SRX1134694 GSM1845088 SRP062097 PRJNA292069 SRS1026767 SAMN03979101 ChIP-Seq GENOMIC ChIP Genomic DNA was isolated from control sh ovaries, sheared to average 400bp, size selected to 200-600bp, cloned and sequenced (paired-end 100nts) gDNA-seq library was generated using the NEBNext Ultra DNA Library Prep Kit for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845088 GSM1845088 GEO Accession GSM1845088 SRX1134695 GSM1845089 SRP062097 PRJNA292069 SRS1026766 SAMN03979102 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845089 GSM1845089 GEO Accession GSM1845089 SRX1134696 GSM1845090 SRP062097 PRJNA292069 SRS1026765 SAMN03979103 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845090 GSM1845090 GEO Accession GSM1845090 SRX1134697 GSM1845091 SRP062097 PRJNA292069 SRS1026764 SAMN03979104 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845091 GSM1845091 GEO Accession GSM1845091 SRX1134698 GSM1845092 SRP062097 PRJNA292069 SRS1026763 SAMN03979105 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845092 GSM1845092 GEO Accession GSM1845092 SRX1134699 GSM1845093 SRP062097 PRJNA292069 SRS1026762 SAMN03979106 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845093 GSM1845093 GEO Accession GSM1845093 SRX1134700 GSM1845094 SRP062097 PRJNA292069 SRS1026761 SAMN03979107 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845094 GSM1845094 GEO Accession GSM1845094 SRX1134701 GSM1845095 SRP062097 PRJNA292069 SRS1026760 SAMN03979108 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845095 GSM1845095 GEO Accession GSM1845095 SRX1134702 GSM1845096 SRP062097 PRJNA292069 SRS1026759 SAMN03979109 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845096 GSM1845096 GEO Accession GSM1845096 SRX1134703 GSM1845097 SRP062097 PRJNA292069 SRS1026758 SAMN03979110 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845097 GSM1845097 GEO Accession GSM1845097 SRX1134704 GSM1845098 SRP062097 PRJNA292069 SRS1026757 SAMN03979078 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845098 GSM1845098 GEO Accession GSM1845098 SRX1134705 GSM1845099 SRP062097 PRJNA292069 SRS1026756 SAMN03979079 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845099 GSM1845099 GEO Accession GSM1845099 SRX1134706 GSM1845100 SRP062097 PRJNA292069 SRS1026755 SAMN03979080 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845100 GSM1845100 GEO Accession GSM1845100 SRX1134707 GSM1845101 SRP062097 PRJNA292069 SRS1026754 SAMN03979052 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845101 GSM1845101 GEO Accession GSM1845101 SRX1134708 GSM1845102 SRP062097 PRJNA292069 SRS1026753 SAMN03979053 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845102 GSM1845102 GEO Accession GSM1845102 SRX1134709 GSM1845103 SRP062097 PRJNA292069 SRS1026752 SAMN03979054 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845103 GSM1845103 GEO Accession GSM1845103 SRX1134710 GSM1845104 SRP062097 PRJNA292069 SRS1026751 SAMN03979055 ChIP-Seq GENOMIC ChIP ChIP-seq was performed according to Lee et al, Nat Protoc, 2006 ChIP-seq libraries were generated using the NEBNext™ DNA Sample Prep Reagent Set 1 for Illumina (NEB) and the Kapa HiFi Library Amp Real-Time Kit (Peqlab) for amplification. Illumina HiSeq 2000 gds 301845104 GSM1845104 GEO Accession GSM1845104 SRX1134711 GSM1845105 SRP062097 PRJNA292069 SRS1026750 SAMN03979056 RNA-Seq TRANSCRIPTOMIC cDNA RNA-seq was performed according to Zhang et al, Silence, 2012 Total RNA was extracted using Trizol and polA RNA was purified with oligo-dT beads. For 2nd strand synthesis, dUTP was added to generate stranded libraries using the NEBNext Ultra DNA Library Prep Kit for Illumina (NEB). The Kapa HiFi Library Amp Real-Time Kit (Peqlab) with Illumina TruSeq compatible primers was used to amplify the library. Illumina HiSeq 2000 gds 301845105 GSM1845105 GEO Accession GSM1845105 SRX1134712 GSM1845106 SRP062097 PRJNA292069 