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Thomas A. Jones

Researcher at Harvard University

Publications -  15
Citations -  31798

Thomas A. Jones is an academic researcher from Harvard University. The author has contributed to research in topics: Genome & RNA. The author has an hindex of 13, co-authored 15 publications receiving 29894 citations. Previous affiliations of Thomas A. Jones include Janelia Farm Research Campus & Washington University in St. Louis.

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Journal ArticleDOI

Initial sequencing and analysis of the human genome.

Eric S. Lander, +248 more
- 15 Feb 2001 - 
TL;DR: The results of an international collaboration to produce and make freely available a draft sequence of the human genome are reported and an initial analysis is presented, describing some of the insights that can be gleaned from the sequence.
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Initial sequencing and comparative analysis of the mouse genome.

Robert H. Waterston, +222 more
- 05 Dec 2002 - 
TL;DR: The results of an international collaboration to produce a high-quality draft sequence of the mouse genome are reported and an initial comparative analysis of the Mouse and human genomes is presented, describing some of the insights that can be gleaned from the two sequences.
Journal ArticleDOI

Rfam 12.0: updates to the RNA families database

TL;DR: The upgrade of the authors' search pipeline to use Infernal 1.1 is described and improved homology detection ability is demonstrated by comparison with the previous version, and the new pipeline is easier for users to apply to their own data sets, and its ability to annotate RNAs in genomic and metagenomic data sets of various sizes is illustrated.
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The Dfam database of repetitive DNA families

TL;DR: Recent advances in Dfam are described, most notably expansion to 4150 total families including a comprehensive set of known repeat families from four new organisms (mouse, zebrafish, fly and nematode).
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Computational identification of noncoding RNAs in E. coli by comparative genomics.

TL;DR: A computational comparative genomic screen for ncRNA genes is described, to distinguish conserved RNA secondary structures from a background of other conserved sequences using probabilistic models of expected mutational patterns in pairwise sequence alignments.