SRX870169 GSM1605510 SRP053397 SRS841167 GSM1605510 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605510 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605510 gds 301605510 GEO Accession GSM1605510 SRX870170 GSM1605511 SRP053397 SRS841166 GSM1605511 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605511 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605511 gds 301605511 GEO Accession GSM1605511 SRX870171 GSM1605512 SRP053397 SRS841165 GSM1605512 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605512 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605512 gds 301605512 GEO Accession GSM1605512 SRX870172 GSM1605513 SRP053397 SRS841164 GSM1605513 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605513 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605513 gds 301605513 GEO Accession GSM1605513 SRX870173 GSM1605514 SRP053397 SRS841163 GSM1605514 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605514 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605514 gds 301605514 GEO Accession GSM1605514 SRX870174 GSM1605515 SRP053397 SRS841161 GSM1605515 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605515 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605515 gds 301605515 GEO Accession GSM1605515 SRX870175 GSM1605516 SRP053397 SRS841162 GSM1605516 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605516 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605516 gds 301605516 GEO Accession GSM1605516 SRX870176 GSM1605517 SRP053397 SRS841160 GSM1605517 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605517 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605517 gds 301605517 GEO Accession GSM1605517 SRX870177 GSM1605518 SRP053397 SRS841158 GSM1605518 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605518 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605518 gds 301605518 GEO Accession GSM1605518 SRX870178 GSM1605519 SRP053397 SRS841159 GSM1605519 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605519 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605519 gds 301605519 GEO Accession GSM1605519 SRX870179 GSM1605520 SRP053397 SRS841157 GSM1605520 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605520 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605520 gds 301605520 GEO Accession GSM1605520 SRX870180 GSM1605521 SRP053397 SRS841156 GSM1605521 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605521 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605521 gds 301605521 GEO Accession GSM1605521 SRX870181 GSM1605522 SRP053397 SRS841155 GSM1605522 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605522 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605522 gds 301605522 GEO Accession GSM1605522 SRX870182 GSM1605523 SRP053397 SRS841154 GSM1605523 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605523 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605523 gds 301605523 GEO Accession GSM1605523 SRX870183 GSM1605524 SRP053397 SRS841152 GSM1605524 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605524 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605524 gds 301605524 GEO Accession GSM1605524 SRX870184 GSM1605525 SRP053397 SRS841153 GSM1605525 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605525 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605525 gds 301605525 GEO Accession GSM1605525 SRX870185 GSM1605526 SRP053397 SRS841151 GSM1605526 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605526 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605526 gds 301605526 GEO Accession GSM1605526 SRX870186 GSM1605527 SRP053397 SRS841148 GSM1605527 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605527 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605527 gds 301605527 GEO Accession GSM1605527 SRX870187 GSM1605528 SRP053397 SRS841150 GSM1605528 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605528 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605528 gds 301605528 GEO Accession GSM1605528 SRX870188 GSM1605529 SRP053397 SRS841149 GSM1605529 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605529 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605529 gds 301605529 GEO Accession GSM1605529 SRX870189 GSM1605530 SRP053397 SRS841147 GSM1605530 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605530 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605530 gds 301605530 GEO Accession GSM1605530 SRX870190 GSM1605531 SRP053397 SRS841144 GSM1605531 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605531 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605531 gds 301605531 GEO Accession GSM1605531 SRX870191 GSM1605532 SRP053397 SRS841146 GSM1605532 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605532 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605532 gds 301605532 GEO Accession GSM1605532 SRX870192 GSM1605533 SRP053397 SRS840965 GSM1605533 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605533 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605533 gds 301605533 GEO Accession GSM1605533 SRX870193 GSM1605534 SRP053397 SRS840964 GSM1605534 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605534 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605534 gds 301605534 GEO Accession GSM1605534 SRX870194 GSM1605535 SRP053397 SRS840963 GSM1605535 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605535 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605535 gds 301605535 GEO Accession GSM1605535 SRX870195 GSM1605536 SRP053397 SRS840962 