Genetic variation in 1000 Indian individuals
circad is a comprehensive manually curated resource of circular RNA associated with diseases. Circular RNAs (circRNAs) are unique transcript isoforms characterised by back splicing of exon ends to for ...
Esc (Immune escape variants in SARS-CoV-2) is a comprehensive and manually curated compendium of genetic variants in SARS-CoV-2 associated with immune escape. The data on variants and associations hav ...
Comprehensive peptide signature database
Middle East and North Africa (MENA) encompass very unique populations, with a rich history and encompasses characteristic ethnic, linguistic and genetic diversity. The genetic diversity of MENA region ...
Knowledgebase of Microbes’ Battling Agents for Therapeutics.
Genetic variation in Trypanosoma cruzi
Indian Genetic Disease 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. ...
Indian Biodiversity Ontology contains the semantic information about the domain of Indian Biodiversity
ClinGen Variant Curation Interface is a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines.
Whole-genome sequence data, variant calls, and annotations of natural genetic variation in C. elegans species.
ClinGen is a National Institutes of Health (NIH)-funded resource dedicated to building an authoritative central resource that defines the clinical relevance of genes and variants for usein precision m ...
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 ...
The International Genome Sample Resource (IGSR) was established to ensure the ongoing usability of data generated by the 1000 Genomes Project and to extend the data set. The 1000 Genomes Project ran b ...
Interpreting Genetic Variation in Human and Cancer Genomes Using Post-translational Modification Sites and Signaling Networks (2021 Update). Find your mutation or gene of interest. You are viewing a ...
InBiodiv-O: An Ontology for Indian Biodiversity Knowledge Management
InBan-CIDO ontology is an extension of the CIDO ontology to show the impact of Covid-19 on the Indian economy sector.
The 1000 Genomes Project (1000GP) represents the most comprehensive world-wide nucleotide variation data set so far in humans, providing the sequencing and analysis of 2504 genomes from 26 populations ...
A generic integrated web-based workflow system to evaluate genotype-phenotype correlations in human mitochondrial diseases.
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 — ...