Welcome to the Open Genomics Engine Discussion Forum
Welcome to the Tynon General Discussion Forum
Use this forum for any discussion relating to Tynon you like Feel free to discuss anything going on in the game, talk smack or anything else. Just keep it clean and constructive
Header Leaderboard Ad
Collapse
Welcome to the Open Genomics Engine Discussion Forum
Collapse
Announcement
Collapse
No announcement yet.
X
-
Yepp, .. project development has been discontinued..
Latest news is:
Download OpenGE version 0.4
May 23, 2013
OpenGE 0.4 features improved speed and stability…
Leave a comment:
-
Originally posted by ECO View PostHi all,
I'm excited to announce that SEQanswers will act as the official discussion host for the Open Genomics Engine project. See the official announcement below:
As always, feedback and input are welcome.
-=Eric
in what language are the programs written, what compiler is needed,
what operation system, do the programs work from command line,
can they be joined in batch files, is there a simple example of some
such program, and the typical size of a data-file which it handles
Leave a comment:
-
Originally posted by adaptivegenome View PostIt has been a year since I posted that message and since then we decided against developing a GUI. We have functionality that allows you to plug-in external tools into OpenGE (bpipe style) and this is great for simple command-line based workflows. It is definitely not intended to be a replacement for Galaxy, which is one the best workflow managers around.
The focus of OpenGE was to speed up and optimize certain steps of the genome analysis pipeline. I think we achieved that. The code is not 100% bug-free but it has been a continuous work in progress
Leave a comment:
-
Originally posted by BobFreemanMA View PostThis seems very exciting and promising, but I hope that you can tell me how this project is different from Galaxy. And it seems to have a significant advantage in terms of release time, users, development, etc.
Tx,
Bob
The focus of OpenGE was to speed up and optimize certain steps of the genome analysis pipeline. I think we achieved that. The code is not 100% bug-free but it has been a continuous work in progress
Leave a comment:
-
And this is different from Galaxy in what ways???
Originally posted by adaptivegenome View PostHi gringer,
Certainly one aspect of OpenGE will be the management of analysis pipelines composed of existing tools. Much like the recently released bpipe project, the aim would be to incorporate existing tools into workflows. We want to eventually build a web-based GUI (in development right now) that allows for the dynamic creation of workflows (currently this is implemented at the command line) and we would like it to feature things like: versioning of tools, progress tracking, recovery and restarting from errors, etc.
Rewriting everyone's code is inefficient and unnecessary, but OpenGE also will feature modifications of existing code from projects like bamtools. We have implemented a multithreaded BAM compression method, a multithread combined merge-sort, and some other low-level tools for operating on BAM files. I know Heng Li has begun introducing some of this into samtools and I believe Nils Homer may be working on this as well. I would love to see how our code stacks up since a secondary goal of the project is to accelerate the analysis of genomes.
One nice thing about the project is that we will have funding to continue development of the GUI as well as optimization and addition of other tools to the software. I am hoping that via SEQanswers we can get direction from the community on prioritizing what to do next. Furthermore we hope to write adapters/plugins for existing tools and to encourage others to join in the development, etc.
The project is completely open source and will be hosted on GitHub. We are hoping that the combination of fast code and a easy to use package manager/workflow GUI will put all this analysis in the hands everyone...
Sorry for the long post, but hopefully that sort answers your question?
Tx,
Bob
Leave a comment:
-
Originally posted by rezaf_2000 View PostSo, what is the role of NVIDIA in Open GE?
The foundation will continue to fund us in the short-term but we will need to recruit additional sources of extramural funding from the NIH, NSF, etc. for the long-term sustainment of the project.
Leave a comment:
-
Although the project officially goes live on Monday, June 4th, the code is available on github now.
The main code featuring multithreaded processing of BAM files is located here:
An accelerated framework for manipulating and interpreting high-throughput sequencing data - GitHub - adaptivegenome/openge: An accelerated framework for manipulating and interpreting high-throughp...
Binaries are here:
The preliminary release of a bpipe-compatible workflow system is located:
GitHub is where people build software. More than 100 million people use GitHub to discover, fork, and contribute to over 330 million projects.
The main code is based on bamtools and so for those that are familiar with samtools or bamtools, it should be easy to start using right away. Please feel free to submit comments/suggestions via the github site (under Issues) or discuss here in this forum. We would be grateful to hear of bugs or simply feedback on speed increases with different input data.Last edited by adaptivegenome; 06-02-2012, 03:33 AM.
