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Open AccessJournal ArticleDOI

tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence.

Todd M. Lowe, +1 more
- 01 Mar 1997 - 
- Vol. 25, Iss: 5, pp 955-964
TLDR
A program is described, tRNAscan-SE, which identifies 99-100% of transfer RNA genes in DNA sequence while giving less than one false positive per 15 gigabases.
Abstract
We describe a program, tRNAscan-SE, which identifies 99-100% of transfer RNA genes in DNA sequence while giving less than one false positive per 15 gigabases. Two previously described tRNA detection programs are used as fast, first-pass prefilters to identify candidate tRNAs, which are then analyzed by a highly selective tRNA covariance model. This work represents a practical application of RNA covariance models, which are general, probabilistic secondary structure profiles based on stochastic context-free grammars. tRNAscan-SE searches at approximately 30 000 bp/s. Additional extensions to tRNAscan-SE detect unusual tRNA homologues such as selenocysteine tRNAs, tRNA-derived repetitive elements and tRNA pseudogenes.

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Citations
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Journal ArticleDOI

Exploring patterns and extent of bias in estimating divergence time from mitochondrial DNA sequence data in a particular lineage: A case study of salamanders (Order Caudata)

TL;DR: Assessment of the effects of saturation on dating divergences using mitochondrial genome sequences on a timescale of ~200-300 My indicated that dates derived from the mitochondrial data were considerably overestimated and systematically biased toward the calibration point for the ingroup root.
Journal ArticleDOI

Frequent mitochondrial gene rearrangements at the hymenopteran nad3-nad5 junction.

TL;DR: The organization of mitochondrial genes from a diverse range of hymenopterans was characterized, and local inversions were relatively common, i.e., rearrangements characterized by the movement of genes from one mitochondrial strand to the other, opposite or close to their ancestral position.
Journal ArticleDOI

HAMR: high-throughput annotation of modified ribonucleotides

TL;DR: A method that can not only locate these modifications transcriptome-wide with single nucleotide resolution, but can also differentiate between different classes of modifications is developed, finding that different modifications produce distinct patterns of cDNA sequence.
Journal ArticleDOI

Genes adopt non-optimal codon usage to generate cell cycle-dependent oscillations in protein levels.

TL;DR: The data indicate that cells exploit wobbling to generate cell cycle‐dependent dynamics of proteins, and it is proposed that non‐optimal (wobbly) matching codons influence protein synthesis during the cell cycle.
References
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Journal ArticleDOI

Basic Local Alignment Search Tool

TL;DR: A new approach to rapid sequence comparison, basic local alignment search tool (BLAST), directly approximates alignments that optimize a measure of local similarity, the maximal segment pair (MSP) score.
Journal ArticleDOI

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TL;DR: Three computer programs for comparisons of protein and DNA sequences can be used to search sequence data bases, evaluate similarity scores, and identify periodic structures based on local sequence similarity.
Journal ArticleDOI

Whole-genome random sequencing and assembly of Haemophilus influenzae Rd.

TL;DR: An approach for genome analysis based on sequencing and assembly of unselected pieces of DNA from the whole chromosome has been applied to obtain the complete nucleotide sequence of the genome from the bacterium Haemophilus influenzae Rd.
PatentDOI

COMPLETE GENOME SEQUENCE OF THE METHANOGENIC ARCHAEON, $i(METHANOCOCCUS JANNASCHII)

TL;DR: In this article, the complete 1.66-megabase pair genome sequence of an autotrophic archaeon, Methanococcus jannaschii, and its 58 and 16-kilobase pair extrachromosomal elements are described.
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