SRS1026749 SAMN03979057 RNA-Seq TRANSCRIPTOMIC cDNA RNA-seq was performed according to Zhang et al, Silence, 2012 Total RNA was extracted using Trizol and polA RNA was purified with oligo-dT beads. For 2nd strand synthesis, dUTP was added to generate stranded libraries using the NEBNext Ultra DNA Library Prep Kit for Illumina (NEB). The Kapa HiFi Library Amp Real-Time Kit (Peqlab) with Illumina TruSeq compatible primers was used to amplify the library. Illumina HiSeq 2000 gds 301845106 GSM1845106 GEO Accession GSM1845106 SRX1134713 GSM1845107 SRP062097 PRJNA292069 SRS1026748 SAMN03979058 RNA-Seq TRANSCRIPTOMIC cDNA RNA-seq was performed according to Zhang et al, Silence, 2012 Total RNA was extracted using Trizol and polA RNA was purified with oligo-dT beads. For 2nd strand synthesis, dUTP was added to generate stranded libraries using the NEBNext Ultra DNA Library Prep Kit for Illumina (NEB). The Kapa HiFi Library Amp Real-Time Kit (Peqlab) with Illumina TruSeq compatible primers was used to amplify the library. Illumina HiSeq 2000 gds 301845107 GSM1845107 GEO Accession GSM1845107 SRX1134714 GSM1845108 SRP062097 PRJNA292069 SRS1026747 SAMN03979059 RNA-Seq TRANSCRIPTOMIC cDNA RNA-seq was performed according to Zhang et al, Silence, 2012 Total RNA was extracted using Trizol and polA RNA was purified with oligo-dT beads. For 2nd strand synthesis, dUTP was added to generate stranded libraries using the NEBNext Ultra DNA Library Prep Kit for Illumina (NEB). The Kapa HiFi Library Amp Real-Time Kit (Peqlab) with Illumina TruSeq compatible primers was used to amplify the library. Illumina HiSeq 2000 gds 301845108 GSM1845108 GEO Accession GSM1845108 SRX1134715 GSM1845109 SRP062097 PRJNA292069 SRS1026746 SAMN03979060 RNA-Seq TRANSCRIPTOMIC cDNA RNA-seq was performed according to Zhang et al, Silence, 2012 Total RNA was extracted using Trizol and polA RNA was purified with oligo-dT beads. For 2nd strand synthesis, dUTP was added to generate stranded libraries using the NEBNext Ultra DNA Library Prep Kit for Illumina (NEB). The Kapa HiFi Library Amp Real-Time Kit (Peqlab) with Illumina TruSeq compatible primers was used to amplify the library. Illumina HiSeq 2000 gds 301845109 GSM1845109 GEO Accession GSM1845109 SRX1134716 GSM1845110 SRP062097 PRJNA292069 SRS1026745 SAMN03979061 RNA-Seq TRANSCRIPTOMIC cDNA RNA-seq was performed according to Zhang et al, Silence, 2012 Total RNA was extracted using Trizol and depleted for ribosomal RNA (Ribo-Zero Kit, Epicentre). For 2nd strand synthesis, dUTP was added to generate stranded libraries. UDG digested dsDNA was cloned using the NEBNext™ DNA Sample Prep Reagent Set 1 (NEB). The Kapa HiFi Library Amp Real-Time Kit (Peqlab) with Illumina TruSeq compatible primers was used to amplify the library. Illumina HiSeq 2000 gds 301845110 GSM1845110 GEO Accession GSM1845110 SRX1134717 GSM1845111 SRP062097 PRJNA292069 SRS1026744 SAMN03979062 OTHER TRANSCRIPTOMIC other Cap-seq was performed according to Nachaev et al, Science, 2010 and Gu et al, Cell, 2013 Purified Capped RNA fragments were ligated with 3' and 5' linkers. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. Illumina HiSeq 2000 gds 301845111 GSM1845111 GEO Accession GSM1845111 SRX1134718 GSM1845112 SRP062097 PRJNA292069 SRS1026743 SAMN03979063 ncRNA-Seq TRANSCRIPTOMIC size fractionation smallRNA cloning was performed according to Brennecke et al, Cell, 2007 total RNA was isolated with Trizol. small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. sizeselected 18-29nt smallRNA cloning Illumina HiSeq 2000 gds 301845112 GSM1845112 GEO Accession GSM1845112 SRX1134719 GSM1845113 SRP062097 PRJNA292069 SRS1026742 SAMN03979064 ncRNA-Seq TRANSCRIPTOMIC size fractionation smallRNA cloning was performed according to Brennecke et al, Cell, 2007 small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. sizeselected 18-29nt