AmalgamScope: Merging Annotations Data across the Human Genome

The past years have shown an enormous advancement in sequencing and array-based technologies, producing supplementary or alternative views of the genome stored in various formats and databases. Their sheer volume and different data scope pose a challenge to jointly visualize and integrate diverse da...

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Main Authors: Georgia Tsiliki, Konstantinos Tsaramirsis, Sophia Kossida
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2014/893501
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spelling doaj-e5496508dc204098a99bc2aaa9686f652020-11-25T01:05:34ZengHindawi LimitedBioMed Research International2314-61332314-61412014-01-01201410.1155/2014/893501893501AmalgamScope: Merging Annotations Data across the Human GenomeGeorgia Tsiliki0Konstantinos Tsaramirsis1Sophia Kossida2Bioinformatics and Medical Informatics Team, Biomedical Research Foundation, Academy of Athens, 115 27 Athens, GreeceBioinformatics and Medical Informatics Team, Biomedical Research Foundation, Academy of Athens, 115 27 Athens, GreeceBioinformatics and Medical Informatics Team, Biomedical Research Foundation, Academy of Athens, 115 27 Athens, GreeceThe past years have shown an enormous advancement in sequencing and array-based technologies, producing supplementary or alternative views of the genome stored in various formats and databases. Their sheer volume and different data scope pose a challenge to jointly visualize and integrate diverse data types. We present AmalgamScope a new interactive software tool focusing on assisting scientists with the annotation of the human genome and particularly the integration of the annotation files from multiple data types, using gene identifiers and genomic coordinates. Supported platforms include next-generation sequencing and microarray technologies. The available features of AmalgamScope range from the annotation of diverse data types across the human genome to integration of the data based on the annotational information and visualization of the merged files within chromosomal regions or the whole genome. Additionally, users can define custom transcriptome library files for any species and use the file exchanging distant server options of the tool.http://dx.doi.org/10.1155/2014/893501
collection DOAJ
language English
format Article
sources DOAJ
author Georgia Tsiliki
Konstantinos Tsaramirsis
Sophia Kossida
spellingShingle Georgia Tsiliki
Konstantinos Tsaramirsis
Sophia Kossida
AmalgamScope: Merging Annotations Data across the Human Genome
BioMed Research International
author_facet Georgia Tsiliki
Konstantinos Tsaramirsis
Sophia Kossida
author_sort Georgia Tsiliki
title AmalgamScope: Merging Annotations Data across the Human Genome
title_short AmalgamScope: Merging Annotations Data across the Human Genome
title_full AmalgamScope: Merging Annotations Data across the Human Genome
title_fullStr AmalgamScope: Merging Annotations Data across the Human Genome
title_full_unstemmed AmalgamScope: Merging Annotations Data across the Human Genome
title_sort amalgamscope: merging annotations data across the human genome
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2014-01-01
description The past years have shown an enormous advancement in sequencing and array-based technologies, producing supplementary or alternative views of the genome stored in various formats and databases. Their sheer volume and different data scope pose a challenge to jointly visualize and integrate diverse data types. We present AmalgamScope a new interactive software tool focusing on assisting scientists with the annotation of the human genome and particularly the integration of the annotation files from multiple data types, using gene identifiers and genomic coordinates. Supported platforms include next-generation sequencing and microarray technologies. The available features of AmalgamScope range from the annotation of diverse data types across the human genome to integration of the data based on the annotational information and visualization of the merged files within chromosomal regions or the whole genome. Additionally, users can define custom transcriptome library files for any species and use the file exchanging distant server options of the tool.
url http://dx.doi.org/10.1155/2014/893501
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