about
Next-generation sequencing in aging research: emerging applications, problems, pitfalls and possible solutionsAdaptive seeds tame genomic sequence comparisonAlignment of Short Reads: A Crucial Step for Application of Next-Generation Sequencing Data in Precision MedicineChallenges and opportunities in understanding microbial communities with metagenome assembly (accompanied by IPython Notebook tutorial)Applications of next-generation sequencing to blood and marrow transplantationA field guide to whole-genome sequencing, assembly and annotationAlgorithms in nature: the convergence of systems biology and computational thinkingAdvanced Applications of RNA Sequencing and ChallengesDynamic transcriptional and epigenomic reprogramming from pediatric nasal epithelial cells to induced pluripotent stem cellsGenotyping by sequencing approaches to characterise crop genomes: choosing the right tool for the right applicationIdentifying disease mutations in genomic medicine settings: current challenges and how to accelerate progressStem cells. m6A mRNA methylation facilitates resolution of naïve pluripotency toward differentiationBioassay-guided fractionation of extracts from Codiaeum variegatum against Entamoeba histolytica discovers compounds that modify expression of ceramide biosynthesis related genesUsing genome-wide expression profiling to define gene networks relevant to the study of complex traits: from RNA integrity to network topologyBioinformatics of prokaryotic RNAsSingle Nucleotide Polymorphism (SNP) Detection and Genotype Calling from Massively Parallel Sequencing (MPS) DataChallenges and opportunities in estimating viral genetic diversity from next-generation sequencing dataApplications of next generation sequencing in molecular ecology of non-model organismsinGAP: an integrated next-generation genome analysis pipelineANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataCount-based differential expression analysis of RNA sequencing data using R and BioconductorChIP-seq: advantages and challenges of a maturing technologyEpigenetic methodologies for behavioral scientists.Qualimap: evaluating next-generation sequencing alignment data.Tools for mapping high-throughput sequencing data.Next-generation technologies and data analytical approaches for epigenomics.Evaluation and comparison of multiple aligners for next-generation sequencing data analysis.Identification of mutations in laboratory-evolved microbes from next-generation sequencing data using breseq.miRIAD-integrating microRNA inter- and intragenic data.Analysis of genomic rearrangements by using the Burrows-Wheeler transform of short-read data.Noncoding RNA: Current Deep Sequencing Data Analysis Approaches and Challenges.Analysis of Microarray and RNA-seq Expression Profiling Data.NGSView: an extensible open source editor for next-generation sequencing data.Identification of differentially expressed microRNAs in metastatic melanoma using next-generation sequencing technologySAMStat: monitoring biases in next generation sequencing data.Massive parallel sequencing of mRNA in identification of unannotated salinity stress-inducible transcripts in rice (Oryza sativa L.).RSEQtools: a modular framework to analyze RNA-Seq data using compact, anonymized data summaries.X-MATE: a flexible system for mapping short read data.A comparison of massively parallel nucleotide sequencing with oligonucleotide microarrays for global transcription profilingIntegration of signals along orthogonal axes of the vertebrate neural tube controls progenitor competence and increases cell diversity
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
How to map billions of short reads onto genomes
@ast
How to map billions of short reads onto genomes
@en
How to map billions of short reads onto genomes
@nl
type
label
How to map billions of short reads onto genomes
@ast
How to map billions of short reads onto genomes
@en
How to map billions of short reads onto genomes
@nl
prefLabel
How to map billions of short reads onto genomes
@ast
How to map billions of short reads onto genomes
@en
How to map billions of short reads onto genomes
@nl
P2860
P3181
P356
P1433
P1476
How to map billions of short reads onto genomes
@en
P2093
Cole Trapnell
P2860
P2888
P3181
P356
10.1038/NBT0509-455
P407
P577
2009-05-01T00:00:00Z