<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<SAMPLE_SET>
    <SAMPLE accession="DRS026763" center_name="TOTTORI" alias="DRS026763">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00026080</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>6211</TAXON_ID>
            <SCIENTIFIC_NAME>Echinococcus multilocularis</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Activated eggs [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>The hatched eggs were activated with 1% pancreatin, 1% fresh pig bile and 0.2% Na2CO3 in RPMI 1640 at 38 degree C for 20 min, and cultivated at 38 degree C for 24 hr RPMI 1640 with fetal calf serum. The RNA were extracted from these activated and incubated eggs using Trizol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Activated eggs [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>geo_loc_name</TAG>
                <VALUE>Japan: Hokkaido</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3524</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS026764" center_name="TOTTORI" alias="DRS026764">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00026081</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>6211</TAXON_ID>
            <SCIENTIFIC_NAME>Echinococcus multilocularis</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Four weeks old larvae [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Small lesions with the early stage larvae were collected from the liver of DBA/2 mice at 4 weeks after the oral infection with eggs. The RNA were extracted from the small lesions with the early stage larvae using Trizol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Four weeks old larvae [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>geo_loc_name</TAG>
                <VALUE>Japan: Hokkaido</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3524</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS026765" center_name="TOTTORI" alias="DRS026765">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00026082</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>6211</TAXON_ID>
            <SCIENTIFIC_NAME>Echinococcus multilocularis</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>In vitro-cultured small vesicles [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Cyst mass of metacestodes from a DBA/2 mouse  were cut into small pieces and cultured in RPMI 1640 with fetal calf serum. Miniature cyst developed to small vesicles (2-4 mm in diameter) after several weeks. These small vesicles did not showed any brood capsules or protoscoleces. The RNA were extracted from these small vesicles using Trizol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>In vitro-cultured small vesicles [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>geo_loc_name</TAG>
                <VALUE>Japan: Hokkaido</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3524</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS026766" center_name="TOTTORI" alias="DRS026766">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00026083</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>6211</TAXON_ID>
            <SCIENTIFIC_NAME>Echinococcus multilocularis</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Nonactivated eggs [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Feces with eggs were collected from infected dogs at 35 days after infection. Eggs were isolated from the feces by filtering by mesh, natural sedimentation and flotation with sugar solution. The isolated eggs were treated with 3% sodium hypochlorite for the removal of embryophore and sterilization. The RNA were extracted from these hatched eggs using Trizol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Nonactivated eggs [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>geo_loc_name</TAG>
                <VALUE>Japan: Hokkaido</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3524</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS032367" center_name="TOTTORI" alias="DRS032367">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00054236</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>6211</TAXON_ID>
            <SCIENTIFIC_NAME>Echinococcus multilocularis</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>Nonactivated eggs No6  [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>label</TAG>
                <VALUE>No6</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>Nonactivated eggs  No6 [Echinococcus multilocularis RNAseq]</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>geo_loc_name</TAG>
                <VALUE>Japan:Hokkaido</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Feces with eggs were collected from infected dogs at 35 days after infection. Eggs were isolated from the feces by filtering by mesh, natural sedimentation and flotation with sugar solution. The isolated eggs were treated with 3% sodium hypochlorite for the removal of embryophore and sterilization. The RNA were extracted from these hatched eggs using Trizol.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB3524</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
</SAMPLE_SET>
