<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pankhurst LJ</submitter><funding>Medical Research Council</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Wellcome Trust</funding><pagination>49-58</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4698465</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Slow and cumbersome laboratory diagnostics for Mycobacterium tuberculosis complex (MTBC) risk delayed treatment and poor patient outcomes. Whole-genome sequencing (WGS) could potentially provide a rapid and comprehensive diagnostic solution. In this prospective study, we compare real-time WGS with routine MTBC diagnostic workflows.&lt;h4>Methods&lt;/h4>We compared sequencing mycobacteria from all newly positive liquid cultures with routine laboratory diagnostic workflows across eight laboratories in Europe and North America for diagnostic accuracy, processing times, and cost between Sept 6, 2013, and April 14, 2014. We sequenced specimens once using local Illumina MiSeq platforms and processed data centrally using a semi-automated bioinformatics pipeline. We identified species</pubmed_abstract><journal>The Lancet. Respiratory medicine</journal><pubmed_title>Rapid, comprehensive, and affordable mycobacterial diagnosis with whole-genome sequencing: a prospective study.</pubmed_title><pmcid>PMC4698465</pmcid><funding_grant_id>HPRU-2012-10080</funding_grant_id><funding_grant_id>MR/J011398/1</funding_grant_id><funding_grant_id>G0800778</funding_grant_id><funding_grant_id>NF-SI-0512-10047</funding_grant_id><funding_grant_id>098615</funding_grant_id><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>COMPASS-TB Study Group</pubmed_authors><pubmed_authors>Votintseva AA</pubmed_authors><pubmed_authors>Paul J</pubmed_authors><pubmed_authors>Niemann S</pubmed_authors><pubmed_authors>Wyllie D</pubmed_authors><pubmed_authors>Rogers TR</pubmed_authors><pubmed_authors>Fermont JM</pubmed_authors><pubmed_authors>Wilcox MH</pubmed_authors><pubmed_authors>Gascoyne-Binzi DM</pubmed_authors><pubmed_authors>Roycroft E</pubmed_authors><pubmed_authors>Supply P</pubmed_authors><pubmed_authors>Kong C</pubmed_authors><pubmed_authors>Walker TM</pubmed_authors><pubmed_authors>Kohl TA</pubmed_authors><pubmed_authors>Cole K</pubmed_authors><pubmed_authors>Wordsworth S</pubmed_authors><pubmed_authors>Del Ojo Elias C</pubmed_authors><pubmed_authors>Davies J</pubmed_authors><pubmed_authors>Lemaitre N</pubmed_authors><pubmed_authors>Smith EG</pubmed_authors><pubmed_authors>Tang P</pubmed_authors><pubmed_authors>Crook DW</pubmed_authors><pubmed_authors>Pankhurst LJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rapid, comprehensive, and affordable mycobacterial diagnosis with whole-genome sequencing: a prospective study.</name><description>&lt;h4>Background&lt;/h4>Slow and cumbersome laboratory diagnostics for Mycobacterium tuberculosis complex (MTBC) risk delayed treatment and poor patient outcomes. Whole-genome sequencing (WGS) could potentially provide a rapid and comprehensive diagnostic solution. In this prospective study, we compare real-time WGS with routine MTBC diagnostic workflows.&lt;h4>Methods&lt;/h4>We compared sequencing mycobacteria from all newly positive liquid cultures with routine laboratory diagnostic workflows across eight laboratories in Europe and North America for diagnostic accuracy, processing times, and cost between Sept 6, 2013, and April 14, 2014. We sequenced specimens once using local Illumina MiSeq platforms and processed data centrally using a semi-automated bioinformatics pipeline. We identified species</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2026-05-05T07:36:13.834Z</modification><creation>2019-03-27T02:06:08Z</creation></dates><accession>S-EPMC4698465</accession><cross_references><pubmed>26669893</pubmed><doi>10.1016/S2213-2600(15)00466-X</doi></cross_references></HashMap>