Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding - Wikidata - wikimedia - TriplyDB

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

http://www.wikidata.org/entity/Q24647100

about

U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line Towards a comprehensive structural variation map of an individual human genome Human genetics and genomics a decade after the release of the draft sequence of the human genome Human genome sequencing in health and disease Personal genome sequencing: current approaches and challenges De novo genome sequencing and comparative genomics of date palm (Phoenix dactylifera)Next-generation sequencing in aging research: emerging applications, problems, pitfalls and possible solutions Accurate and comprehensive sequencing of personal genomes TIARA: a database for accurate analysis of multiple personal genomes based on cross-technology Mapping copy number variation by population-scale genome sequencing High-fidelity gene synthesis by retrieval of sequence-verified DNA identified using high-throughput pyrosequencing Targeted enrichment of genomic DNA regions for next-generation sequencing Sequencing technologies and genome sequencing The sequence of sequencers: The history of sequencing DNA Advances in BAC-based physical mapping and map integration strategies in plants Massively parallel sequencing: the new frontier of hematologic genomics Epigenetic genome-wide association methylation in aging and longevity Stepping stones in DNA sequencing The case for cloud computing in genome informatics The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data Application of Genomic Technologies to the Breeding of Trees A copy number variation map of the human genome Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays Development of personalized tumor biomarkers using massively parallel sequencing Analysis of next-generation genomic data in cancer: accomplishments and challenges Linking Genes to Cardiovascular Diseases: Gene Action and Gene-Environment Interactions.Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects LINE-1 elements in structural variation and disease Whole-genome sequencing and analysis of the Malaysian cynomolgus macaque (Macaca fascicularis) genome Characterization of a biogas-producing microbial community by short-read next generation DNA sequencing Structural alterations from multiple displacement amplification of a human genome revealed by mate-pair sequencing Genome sequence and global sequence variation map with 5.5 million SNPs in Chinese rhesus macaque A reduced representation approach to population genetic analyses and applications to human evolution LINE-1 retrotransposition activity in human genomes Gene inactivation and its implications for annotation in the era of personal genomics Whole methylome analysis by ultra-deep sequencing using two-base encoding Experimental generation of SNP haplotype signatures in patients with sickle cell anaemia Exome sequencing of a multigenerational human pedigree A standard variation file format for human genome sequences A framework for variation discovery and genotyping using next-generation DNA sequencing data

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Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

http://www.wikidata.org/entity/Q24647100

description

2009 nî lūn-bûn

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2009 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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Genome Research

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Adam E Sannicandro

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Alena A Antipova

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Ali Bashir

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Andrew Sheridan

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Bin Li

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Brittany E Coleman

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Christopher R Clouser

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Cisyla Duncan

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Clarence C Lee

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P2860

Initial sequencing and analysis of the human genome

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

The diploid genome sequence of an individual human

Evaluation of paired-end sequencing strategies for detection of genome rearrangements in cancer

Population stratification of a common APOBEC gene deletion polymorphism

The diploid genome sequence of an Asian individual

The Sequence of the Human Genome

Evolutionary and Biomedical Insights from the Rhesus Macaque Genome

Fine-scale structural variation of the human genome

Mapping and sequencing of structural variation from eight human genomes

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1527-1541

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scholarly article

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2554501

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10.1101/GR.091868.109

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9

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19

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Jeffrey M. Kidd

Alan P Blanchard

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26310744

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