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...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2014-01-01
|
Series: | BioMed Research International |
Online Access: | http://dx.doi.org/10.1155/2014/893501 |
id |
doaj-e5496508dc204098a99bc2aaa9686f65 |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT georgiatsiliki amalgamscopemergingannotationsdataacrossthehumangenome AT konstantinostsaramirsis amalgamscopemergingannotationsdataacrossthehumangenome AT sophiakossida amalgamscopemergingannotationsdataacrossthehumangenome |
_version_ |
1725193827653779456 |