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BC SNPmax

Names
More detailed information about this field from each metasource.

BC SNPmax
metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

bc_snpmax
metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

Other names: bc_snpmax

Names

More detailed information about this field from each metasource.

BC SNPmax

metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

bc_snpmax

metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

This source may no longer be available. No known URL could be resolved successfully.

Database platform for managing molecular data (sequence variants and DNA array) with associated phenotypes and analyzing the data for QTL mapping.

Description

More detailed information about this field from each metasource.

Database platform for managing molecular data (sequence variants and DNA array) with associated phenotypes and analyzing the data for QTL mapping.

metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

Webpage:

http://www.bcplatforms.com/

Webpage

More detailed information about this field from each metasource.

http://www.bcplatforms.com/

metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

Licence:

Name: Proprietary

Licence name

More detailed information about this field from each metasource.

Proprietary

metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

Tags:

Tags
More detailed information about this field from each metasource.

genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

genetic variation

More to explore:

1/20

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. ...

bc-GenExMiner

Breast cancer gene-expression miner (bc-GenExMiner) 4.5 is a mining module computes breast cancer differential gene expression analyses. It is a statistical mining tool of published annotated breast c ...

Chicken Variation Database

The chicken Variation Database (ChickVD) is an integrated information system for storage, retrieval, visualization and analysis of chicken variation data.

Pompe

Novel disease-associated variants, common sequence variants, and results from newborn screening. The Pompe disease GAA variant database represents an effort to collect all known variants in the GAA g ...

QTL Matchmaker

QTL MatchMaker system is designed to integrate and mine QTL information across human, mouse and rat genomes and to annotate functional genomic data. It combines and organizes information from relevant ...

Animal Quantitative Trait Loci (QTL) Database

The Animal Quantitative Trait Loci (QTL) Database (Animal QTLdb) strives to collect all publicly available trait mapping data, i.e. QTL (phenotype/expression, eQTL), candidate gene and association dat ...

Pharmacogenomics Knowledge Base

PharmGKB is a resource that provides information about how human genetic variation affects response to medications. PharmGKB collects, curates and disseminates knowledge about clinically actionable ge ...

SoyBase

SoyBase, the USDA-ARS soybean genetic database, is a comprehensive repository for professionally curated genetics, genomics and related data resources for soybean. SoyBase contains genetic, physical a ...

Hierarchical Data Format

HDF5 is a data model, library, and file format for storing and managing data. It supports an unlimited variety of datatypes, and is designed for flexible and efficient I/O and for high volume and comp ...

The conserved clinical variation visualization tool

The availability of genetic variants, together with phenotypic annotations from model organisms, facilitates comparing these variants with equivalent variants in humans. However, existing databases an ...

MSV3d

Database of human missense variants mapped to 3D protein structures.

NucPosDB

A database of nucleosome positioning in vivo and nucleosomics of cell-free DNA.

European Variation Archive

The European Variation Archive is an open-access archive that accepts submission of, and provides access to, all types of genetic variation data from all species. All users are able to download any da ...

Gramene: A curated, open-source, integrated data resource for comparative functional genomics in plants

Gramene's purpose is to provide added value to plant genomics data sets available within the public sector, which will facilitate researchers' ability to understand the plant genomes and take advantag ...

Gephebase

Gephebase is a manually-curated database compiling our accumulated knowledge of the genes and mutations that underlie natural, domesticated and experimental phenotypic variation in all Eukaryotes â€” ...

Leiden Open Variation Database

The Leiden Open Variation Database (LOVD) provides a flexible, freely available tool for gene-centered collection and display of DNA variations. LOVD also stores patient-centered data, NGS data, and v ...

KVarPredDB

A database for predicting pathogenicity of missense sequence variants of keratin genes associated with genodermatoses.

Minimum Information about an fMRI Study

These reporting guidelines were developed by the Committee on Best Practices in Data Analysis and Sharing (COBIDAS) of the Organization for Human Brain Mapping.

ClinVar

ClinVar is a freely accessible, public archive of reports of the relationships among human variations and phenotypes, with supporting evidence. ClinVar thus facilitates access to and communication abo ...

Bovine Genome Variation Database (BGVD)

An integrated Web-database for bovine sequencing variations and selective signatures.

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Service status

Reach us:
[email protected]

Data is amalgamated and only retrieved periodically.
Some of the resources used by the system:

® FAIRsharing.org
® Bioontology/Bioportal Terms
® Nucleic Acid Research - Database
® re3data.org
® bio.tools
® PubMed - Courtesy of the U.S. National Library of Medicine

BC SNPmax Names More detailed information about this field from each metasource. × BC SNPmax metasource: bio.tools version: extracted_at: 2022-11-04T11:24:43.813232 bc_snpmax metasource: bio.tools version: extracted_at: 2022-11-04T11:24:43.813232 Close

Webpage:

Licence:

Tags: Tags More detailed information about this field from each metasource. × genetic variation metasource: bio.tools version: extracted_at: 2022-11-04T11:24:43.813232 Close

More to explore:

1/20

Human Genetic Variation Database

bc-GenExMiner

Chicken Variation Database

Pompe

QTL Matchmaker

Animal Quantitative Trait Loci (QTL) Database

Pharmacogenomics Knowledge Base

SoyBase

Hierarchical Data Format

The conserved clinical variation visualization tool

MSV3d

NucPosDB

European Variation Archive

Gramene: A curated, open-source, integrated data resource for comparative functional genomics in plants

Gephebase

Leiden Open Variation Database

KVarPredDB

Minimum Information about an fMRI Study

ClinVar

Bovine Genome Variation Database (BGVD)

BC SNPmax

Names
More detailed information about this field from each metasource.

BC SNPmax
metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

bc_snpmax
metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232

Tags:

Tags
More detailed information about this field from each metasource.

genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:24:43.813232