GSM3552955: ko_heart_0; Mus musculus; RNA-Seq

SRX5213466 GSM3552955 GSM3552955: ko_heart_0; Mus musculus; RNA-Seq SRP176442 SRS4217498 GSM3552955 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552955 GSM3552955 GEO Accession GSM3552955 SRX5213467 GSM3552956 GSM3552956: wt_heart_1; Mus musculus; RNA-Seq SRP176442 SRS4217499 GSM3552956 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552956 GSM3552956 GEO Accession GSM3552956 SRX5213468 GSM3552957 GSM3552957: ko_heart_1; Mus musculus; RNA-Seq SRP176442 SRS4217500 GSM3552957 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552957 GSM3552957 GEO Accession GSM3552957 SRX5213469 GSM3552958 GSM3552958: ko_heart_2; Mus musculus; RNA-Seq SRP176442 SRS4217501 GSM3552958 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552958 GSM3552958 GEO Accession GSM3552958 SRX5213470 GSM3552959 GSM3552959: wt_heart_2; Mus musculus; RNA-Seq SRP176442 SRS4217502 GSM3552959 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552959 GSM3552959 GEO Accession GSM3552959 SRX5213471 GSM3552960 GSM3552960: wt_heart_0; Mus musculus; RNA-Seq SRP176442 SRS4217503 GSM3552960 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552960 GSM3552960 GEO Accession GSM3552960 SRX5213472 GSM3552961 GSM3552961: wt_liver_0; Mus musculus; RNA-Seq SRP176442 SRS4217504 GSM3552961 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552961 GSM3552961 GEO Accession GSM3552961 SRX5213473 GSM3552962 GSM3552962: wt_liver_1; Mus musculus; RNA-Seq SRP176442 SRS4217505 GSM3552962 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552962 GSM3552962 GEO Accession GSM3552962 SRX5213474 GSM3552963 GSM3552963: ko_liver_0; Mus musculus; RNA-Seq SRP176442 SRS4217506 GSM3552963 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552963 GSM3552963 GEO Accession GSM3552963 SRX5213475 GSM3552964 GSM3552964: ko_liver_1; Mus musculus; RNA-Seq SRP176442 SRS4217507 GSM3552964 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552964 GSM3552964 GEO Accession GSM3552964 SRX5213476 GSM3552965 GSM3552965: wt_liver_2; Mus musculus; RNA-Seq SRP176442 SRS4217508 GSM3552965 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552965 GSM3552965 GEO Accession GSM3552965 SRX5213477 GSM3552966 GSM3552966: ko_liver_2; Mus musculus; RNA-Seq SRP176442 SRS4217509 GSM3552966 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552966 GSM3552966 GEO Accession GSM3552966 SRX5213478 GSM3552967 GSM3552967: ko_spleen_2; Mus musculus; RNA-Seq SRP176442 SRS4217510 GSM3552967 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552967 GSM3552967 GEO Accession GSM3552967 SRX5213479 GSM3552968 GSM3552968: wt_spleen_1; Mus musculus; RNA-Seq SRP176442 SRS4217511 GSM3552968 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552968 GSM3552968 GEO Accession GSM3552968 SRX5213480 GSM3552969 GSM3552969: ko_spleen_0; Mus musculus; RNA-Seq SRP176442 SRS4217512 GSM3552969 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552969 GSM3552969 GEO Accession GSM3552969 SRX5213481 GSM3552970 GSM3552970: ko_spleen_1; Mus musculus; RNA-Seq SRP176442 SRS4217513 GSM3552970 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552970 GSM3552970 GEO Accession GSM3552970 SRX5213482 GSM3552971 GSM3552971: wt_spleen_2; Mus musculus; RNA-Seq SRP176442 SRS4217514 GSM3552971 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552971 GSM3552971 GEO Accession GSM3552971 SRX5213483 GSM3552972 GSM3552972: wt_spleen_0; Mus musculus; RNA-Seq SRP176442 SRS4217515 GSM3552972 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552972 GSM3552972 GEO Accession GSM3552972 SRX5213484 GSM3552973 GSM3552973: ko_eye_2; Mus musculus; RNA-Seq SRP176442 SRS4217516 GSM3552973 