author_facet Orgeur, Mickael
Martens, Marvin
Börno, Stefan T.
Timmermann, Bernd
Duprez, Delphine
Stricker, Sigmar
Orgeur, Mickael
Martens, Marvin
Börno, Stefan T.
Timmermann, Bernd
Duprez, Delphine
Stricker, Sigmar
author Orgeur, Mickael
Martens, Marvin
Börno, Stefan T.
Timmermann, Bernd
Duprez, Delphine
Stricker, Sigmar
spellingShingle Orgeur, Mickael
Martens, Marvin
Börno, Stefan T.
Timmermann, Bernd
Duprez, Delphine
Stricker, Sigmar
Biology Open
A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
General Agricultural and Biological Sciences
General Biochemistry, Genetics and Molecular Biology
author_sort orgeur, mickael
spelling Orgeur, Mickael Martens, Marvin Börno, Stefan T. Timmermann, Bernd Duprez, Delphine Stricker, Sigmar 2046-6390 The Company of Biologists General Agricultural and Biological Sciences General Biochemistry, Genetics and Molecular Biology http://dx.doi.org/10.1242/bio.028498 <jats:p>The sequence of the chicken genome, like several other draft genome sequences, is presently not fully covered. Gaps, contigs assigned with low confidence and uncharacterized chromosomes result in gene fragmentation and imprecise gene annotation. Transcript abundance estimation from RNA sequencing (RNA-seq) data relies on read quality, library complexity and expression normalization. In addition, the quality of the genome sequence used to map sequencing reads and the gene annotation that defines gene features must also be taken into account. Partially covered genome sequence causes the loss of sequencing reads from the mapping step, while an inaccurate definition of gene features induces imprecise read counts from the assignment step. Both steps can significantly bias interpretation of RNA-seq data. Here, we describe a dual transcript-discovery approach combining a genome-guided gene prediction and a de novo transcriptome assembly. This dual approach enabled us to increase the assignment rate of RNA-seq data by nearly 20% as compared to when using only the chicken reference annotation, contributing therefore to a more accurate estimation of transcript abundance. More generally, this strategy could be applied to any organism with partial genome sequence and/or lacking a manually-curated reference annotation in order to improve the accuracy of gene expression studies.</jats:p> A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model Biology Open
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title A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_unstemmed A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_full A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_fullStr A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_full_unstemmed A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_short A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_sort a dual transcript-discovery approach to improve the delimitation of gene features from rna-seq data in the chicken model
topic General Agricultural and Biological Sciences
General Biochemistry, Genetics and Molecular Biology
url http://dx.doi.org/10.1242/bio.028498
publishDate 2017
physical
description <jats:p>The sequence of the chicken genome, like several other draft genome sequences, is presently not fully covered. Gaps, contigs assigned with low confidence and uncharacterized chromosomes result in gene fragmentation and imprecise gene annotation. Transcript abundance estimation from RNA sequencing (RNA-seq) data relies on read quality, library complexity and expression normalization. In addition, the quality of the genome sequence used to map sequencing reads and the gene annotation that defines gene features must also be taken into account. Partially covered genome sequence causes the loss of sequencing reads from the mapping step, while an inaccurate definition of gene features induces imprecise read counts from the assignment step. Both steps can significantly bias interpretation of RNA-seq data. Here, we describe a dual transcript-discovery approach combining a genome-guided gene prediction and a de novo transcriptome assembly. This dual approach enabled us to increase the assignment rate of RNA-seq data by nearly 20% as compared to when using only the chicken reference annotation, contributing therefore to a more accurate estimation of transcript abundance. More generally, this strategy could be applied to any organism with partial genome sequence and/or lacking a manually-curated reference annotation in order to improve the accuracy of gene expression studies.</jats:p>
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author Orgeur, Mickael, Martens, Marvin, Börno, Stefan T., Timmermann, Bernd, Duprez, Delphine, Stricker, Sigmar
author_facet Orgeur, Mickael, Martens, Marvin, Börno, Stefan T., Timmermann, Bernd, Duprez, Delphine, Stricker, Sigmar, Orgeur, Mickael, Martens, Marvin, Börno, Stefan T., Timmermann, Bernd, Duprez, Delphine, Stricker, Sigmar
author_sort orgeur, mickael
container_start_page 0
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description <jats:p>The sequence of the chicken genome, like several other draft genome sequences, is presently not fully covered. Gaps, contigs assigned with low confidence and uncharacterized chromosomes result in gene fragmentation and imprecise gene annotation. Transcript abundance estimation from RNA sequencing (RNA-seq) data relies on read quality, library complexity and expression normalization. In addition, the quality of the genome sequence used to map sequencing reads and the gene annotation that defines gene features must also be taken into account. Partially covered genome sequence causes the loss of sequencing reads from the mapping step, while an inaccurate definition of gene features induces imprecise read counts from the assignment step. Both steps can significantly bias interpretation of RNA-seq data. Here, we describe a dual transcript-discovery approach combining a genome-guided gene prediction and a de novo transcriptome assembly. This dual approach enabled us to increase the assignment rate of RNA-seq data by nearly 20% as compared to when using only the chicken reference annotation, contributing therefore to a more accurate estimation of transcript abundance. More generally, this strategy could be applied to any organism with partial genome sequence and/or lacking a manually-curated reference annotation in order to improve the accuracy of gene expression studies.</jats:p>
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spelling Orgeur, Mickael Martens, Marvin Börno, Stefan T. Timmermann, Bernd Duprez, Delphine Stricker, Sigmar 2046-6390 The Company of Biologists General Agricultural and Biological Sciences General Biochemistry, Genetics and Molecular Biology http://dx.doi.org/10.1242/bio.028498 <jats:p>The sequence of the chicken genome, like several other draft genome sequences, is presently not fully covered. Gaps, contigs assigned with low confidence and uncharacterized chromosomes result in gene fragmentation and imprecise gene annotation. Transcript abundance estimation from RNA sequencing (RNA-seq) data relies on read quality, library complexity and expression normalization. In addition, the quality of the genome sequence used to map sequencing reads and the gene annotation that defines gene features must also be taken into account. Partially covered genome sequence causes the loss of sequencing reads from the mapping step, while an inaccurate definition of gene features induces imprecise read counts from the assignment step. Both steps can significantly bias interpretation of RNA-seq data. Here, we describe a dual transcript-discovery approach combining a genome-guided gene prediction and a de novo transcriptome assembly. This dual approach enabled us to increase the assignment rate of RNA-seq data by nearly 20% as compared to when using only the chicken reference annotation, contributing therefore to a more accurate estimation of transcript abundance. More generally, this strategy could be applied to any organism with partial genome sequence and/or lacking a manually-curated reference annotation in order to improve the accuracy of gene expression studies.</jats:p> A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model Biology Open
spellingShingle Orgeur, Mickael, Martens, Marvin, Börno, Stefan T., Timmermann, Bernd, Duprez, Delphine, Stricker, Sigmar, Biology Open, A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model, General Agricultural and Biological Sciences, General Biochemistry, Genetics and Molecular Biology
title A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_full A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_fullStr A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_full_unstemmed A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_short A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
title_sort a dual transcript-discovery approach to improve the delimitation of gene features from rna-seq data in the chicken model
title_unstemmed A dual transcript-discovery approach to improve the delimitation of gene features from RNA-seq data in the chicken model
topic General Agricultural and Biological Sciences, General Biochemistry, Genetics and Molecular Biology
url http://dx.doi.org/10.1242/bio.028498