Leave a comment:
-
Thanks for the feedback. I'll see if we can get the website updated a bit.
Leave a comment:
-
Sorry for the long post, but hopefully that sort answers your question?
Leave a comment:
-
Hi gringer,
Certainly one aspect of OpenGE will be the management of analysis pipelines composed of existing tools. Much like the recently released bpipe project, the aim would be to incorporate existing tools into workflows. We want to eventually build a web-based GUI (in development right now) that allows for the dynamic creation of workflows (currently this is implemented at the command line) and we would like it to feature things like: versioning of tools, progress tracking, recovery and restarting from errors, etc.
Rewriting everyone's code is inefficient and unnecessary, but OpenGE also will feature modifications of existing code from projects like bamtools. We have implemented a multithreaded BAM compression method, a multithread combined merge-sort, and some other low-level tools for operating on BAM files. I know Heng Li has begun introducing some of this into samtools and I believe Nils Homer may be working on this as well. I would love to see how our code stacks up since a secondary goal of the project is to accelerate the analysis of genomes.
One nice thing about the project is that we will have funding to continue development of the GUI as well as optimization and addition of other tools to the software. I am hoping that via SEQanswers we can get direction from the community on prioritizing what to do next. Furthermore we hope to write adapters/plugins for existing tools and to encourage others to join in the development, etc.
The project is completely open source and will be hosted on GitHub. We are hoping that the combination of fast code and a easy to use package manager/workflow GUI will put all this analysis in the hands everyone...
Sorry for the long post, but hopefully that sort answers your question?
Leave a comment:
-
Will this be a frontend to manage a number of different FOSS HTS analysis packages with one program, or a rebuilt chariot for HTS analysis?
Leave a comment:
Latest Articles
Collapse
-
Differential Expression and Data Visualization: Recommended Tools for Next-Level Sequencing Analysisby seqadmin
After covering QC and alignment tools in the first segment and variant analysis and genome assembly in the second segment, we’re wrapping up with a discussion about tools for differential gene expression analysis and data visualization. In this article, we include recommendations from the following experts: Dr. Mark Ziemann, Senior Lecturer in Biotechnology and Bioinformatics, Deakin University; Dr. Medhat Mahmoud Postdoctoral Research Fellow at Baylor College of Medicine;...-
Channel: Articles
05-23-2023, 12:26 PM -
-
by seqadmin
Continuing from our previous article, we share variant analysis and genome assembly tools recommended by our experts Dr. Medhat Mahmoud, Postdoctoral Research Fellow at Baylor College of Medicine, and Dr. Ming "Tommy" Tang, Director of Computational Biology at Immunitas and author of From Cell Line to Command Line.
Variant detection and analysis tools
Mahmoud classifies variant detection work into two main groups: short variants (<50...-
Channel: Articles
05-19-2023, 10:03 AM -
-
by seqadmin
With new tools and computational resources being released regularly, it can be hard to determine which are best suited for the analysis process and which older tools continue to be maintained. In an effort to assist the sequencing community, we interviewed three highly skilled bioinformaticians about their recommended tools for several important analysis applications.
Quality control and preprocessing tools
“Garbage in, garbage out” is a popular...-
Channel: Articles
05-16-2023, 10:11 AM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Exploring French-Canadian Ancestry: Insights into Migration, Settlement Patterns, and Genetic Structure
by seqadmin
Started by seqadmin, 05-26-2023, 09:22 AM
|
0 responses
8 views
0 likes
|
Last Post
by seqadmin
05-26-2023, 09:22 AM
|
||
Started by seqadmin, 05-24-2023, 09:49 AM
|
0 responses
14 views
0 likes
|
Last Post
by seqadmin
05-24-2023, 09:49 AM
|
||
Introducing ProtVar: A Web Tool for Contextualizing and Interpreting Human Missense Variation in Proteins
by seqadmin
Started by seqadmin, 05-23-2023, 07:14 AM
|
0 responses
30 views
0 likes
|
Last Post
by seqadmin
05-23-2023, 07:14 AM
|
||
Started by seqadmin, 05-18-2023, 11:36 AM
|
0 responses
116 views
0 likes
|
Last Post
by seqadmin
05-18-2023, 11:36 AM
|
Leave a comment: