Sequencing technologies — the next generation

By Michael L. Metzker. Nature reviews genetics, 2010

7,174 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/4aacf3335fca0a67c8f7034aaf2e74b5d300d771

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In Molecular Biology

Citations in the corpus

MaxBin: an automated binning method to recover individual genomes from metagenomes using an expectation-maximization algorithm (2014, background): “Background The development of high-throughput genomic sequencing technologies has enabled the recovery of genomes directly from microbial communities in natural and engineered environments [1].”
De novo identification of differentially methylated regions in the human genome (2015, methodology): “With the proliferation and decreasing cost of nextgeneration sequencing technology and data generation [61-63], fitting WGBS data is a likely future application.”
Inferring Population Structure and Admixture Proportions in Low-Depth NGS Data (2018, background): “Next-generation sequencing (NGS) methods [15] produce a large amount of reliable DNA sequencing data at low cost and are commonly used in population genetic studies [16].”
RNA Sequencing and Analysis (2015, neutral): “Various single-cell RNA ampli ﬁ cation methods have been developed to accommodate less input RNA (Tang et al. 2009, 2010; Hashimshony et al. 2012; Islam et al. 2012; Picelli et al. 2013; Sasagawa et al. 2013; Shalek et al. 2013).”
Next generation sequencing technology: Advances and applications. (2014, background): “The template sequence is subsequently decoded from the color labels from the two ligation events per base [65].”
A Robust, Simple Genotyping-by-Sequencing (GBS) Approach for High Diversity Species (2011, methodology): “Next-generation sequencing (NGS) technologies have been recently used for whole genome sequencing and for re-sequencing projects where the genomes of several specimens are sequenced to discover large numbers of single nucleotide polymorphisms (SNPs) for exploring within-species diversity, constructi”
A survey of tools for variant analysis of next-generation genome sequencing data (2013, neutral): “DNA fragments in parallel [50, 51].”