smallRNA cloning Illumina HiSeq 2000 gds 301845113 GSM1845113 GEO Accession GSM1845113 SRX1134720 GSM1845114 SRP062097 PRJNA292069 SRS1026741 SAMN03979065 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845114 GSM1845114 GEO Accession GSM1845114 SRX1134721 GSM1845115 SRP062097 PRJNA292069 SRS1026740 SAMN03979066 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845115 GSM1845115 GEO Accession GSM1845115 SRX1134722 GSM1845116 SRP062097 PRJNA292069 SRS1026739 SAMN03979067 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845116 GSM1845116 GEO Accession GSM1845116 SRX1134723 GSM1845117 SRP062097 PRJNA292069 SRS1026738 SAMN03979068 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845117 GSM1845117 GEO Accession GSM1845117 SRX1134724 GSM1845118 SRP062097 PRJNA292069 SRS1026737 SAMN03979069 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845118 GSM1845118 GEO Accession GSM1845118 SRX1134725 GSM1845119 SRP062097 PRJNA292069 SRS1026736 SAMN03979070 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845119 GSM1845119 GEO Accession GSM1845119 SRX1134726 GSM1845120 SRP062097 PRJNA292069 SRS1026735 SAMN03979071 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845120 GSM1845120 GEO Accession GSM1845120 SRX1134727 GSM1845121 SRP062097 PRJNA292069 SRS1026734 SAMN03979072 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845121 GSM1845121 GEO Accession GSM1845121 SRX1134728 GSM1845122 SRP062097 PRJNA292069 SRS1026733 SAMN03979073 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845122 GSM1845122 GEO Accession GSM1845122 SRX1134729 GSM1845123 SRP062097 PRJNA292069 SRS1026732 SAMN03979074 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845123 GSM1845123 GEO Accession GSM1845123 SRX1134730 GSM1845124 SRP062097 PRJNA292069 SRS1026731 SAMN03979075 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845124 GSM1845124 GEO Accession GSM1845124 SRX1134731 GSM1845125 SRP062097 PRJNA292069 SRS1026730 SAMN03979572 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845125 GSM1845125 GEO Accession GSM1845125 SRX1134732 GSM1845126 SRP062097 PRJNA292069 SRS1026729 SAMN03979076 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845126 GSM1845126 GEO Accession GSM1845126 SRX1134733 GSM1845127 SRP062097 PRJNA292069 SRS1026728 SAMN03979077 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845127 GSM1845127 GEO Accession GSM1845127 SRX1134734 GSM1845128 SRP062097 PRJNA292069 SRS1026727 SAMN03979573 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845128 GSM1845128 GEO Accession GSM1845128 SRX1134735 GSM1845129 SRP062097 PRJNA292069 SRS1026726 SAMN03979574 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845129 GSM1845129 GEO Accession GSM1845129 SRX1134736 GSM1845130 SRP062097 PRJNA292069 SRS1026725 SAMN03979575 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845130 GSM1845130 GEO Accession GSM1845130 SRX1134737 GSM1845131 SRP062097 PRJNA292069 SRS1026724 SAMN03979576 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845131 GSM1845131 GEO Accession GSM1845131 SRX1134738 GSM1845132 SRP062097 PRJNA292069 SRS1026723 SAMN03979577 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845132 GSM1845132 GEO Accession GSM1845132 SRX1137152 GSM1845374 SRP062097 PRJNA292069 SRS1028608 SAMN03979685 RIP-Seq TRANSCRIPTOMIC other small RNAs from beads were isolated by acid phenol extraction and Ethanol precipitation, further cloning of small RNAs was done as for total small RNA-seq small RNAs were PAGE selected and 3' and 5' linkers was ligated. 1st strand cDNA synthesis was performed using SuperScript III (Invitrogen) and the library was amplified using the Kapa HiFi Library Amp real time Kit (Peqlab) with Illumina TruSeq compatible primers. IP from ovary lysate/acid Phenol RNA extraction from beads/ sizeselected small RNA cloning Illumina HiSeq 2000 gds 301845374 GSM1845374 GEO Accession GSM1845374