<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<SAMPLE_SET>
    <SAMPLE accession="DRS019017" center_name="KYOTO_SC" alias="DRS019017">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018750</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>F2C_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>fertilized 2-cell embryos</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>F2C_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019018" center_name="KYOTO_SC" alias="DRS019018">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018751</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>F2C_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>fertilized 2-cell embryos</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>F2C_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
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    <SAMPLE accession="DRS019019" center_name="KYOTO_SC" alias="DRS019019">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018752</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>F2C_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>fertilized 2-cell embryos</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>F2C_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019020" center_name="KYOTO_SC" alias="DRS019020">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018753</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>F2C_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>fertilized 2-cell embryos</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>F2C_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
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    <SAMPLE accession="DRS019021" center_name="KYOTO_SC" alias="DRS019021">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018754</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>MII_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>MII oocyte</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>MII_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019022" center_name="KYOTO_SC" alias="DRS019022">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018755</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>MII_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>MII oocyte</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>MII_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019023" center_name="KYOTO_SC" alias="DRS019023">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018756</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>MII_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>MII oocyte</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>MII_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019024" center_name="KYOTO_SC" alias="DRS019024">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00018757</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>MII_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>host_body_site</TAG>
                <VALUE>MII oocyte</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer?fs instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>MII_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019025" center_name="KYOTO_SC" alias="DRS019025">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023316</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>siC_morula_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>siC_morula_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019026" center_name="KYOTO_SC" alias="DRS019026">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023317</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>siC_morula_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>siC_morula_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019027" center_name="KYOTO_SC" alias="DRS019027">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023318</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>siC_morula_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>siC_morula_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019028" center_name="KYOTO_SC" alias="DRS019028">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023319</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>siC_morula_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>siC_morula_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019029" center_name="KYOTO_SC" alias="DRS019029">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023320</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>si_pIl_morula_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>si_pIl_morula_1</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019030" center_name="KYOTO_SC" alias="DRS019030">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023321</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>si_pIl_morula_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>si_pIl_morula_2</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019031" center_name="KYOTO_SC" alias="DRS019031">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023322</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>si_pIl_morula_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>si_pIl_morula_3</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
    <SAMPLE accession="DRS019032" center_name="KYOTO_SC" alias="DRS019032">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioSample ID">SAMD00023323</PRIMARY_ID>
        </IDENTIFIERS>
        <SAMPLE_NAME>
            <TAXON_ID>10090</TAXON_ID>
            <SCIENTIFIC_NAME>Mus musculus</SCIENTIFIC_NAME>
        </SAMPLE_NAME>
        <SAMPLE_ATTRIBUTES>
            <SAMPLE_ATTRIBUTE>
                <TAG>strain</TAG>
                <VALUE>C57BL/6 X ICR</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_title</TAG>
                <VALUE>si_pIl_morula_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>description</TAG>
                <VALUE>Total RNA and polyA+ RNA were extracted from pools, each of which contained one hundred MII oocytes or 2-cell embryos (C57BL/6 X ICR), by using a Dynabeads mRNA DIRECT Micro Kit (Invitrogen). Four replicates were made for directional RNA-seq library construction by using an NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB). In this library preparation, cDNAs were enriched by 15-cycle PCR. Illumina HiSeq 2000 was used to perform 50-bp single-end sequencing according to the manufacturer's instructions.</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>isolate</TAG>
                <VALUE>Dynabeads</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>sample_name</TAG>
                <VALUE>si_pIl_morula_4</VALUE>
            </SAMPLE_ATTRIBUTE>
            <SAMPLE_ATTRIBUTE>
                <TAG>bioproject_id</TAG>
                <VALUE>PRJDB2994</VALUE>
            </SAMPLE_ATTRIBUTE>
        </SAMPLE_ATTRIBUTES>
    </SAMPLE>
</SAMPLE_SET>
