{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,17]],"date-time":"2026-04-17T04:31:09Z","timestamp":1776400269136,"version":"3.51.2"},"reference-count":22,"publisher":"Oxford University Press (OUP)","issue":"22","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2011,11,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Summary: With the rapidly expanding availability of data from personal genomes, exomes and transcriptomes, medical researchers will frequently need to test whether observed genomic variants are novel or known. This task requires downloading and handling large and diverse datasets from a variety of sources, and processing them with bioinformatics tools and pipelines. Alternatively, researchers can upload data to online tools, which may conflict with privacy requirements. We present here Kaviar, a tool that greatly simplifies the assessment of novel variants. Kaviar includes: (i) an integrated and growing database of genomic variation from diverse sources, including over 55 million variants from personal genomes, family genomes, transcriptomes, SNV databases and population surveys; and (ii) software for querying the database efficiently.<\/jats:p>\n               <jats:p>Availability: Kaviar is programmed in Perl and offered free of charge as Open Source Software. Kaviar may be used online as a programmatic web service or downloaded for local use from http:\/\/db.systemsbiology.net\/kaviar. The database is also provided.<\/jats:p>\n               <jats:p>Contact: \u00a0gustavo@systemsbiology.org<\/jats:p>\n               <jats:p>Supplementary Information: \u00a0Supplementary data are available at Bioinformatics online.<\/jats:p>","DOI":"10.1093\/bioinformatics\/btr540","type":"journal-article","created":{"date-parts":[[2011,9,30]],"date-time":"2011-09-30T10:29:20Z","timestamp":1317378560000},"page":"3216-3217","source":"Crossref","is-referenced-by-count":198,"title":["Kaviar: an accessible system for testing SNV novelty"],"prefix":"10.1093","volume":"27","author":[{"given":"Gustavo","family":"Glusman","sequence":"first","affiliation":[{"name":"Institute for Systems Biology, Seattle, WA 98109, USA"}]},{"given":"Juan","family":"Caballero","sequence":"additional","affiliation":[{"name":"Institute for Systems Biology, Seattle, WA 98109, USA"}]},{"given":"Denise E.","family":"Mauldin","sequence":"additional","affiliation":[{"name":"Institute for Systems Biology, Seattle, WA 98109, USA"}]},{"given":"Leroy","family":"Hood","sequence":"additional","affiliation":[{"name":"Institute for Systems Biology, Seattle, WA 98109, USA"}]},{"given":"Jared C.","family":"Roach","sequence":"additional","affiliation":[{"name":"Institute for Systems Biology, Seattle, WA 98109, USA"}]}],"member":"286","published-online":{"date-parts":[[2011,9,28]]},"reference":[{"key":"2023012511332363400_B1","doi-asserted-by":"crossref","first-page":"1061","DOI":"10.1038\/nature09534","article-title":"A map of human genome variation from population-scale sequencing","volume":"467","author":"1000","year":"2010","journal-title":"Nature"},{"key":"2023012511332363400_B2","doi-asserted-by":"crossref","first-page":"105","DOI":"10.1186\/1471-2105-12-105","article-title":"ENGINES: exploring single nucleotide variation in entire human genomes","volume":"12","author":"Amigo","year":"2011","journal-title":"BMC Bioinformatics"},{"key":"2023012511332363400_B3","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1186\/gm2","article-title":"Systems medicine: the future of medical genomics and healthcare","volume":"1","author":"Auffray","year":"2009","journal-title":"Genome Med."},{"key":"2023012511332363400_B4","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1101\/gr.099226.109","article-title":"Sex-specific and lineage-specific alternative splicing in primates","volume":"20","author":"Blekhman","year":"2010","journal-title":"Genome Res."},{"key":"2023012511332363400_B5","doi-asserted-by":"crossref","first-page":"2156","DOI":"10.1093\/bioinformatics\/btr330","article-title":"The variant call format and VCFtools","volume":"27","author":"Danecek","year":"2011","journal-title":"Bioinformatics"},{"key":"2023012511332363400_B6","doi-asserted-by":"crossref","first-page":"2","DOI":"10.1002\/humu.21149","article-title":"dbSNP in the detail and copy number complexities","volume":"31","author":"Day","year":"2010","journal-title":"Hum. 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