OmicBrowse - Browse /OmicBrowse/1.4 at SourceForge.net

The interactive file manager requires Javascript. Please enable it or use sftp or scp.
You may still browse the files here.

Name	Modified	Size	InfoDownloads / Week
Parent folder
1.4.4	2009-12-24		0
1.4.3	2009-12-04		0
1.4.2	2009-10-21		0
1.4.1	2009-10-09		0
OmicBrowse-win-1.4.zip	2009-09-11	37.9 MB	0
OmicBrowse-1.4.tar.gz	2009-09-11	35.0 MB	0
Totals: 6 Items		72.9 MB	0

Other Useful Business Software

Go from Data Warehouse to Data and AI platform with BigQuery

Build, train, and run ML models with simple SQL. Automate data prep, analysis, and predictions with built-in AI assistance from Gemini.

BigQuery is more than a data warehouse—it's an autonomous data-to-AI platform. Use familiar SQL to train ML models, run time-series forecasts, and generate AI-powered insights with native Gemini integration. Built-in agents handle data engineering and data science workflows automatically. Get $300 in free credit, query 1 TB, and store 10 GB free monthly.

Try BigQuery Free

Build on Google Cloud with $300 in Free Credit

New to Google Cloud? Get $300 in free credit to explore Compute Engine, BigQuery, Cloud Run, Vertex AI, and 150+ other products.

Start your next project with $300 in free Google Cloud credit. Spin up VMs, run containers, query exabytes in BigQuery, or build AI apps with Vertex AI and Gemini. Once your credits are used, keep building with 20+ products with free monthly usage, including Compute Engine, Cloud Storage, GKE, and Cloud Run functions. Sign up to start building right away.

Start Free Trial

Recommended Projects

FragGeneScan
FragGeneScan is an application for finding (fragmented) genes in short reads. It can also be applied to predict prokaryotic genes in incomplete assemblies or complete genomes. FragGeneScan was first released through omics website (http://omics.informatics.indiana.edu/FragGeneScan/) in March 2010, where you can find its old releases. FragGeneScan migrated to SourceForge in October, 2013.
MitoSAlt
Identification of mitochondrial structural alterations
kSNP
kSNP4 does SNP discovery and SNP annotation from whole genomes
VCF Explorer
A desktop application for analyzing whole genome VCF files
ArrayOligoSelector
ArrayOligoSelector (AOS) systematically designs gene specific long oligo probes for entire genomes. The program optimizes the oligo selections for several parameters, including uniqueness in the genome, internal repeats, self-binding, and GC content.

OmicBrowse Files

Get an email when there's a new version of OmicBrowse