{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE345nnn/GSE345400/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Bemisia tabaci"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE345400"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Transcriptomic analysis of Bemisia tabaci MED adults exposed to soybean-derived lecithin","description":"This study performed transcriptome sequencing of Bemisia tabaci MED adults (provided by Professor Youjun Zhang) treated with soybean-derived lecithin and a water control. Six samples (three per group) were sequenced, yielding a total of 42.74 Gb of clean data (ranging from 6.76 to 7.36 Gb per sample). Q30 bases ranged from 92.89% to 93.10%, and the average GC content was 41.20%. Clean reads were mapped to the B. tabaci reference genome (NCBI Assembly ASM185493v1), with overall alignment rates ranging from 81.08% to 82.58%. Differential expression analysis (DESeq2) identified a total of 135 differentially expressed genes (DEGs) between the lecithin treatment and control groups.","dates":{"publication":"2026/09/02"},"accession":"GSE345400","cross_references":{"GSM":["GSM10002719","GSM10002718","GSM10002720","GSM10002723","GSM10002722","GSM10002721"],"GPL":["37448"],"GSE":["345400"],"taxon":["Bemisia tabaci"]}}