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552973 GSM3552973 GEO Accession GSM3552973 SRX5213485 GSM3552974 GSM3552974: wt_eye_1; Mus musculus; RNA-Seq SRP176442 SRS4217517 GSM3552974 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552974 GSM3552974 GEO Accession GSM3552974 SRX5213486 GSM3552975 GSM3552975: ko_eye_0; Mus musculus; RNA-Seq SRP176442 SRS4217518 GSM3552975 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552975 GSM3552975 GEO Accession GSM3552975 SRX5213487 GSM3552976 GSM3552976: ko_eye_1; Mus musculus; RNA-Seq SRP176442 SRS4217519 GSM3552976 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552976 GSM3552976 GEO Accession GSM3552976 SRX5213488 GSM3552977 GSM3552977: wt_eye_2; Mus musculus; RNA-Seq SRP176442 SRS4217520 GSM3552977 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552977 GSM3552977 GEO Accession GSM3552977 SRX5213489 GSM3552978 GSM3552978: wt_eye_0; Mus musculus; RNA-Seq SRP176442 SRS4217521 GSM3552978 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552978 GSM3552978 GEO Accession GSM3552978 SRX5213490 GSM3552979 GSM3552979: ko_prostate_0; Mus musculus; RNA-Seq SRP176442 SRS4217522 GSM3552979 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552979 GSM3552979 GEO Accession GSM3552979 SRX5213491 GSM3552980 GSM3552980: ko_prostate_1; Mus musculus; RNA-Seq SRP176442 SRS4217523 GSM3552980 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552980 GSM3552980 GEO Accession GSM3552980 SRX5213492 GSM3552981 GSM3552981: wt_prostate_0; Mus musculus; RNA-Seq SRP176442 SRS4217524 GSM3552981 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552981 GSM3552981 GEO Accession GSM3552981 SRX5213493 GSM3552982 GSM3552982: wt_prostate_1; Mus musculus; RNA-Seq SRP176442 SRS4217525 GSM3552982 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552982 GSM3552982 GEO Accession GSM3552982 SRX5213494 GSM3552983 GSM3552983: wt_prostate_2; Mus musculus; RNA-Seq SRP176442 SRS4217526 GSM3552983 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552983 GSM3552983 GEO Accession GSM3552983 SRX5213495 GSM3552984 GSM3552984: wt_mef_0; Mus musculus; RNA-Seq SRP176442 SRS4217527 GSM3552984 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2000 gds 303552984 GSM3552984 GEO Accession GSM3552984 SRX5213496 GSM3552985 GSM3552985: wt_mef_1; Mus musculus; RNA-Seq SRP176442 SRS4217528 GSM3552985 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2000 gds 303552985 GSM3552985 GEO Accession GSM3552985 SRX5213497 GSM3552986 GSM3552986: wt_mef_2; Mus musculus; RNA-Seq SRP176442 SRS4217529 GSM3552986 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2000 gds 303552986 GSM3552986 GEO Accession GSM3552986 SRX5213498 GSM3552987 GSM3552987: ko_mef_0; Mus musculus; RNA-Seq SRP176442 SRS4217530 GSM3552987 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2000 gds 303552987 GSM3552987 GEO Accession GSM3552987 SRX5213499 GSM3552988 GSM3552988: ko_mef_1; Mus musculus; RNA-Seq SRP176442 SRS4217531 GSM3552988 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2000 gds 303552988 GSM3552988 GEO Accession GSM3552988 SRX5213500 GSM3552989 GSM3552989: ko_mef_2; Mus musculus; RNA-Seq SRP176442 SRS4217532 GSM3552989 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2000 gds 303552989 GSM3552989 GEO Accession GSM3552989 SRX5213501 GSM3552990 GSM3552990: WT-L223-61_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217533 GSM3552990 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552990 GSM3552990 GEO Accession GSM3552990 SRX5213502 GSM3552991 GSM3552991: KO-63_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217534 GSM3552991 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552991 GSM3552991 GEO