Increment_Ratio_of_Coverage_V2.0 download | SourceForge.net

Increment_Ratio_of_Coverage_V2.0

Brought to you by: zhenjunyang

Add a Review

Downloads: 4 This Week

Last Update: 2020-05-28

Download

Add to Preferred Sources

A program for CNV detection with whole-genome low-coverage sequencing data.

md5 of Increment_Ratio_of_Coverage_V2.0.tar.gz: c8dda5fbd5b43527538f5c410a303a74

Project Activity

See All Activity >

Follow Increment_Ratio_of_Coverage_V2.0

Increment_Ratio_of_Coverage_V2.0 Web Site

Other Useful Business Software

Endpoint Management with Remote Control Built In

Patch, monitor, and connect to Windows and macOS devices from one console

Splashtop AEM handles patching, alerts, scripts, and inventory, and unattended remote control is included. When something needs hands-on work, you’re one click away instead of switching tools.

Start Free Trial

Rate This Project

User Reviews

Be the first to post a review of Increment_Ratio_of_Coverage_V2.0!

Additional Project Details

Registered

2019-07-05

Report inappropriate content

Build Agents and Models on One Platform

Everything you need to build production-ready agents and models. Access 200+ Google and third-party AI models and tools.

Gemini Enterprise Agent Platform is Google Cloud's comprehensive platform for developers to build, scale, govern, and optimize agents and models. Choose from Google's most advanced models and third-party models like Anthropic's Claude Model Family.

Start Free

Recommended Projects

RDXplorer
The RDXplorer is a computational tool for copy number variants (CNV) detection in whole human genome sequence data using read depth (RD) coverage. CNV detection is based on the Event-Wise Testing (EWT) algorithm recently published by our group.
cnvOffSeq
detecting & genotyping intergenic CNVs using off-target exome data
Lep-MAP3
Lep-MAP3 is a novel and free software for linkage mapping. It can construct linkage maps on very large number of markers and individuals on single or multiple families. Especially, it supports whole genome sequencing data even with low sequencing depth. If you use Lep-MAP3, please cite P. Rastas. Lep-MAP3: Robust linkage mapping even for low-coverage whole genome sequencing data, Bioinformatics. 2017, 33(23):3726-3732. https://doi.org/10.1093/bioinformatics/btx494. Please note Lep-Anchor for anchoring genomes with Lep-MAP3 linkage maps http://sourceforge.net/projects/lep-anchor
Vancouver Short Read Analysis Package
This package contains code for use with Short Read DNA Sequencing technologies, and includes packages for ChIP-Seq, Whole Transcriptome Shotgun Sequencing, Whole Genome Shotgun Sequencing, SNP Detection, Transcript expression and file conversion.
ADTEx
Aberration detection in tumour exome