GSM1605536 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605536 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605536 gds 301605536 GEO Accession GSM1605536 SRX870196 GSM1605537 SRP053397 SRS840961 GSM1605537 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605537 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605537 gds 301605537 GEO Accession GSM1605537 SRX870197 GSM1605538 SRP053397 SRS840960 GSM1605538 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605538 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605538 gds 301605538 GEO Accession GSM1605538 SRX870198 GSM1605539 SRP053397 SRS840966 GSM1605539 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605539 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605539 gds 301605539 GEO Accession GSM1605539 SRX870199 GSM1605540 SRP053397 SRS841145 GSM1605540 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605540 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605540 gds 301605540 GEO Accession GSM1605540 SRX870200 GSM1605541 SRP053397 SRS841142 GSM1605541 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605541 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605541 gds 301605541 GEO Accession GSM1605541 SRX870201 GSM1605542 SRP053397 SRS841143 GSM1605542 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605542 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605542 gds 301605542 GEO Accession GSM1605542 SRX870202 GSM1605543 SRP053397 SRS841140 GSM1605543 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605543 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605543 gds 301605543 GEO Accession GSM1605543 SRX870203 GSM1605544 SRP053397 SRS841141 GSM1605544 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605544 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605544 gds 301605544 GEO Accession GSM1605544 SRX870204 GSM1605545 SRP053397 SRS841138 GSM1605545 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605545 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605545 gds 301605545 GEO Accession GSM1605545 SRX870205 GSM1605546 SRP053397 SRS841137 GSM1605546 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605546 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605546 gds 301605546 GEO Accession GSM1605546 SRX870206 GSM1605547 SRP053397 SRS841139 GSM1605547 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605547 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605547 gds 301605547 GEO Accession GSM1605547 SRX870207 GSM1605548 SRP053397 SRS841136 GSM1605548 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605548 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605548 gds 301605548 GEO Accession GSM1605548 SRX870208 GSM1605549 SRP053397 SRS841134 GSM1605549 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605549 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605549 gds 301605549 GEO Accession GSM1605549 SRX870209 GSM1605550 SRP053397 SRS841135 GSM1605550 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605550 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605550 gds 301605550 GEO Accession GSM1605550 SRX870210 GSM1605551 SRP053397 SRS841133 GSM1605551 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605551 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605551 gds 301605551 GEO Accession GSM1605551 SRX870211 GSM1605552 SRP053397 SRS841131 GSM1605552 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605552 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605552 gds 301605552 GEO Accession GSM1605552 SRX870212 GSM1605553 SRP053397 SRS841132 GSM1605553 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605553 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605553 gds 301605553 GEO Accession GSM1605553 SRX870213 GSM1605554 SRP053397 SRS841128 GSM1605554 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605554 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605554 gds 301605554 GEO Accession GSM1605554 SRX870214 GSM1605555 SRP053397 SRS841129 GSM1605555 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605555 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605555 gds 301605555 GEO Accession GSM1605555 SRX870215 GSM1605556 SRP053397 SRS841130 GSM1605556 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605556 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605556 gds 301605556 GEO Accession GSM1605556 SRX870216 GSM1605557 SRP053397 SRS841126 GSM1605557 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605557 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605557 gds 301605557 GEO Accession GSM1605557 SRX870217 GSM1605558 SRP053397 SRS841125 GSM1605558 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605558 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605558 gds 301605558 GEO Accession GSM1605558 SRX870218 GSM1605559 SRP053397 SRS841123 GSM1605559 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605559 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605559 gds 301605559 GEO Accession GSM1605559 SRX870219 GSM1605560 SRP053397 SRS841127 GSM1605560 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605560 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605560 gds 301605560 GEO Accession GSM1605560 SRX870220 GSM1605561 SRP053397 SRS841122 GSM1605561 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605561 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605561 gds 301605561 GEO Accession GSM1605561 SRX870221 GSM1605562 SRP053397 SRS841124 GSM1605562 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605562 