GSM3373941: VSV-1 m; Cricetulus griseus; RNA-Seq

SRX4634288 GSM3373941 GSM3373941: VSV-1 m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734914 GSM3373941 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373941 GSM3373941 GEO Accession GSM3373941 SRX4634289 GSM3373942 GSM3373942: VSV-1 poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734915 GSM3373942 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373942 GSM3373942 GEO Accession GSM3373942 SRX4634290 GSM3373943 GSM3373943: VSV-1 ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734916 GSM3373943 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373943 GSM3373943 GEO Accession GSM3373943 SRX4634291 GSM3373944 GSM3373944: VSV-1 V+m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734917 GSM3373944 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373944 GSM3373944 GEO Accession GSM3373944 SRX4634292 GSM3373945 GSM3373945: VSV-1 V+poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734918 GSM3373945 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373945 GSM3373945 GEO Accession GSM3373945 SRX4634293 GSM3373946 GSM3373946: VSV-1 V+ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734919 GSM3373946 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373946 GSM3373946 GEO Accession GSM3373946 SRX4634294 GSM3373947 GSM3373947: VSV-2 m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734920 GSM3373947 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373947 GSM3373947 GEO Accession GSM3373947 SRX4634295 GSM3373948 GSM3373948: VSV-2 poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734925 GSM3373948 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373948 GSM3373948 GEO Accession GSM3373948 SRX4634296 GSM3373949 GSM3373949: VSV-2 ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734921 GSM3373949 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373949 GSM3373949 GEO Accession GSM3373949 SRX4634297 GSM3373950 GSM3373950: VSV-2 V+m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734922 GSM3373950 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373950 GSM3373950 GEO Accession GSM3373950 SRX4634298 GSM3373951 GSM3373951: VSV-2 V+poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734923 GSM3373951 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373951 GSM3373951 GEO Accession GSM3373951 SRX4634299 GSM3373952 GSM3373952: VSV-2 V+ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734924 GSM3373952 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373952 GSM3373952 GEO Accession GSM3373952 SRX4634300 GSM3373953 GSM3373953: EMCV-1 m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734926 GSM3373953 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373953 GSM3373953 GEO Accession GSM3373953 SRX4634301 GSM3373954 GSM3373954: EMCV-1 poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734927 GSM3373954 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373954 GSM3373954 GEO Accession GSM3373954 SRX4634302 GSM3373955 GSM3373955: EMCV-1 ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734928 GSM3373955 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373955 GSM3373955 GEO Accession GSM3373955 SRX4634303 GSM3373956 GSM3373956: EMCV-1 V+m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734929 GSM3373956 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373956 GSM3373956 GEO Accession GSM3373956 SRX4634304 GSM3373957 GSM3373957: EMCV-1 V+poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734930 GSM3373957 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373957 GSM3373957 GEO Accession GSM3373957 SRX4634305 GSM3373958 GSM3373958: EMCV-1 V+ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734948 GSM3373958 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373958 GSM3373958 GEO Accession GSM3373958 SRX4634306 GSM3373959 GSM3373959: EMCV-2 m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734931 GSM3373959 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373959 GSM3373959 GEO Accession GSM3373959 SRX4634307 GSM3373960 GSM3373960: EMCV-2 poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734932 GSM3373960 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373960 GSM3373960 GEO Accession GSM3373960 SRX4634308 GSM3373961 GSM3373961: EMCV-2 ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734933 GSM3373961 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373961 GSM3373961 GEO Accession GSM3373961 SRX4634309 GSM3373962 GSM3373962: EMCV-2 V+m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734934 GSM3373962 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373962 GSM3373962 GEO Accession GSM3373962 SRX4634310 GSM3373963 GSM3373963: EMCV-2 V+poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734935 GSM3373963 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373963 GSM3373963 GEO Accession GSM3373963 SRX4634311 GSM3373964 GSM3373964: EMCV-2 V+ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734936 GSM3373964 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373964 GSM3373964 GEO Accession GSM3373964 SRX4634312 GSM3373965 GSM3373965: Reo-1 m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734937 GSM3373965 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373965 GSM3373965 GEO Accession GSM3373965 SRX4634313 GSM3373966 GSM3373966: Reo-1 poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734938 GSM3373966 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373966 GSM3373966 GEO Accession GSM3373966 SRX4634314 GSM3373967 GSM3373967: Reo-1 ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734939 GSM3373967 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373967 GSM3373967 GEO Accession GSM3373967 SRX4634315 GSM3373968 GSM3373968: Reo-1 V+m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734940 GSM3373968 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373968 GSM3373968 GEO Accession GSM3373968 SRX4634316 GSM3373969 GSM3373969: Reo-1 V+poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734941 GSM3373969 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373969 GSM3373969 GEO Accession GSM3373969 SRX4634317 GSM3373970 GSM3373970: Reo-1 V+ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734942 GSM3373970 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373970 GSM3373970 GEO Accession GSM3373970 SRX4634318 GSM3373971 GSM3373971: Reo-2 m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734943 GSM3373971 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373971 GSM3373971 GEO Accession GSM3373971 SRX4634319 GSM3373972 GSM3373972: Reo-2 poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734949 GSM3373972 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373972 GSM3373972 GEO Accession GSM3373972 SRX4634320 GSM3373973 GSM3373973: Reo-2 ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734944 GSM3373973 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373973 GSM3373973 GEO Accession GSM3373973 SRX4634321 GSM3373974 GSM3373974: Reo-2 V+m; Cricetulus griseus; RNA-Seq SRP159459 SRS3734945 GSM3373974 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373974 GSM3373974 GEO Accession GSM3373974 SRX4634322 GSM3373975 GSM3373975: Reo-2 V+poly; Cricetulus griseus; RNA-Seq SRP159459 SRS3734946 GSM3373975 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373975 GSM3373975 GEO Accession GSM3373975 SRX4634323 GSM3373976 GSM3373976: Reo-2 V+ifn; Cricetulus griseus; RNA-Seq SRP159459 SRS3734947 GSM3373976 RNA-Seq TRANSCRIPTOMIC cDNA Cell cultures were resuspended in RLT buffer (Qiagen) and kept at -80°C until RNA was extracted using the RNeasy kit (Qiagen) and on-column DNAse digestion. RNA libraries were prepared for sequencing using standard Illumina protocols NextSeq 500 gds 303373976 GSM3373976 GEO Accession GSM3373976