update of molecular diagnostics for infectious diseasesPlant Microbe Interactions in Post Genomic Era: Perspectives and ApplicationsThe future of human cerebral cartography: a novel approachThe minimum information about a genome sequence (MIGS) specificationCirculating mutant DNA to assess tumor dynamicsAccurate multiplex gene synthesis from programmable DNA microchipsDesign constraints on a synthetic metabolismSingle Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) DataPhylogenetic analyses: A toolbox expanding towards Bayesian methodsFinding the needles in the metagenome haystackGenome-wide association studies for common diseases and complex traitsThe colorectal microRNAomeOpen sharing of genomic data: Who does it and why?Genome assembly comparison identifies structural variants in the human genome.Nanopore Sequencing: Electrical Measurements of the Code of Life.On the Feasibility of Using the Intrinsic Fluorescence of Nucleotides for DNA SequencingA fast and accurate SNP detection algorithm for next-generation sequencing data.Comparing a few SNP calling algorithms using low-coverage sequencing data.GenHtr: a tool for comparative assessment of genetic heterogeneity in microbial genomes generated by massive short-read sequencing.Inference of population genetic parameters in metagenomics: a clean look at messy data.A comparison of tools for the simulation of genomic next-generation sequencing data.Genomics pipelines and data integration: challenges and opportunities in the research setting.GenePING: secure, scalable management of personal genomic data.
P2860
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P2860
description
2004 nî lūn-bûn
@nan
2004 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Advanced sequencing technologies: methods and goals
@ast
Advanced sequencing technologies: methods and goals
@en
Advanced sequencing technologies: methods and goals
@nl
type
label
Advanced sequencing technologies: methods and goals
@ast
Advanced sequencing technologies: methods and goals
@en
Advanced sequencing technologies: methods and goals
@nl
prefLabel
Advanced sequencing technologies: methods and goals
@ast
Advanced sequencing technologies: methods and goals
@en
Advanced sequencing technologies: methods and goals
@nl
P2860
P50
P3181
P356
P1476
Advanced sequencing technologies: methods and goals
@en
P2093
Chris Varma
P2860
P2888
P304
P3181
P356
10.1038/NRG1325
P407
P577
2004-05-01T00:00:00Z
P5875
P6179
1041884975