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Filovirus RefSeq entries: evaluation and selection of filovirus type variants, type sequences, and names.


ABSTRACT: Sequence determination of complete or coding-complete genomes of viruses is becoming common practice for supporting the work of epidemiologists, ecologists, virologists, and taxonomists. Sequencing duration and costs are rapidly decreasing, sequencing hardware is under modification for use by non-experts, and software is constantly being improved to simplify sequence data management and analysis. Thus, analysis of virus disease outbreaks on the molecular level is now feasible, including characterization of the evolution of individual virus populations in single patients over time. The increasing accumulation of sequencing data creates a management problem for the curators of commonly used sequence databases and an entry retrieval problem for end users. Therefore, utilizing the data to their fullest potential will require setting nomenclature and annotation standards for virus isolates and associated genomic sequences. The National Center for Biotechnology Information's (NCBI's) RefSeq is a non-redundant, curated database for reference (or type) nucleotide sequence records that supplies source data to numerous other databases. Building on recently proposed templates for filovirus variant naming [ ()////-], we report consensus decisions from a majority of past and currently active filovirus experts on the eight filovirus type variants and isolates to be represented in RefSeq, their final designations, and their associated sequences.

SUBMITTER: Kuhn JH 

PROVIDER: S-EPMC4189044 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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Filovirus RefSeq entries: evaluation and selection of filovirus type variants, type sequences, and names.

Kuhn Jens H JH   Andersen Kristian G KG   Bào Yīmíng Y   Bavari Sina S   Becker Stephan S   Bennett Richard S RS   Bergman Nicholas H NH   Blinkova Olga O   Bradfute Steven S   Brister J Rodney JR   Bukreyev Alexander A   Chandran Kartik K   Chepurnov Alexander A AA   Davey Robert A RA   Dietzgen Ralf G RG   Doggett Norman A NA   Dolnik Olga O   Dye John M JM   Enterlein Sven S   Fenimore Paul W PW   Formenty Pierre P   Freiberg Alexander N AN   Garry Robert F RF   Garza Nicole L NL   Gire Stephen K SK   Gonzalez Jean-Paul JP   Griffiths Anthony A   Happi Christian T CT   Hensley Lisa E LE   Herbert Andrew S AS   Hevey Michael C MC   Hoenen Thomas T   Honko Anna N AN   Ignatyev Georgy M GM   Jahrling Peter B PB   Johnson Joshua C JC   Johnson Karl M KM   Kindrachuk Jason J   Klenk Hans-Dieter HD   Kobinger Gary G   Kochel Tadeusz J TJ   Lackemeyer Matthew G MG   Lackner Daniel F DF   Leroy Eric M EM   Lever Mark S MS   Mühlberger Elke E   Netesov Sergey V SV   Olinger Gene G GG   Omilabu Sunday A SA   Palacios Gustavo G   Panchal Rekha G RG   Park Daniel J DJ   Patterson Jean L JL   Paweska Janusz T JT   Peters Clarence J CJ   Pettitt James J   Pitt Louise L   Radoshitzky Sheli R SR   Ryabchikova Elena I EI   Saphire Erica Ollmann EO   Sabeti Pardis C PC   Sealfon Rachel R   Shestopalov Aleksandr M AM   Smither Sophie J SJ   Sullivan Nancy J NJ   Swanepoel Robert R   Takada Ayato A   Towner Jonathan S JS   van der Groen Guido G   Volchkov Viktor E VE   Volchkova Valentina A VA   Wahl-Jensen Victoria V   Warren Travis K TK   Warfield Kelly L KL   Weidmann Manfred M   Nichol Stuart T ST  

Viruses 20140926 9


Sequence determination of complete or coding-complete genomes of viruses is becoming common practice for supporting the work of epidemiologists, ecologists, virologists, and taxonomists. Sequencing duration and costs are rapidly decreasing, sequencing hardware is under modification for use by non-experts, and software is constantly being improved to simplify sequence data management and analysis. Thus, analysis of virus disease outbreaks on the molecular level is now feasible, including characte  ...[more]

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