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1.
BMC Bioinformatics ; 6: 131, 2005 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-15924626

RESUMO

BACKGROUND: Despite the continuous production of genome sequence for a number of organisms, reliable, comprehensive, and cost effective gene prediction remains problematic. This is particularly true for genomes for which there is not a large collection of known gene sequences, such as the recently published chicken genome. We used the chicken sequence to test comparative and homology-based gene-finding methods followed by experimental validation as an effective genome annotation method. RESULTS: We performed experimental evaluation by RT-PCR of three different computational gene finders, Ensembl, SGP2 and TWINSCAN, applied to the chicken genome. A Venn diagram was computed and each component of it was evaluated. The results showed that de novo comparative methods can identify up to about 700 chicken genes with no previous evidence of expression, and can correctly extend about 40% of homology-based predictions at the 5' end. CONCLUSIONS: De novo comparative gene prediction followed by experimental verification is effective at enhancing the annotation of the newly sequenced genomes provided by standard homology-based methods.


Assuntos
Biologia Computacional/métodos , Genoma , Animais , Galinhas , Mapeamento Cromossômico , Primers do DNA , DNA Complementar/metabolismo , Interpretação Estatística de Dados , Bases de Dados Genéticas , Éxons , Etiquetas de Sequências Expressas , Perfilação da Expressão Gênica , Íntrons , Modelos Estatísticos , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Alinhamento de Sequência , Análise de Sequência de DNA , Software , Distribuição Tecidual
2.
Genome Res ; 13(1): 27-36, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12529303

RESUMO

We report a second-generation gene annotation of human chromosome 22. Using expressed sequence databases, comparative sequence analysis, and experimental verification, we have extended genes, fused previously fragmented structures, and identified new genes. The total length in exons of annotation was increased by 74% over our previously published annotation and includes 546 protein-coding genes and 234 pseudogenes. Thirty-two potential protein-coding annotations are partial copies of other genes, and may represent duplications on an evolutionary path to change or loss of function. We also identified 31 non-protein-coding transcripts, including 16 possible antisense RNAs. By extrapolation, we estimate the human genome contains 29,000-36,000 protein-coding genes, 21,300 pseudogenes, and 1500 antisense RNAs. We suggest that our revised annotation criteria provide a paradigm for future annotation of the human genome.


Assuntos
Mapeamento Cromossômico/métodos , Cromossomos Humanos Par 22/genética , Genes/genética , Animais , Humanos , Camundongos , Dados de Sequência Molecular
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