Salmonella enterica is the second most reported bacterial cause of food-borne infections in europe. therefore molecular surveillance activities based on pathogen subtyping are an important measure of controlling Salmonellosis by public health agencies. In Germany, at the federal level, this work is carried out by the national Reference center for Salmonella and other Bacterial enteric pathogens (nRc). With rise of next generation sequencing techniques, the NRC has introduced whole-genome-based typing methods for S. enterica in 2016. In this study we report on the feasibility of genome-based in silico serotyping in the German setting using raw sequence reads. We found that SeqSero and seven gene MLST showed 98% and 95% concordance, respectively, with classical serotyping for the here evaluated serotypes, including the most common German serotypes S. enteritidis and S. typhimurium as well as less frequently found serotypes. the level of concordance increased to >99% when the results of both in silico methods were combined. However, both tools exhibited misidentification of monophasic variants, in particular monophasic S. Typhimurium and therefore need to be fine-tuned for reliable detection of this epidemiologically important variant. We conclude that with adjustments Salmonella genomebased serotyping might become the new gold standard.Subtyping of bacterial enteric pathogens, such as Salmonella enterica, traditionally relies on serotyping. The species Salmonella enterica is divided into six subspecies and consists of more than 2600 serovars, which are classified according to the White-Kauffmann-Le Minor Scheme 1 . Serotyping is based on determination of somatic O antigens and flagellin H antigens by reaction with specific antisera. Most S. enterica serovars have two alternately expressed H antigens, also referred to as 'phases' . The phase-1 and phase-2 flagellin proteins are encoded by fliC and fljB, respectively. The phase switch is regulated by the invertase hin and the fliC repressor gene fljA 2 . Therefore, the specific antigenic formula consists of three positions: the first position represents the O antigens, the second and third positions the two different flagellin H antigens. Each antigen position is separated by a colon, i.e. O:H1:H2. The antigenic formula for S. Typhimurium for example is accordingly 1,4,[5],12:i:1,2. There are variants of S. Typhimurium, which express only one flagellin and which therefore are referred to as monophasic S. Typhimurium. S. Enteritidis on the other hand does not possess a second flagellin per se, which is reflected in the antigenic formula: 1,9,12:g,m:-. It should be noted that some serovars share the same antigenic formula and require additional testing for unambiguous identification, e.g. the clinically important serovar S. Chloeraesuis shares its antigenic formula 6,7:c:1,5 with serovars S. Paratyphi C and S. Typhisuis. A differentiation is possible based on biochemical characteristics or PCR 3 .With rise of next generation sequencing (NGS) techniques, genomic typing ...