Results 31 to 40 of about 108,343 (213)
WGS-derived MLVA profiles extracted with MLVAtype without taking into account the MNTR value.
Mismatches between WGS- and Sanger-derived values are indicated in bold. n/a: not applicable. Read lengths obtained with DRC and Ugandan isolates were 300 and 150 nt, respectively.
O. Colin Stine (7444409) +6 more
core +1 more source
Preferences for the provision of whole genome sequencing services among young adults. [PDF]
OBJECTIVES:As whole genome sequencing (WGS) becomes increasingly available, clinicians will be faced with conveying complex information to individuals at different stages in life.
Christopher H Wade, Kailyn R Elliott
doaj +1 more source
Budućnost cjelogenomskog sekvenciranja u pedijatriji
Sekvenciranje cijeloga genoma (eng. Whole genome sequencing – WGS) postaje sve zastupljeniji genetički dijagnostički test u svakodnevnoj kliničkoj praksi. Inicijativa za medicinski genom (eng.
Petar Brlek, Dragan Primorac
doaj +1 more source
BACKGROUND: Multidrug- and extensively drug-resistant strains of Mycobacterium tuberculosis complex (MTBC) remain a significant global health challenge.
A. Ghodousi +6 more
doaj +1 more source
Sup. Table 6 Tissue specific variants WGS.
Sup. Table 6 Tissue specific variants WGS.
Markus Grosch (14303462)
core +1 more source
Human infections with Brucella melitensis are occasionally reported in Sweden, despite the fact that the national flocks of sheep and goats are officially free from brucellosis. The aim of our study was to analyze 103 isolates of B.
Lorena Sacchini +6 more
doaj +1 more source
BACKGROUND: Molecular typing of Mycobacterium tuberculosis isolates provides insight into TB transmission by identifying clustering isolates. However, clustering alone does not necessarily indicate ongoing in-country transmission, as infections may have ...
W. Frederiks, R.M. Anthony, G. de Vries
doaj +1 more source
Compound heterozygosity as a cause of diagnostic difficulties in patients with hereditary diseases
Background. Up to 40 % of patients with suspected monogenic disorders remain undiagnosed when using targeted gene panels or exome sequencing, particularly in cases of compound heterozygosity where one pathogenic variant goes undetected.The aim.
M. E. Lobanov +9 more
doaj +1 more source

