Cargando…

Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server

BACKGROUND: DNA sequencing is used ubiquitously: from deciphering genomes[1] to determining the primary sequence of small RNAs (smRNAs) [2-5]. The cloning of smRNAs is currently the most conventional method to determine the actual sequence of these important regulators of gene expression. Typical sm...

Descripción completa

Detalles Bibliográficos
Autores principales: Ebhardt, H Alexander, Wiese, Kay C, Unrau, Peter J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1450305/
https://www.ncbi.nlm.nih.gov/pubmed/16584563
http://dx.doi.org/10.1186/1471-2105-7-185
_version_ 1782127393521008640
author Ebhardt, H Alexander
Wiese, Kay C
Unrau, Peter J
author_facet Ebhardt, H Alexander
Wiese, Kay C
Unrau, Peter J
author_sort Ebhardt, H Alexander
collection PubMed
description BACKGROUND: DNA sequencing is used ubiquitously: from deciphering genomes[1] to determining the primary sequence of small RNAs (smRNAs) [2-5]. The cloning of smRNAs is currently the most conventional method to determine the actual sequence of these important regulators of gene expression. Typical smRNA cloning projects involve the sequencing of hundreds to thousands of smRNA clones that are delimited at their 5' and 3' ends by fixed sequence regions. These primers result from the biochemical protocol used to isolate and convert the smRNA into clonable PCR products. Recently we completed a smRNA cloning project involving tobacco plants, where analysis was required for ~700 smRNA sequences[6]. Finding no easily accessible research tool to enter and analyze smRNA sequences we developed Ebbie to assist us with our study. RESULTS: Ebbie is a semi-automated smRNA cloning data processing algorithm, which initially searches for any substring within a DNA sequencing text file, which is flanked by two constant strings. The substring, also termed smRNA or insert, is stored in a MySQL and BlastN database. These inserts are then compared using BlastN to locally installed databases allowing the rapid comparison of the insert to both the growing smRNA database and to other static sequence databases. Our laboratory used Ebbie to analyze scores of DNA sequencing data originating from an smRNA cloning project[6]. Through its built-in instant analysis of all inserts using BlastN, we were able to quickly identify 33 groups of smRNAs from ~700 database entries. This clustering allowed the easy identification of novel and highly expressed clusters of smRNAs. Ebbie is available under GNU GPL and currently implemented on CONCLUSION: Ebbie was designed for medium sized smRNA cloning projects with about 1,000 database entries [6-8].Ebbie can be used for any type of sequence analysis where two constant primer regions flank a sequence of interest. The reliable storage of inserts, and their annotation in a MySQL database, BlastN[9] comparison of new inserts to dynamic and static databases make it a powerful new tool in any laboratory using DNA sequencing. Ebbie also prevents manual mistakes during the excision process and speeds up annotation and data-entry. Once the server is installed locally, its access can be restricted to protect sensitive new DNA sequencing data. Ebbie was primarily designed for smRNA cloning projects, but can be applied to a variety of RNA and DNA cloning projects[2,3,10,11].
format Text
id pubmed-1450305
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-14503052006-04-29 Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server Ebhardt, H Alexander Wiese, Kay C Unrau, Peter J BMC Bioinformatics Software BACKGROUND: DNA sequencing is used ubiquitously: from deciphering genomes[1] to determining the primary sequence of small RNAs (smRNAs) [2-5]. The cloning of smRNAs is currently the most conventional method to determine the actual sequence of these important regulators of gene expression. Typical smRNA cloning projects involve the sequencing of hundreds to thousands of smRNA clones that are delimited at their 5' and 3' ends by fixed sequence regions. These primers result from the biochemical protocol used to isolate and convert the smRNA into clonable PCR products. Recently we completed a smRNA cloning project involving tobacco plants, where analysis was required for ~700 smRNA sequences[6]. Finding no easily accessible research tool to enter and analyze smRNA sequences we developed Ebbie to assist us with our study. RESULTS: Ebbie is a semi-automated smRNA cloning data processing algorithm, which initially searches for any substring within a DNA sequencing text file, which is flanked by two constant strings. The substring, also termed smRNA or insert, is stored in a MySQL and BlastN database. These inserts are then compared using BlastN to locally installed databases allowing the rapid comparison of the insert to both the growing smRNA database and to other static sequence databases. Our laboratory used Ebbie to analyze scores of DNA sequencing data originating from an smRNA cloning project[6]. Through its built-in instant analysis of all inserts using BlastN, we were able to quickly identify 33 groups of smRNAs from ~700 database entries. This clustering allowed the easy identification of novel and highly expressed clusters of smRNAs. Ebbie is available under GNU GPL and currently implemented on CONCLUSION: Ebbie was designed for medium sized smRNA cloning projects with about 1,000 database entries [6-8].Ebbie can be used for any type of sequence analysis where two constant primer regions flank a sequence of interest. The reliable storage of inserts, and their annotation in a MySQL database, BlastN[9] comparison of new inserts to dynamic and static databases make it a powerful new tool in any laboratory using DNA sequencing. Ebbie also prevents manual mistakes during the excision process and speeds up annotation and data-entry. Once the server is installed locally, its access can be restricted to protect sensitive new DNA sequencing data. Ebbie was primarily designed for smRNA cloning projects, but can be applied to a variety of RNA and DNA cloning projects[2,3,10,11]. BioMed Central 2006-04-03 /pmc/articles/PMC1450305/ /pubmed/16584563 http://dx.doi.org/10.1186/1471-2105-7-185 Text en Copyright © 2006 Ebhardt et al; licensee BioMed Central Ltd.
spellingShingle Software
Ebhardt, H Alexander
Wiese, Kay C
Unrau, Peter J
Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server
title Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server
title_full Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server
title_fullStr Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server
title_full_unstemmed Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server
title_short Ebbie: automated analysis and storage of small RNA cloning data using a dynamic web server
title_sort ebbie: automated analysis and storage of small rna cloning data using a dynamic web server
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1450305/
https://www.ncbi.nlm.nih.gov/pubmed/16584563
http://dx.doi.org/10.1186/1471-2105-7-185
work_keys_str_mv AT ebhardthalexander ebbieautomatedanalysisandstorageofsmallrnacloningdatausingadynamicwebserver
AT wiesekayc ebbieautomatedanalysisandstorageofsmallrnacloningdatausingadynamicwebserver
AT unraupeterj ebbieautomatedanalysisandstorageofsmallrnacloningdatausingadynamicwebserver