INTSIM

Brought to you by: andi210

Last Update: 2016-03-28

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

The IntSim software package has been developed to simulate various genome mutations including germline and somatic variations from next generation sequencing data, and also to generate read data from mixed genomes by considering moderate levels of tumor purity.

Project Activity

See All Activity >

Follow INTSIM

INTSIM Web Site

Other Useful Business Software

Fully Managed MySQL, PostgreSQL, and SQL Server

Automatic backups, patching, replication, and failover. Focus on your app, not your database.

Cloud SQL handles your database ops end to end, so you can focus on your app.

Try Free

Rate This Project

User Reviews

Be the first to post a review of INTSIM!

Additional Project Details

Registered

2015-06-03

Report inappropriate content

$300 Free Credits for Your Google Cloud Projects

Start building on Google Cloud with $300 in free credits. No commitment, no credit card required until you're ready to scale.

Launch your next project with $300 in free Google Cloud credits—no strings attached. Test, build, and deploy without risk. Use your credits across the entire Google Cloud platform to find what works best for your needs. After your credits are used, continue with always-free tier services. Only pay when you're ready to scale. Sign up in minutes and start exploring.

Start Free Trial

Recommended Projects

VarScan
Variant detection in next-generation sequencing data
MitoSAlt
Identification of mitochondrial structural alterations
CONDEL
CONDEL is a method for detecting CNVs and deletion types from single samples using high-throughput sequence data. It can be used for analyzing genomes from tumor cells or normal cells with an input of genome reference, reference index, SAM file, and read counts.
cFinder
Tool for automatic definition and quantification of haplotypes in a mixed sample. Supports ultra-deep sequencing with data from any next-generation sequencing strategy. Detailed manual is included in the zip package.
BreakDancer
BreakDancer-0.0.1 is a Perl package that provides genome-wide detection of structural variants from next generation paired-end sequencing reads.