Accession GSM3552991 SRX5213503 GSM3552992 GSM3552992: R-8_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217535 GSM3552992 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552992 GSM3552992 GEO Accession GSM3552992 SRX5213504 GSM3552993 GSM3552993: WT-L233-47_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217536 GSM3552993 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552993 GSM3552993 GEO Accession GSM3552993 SRX5213505 GSM3552994 GSM3552994: KO-9_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217537 GSM3552994 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552994 GSM3552994 GEO Accession GSM3552994 SRX5213506 GSM3552995 GSM3552995: WT-L233-65_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217538 GSM3552995 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552995 GSM3552995 GEO Accession GSM3552995 SRX5213507 GSM3552996 GSM3552996: KO-1_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217539 GSM3552996 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552996 GSM3552996 GEO Accession GSM3552996 SRX5213508 GSM3552997 GSM3552997: Tug1-WT_L15-73_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217540 GSM3552997 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552997 GSM3552997 GEO Accession GSM3552997 SRX5213509 GSM3552998 GSM3552998: Tug1-KO_L14-65_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217541 GSM3552998 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552998 GSM3552998 GEO Accession GSM3552998 SRX5213510 GSM3552999 GSM3552999: Tug1-Rescue_34_G2_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217542 GSM3552999 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303552999 GSM3552999 GEO Accession GSM3552999 SRX5213511 GSM3553000 GSM3553000: Tug1-Rescue_88_G3_Testis; Mus musculus; RNA-Seq SRP176442 SRS4217543 GSM3553000 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553000 GSM3553000 GEO Accession GSM3553000 SRX5213512 GSM3553001 GSM3553001: C57BL/6J.WT_Cast.WT_testes_0; Mus musculus; RNA-Seq SRP176442 SRS4217544 GSM3553001 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553001 GSM3553001 GEO Accession GSM3553001 SRX5213513 GSM3553002 GSM3553002: C57BL/6J.WT_Cast.WT_testes_1; Mus musculus; RNA-Seq SRP176442 SRS4217545 GSM3553002 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553002 GSM3553002 GEO Accession GSM3553002 SRX5213514 GSM3553003 GSM3553003: C57BL/6J.WT_Cast.WT_testes_2; Mus musculus; RNA-Seq SRP176442 SRS4217546 GSM3553003 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553003 GSM3553003 GEO Accession GSM3553003 SRX5213515 GSM3553004 GSM3553004: C57BL/6J.Tug1KO_Cast.WT_testes_0; Mus musculus; RNA-Seq SRP176442 SRS4217547 GSM3553004 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553004 GSM3553004 GEO Accession GSM3553004 SRX5213516 GSM3553005 GSM3553005: C57BL/6J.Tug1KO_Cast.WT_testes_1; Mus musculus; RNA-Seq SRP176442 SRS4217548 GSM3553005 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553005 GSM3553005 GEO Accession GSM3553005 SRX5213517 GSM3553006 GSM3553006: C57BL/6J.Tug1KO_Cast.WT_testes_2; Mus musculus; RNA-Seq SRP176442 SRS4217549 GSM3553006 RNA-Seq TRANSCRIPTOMIC cDNA Tissues were harvested immediately after euthanasia, snap frozen in liquid nitrogen and stored at -80˚C. Tissues were subsequently pulverized in liquid nitrogen and homogenized in TRIzol. Embryonic Mouse Fibroblasts (MEF, passage 2) and mouse embryonic stem cells (ESC) were cultured in 10cm dishes in normal conditions (37˚C, 5% CO2) and homogenized directly in Trizol. Standard illumina protocols were used to make libraries (TruSeq RNA Sample Preparation Kit v2) Illumina HiSeq 2500 gds 303553006 GSM3553006 GEO Accession GSM3553006