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605562 gds 301605562 GEO Accession GSM1605562 SRX870222 GSM1605563 SRP053397 SRS841121 GSM1605563 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605563 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605563 gds 301605563 GEO Accession GSM1605563 SRX870223 GSM1605564 SRP053397 SRS841119 GSM1605564 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605564 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605564 gds 301605564 GEO Accession GSM1605564 SRX870224 GSM1605565 SRP053397 SRS841120 GSM1605565 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605565 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605565 gds 301605565 GEO Accession GSM1605565 SRX870225 GSM1605566 SRP053397 SRS841117 GSM1605566 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605566 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605566 gds 301605566 GEO Accession GSM1605566 SRX870226 GSM1605567 SRP053397 SRS841118 GSM1605567 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605567 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605567 gds 301605567 GEO Accession GSM1605567 SRX870227 GSM1605568 SRP053397 SRS841116 GSM1605568 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605568 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605568 gds 301605568 GEO Accession GSM1605568 SRX870228 GSM1605569 SRP053397 SRS841114 GSM1605569 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605569 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605569 gds 301605569 GEO Accession GSM1605569 SRX870229 GSM1605570 SRP053397 SRS841115 GSM1605570 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605570 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605570 gds 301605570 GEO Accession GSM1605570 SRX870230 GSM1605571 SRP053397 SRS841111 GSM1605571 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605571 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605571 gds 301605571 GEO Accession GSM1605571 SRX870231 GSM1605572 SRP053397 SRS841112 GSM1605572 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605572 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605572 gds 301605572 GEO Accession GSM1605572 SRX870232 GSM1605573 SRP053397 SRS841113 GSM1605573 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605573 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605573 gds 301605573 GEO Accession GSM1605573 SRX870233 GSM1605574 SRP053397 SRS841109 GSM1605574 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605574 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605574 gds 301605574 GEO Accession GSM1605574 SRX870234 GSM1605575 SRP053397 SRS841110 GSM1605575 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605575 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605575 gds 301605575 GEO Accession GSM1605575 SRX870235 GSM1605576 SRP053397 SRS841108 GSM1605576 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605576 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605576 gds 301605576 GEO Accession GSM1605576 SRX870236 GSM1605577 SRP053397 SRS841107 GSM1605577 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605577 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605577 gds 301605577 GEO Accession GSM1605577 SRX870237 GSM1605578 SRP053397 SRS841106 GSM1605578 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605578 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605578 gds 301605578 GEO Accession GSM1605578 SRX870238 GSM1605579 SRP053397 SRS841105 GSM1605579 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605579 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605579 gds 301605579 GEO Accession GSM1605579 SRX870239 GSM1605580 SRP053397 SRS841103 GSM1605580 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605580 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605580 gds 301605580 GEO Accession GSM1605580 SRX870240 GSM1605581 SRP053397 SRS841104 GSM1605581 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605581 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605581 gds 301605581 GEO Accession GSM1605581 SRX870241 GSM1605582 SRP053397 SRS841102 GSM1605582 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605582 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605582 gds 301605582 GEO Accession GSM1605582 SRX870242 GSM1605583 SRP053397 SRS841101 GSM1605583 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605583 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605583 gds 301605583 GEO Accession GSM1605583 SRX870243 GSM1605584 SRP053397 SRS841099 GSM1605584 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605584 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605584 gds 301605584 GEO Accession GSM1605584 SRX870244 GSM1605585 SRP053397 SRS841100 GSM1605585 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605585 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605585 gds 301605585 GEO Accession GSM1605585 SRX870245 GSM1605586 SRP053397 SRS841097 GSM1605586 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605586 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605586 gds 301605586 GEO Accession GSM1605586 SRX870246 GSM1605587 SRP053397 SRS841098 GSM1605587 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605587 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605587 gds 301605587 GEO Accession GSM1605587 SRX870247 GSM1605588 SRP053397 SRS841096 GSM1605588 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605588 