<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE345nnn/GSE345400/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Bemisia tabaci</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE345400</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic analysis of Bemisia tabaci MED adults exposed to soybean-derived lecithin</name><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.</description><dates><publication>2026/09/02</publication></dates><accession>GSE345400</accession><cross_references><GSM>GSM10002719</GSM><GSM>GSM10002718</GSM><GSM>GSM10002720</GSM><GSM>GSM10002723</GSM><GSM>GSM10002722</GSM><GSM>GSM10002721</GSM><GPL>37448</GPL><GSE>345400</GSE><taxon>Bemisia tabaci</taxon></cross_references></HashMap>