about
Nanopore-CMOS Interfaces for DNA SequencingBioinformatics Resources for MicroRNA DiscoveryTranslating cancer genomes and transcriptomes for precision oncologyCurrent strategies for mutation detection in phenotype-driven screens utilising next generation sequencingMicrobiome analysis - from technical advances to biological relevanceA field guide to whole-genome sequencing, assembly and annotationThe female gametophyte: an emerging model for cell type-specific systems biology in plant developmentSomatic mosaicism: implications for disease and transmission geneticsThe evolution of Ebola virus: Insights from the 2013–2016 epidemicIntegrating next-generation sequencing into clinical oncology: strategies, promises and pitfallsOmics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism InvestigationsPlant Microbe Interactions in Post Genomic Era: Perspectives and ApplicationsHost-Microbiome Interaction and Cancer: Potential Application in Precision MedicineThe genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discoveryEmerging platforms using liquid biopsy to detect EGFR mutations in lung cancerTumor neoantigens: building a framework for personalized cancer immunotherapyDNA barcoding: an efficient tool to overcome authentication challenges in the herbal marketNext Gen Pop Gen: implementing a high-throughput approach to population genetics in boarfish (Capros aper)Lineage-specific genomics: Frequent birth and death in the human genome: The human genome contains many lineage-specific elements created by both sequence and functional turnoverA novel method of microsatellite genotyping-by-sequencing using individual combinatorial barcodingThe use of museum specimens with high-throughput DNA sequencersImpacts of low coverage depths and post-mortem DNA damage on variant calling: a simulation studyTipping points in seaweed genetic engineering: scaling up opportunities in the next decadeNaming and outline of Dothideomycetes-2014 including proposals for the protection or suppression of generic namesA genomic perspective on hybridization and speciationMicrofluidics in systems biology-hype or truly useful?Using homology relations within a database markedly boosts protein sequence similarity search.Building International Genomics Collaboration for Global Health Security.Investigation into the annotation of protocol sequencing steps in the sequence read archive.Transcriptomic Analysis of C. elegans RNA Sequencing Data Through the Tuxedo Suite on the Galaxy Project.DNA sequencing using polymerase substrate-binding kinetics.Detection of structural DNA variation from next generation sequencing data: a review of informatic approaches.Prevention, diagnosis and treatment of high-throughput sequencing data pathologies.Navigating and mining modENCODE data.Genomic sequencing: assessing the health care system, policy, and big-data implications.An evaluation of alternative methods for constructing phylogenies from whole genome sequence data: a case study with SalmonellaSeqAssist: a novel toolkit for preliminary analysis of next-generation sequencing data.The Impact of Missing Data on Species Tree Estimation.Third generation sequencing technologies applied to diagnostic microbiology: benefits and challenges in applications and data analysis.TCGA Expedition: A Data Acquisition and Management System for TCGA Data.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Next-generation sequencing platforms.
@en
type
label
Next-generation sequencing platforms.
@en
prefLabel
Next-generation sequencing platforms.
@en
P1476
Next-generation sequencing platforms.
@en
P2093
Elaine R Mardis
P304
P356
10.1146/ANNUREV-ANCHEM-062012-092628
P577
2013-01-01T00:00:00Z