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605588 gds 301605588 GEO Accession GSM1605588 SRX870248 GSM1605589 SRP053397 SRS841093 GSM1605589 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605589 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605589 gds 301605589 GEO Accession GSM1605589 SRX870249 GSM1605590 SRP053397 SRS841094 GSM1605590 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605590 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605590 gds 301605590 GEO Accession GSM1605590 SRX870250 GSM1605591 SRP053397 SRS841095 GSM1605591 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605591 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605591 gds 301605591 GEO Accession GSM1605591 SRX870251 GSM1605592 SRP053397 SRS841092 GSM1605592 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605592 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605592 gds 301605592 GEO Accession GSM1605592 SRX870252 GSM1605593 SRP053397 SRS841091 GSM1605593 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605593 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605593 gds 301605593 GEO Accession GSM1605593 SRX870253 GSM1605594 SRP053397 SRS841090 GSM1605594 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605594 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605594 gds 301605594 GEO Accession GSM1605594 SRX870254 GSM1605595 SRP053397 SRS841088 GSM1605595 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605595 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605595 gds 301605595 GEO Accession GSM1605595 SRX870255 GSM1605596 SRP053397 SRS840967 GSM1605596 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605596 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605596 gds 301605596 GEO Accession GSM1605596 SRX870256 GSM1605597 SRP053397 SRS841087 GSM1605597 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605597 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605597 gds 301605597 GEO Accession GSM1605597 SRX870257 GSM1605598 SRP053397 SRS841089 GSM1605598 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605598 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605598 gds 301605598 GEO Accession GSM1605598 SRX870258 GSM1605599 SRP053397 SRS841086 GSM1605599 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605599 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605599 gds 301605599 GEO Accession GSM1605599 SRX870259 GSM1605600 SRP053397 SRS841084 GSM1605600 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605600 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605600 gds 301605600 GEO Accession GSM1605600 SRX870260 GSM1605601 SRP053397 SRS841082 GSM1605601 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605601 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605601 gds 301605601 GEO Accession GSM1605601 SRX870261 GSM1605602 SRP053397 SRS841081 GSM1605602 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605602 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605602 gds 301605602 GEO Accession GSM1605602 SRX870262 GSM1605603 SRP053397 SRS841085 GSM1605603 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605603 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605603 gds 301605603 GEO Accession GSM1605603 SRX870263 GSM1605604 SRP053397 SRS841079 GSM1605604 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605604 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605604 gds 301605604 GEO Accession GSM1605604 SRX870264 GSM1605605 SRP053397 SRS841083 GSM1605605 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605605 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605605 gds 301605605 GEO Accession GSM1605605 SRX870265 GSM1605606 SRP053397 SRS841080 GSM1605606 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605606 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605606 gds 301605606 GEO Accession GSM1605606 SRX870266 GSM1605607 SRP053397 SRS841077 GSM1605607 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605607 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605607 gds 301605607 GEO Accession GSM1605607 SRX870267 GSM1605608 SRP053397 SRS841076 GSM1605608 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605608 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605608 gds 301605608 GEO Accession GSM1605608 SRX870268 GSM1605609 SRP053397 SRS841078 GSM1605609 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605609 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605609 gds 301605609 GEO Accession GSM1605609 SRX870269 GSM1605610 SRP053397 SRS841075 GSM1605610 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605610 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605610 gds 301605610 GEO Accession GSM1605610 SRX870270 GSM1605611 SRP053397 SRS841073 GSM1605611 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605611 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605611 gds 301605611 GEO Accession GSM1605611 SRX870271 GSM1605612 SRP053397 SRS841074 GSM1605612 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605612 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605612 gds 301605612 GEO Accession GSM1605612 SRX870272 GSM1605613 SRP053397 SRS841072 GSM1605613 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605613 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605613 gds 301605613 GEO Accession GSM1605613 SRX870273 GSM1605614 SRP053397 SRS841071 GSM1605614 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605614 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605614 