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GENCODE is a scientific project in genome research and part of the ENCODE (ENCyclopedia Of DNA Elements) scale-up project.. The GENCODE consortium was initially formed as part of the pilot phase of the ENCODE project to identify and map all protein-coding genes within the ENCODE regions (approx. 1% of Human genome). [2]
The CCDS dataset is an integral part of the GENCODE gene annotation project [11] and it is used as a standard for high-quality coding exon definition in various research fields, including clinical studies, large-scale epigenomic studies, exome projects and exon array design. [3]
v10–v19 Persons with potential health hazards related to personal and family history V10 Personal history of malignant neoplasm (i.e. cancer) V11 Personal history of mental disorder; V12 Personal history of certain other diseases; V13 Personal history of other diseases; V14 Personal history of allergy to medicinal agents
Several projects to improve RefSeq services are currently in development by the NCBI, often in collaboration with research centers such as EMBL-EBI: . Consensus CDS (CCDS): This project aims to identify a core set of human and mouse protein-coding regions and standardize sets of genes with high and consistent levels of genomic annotation quality.
V19, a family history of other conditions, in the ICD-9 V codes Topics referred to by the same term This disambiguation page lists articles associated with the same title formed as a letter–number combination.
The Encyclopedia of DNA Elements (ENCODE) is a public research project which aims "to build a comprehensive parts list of functional elements in the human genome." [2]ENCODE also supports further biomedical research by "generating community resources of genomics data, software, tools and methods for genomics data analysis, and products resulting from data analyses and interpretations."
This page was last edited on 12 September 2021, at 07:01 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Haplogroup V is a relatively rare mtDNA haplogroup, occurring in around 4% of native Europeans. [5] Its highest concentration is among the Saami people of northern Fennoscandia (~59%).