Advanced sequencing technologies: methods and goals
By Jay Shendure, Robi David Mitra, Chris Varma, George M. Church. Nature reviews genetics, 2004
603 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/aee05137cf6d6a5c1497c91d1b2fadc1c9b75e78
How researchers see this paper
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In Molecular Biology
- Can Alkan
- Süleyman Cenk Sahinalp
- Evan E. Eichler
- Edward S. Buckler
- Fereydoun Hormozdiari
- Steven L. Salzberg
- Todd J. Treangen
- Computational Pan-Genomics Consortium
Citations in the corpus
- GAPIT Version 2: An Enhanced Integrated Tool for Genomic Association and Prediction (2016, background): “Biomedical and agricultural researchers have the unprecedented capacity to generate extremely large amounts of data (Shendure et al., 2004; Ober et al., 2012; Georges, 2014).”
- BLINK: a package for the next level of genome-wide association studies with both individuals and markers in the millions (2018, neutral): “Biomedical innovations have outpaced computing innovations since the completion of the human genome project [1, 2].”
- Combinatorial Algorithms for Structural Variation Detection in High Throughput Sequenced Genomes (2009, methodology): “…(454 Life Sciences [Roche]), sequencing-by-synthesis (Illumina and Helicos), and sequencing-by-ligation (ABI SOLiD) methods produce shorter reads than the traditional capillary sequencing, but they also increase the redundancy by 10-to 100-fold or more (Shendure et al. 2004; Mardis 2008).”