GenDBE
GenDBE enables annotation and assembly of eukaryotic genomes and transcriptomes, supporting intron–exon gene models and integration of Roche/454 and Illumina sequencing data for transcript reconstruction and analysis.
Key Features:
- Eukaryotic gene model support: Handles intron and exon gene structures for eukaryotic genome annotation.
- Transcriptome integration with SAMS: Integrates with SAMS for eukaryotic transcriptome data representation and analysis.
- High-quality transcript assembly: Implements both de novo and reference-based strategies to reconstruct transcripts.
- Sequencing technology support: Accepts and leverages data from Roche/454 and Illumina platforms.
- Assembly toolchain: Employs Trinity and Oases for de novo assembly, ESTScan for CDS screening, cd-hit-est for redundancy filtering, CAP3 for re-assembly, and TopHat/Cufflinks, GMAP, and cuffmerge for reference-based assembly and merging.
Scientific Applications:
- CHO cell line transcriptomics: Enables assembly and analysis of Chinese hamster ovary (CHO) cell transcriptomes to support research on therapeutic protein production and optimization of protein expression.
Methodology:
De novo assembly using Trinity and Oases with varying k-mer sizes; screening of contigs for coding sequences with ESTScan; redundancy removal with cd-hit-est; re-assembly of CDS contigs with CAP3; reference-based assembly using the TopHat/Cufflinks pipeline against the CHO-K1 draft genome; mapping de novo contigs to the reference with GMAP and merging assemblies with cuffmerge.
Topics
Collections
Details
- License:
- GPL-2.0
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- workflow
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- JavaScript
- Added:
- 6/16/2016
- Last Updated:
- 1/10/2019
Operations
Publications
Rupp O, Becker J, Brinkrolf K, Timmermann C, Borth N, Pühler A, Noll T, Goesmann A. Construction of a Public CHO Cell Line Transcript Database Using Versatile Bioinformatics Analysis Pipelines. PLoS ONE. 2014;9(1):e85568. doi:10.1371/journal.pone.0085568. PMID:24427317. PMCID:PMC3888431.