ClinCNV

Brought to you by: oliverdrechsel, stosto77

Last Update: 2016-10-12

Browse Code

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

Ever wanted to predict Copy Number Variants from your Exome data?
Here is CNVler, a tool which is able to predict CNVs in Parent-Child trios, tumor-normal pairs (somatic) and population (germline).

Project Activity

See All Activity >

Follow ClinCNV

ClinCNV Web Site

Other Useful Business Software

$300 in Free Credit Towards Top Cloud Services

Build VMs, containers, AI, databases, storage—all in one place.

Start your project in minutes. After credits run out, 20+ products include free monthly usage. Only pay when you're ready to scale.

Get Started

Rate This Project

User Reviews

Be the first to post a review of ClinCNV!

Additional Project Details

Registered

2014-03-07

Report inappropriate content

$300 in Free Credit Towards Top Cloud Services

Build VMs, containers, AI, databases, storage—all in one place.

Start your project in minutes. After credits run out, 20+ products include free monthly usage. Only pay when you're ready to scale.

Get Started

Recommended Projects

VarScan
Variant detection in next-generation sequencing data
CoNIFER
Homepage for CoNIFER (Copy Number Inference From Exome Reads)
NanoGLADIATOR
Real-time detection of copy number alterations from nanopore data.
EXCAVATOR2tool
Enhanced tool for detecting CNVs from whole-exome sequencing data
hg38 package
hg38 version of the pipelines for whole exome sequencing: exome_test38.sh wole transcription sequencing: rna_test38.sh somatic calling: somatic38.sh SV detect: svdetect38.sh, meerkat38.sh cnv: svdetectcnv38.sh, contra38.sh, cnvkit38.sh *** Mutect2 instead of haptotypecaller is used to call variants in DNA-seq.