ANNOVAR . OPENBIOINFORMATICS . ORG {}

Matching Content Categories {📚}

• Technology & Computing
• Telecommunications
• Mobile Technology & AI

Content Management System {📝}

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Custom-built

No common CMS systems were detected on Annovar.openbioinformatics.org, but we identified it was custom coded using Bootstrap (CSS).

Traffic Estimate {📈}

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🚄 Respectable Traffic: 10k - 20k visitors per month


Based on our best estimate, this website will receive around 10,105 visitors per month in the current month.

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How Does Annovar.openbioinformatics.org Make Money? {💸}

The income method remains a mystery to us.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Annovar.openbioinformatics.org might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

annovar, version, variants, annotation, download, updated, keyword, scores, clinvar, genome, users, gnomad, gene, mar, coordinate, jun, file, oct, hghg, protein, database, databases, exome, data, email, nov, report, genomic, allele, mutations, bug, build, server, change, reference, coordinates, problem, feb, downdb, note, jan, dec, ensgene, files, orfab, argument, user, previous, annotate, identify,

Topics {✒️}

sift/polyphen/lrt/mutationtaster/mutationassessor/fathmm/metasvm/metalr/metarnn scores encode h3k4me1/h3k4me3/h3k27ac/ctcf sites multi-threaded gene-based annotation user-specific genomic positions pre-computed intervar scores genome fathmm-mkl scores encode ccre sites quick startup guide specific cancer types genome sequencing data exome aggregation consortium multi-mapping transcripts allele frequency data exome sequencing data includes gender-specific brazilian genomic variants hg18/hg19/hg38 coordinates gene-disease relationships chip-seq peaks rna-seq peaks learn advanced functions institutional computing clusters ribosome slippage event finding alternative solutions finding replacement servers census-based sample benign/pathogenic categories important features include 2015 acmg-amp guidelines annotation files avgene specific genomic regions gene-based annotation gene definition annotation segmental duplication regions disqus comment form comprehensive/formal calculation filter-based annotation interpro domain annotation genome aggregation database allele frequency calculation directly kaichop gmail ensure backward compatibility downdb command line gff files provided recently published paper generate column headers ucsc genome browser' exome sift dbtype keyword regeneron multiple annotation columns

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Analytics and Tracking {📊}

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Libraries {📚}

• Bootstrap
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Emails and Hosting {✉️}

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Name Servers:

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CDN Services {📦}

• Cloudflare