<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR846/009/SRR8468999/SRR8468999_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR846/009/SRR8468999/SRR8468999_1.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>INRA</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA516327</full_dataset_link><tag>xref:EuropePMC:PMC7658807</tag><long_description>The M. truncatula api mutant exhibits developmental (root hair) and symbiotic (altered infection by Sinorhizobium meliloti) phenotypes (Teillet et al 2008, Mol Plant Microbe Interact. 21:535-46. doi: 10.1094/MPMI-21-5-0535). Genetic analysis indicated that a single recessive mutation controlled the observed phenotype and located the mutation to a 500 kb interval on M. truncatula chromosome 4. To identify a candidate mutation in this interval controlling the api phenotype , the genome of an api mutant is sequenced by Illumina technology.</long_description><repository>ENA</repository><description_synonyms>AAP, YSC1, ALPHA-2-PI, A2AP., API, LAP4, PLI</description_synonyms></additional><is_claimable>false</is_claimable><name></name><description>API mutant sequencing</description><dates><last_updated>2023-05-19</last_updated><first_public>2020-02-22</first_public></dates><accession>PRJNA516327</accession><cross_references/></HashMap>