Ontology highlight
ABSTRACT:
PROVIDER: PRJNA393619 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR5816620_1.fastq.gz | Fastqsanger.gz | |||
| SRR5816620_2.fastq.gz | Fastqsanger.gz | |||
| SRR5816630_1.fastq.gz | Fastqsanger.gz | |||
| SRR5816630_2.fastq.gz | Fastqsanger.gz | |||
| SRR5816640_1.fastq.gz | Fastqsanger.gz |
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2021-10-15 | E-MTAB-9686 | biostudies-arrayexpress
Project description:In this study we developed metaproteomics based methods for quantifying taxonomic composition of microbiomes (microbial communities). We also compared metaproteomics based quantification to other quantification methods, namely metagenomics and 16S rRNA gene amplicon sequencing. The metagenomic and 16S rRNA data can be found in the European Nucleotide Archive (Study number: PRJEB19901). For the method development and comparison of the methods we analyzed three types of mock communities with all three methods. The communities contain between 28 to 32 species and strains of bacteria, archaea, eukaryotes and bacteriophage. For each community type 4 biological replicate communities were generated. All four replicates were analyzed by 16S rRNA sequencing and metaproteomics. Three replicates of each community type were analyzed with metagenomics. The "C" type communities have same cell/phage particle number for all community members (C1 to C4). The "P" type communities have the same protein content for all community members (P1 to P4). The "U" (UNEVEN) type communities cover a large range of protein amounts and cell numbers (U1 to U4). We also generated proteomic data for four pure cultures to test the specificity of the protein inference method. This data is also included in this submission.
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Project description:16S bacterial amplicon sequencing data for Guangzhou cohort
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