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Sequence Analysis with Artemis and Artemis Comparison Tool (ACT) Carribean Bioinformatics Workshop 18 th -29 th January , 2010. atcttttacttttttcatcatctatacaaaaaatcatagaatattcatcatgttgtttaaaataatgtattccattatgaactttattacaaccctcgtt
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Sequence Analysis with Artemis and Artemis Comparison Tool (ACT) Carribean Bioinformatics Workshop 18th-29th January , 2010
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Strategies for sequence annotation • Predictive methods Interpretation of the DNA sequence into genes according to rules • Comparative methods • Experimental methods
Strategies for sequence annotation • Predictive methods Interpretation of the DNA sequence into genes according to rules Interpretation of the DNA sequence into genes according to similarities with other sequences • Comparative methods • Experimental methods
Strategies for sequence annotation • Predictive methods Interpretation of the DNA sequence into genes according to rules Interpretation of the DNA sequence into genes according to similarities with other sequences • Comparative methods Interpretation of the DNA sequence into genes according to experimental results (e.g. cDNA) • Experimental methods
Gene prediction programs: ORFs and CDSs ORFs are not equivalent to CDSs Not all open reading frames are coding sequences
Gene prediction Orpheus PHAT GeneMark Glimmer Gene finder
Gene finding programs • Genefinding software packages use Hidden Markov Models. • Predict coding, intergenic and intron sequences • Need to be trained on a specific organism. • Never perfect!
Gene prediction programs: Problems • ORFs are not equivalent to CDSs • Gene prediction programs find new genes that share properties with a given set of genes. • They can be confounded by: • Sequence constraints (ribosomal proteins etc.) • Sequence biases • Different sets of genes • Horizontal gene transfer • Non-coding DNA
Gene prediction programs: Problems Different gene training sets: Plasmodium falciparum Original annotation Updated annotation
Gene prediction programs: Problems Non-protein coding regions: S. typhi ribosomal RNA genes final genefinder orpheus glimmer glimmer orpheus genefinder final
Gene prediction programs: Problems Non-protein coding regions: N. meningitidis DNA repeats final orpheus glimmer glimmer orpheus final
Gene prediction programs: Problems Pseudogenes M. leprae
Gene prediction programs: Problems Pseudogenes: M. leprae Glimmer
Gene prediction programs: Problems Pseudogenes: M. leprae Pseudogenes: M. leprae ORPHEUS
Gene prediction programs: Problems Pseudogenes: M. leprae WUBLASTX vs. M. tuberculosis
Gene prediction programs: Problems Pseudogenes: M. leprae Final annotation
The Gene Prediction Process ESTs FASTA BlastX DNA SEQUENCE Usefull CDS Prediction ANNALYSIS SOFTWARE Gene finders Codon Usage AT content Annotator
EST Eukaryotic gene stop Exon III Exon II Exon I intron 3’UTR 5’UTR ATGGT AG GT AG CAP AAAAAAAAAA mRNA CAP AAAAAAAAAA TTTTTTTTT cDNA TTTTTTTTT EST
AT content • Coding regions have higher GC content in AT rich genomes
CODON USAGE • Codon bias is different for each organism. • DNA content in coding regions is restricted • but it is not restricted in non coding regions. • The codon usage for any particular gene can influence expression.
Codon usage • All organisms have a preferred set of codons. MalariaTrypanosoma GUU 0.41 GUU 0.28 GUC 0.06 GUC 0.19 GUA 0.42 GUA 0.14 GUG 0.11 GUG 0.39
Codon Usage • http://www.kazusa.or.jp/codon/
Codon Usage in Artemis Forward frames Reverse frames
GC frame plot • Plots the third position GC content of each frame of a DNA sequence. • In coding DNA the GC content of the 3rd base is often higher. • Good prediction of coding in malaria and trypanosomes.
Homology Data • Coding regions are more conserved than non coding regions due to selective pressure. • Comparing all possible translations against all known proteins will give clues to known genes. • Blastx
Gene finding: using ACT P. yoelii TBLASTX comparisons P. falciparum P. knowlesi
Gene finding by RNA-Seq (Transcriptional landscape of Neosporacaninum Tachyzoites Day 3 Tachyzoites (RNAseq) Day 4 Tachyzoites (RNAseq)
Transcriptome sequencing in Neospora (RNAseq is useful for predicting/confirming UTR boundaries) Day 3 Tachyzoites (RNAseq) Day 4 Tachyzoites (RNAseq) N. caninum Chr08 TBLASTX matches visualised in ACT T. gondii Chr08 3’ UTR 5’ UTR
RNA-Seq: correcting gene models After Before __16hr, __32hr, __48hr %GC %GC