<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="Bee12" center_name="University of Illinois" accession="SRP005626">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP005626</PRIMARY_ID>
      <SUBMITTER_ID namespace="University of Illinois">Bee12</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Transcriptomic data for 12 bee species.</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>mRNA from 12 bee species was extracted and sequenced on a GS-FLX platform. The resulting EST sequences were assembled using phrap to produce a non-redundant EST dataset for each of the species.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Bee12</CENTER_PROJECT_NAME>
      <STUDY_DESCRIPTION>Bees used for sequencing were free-flying or collected from nests. They were placed directly into liquid Nitrogen for RNA preservation. *Different ages, behavioral groups, and castes (when applicable) were used to maximize transcript diversity. RNA was extracted from brains and abdomens of 50  females per species. *Pooled mRNA (90% brain, 10% abdomen) was sequenced by 454 Life Science/Roche platform on the GS-FLX platform. EST reads were assembled using Phrap to generate species-specific, non-redundant contigs and singletons.</STUDY_DESCRIPTION>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
