FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Issue Volume 51:Issue D1(2023) (9th November 2022)
- Record Type:
- Journal Article
- Title:
- FAVOR: functional annotation of variants online resource and annotator for variation across the human genome. Issue Volume 51:Issue D1(2023) (9th November 2022)
- Main Title:
- FAVOR: functional annotation of variants online resource and annotator for variation across the human genome
- Authors:
- Zhou, Hufeng
Arapoglou, Theodore
Li, Xihao
Li, Zilin
Zheng, Xiuwen
Moore, Jill
Asok, Abhijith
Kumar, Sushant
Blue, Elizabeth E
Buyske, Steven
Cox, Nancy
Felsenfeld, Adam
Gerstein, Mark
Kenny, Eimear
Li, Bingshan
Matise, Tara
Philippakis, Anthony
Rehm, Heidi L
Sofia, Heidi J
Snyder, Grace
Weng, Zhiping
Neale, Benjamin
Sunyaev, Shamil R
Lin, Xihong - Abstract:
- Abstract: Large biobank-scale whole genome sequencing (WGS) studies are rapidly identifying a multitude of coding and non-coding variants. They provide an unprecedented resource for illuminating the genetic basis of human diseases. Variant functional annotations play a critical role in WGS analysis, result interpretation, and prioritization of disease- or trait-associated causal variants. Existing functional annotation databases have limited scope to perform online queries and functionally annotate the genotype data of large biobank-scale WGS studies. We develop the Functional Annotation of Variants Online Resources (FAVOR) to meet these pressing needs. FAVOR provides a comprehensive multi-faceted variant functional annotation online portal that summarizes and visualizes findings of all possible nine billion single nucleotide variants (SNVs) across the genome. It allows for rapid variant-, gene- and region-level queries of variant functional annotations. FAVOR integrates variant functional information from multiple sources to describe the functional characteristics of variants and facilitates prioritizing plausible causal variants influencing human phenotypes. Furthermore, we provide a scalable annotation tool, FAVORannotator, to functionally annotate large-scale WGS studies and efficiently store the genotype and their variant functional annotation data in a single file using the annotated Genomic Data Structure (aGDS) format, making downstream analysis more convenient.Abstract: Large biobank-scale whole genome sequencing (WGS) studies are rapidly identifying a multitude of coding and non-coding variants. They provide an unprecedented resource for illuminating the genetic basis of human diseases. Variant functional annotations play a critical role in WGS analysis, result interpretation, and prioritization of disease- or trait-associated causal variants. Existing functional annotation databases have limited scope to perform online queries and functionally annotate the genotype data of large biobank-scale WGS studies. We develop the Functional Annotation of Variants Online Resources (FAVOR) to meet these pressing needs. FAVOR provides a comprehensive multi-faceted variant functional annotation online portal that summarizes and visualizes findings of all possible nine billion single nucleotide variants (SNVs) across the genome. It allows for rapid variant-, gene- and region-level queries of variant functional annotations. FAVOR integrates variant functional information from multiple sources to describe the functional characteristics of variants and facilitates prioritizing plausible causal variants influencing human phenotypes. Furthermore, we provide a scalable annotation tool, FAVORannotator, to functionally annotate large-scale WGS studies and efficiently store the genotype and their variant functional annotation data in a single file using the annotated Genomic Data Structure (aGDS) format, making downstream analysis more convenient. FAVOR and FAVORannotator are available at https://favor.genohub.org . … (more)
- Is Part Of:
- Nucleic acids research. Volume 51:Issue D1(2023)
- Journal:
- Nucleic acids research
- Issue:
- Volume 51:Issue D1(2023)
- Issue Display:
- Volume 51, Issue 1 (2023)
- Year:
- 2023
- Volume:
- 51
- Issue:
- 1
- Issue Sort Value:
- 2023-0051-0001-0000
- Page Start:
- D1300
- Page End:
- D1311
- Publication Date:
- 2022-11-09
- Subjects:
- Nucleic acids -- Periodicals
Molecular biology -- Periodicals
572.805 - Journal URLs:
- http://nar.oxfordjournals.org/ ↗
http://www.ncbi.nlm.nih.gov/pmc/journals/4 ↗
http://ukcatalogue.oup.com/ ↗
http://firstsearch.oclc.org ↗ - DOI:
- 10.1093/nar/gkac966 ↗
- Languages:
- English
- ISSNs:
- 0305-1048
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6183.850000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26689.xml