CNVIntegrate

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CNVIntegrate

metasource: bio.tools
version: extracted_at: 2022-11-04T11:25:34.652187

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cnvintegrate

metasource: bio.tools
version: extracted_at: 2022-11-04T11:25:34.652187

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CancerImmunityQTL

immunQTLs across multiple cancer types

CaSNP

Cancer SNP data on copy number alterations

Progenetix - genomic copy number aberrations in cancer

The Progenetix database provides an overview of copy number abnormalities in human cancer from Comparative Genomic Hybridization (CGH) experiments. With 30817 cases from 1016 publications (Oct 2013), ...

The ribosomal RNA operon copy number database

The ribosomal RNA operon copy number database is a publicly available, curated resource for ribosomal operon (rrn) copy number information for Bacteria and Archaea.

CCAS

One-stop and comprehensive annotation system for individual cancer genome at multi-omics level.

VariED

The first integrated database of gene annotation and expression profiles for variants related to human diseases. An integrated database of variants and gene expression profiles for genetic diseases.

CanGEM

Gene copy number changes in cancer

CNAdbCC

CNAdbCC is a curated database for copy number aberrations analysis and visualization of cervical cancer. Currently, the database contains about 1,000 dataset samples mainly integrated by affymetrix an ...

TaiwanGenomes

Complete genomic profiles of 1,496 Taiwanese reveal curated medical insights.

InvFEST

Polymorphic inversions in the human genome

LncVar

Database of genetic variations associated with long noncoding genes.

Exome Aggregation Consortium Browser

The Exome Aggregation Consortium (ExAC) is a coalition of investigators seeking to aggregate and harmonize exome sequencing data from a variety of large-scale sequencing projects, and to make summary ...

cBioPortal for Cancer Genomics

The cBioPortal for Cancer Genomics provides visualization, analysis and download of large-scale cancer genomics data sets.

DriverDBv2

DriverDB, a database that incorporates >9500 cancer-related RNA-seq datasets and >7000 more exome-seq datasets, in addition to annotation databases and published bioinformatics algorithms dedicated to ...

ICGC Data Portal

The International Cancer Genome Consortium (ICGC) is a collaborative effort to characterize genomic abnormalities in 50 different cancer types. Currently has data from 24 cancer projects. Open access ...

ESP

NHLBI Exome Sequencing Project (ESP): Exome Variant Server (EVS) for browsing single nucleotide variation data from exome sequencing experiments mainly focused on heart, lung and blood disorders.

arrayMap - Genomic Array Data for Cancer CNV Profiles

Part of the Progenetix project, the arrayMap database facilitates the study of the genetics of human cancer. The Progenetix project provides the data customisation and visualization tools to mine the ...

Human Genetic Variation Database

The Human Genetic Variation Database (HGVD) aims to provide a central resource to archive and display Japanese genetic variation and association between the variation and transcription level of genes. ...

SynLethDB