Difference between revisions of "TXGP ens63 reference"

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(Overview)
(Overview)
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= Overview =
 
= Overview =
One of the most interesting questions we can ask with ''X. laevis'' genome would be how many genes it has. To construct gene models, we are mainly focusing on de novo transcriptome assembly approach with our RNA-seq data. However, many de novo transcriptome assembly program generates 'false positive' transcripts. Also, because of allotetraploidy in ''X. laevis'', transcriptome data may contain many transcript variants for each gene. So, to estimate the gene model from transcriptome data, it would be helpful to combine all transcripts derived from the same gene, and analyze them separately. Sequence-based clustering is natural way to do this, but we need to optimize parameters, such as %identity to define a cluster.   
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One of the most interesting questions we can ask with ''X. laevis'' genome would be how many genes it has. To construct gene models, we are mainly focusing on ''de novo'' transcriptome assembly approach with our RNA-seq data. However, de novo transcriptome assembly programs generate many 'false positive' transcripts. Also, because of allotetraploidy in ''X. laevis'', transcriptome data may contain many transcript variants for each gene. So, to estimate the gene model from transcriptome data precisely, we would like to combine all transcripts candidates foe each gene together, and analyze them separately. Sequence-based clustering is natural way to do this, but we need to optimize parameters, such as %identity to define a cluster.   
  
 
To get some ideas for this, we have looked at genes and transcripts of several well-studied organisms.
 
To get some ideas for this, we have looked at genes and transcripts of several well-studied organisms.

Revision as of 11:18, 13 October 2011

Overview

One of the most interesting questions we can ask with X. laevis genome would be how many genes it has. To construct gene models, we are mainly focusing on de novo transcriptome assembly approach with our RNA-seq data. However, de novo transcriptome assembly programs generate many 'false positive' transcripts. Also, because of allotetraploidy in X. laevis, transcriptome data may contain many transcript variants for each gene. So, to estimate the gene model from transcriptome data precisely, we would like to combine all transcripts candidates foe each gene together, and analyze them separately. Sequence-based clustering is natural way to do this, but we need to optimize parameters, such as %identity to define a cluster.

To get some ideas for this, we have looked at genes and transcripts of several well-studied organisms.

Genes & Transcripts

ens63_gene_tx.small.png

= Clustering of transcripts to gene