<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>531</volume><submitter>Maurier F</submitter><funding>Lille Hospital University</funding><pubmed_abstract>Genome sequencing of virus has become a useful tool for better understanding of virus pathogenicity and epidemiological surveillance. Obtaining virus genome sequence directly from clinical samples is still a challenging task due to the low load of virus genetic material compared to the host DNA, and to the difficulty to get an accurate genome assembly. Here we introduce a complete sequencing and analyzing protocol called V-ASAP for Virus Amplicon Sequencing Assembly Pipeline. Our protocol is able to generate the viral dominant genome sequence starting from clinical samples. It is based on a multiplex PCR amplicon sequencing coupled with a reference-free analytical pipeline. This protocol was applied to 11 clinical samples infected with coronavirus OC43 (HcoV-OC43), and led to seven complet</pubmed_abstract><journal>Virology</journal><pagination>141-148</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7112119</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A complete protocol for whole-genome sequencing of virus from clinical samples: Application to coronavirus OC43.</pubmed_title><pmcid>PMC7112119</pmcid><pubmed_authors>Varre JS</pubmed_authors><pubmed_authors>Touzet H</pubmed_authors><pubmed_authors>Caboche S</pubmed_authors><pubmed_authors>Beury D</pubmed_authors><pubmed_authors>Flechon L</pubmed_authors><pubmed_authors>Maurier F</pubmed_authors><pubmed_authors>Hot D</pubmed_authors><pubmed_authors>Goffard A</pubmed_authors></additional><is_claimable>false</is_claimable><name>A complete protocol for whole-genome sequencing of virus from clinical samples: Application to coronavirus OC43.</name><description>Genome sequencing of virus has become a useful tool for better understanding of virus pathogenicity and epidemiological surveillance. Obtaining virus genome sequence directly from clinical samples is still a challenging task due to the low load of virus genetic material compared to the host DNA, and to the difficulty to get an accurate genome assembly. Here we introduce a complete sequencing and analyzing protocol called V-ASAP for Virus Amplicon Sequencing Assembly Pipeline. Our protocol is able to generate the viral dominant genome sequence starting from clinical samples. It is based on a multiplex PCR amplicon sequencing coupled with a reference-free analytical pipeline. This protocol was applied to 11 clinical samples infected with coronavirus OC43 (HcoV-OC43), and led to seven complet</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May</publication><modification>2026-04-28T22:39:35.18Z</modification><creation>2020-05-22T18:54:25Z</creation></dates><accession>S-EPMC7112119</accession><cross_references><pubmed>30878524</pubmed><doi>10.1016/j.virol.2019.03.006</doi></cross_references></HashMap>