<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/GSE338nnn/GSE338396/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Arabidopsis thaliana</species><gds_type>Methylation profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE338396</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Protocol for low-input whole-genome bisulfite sequencing in plants</name><description>DNA methylation profiling of rare plant samples is limited by the scarcity of input DNA. This protocol uses Arabidopsis leaf to describe tissue cryo-milling, proteinase K lysis, direct bisulfite conversion, post-bisulfite adapter tagging library construction with random priming and adapter ligation, and MethylStar-based alignment and methylation calling. DNA inputs as low as 50 pg generate methylomes comparable to conventional 50-ng WGBS.</description><dates><publication>2026/07/13</publication></dates><accession>GSE338396</accession><cross_references><GSM>GSM9872896</GSM><GSM>GSM9872897</GSM><GSM>GSM9872895</GSM><GSM>GSM9872900</GSM><GSM>GSM9872911</GSM><GSM>GSM9872912</GSM><GSM>GSM9872901</GSM><GSM>GSM9872898</GSM><GSM>GSM9872899</GSM><GSM>GSM9872910</GSM><GSM>GSM9872904</GSM><GSM>GSM9872905</GSM><GSM>GSM9872902</GSM><GSM>GSM9872903</GSM><GSM>GSM9872908</GSM><GSM>GSM9872909</GSM><GSM>GSM9872906</GSM><GSM>GSM9872907</GSM><GPL>34544</GPL><GSE>338396</GSE><taxon>Arabidopsis thaliana</taxon></cross_references></HashMap>