gds 301605614 GEO Accession GSM1605614 SRX870274 GSM1605615 SRP053397 SRS841069 GSM1605615 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605615 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605615 gds 301605615 GEO Accession GSM1605615 SRX870275 GSM1605616 SRP053397 SRS841070 GSM1605616 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605616 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605616 gds 301605616 GEO Accession GSM1605616 SRX870276 GSM1605617 SRP053397 SRS841068 GSM1605617 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605617 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605617 gds 301605617 GEO Accession GSM1605617 SRX870277 GSM1605618 SRP053397 SRS841066 GSM1605618 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605618 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605618 gds 301605618 GEO Accession GSM1605618 SRX870278 GSM1605619 SRP053397 SRS841064 GSM1605619 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605619 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605619 gds 301605619 GEO Accession GSM1605619 SRX870279 GSM1605620 SRP053397 SRS841067 GSM1605620 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605620 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605620 gds 301605620 GEO Accession GSM1605620 SRX870280 GSM1605621 SRP053397 SRS841063 GSM1605621 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605621 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605621 gds 301605621 GEO Accession GSM1605621 SRX870281 GSM1605622 SRP053397 SRS841065 GSM1605622 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605622 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605622 gds 301605622 GEO Accession GSM1605622 SRX870282 GSM1605623 SRP053397 SRS841062 GSM1605623 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605623 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605623 gds 301605623 GEO Accession GSM1605623 SRX870283 GSM1605624 SRP053397 SRS841061 GSM1605624 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605624 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605624 gds 301605624 GEO Accession GSM1605624 SRX870284 GSM1605625 SRP053397 SRS841060 GSM1605625 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605625 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605625 gds 301605625 GEO Accession GSM1605625 SRX870285 GSM1605626 SRP053397 SRS841057 GSM1605626 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605626 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605626 gds 301605626 GEO Accession GSM1605626 SRX870286 GSM1605627 SRP053397 SRS841055 GSM1605627 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605627 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605627 gds 301605627 GEO Accession GSM1605627 SRX870287 GSM1605628 SRP053397 SRS841056 GSM1605628 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605628 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605628 gds 301605628 GEO Accession GSM1605628 SRX870288 GSM1605629 SRP053397 SRS841059 GSM1605629 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605629 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605629 gds 301605629 GEO Accession GSM1605629 SRX870289 GSM1605630 SRP053397 SRS841053 GSM1605630 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605630 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605630 gds 301605630 GEO Accession GSM1605630 SRX870290 GSM1605631 SRP053397 SRS841058 GSM1605631 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605631 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605631 gds 301605631 GEO Accession GSM1605631 SRX870291 GSM1605632 SRP053397 SRS841054 GSM1605632 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605632 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605632 gds 301605632 GEO Accession GSM1605632 SRX870292 GSM1605633 SRP053397 SRS841052 GSM1605633 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605633 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605633 gds 301605633 GEO Accession GSM1605633 SRX870293 GSM1605634 SRP053397 SRS841049 GSM1605634 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605634 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605634 gds 301605634 GEO Accession GSM1605634 SRX870294 GSM1605635 SRP053397 SRS841051 GSM1605635 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605635 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605635 gds 301605635 GEO Accession GSM1605635 SRX870295 GSM1605636 SRP053397 SRS841050 GSM1605636 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605636 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605636 gds 301605636 GEO Accession GSM1605636 SRX870296 GSM1605637 SRP053397 SRS841048 GSM1605637 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605637 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605637 gds 301605637 GEO Accession GSM1605637 SRX870297 GSM1605638 SRP053397 SRS841047 GSM1605638 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605638 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605638 gds 301605638 GEO Accession GSM1605638 SRX870298 GSM1605639 SRP053397 SRS841044 GSM1605639 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605639 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605639 gds 301605639 GEO Accession GSM1605639 SRX870299 GSM1605640 SRP053397 SRS841045 GSM1605640 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605640 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605640 gds 301605640 GEO Accession GSM1605640 