Project description:Next-Generation-Sequencing (NGS) technologies have led to important improvement in the detection of new or unrecognized infective agents, related to infectious diseases. In this context, NGS high-throughput technology can be used to achieve a comprehensive and unbiased sequencing of the nucleic acids present in a clinical sample (i.e. tissues). Metagenomic shotgun sequencing has emerged as powerful high-throughput approaches to analyze and survey microbial composition in the field of infectious diseases. By directly sequencing millions of nucleic acid molecules in a sample and matching the sequences to those available in databases, pathogens of an infectious disease can be inferred. Despite the large amount of metagenomic shotgun data produced, there is a lack of a comprehensive and easy-use pipeline for data analysis that avoid annoying and complicated bioinformatics steps. Here we present HOME-BIO, a modular and exhaustive pipeline for analysis of biological entity estimation, specific designed for shotgun sequenced clinical samples. HOME-BIO analysis provides comprehensive taxonomy classification by querying different source database and carry out main steps in metagenomic investigation. HOME-BIO is a powerful tool in the hand of biologist without computational experience, which are focused on metagenomic analysis. Its easy-to-use intrinsic characteristic allows users to simply import raw sequenced reads file and obtain taxonomy profile of their samples.
Project description:Sulfoquinovose (SQ) is a major organosulfonate in nature, and thus plays an important role in the biogeochemical sulfur and carbon cycles. We identified a bacterial anaerobic consortium, enriched from lake Konstanz, which degraded SQ to isethionate as intermediate and further into acetate and sulfide. By a metagenomic analysis we identified Faecalicatena sp. DSM22707 as major SQ-degrader in the consortium. Strain DSM22707 degraded SQ in pure culture into isethionate and small amounts of sulfolactate.
2025-05-07 | PXD055296 | Pride
Project description:Methanotrophic bacteria consortium Targeted loci cultured
| PRJNA395142 | ENA
Project description:16S rRNA gene amplicon sequencing of simplified methanotrophic consortium and its initial consortium
Project description:Using Sst and parvalbumin subtype-specific fluorescence activated cell sorting (FACS) and RNA sequencing we identify distinct transcriptome profiles for these interneuron subtypes in the medial PFC. Chronic stress causes significant dysregulation of several key pathways, including sex specific differences in the SST interneuron profiles.
