1999
DOI: 10.1093/bioinformatics/15.11.874
|View full text |Cite
|
Sign up to set email alerts
|

Finding prokaryotic genes by the ‘frame-by-frame’ algorithm: targeting gene starts and overlapping genes

Abstract: mark@amber.gatech.edu.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

1
15
0

Year Published

2000
2000
2015
2015

Publication Types

Select...
5
3
1

Relationship

0
9

Authors

Journals

citations
Cited by 40 publications
(16 citation statements)
references
References 29 publications
1
15
0
Order By: Relevance
“…The insert of pBK129 was sequenced, and analysis of the DNA sequence (GenBank accession no. DQ195264) showed that it contained about 26 kb of nucleotides, including 24 intact genes ranging from traD to mclB as well as a part of traG (27). These genes were positioned in the same order as their counterparts of pTiR10, a wild-type Ti plasmid of octopine strain R10 (40).…”
Section: Resultsmentioning
confidence: 99%
“…The insert of pBK129 was sequenced, and analysis of the DNA sequence (GenBank accession no. DQ195264) showed that it contained about 26 kb of nucleotides, including 24 intact genes ranging from traD to mclB as well as a part of traG (27). These genes were positioned in the same order as their counterparts of pTiR10, a wild-type Ti plasmid of octopine strain R10 (40).…”
Section: Resultsmentioning
confidence: 99%
“…Open reading frames (ORFs) were identified with GeneMark (39), heuristic GeneMark (7), and frame-by-frame GeneMark (48) in combination with ORF Finder (http://www.ncbi.nlm.nih.gov/gorf/gorf.html). If multiple translation initiation sites for an ORF were suggested, manual inspection for the presence of a convincing Shine-Dalgarno sequence and/or close packing with the nearest upstream ORF was used to select the most probable start codon.…”
Section: Methodsmentioning
confidence: 99%
“…The next submodel is the RBS model which models the RBS as well as the nucleotides between the RBS and the start codon. After the start codon we model 3 bases explicitly since it appears that the codon usage immediately downstream of start codons differs from the rest of the gene [13]. Similarly we model the last codon before the stop codon explicitly and 6 bases after the stop in order to capture information present around the stop codon.…”
Section: Methodsmentioning
confidence: 99%
“…Due to their modular structure, HMMs are a suitable frame work for gene finding, and they are now used in GeneMark.hmm [10], GeneMarkS [11,12] and Frame-by-Frame [13]. GeneMarkS uses a mixture of Markov chains of order 0, 1 and 2 in combination with features of already annotated genomes to bootstrap an initial estimation of coding statistics, which is then iteratively improved by the GeneMark.hmm2.1 algorithm.…”
Section: Introductionmentioning
confidence: 99%