SRX870300 GSM1605641 SRP053397 SRS841046 GSM1605641 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605641 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605641 gds 301605641 GEO Accession GSM1605641 SRX870301 GSM1605642 SRP053397 SRS841043 GSM1605642 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605642 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605642 gds 301605642 GEO Accession GSM1605642 SRX870302 GSM1605643 SRP053397 SRS841042 GSM1605643 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605643 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605643 gds 301605643 GEO Accession GSM1605643 SRX870303 GSM1605644 SRP053397 SRS841041 GSM1605644 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605644 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605644 gds 301605644 GEO Accession GSM1605644 SRX870304 GSM1605645 SRP053397 SRS841040 GSM1605645 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605645 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605645 gds 301605645 GEO Accession GSM1605645 SRX870305 GSM1605646 SRP053397 SRS841038 GSM1605646 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605646 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605646 gds 301605646 GEO Accession GSM1605646 SRX870306 GSM1605647 SRP053397 SRS841039 GSM1605647 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605647 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605647 gds 301605647 GEO Accession GSM1605647 SRX870307 GSM1605648 SRP053397 SRS840968 GSM1605648 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605648 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605648 gds 301605648 GEO Accession GSM1605648 SRX870308 GSM1605649 SRP053397 SRS841037 GSM1605649 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605649 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605649 gds 301605649 GEO Accession GSM1605649 SRX870309 GSM1605650 SRP053397 SRS841035 GSM1605650 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605650 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605650 gds 301605650 GEO Accession GSM1605650 SRX870310 GSM1605651 SRP053397 SRS841036 GSM1605651 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605651 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605651 gds 301605651 GEO Accession GSM1605651 SRX870311 GSM1605652 SRP053397 SRS841032 GSM1605652 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605652 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605652 gds 301605652 GEO Accession GSM1605652 SRX870312 GSM1605653 SRP053397 SRS841033 GSM1605653 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605653 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605653 gds 301605653 GEO Accession GSM1605653 SRX870313 GSM1605654 SRP053397 SRS841031 GSM1605654 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605654 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605654 gds 301605654 GEO Accession GSM1605654 SRX870314 GSM1605655 SRP053397 SRS841030 GSM1605655 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605655 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605655 gds 301605655 GEO Accession GSM1605655 SRX870315 GSM1605656 SRP053397 SRS841029 GSM1605656 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605656 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605656 gds 301605656 GEO Accession GSM1605656 SRX870316 GSM1605657 SRP053397 SRS841034 GSM1605657 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605657 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605657 gds 301605657 GEO Accession GSM1605657 SRX870317 GSM1605658 SRP053397 SRS841028 GSM1605658 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605658 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605658 gds 301605658 GEO Accession GSM1605658 SRX870318 GSM1605659 SRP053397 SRS841027 GSM1605659 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605659 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605659 gds 301605659 GEO Accession GSM1605659 SRX870319 GSM1605660 SRP053397 SRS841026 GSM1605660 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605660 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605660 gds 301605660 GEO Accession GSM1605660 SRX870320 GSM1605661 SRP053397 SRS841024 GSM1605661 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605661 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605661 gds 301605661 GEO Accession GSM1605661 SRX870321 GSM1605662 SRP053397 SRS841023 GSM1605662 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605662 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605662 gds 301605662 GEO Accession GSM1605662 SRX870322 GSM1605663 SRP053397 SRS841022 GSM1605663 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605663 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605663 gds 301605663 GEO Accession GSM1605663 SRX870323 GSM1605664 SRP053397 SRS841025 GSM1605664 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605664 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605664 gds 301605664 GEO Accession GSM1605664 SRX870324 GSM1605665 SRP053397 SRS841020 GSM1605665 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605665 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605665 gds 301605665 GEO Accession GSM1605665 SRX870325 GSM1605666 SRP053397 SRS841021 GSM1605666 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605666 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605666 gds 301605666 GEO Accession GSM1605666 SRX870326 GSM1605667 SRP053397 SRS841019 GSM1605667 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605667 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605667 gds 301605667 GEO Accession GSM1605667 SRX870327 GSM1605668 SRP053397 SRS841018 GSM1605668 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605668 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605668 gds 301605668 GEO Accession GSM1605668 SRX870328 GSM1605669 SRP053397 SRS841017 GSM1605669 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605669 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605669 gds 301605669 GEO Accession GSM1605669 SRX870329 GSM1605670 SRP053397 SRS841016 GSM1605670 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605670 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605670 gds 301605670 GEO Accession GSM1605670 SRX870330 GSM1605671 SRP053397 SRS841015 GSM1605671 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605671 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605671 gds 301605671 GEO Accession GSM1605671 SRX870331 GSM1605672 SRP053397 SRS841014 GSM1605672 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605672 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605672 gds 301605672 GEO Accession GSM1605672 SRX870332 GSM1605673 SRP053397 SRS841013 GSM1605673 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605673 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605673 gds 301605673 GEO Accession GSM1605673 SRX870333 GSM1605674 SRP053397 SRS841012 GSM1605674 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605674 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605674 gds 301605674 GEO Accession GSM1605674 SRX870334 GSM1605675 SRP053397 SRS841011 GSM1605675 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605675 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605675 gds 301605675 GEO Accession GSM1605675 SRX870335 GSM1605676 SRP053397 SRS841010 GSM1605676 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605676 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605676 gds 301605676 GEO Accession GSM1605676 SRX870336 GSM1605677 SRP053397 SRS841009 GSM1605677 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605677 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605677 gds 301605677 GEO Accession GSM1605677 SRX870337 GSM1605678 SRP053397 SRS841008 GSM1605678 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605678 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605678 gds 301605678 GEO Accession GSM1605678 SRX870338 GSM1605679 SRP053397 SRS841007 GSM1605679 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605679 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605679 gds 301605679 GEO Accession GSM1605679 SRX870339 GSM1605680 SRP053397 SRS841006 GSM1605680 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605680 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605680 gds 301605680 GEO Accession GSM1605680 SRX870340 GSM1605681 SRP053397 SRS841005 GSM1605681 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605681 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605681 gds 301605681 GEO Accession GSM1605681 SRX870341 GSM1605682 SRP053397 SRS841004 GSM1605682 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605682 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605682 gds 301605682 GEO Accession GSM1605682 SRX870342 GSM1605683 SRP053397 SRS841003 GSM1605683 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605683 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605683 gds 301605683 GEO Accession GSM1605683 SRX870343 GSM1605684 SRP053397 SRS841002 GSM1605684 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605684 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605684 gds 301605684 GEO Accession GSM1605684 SRX870344 GSM1605685 SRP053397 SRS841001 GSM1605685 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605685 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605685 gds 301605685 GEO Accession GSM1605685 SRX870345 GSM1605686 SRP053397 SRS841000 GSM1605686 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605686 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605686 gds 301605686 GEO Accession GSM1605686 SRX870346 GSM1605687 SRP053397 SRS840999 GSM1605687 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605687 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605687 gds 301605687 GEO Accession GSM1605687 SRX870347 GSM1605688 SRP053397 SRS840998 GSM1605688 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605688 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605688 gds 301605688 GEO Accession GSM1605688 SRX870348 GSM1605689 SRP053397 SRS840997 GSM1605689 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605689 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605689 gds 301605689 GEO Accession GSM1605689 SRX870349 GSM1605690 SRP053397 SRS840996 GSM1605690 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605690 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605690 gds 301605690 GEO Accession GSM1605690 SRX870350 GSM1605691 SRP053397 SRS840995 GSM1605691 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605691 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605691 gds 301605691 GEO Accession GSM1605691 SRX870351 GSM1605692 SRP053397 SRS840994 GSM1605692 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605692 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605692 gds 301605692 GEO Accession GSM1605692 SRX870352 GSM1605693 SRP053397 SRS840993 GSM1605693 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605693 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605693 gds 301605693 GEO Accession GSM1605693 SRX870353 GSM1605694 SRP053397 SRS840969 GSM1605694 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605694 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605694 gds 301605694 GEO Accession GSM1605694 SRX870354 GSM1605695 SRP053397 SRS840992 GSM1605695 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605695 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605695 gds 301605695 GEO Accession GSM1605695 SRX870355 GSM1605696 SRP053397 SRS840991 GSM1605696 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605696 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605696 gds 301605696 GEO Accession GSM1605696 SRX870356 GSM1605697 SRP053397 SRS840990 GSM1605697 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605697 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605697 gds 301605697 GEO Accession GSM1605697 SRX870357 GSM1605698 SRP053397 SRS840989 GSM1605698 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605698 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605698 gds 301605698 GEO Accession GSM1605698 SRX870358 GSM1605699 SRP053397 SRS840988 GSM1605699 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605699 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605699 gds 301605699 GEO Accession GSM1605699 SRX870359 GSM1605700 SRP053397 SRS840987 GSM1605700 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605700 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605700 gds 301605700 GEO Accession GSM1605700 SRX870360 GSM1605701 SRP053397 SRS840986 GSM1605701 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605701 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605701 gds 301605701 GEO Accession GSM1605701 SRX870361 GSM1605702 SRP053397 SRS840985 GSM1605702 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605702 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605702 gds 301605702 GEO Accession GSM1605702 SRX870362 GSM1605703 SRP053397 SRS840984 GSM1605703 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605703 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605703 gds 301605703 GEO Accession GSM1605703 SRX870363 GSM1605704 SRP053397 SRS840983 GSM1605704 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605704 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605704 gds 301605704 GEO Accession GSM1605704 SRX870364 GSM1605705 SRP053397 SRS840982 GSM1605705 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605705 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605705 gds 301605705 GEO Accession GSM1605705 SRX870365 GSM1605706 SRP053397 SRS840981 GSM1605706 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605706 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605706 gds 301605706 GEO Accession GSM1605706 SRX870366 GSM1605707 SRP053397 SRS840980 GSM1605707 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605707 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605707 gds 301605707 GEO Accession GSM1605707 SRX870367 GSM1605708 SRP053397 SRS840979 GSM1605708 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605708 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605708 gds 301605708 GEO Accession GSM1605708 SRX870368 GSM1605709 SRP053397 SRS840978 GSM1605709 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605709 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605709 gds 301605709 GEO Accession GSM1605709 SRX870369 GSM1605710 SRP053397 SRS840977 GSM1605710 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605710 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605710 gds 301605710 GEO Accession GSM1605710 SRX870370 GSM1605711 SRP053397 SRS840976 GSM1605711 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605711 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605711 gds 301605711 GEO Accession GSM1605711 SRX870371 GSM1605712 SRP053397 SRS840975 GSM1605712 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605712 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605712 gds 301605712 GEO Accession GSM1605712 SRX870372 GSM1605713 SRP053397 SRS840974 GSM1605713 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605713 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605713 gds 301605713 GEO Accession GSM1605713 SRX870373 GSM1605714 SRP053397 SRS840973 GSM1605714 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605714 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605714 gds 301605714 GEO Accession GSM1605714 SRX870374 GSM1605715 SRP053397 SRS840972 GSM1605715 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605715 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605715 gds 301605715 GEO Accession GSM1605715 SRX870375 GSM1605716 SRP053397 SRS840971 GSM1605716 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605716 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605716 gds 301605716 GEO Accession GSM1605716 SRX870376 GSM1605717 SRP053397 SRS840970 GSM1605717 miRNA-Seq TRANSCRIPTOMIC size fractionation Tissue specimens were removed, flash frozen on dry ice, and total RNA was harvested using the Qiagen miRNeasy kit. RNA quality and integrity were monitored via Agilent Bioanalyzer. A minimum of 3.75 ug of total RNA were used to collect enriched RNA subfractions for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2000 GEO Sample GSM1605717 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1605717 gds 301605717 GEO Accession GSM1605717