bmo_circ_0000129	circRNA	bombyx mori			bmo_circ_0000129			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000131	circRNA	bombyx mori			bmo_circ_0000131			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000257	circRNA	bombyx mori			bmo_circ_0000257			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000654	circRNA	bombyx mori			bmo_circ_0000654			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000674	circRNA	bombyx mori			bmo_circ_0000674			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000681	circRNA	bombyx mori			bmo_circ_0000681			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000832	circRNA	bombyx mori			bmo_circ_0000832			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0000861	circRNA	bombyx mori			bmo_circ_0000861			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001406	circRNA	bombyx mori			bmo_circ_0001406			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001417	circRNA	bombyx mori			bmo_circ_0001417			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001422	circRNA	bombyx mori			bmo_circ_0001422			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001433	circRNA	bombyx mori			bmo_circ_0001433			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001436	circRNA	bombyx mori			bmo_circ_0001436			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001437	circRNA	bombyx mori			bmo_circ_0001437			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001438	circRNA	bombyx mori			bmo_circ_0001438			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001555	circRNA	bombyx mori			bmo_circ_0001555			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0001612	circRNA	bombyx mori			bmo_circ_0001612			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002031	circRNA	bombyx mori			bmo_circ_0002031			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002094	circRNA	bombyx mori			bmo_circ_0002094			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002123	circRNA	bombyx mori			bmo_circ_0002123			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002204	circRNA	bombyx mori			bmo_circ_0002204			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the PSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002365	circRNA	bombyx mori			bmo_circ_0002365			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002389	circRNA	bombyx mori			bmo_circ_0002389			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002460	circRNA	bombyx mori			bmo_circ_0002460			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002462	circRNA	bombyx mori			bmo_circ_0002462			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002508	circRNA	bombyx mori			bmo_circ_0002508			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0002742	circRNA	bombyx mori			bmo_circ_0002742			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully. upregulated in the MSG.	RT-PCR,qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0003025	circRNA	bombyx mori			bmo_circ_0003025			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0003383	circRNA	bombyx mori			bmo_circ_0003383			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	upregulated in the MSG.	qRT-PCR,RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0003518	circRNA	bombyx mori			bmo_circ_0003518			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
bmo_circ_0003542	circRNA	bombyx mori			bmo_circ_0003542			silk gland	28918159	Identification of circular RNA in the Bombyx mori silk gland.	Gan H, Feng T, Wu Y, Liu C, Xia Q, Cheng T.	Insect Biochem Mol Biol.  2017	We further experimentally validated the candidate B. mori circRNAs. Convergent and divergent primers were designed to amplify each circRNA in the RNase R-treated sample (cDNA) and genomic DNA. Convergent primers were designed as a positive control for the corresponding linear transcripts, and divergent primers were designed to detect the circular template. Theoretically, convergent primers should amplify products from both the cDNA and genomic DNA, whereas the divergent primers would only amplify circRNA from cDNA and would fail to amplify a product from the genomic DNA. The reverse transcription PCR amplification results showed that 16 of 38 randomly chosen circRNA were validated successfully.	RT-PCR, RNA-seq	middle silk gland (MSG) and posterior silk gland (PSG)												
circRNA_0827	circRNA	bombyx mori						cytoplasmic polyhedrosis virus infection	29268657	Identification and characterization of circular RNAs in the silkworm midgut following Bombyx mori cytoplasmic polyhedrosis virus infection.	Hu X, Zhu M, Zhang X, Liu B, Liang Z, Huang L, Xu J, Yu L, Li K, Zar MS, Xue R, Cao G, Gong C.	RNA Biol.  2018	According to the sequencing results, 6 circRNAs were selected randomly for validation with divergent primers. Distinct products of the expected size were amplified using the divergent primers and confirmed by Sanger sequencing. The results showed that the selected 6 circRNAs in the silkworm midgut had covalently closed, continuous loop structures with neither 5 to 3 polarity nor a polyadenylated tail, which is consistent with predictions.	qRT-PCR, RNA-seq	silkworm midgut												
circRNA_0962	circRNA	bombyx mori						cytoplasmic polyhedrosis virus infection	29268657	Identification and characterization of circular RNAs in the silkworm midgut following Bombyx mori cytoplasmic polyhedrosis virus infection.	Hu X, Zhu M, Zhang X, Liu B, Liang Z, Huang L, Xu J, Yu L, Li K, Zar MS, Xue R, Cao G, Gong C.	RNA Biol.  2018	According to the sequencing results, 6 circRNAs were selected randomly for validation with divergent primers. Distinct products of the expected size were amplified using the divergent primers and confirmed by Sanger sequencing. The results showed that the selected 6 circRNAs in the silkworm midgut had covalently closed, continuous loop structures with neither 5 to 3 polarity nor a polyadenylated tail, which is consistent with predictions. The expression level was induced by BmCPV infection. The expression tendency was consistent with the CircSeq results.	qRT-PCR, RNA-seq	silkworm midgut												
circRNA_1193	circRNA	bombyx mori						cytoplasmic polyhedrosis virus infection	29268657	Identification and characterization of circular RNAs in the silkworm midgut following Bombyx mori cytoplasmic polyhedrosis virus infection.	Hu X, Zhu M, Zhang X, Liu B, Liang Z, Huang L, Xu J, Yu L, Li K, Zar MS, Xue R, Cao G, Gong C.	RNA Biol.  2018	According to the sequencing results, 6 circRNAs were selected randomly for validation with divergent primers. Distinct products of the expected size were amplified using the divergent primers and confirmed by Sanger sequencing. The results showed that the selected 6 circRNAs in the silkworm midgut had covalently closed, continuous loop structures with neither 5 to 3 polarity nor a polyadenylated tail, which is consistent with predictions. The expression level was induced by BmCPV infection. The expression tendency was consistent with the CircSeq results.	qRT-PCR, RNA-seq	silkworm midgut												
circRNA_5655	circRNA	bombyx mori						cytoplasmic polyhedrosis virus infection	29268657	Identification and characterization of circular RNAs in the silkworm midgut following Bombyx mori cytoplasmic polyhedrosis virus infection.	Hu X, Zhu M, Zhang X, Liu B, Liang Z, Huang L, Xu J, Yu L, Li K, Zar MS, Xue R, Cao G, Gong C.	RNA Biol.  2018	According to the sequencing results, 6 circRNAs were selected randomly for validation with divergent primers. Distinct products of the expected size were amplified using the divergent primers and confirmed by Sanger sequencing. The results showed that the selected 6 circRNAs in the silkworm midgut had covalently closed, continuous loop structures with neither 5 to 3 polarity nor a polyadenylated tail, which is consistent with predictions. The expression level was induced by BmCPV infection. The expression tendency was consistent with the CircSeq results.	qRT-PCR, RNA-seq	silkworm midgut												
circRNA_6031	circRNA	bombyx mori						cytoplasmic polyhedrosis virus infection	29268657	Identification and characterization of circular RNAs in the silkworm midgut following Bombyx mori cytoplasmic polyhedrosis virus infection.	Hu X, Zhu M, Zhang X, Liu B, Liang Z, Huang L, Xu J, Yu L, Li K, Zar MS, Xue R, Cao G, Gong C.	RNA Biol.  2018	According to the sequencing results, 6 circRNAs were selected randomly for validation with divergent primers. Distinct products of the expected size were amplified using the divergent primers and confirmed by Sanger sequencing. The results showed that the selected 6 circRNAs in the silkworm midgut had covalently closed, continuous loop structures with neither 5 to 3 polarity nor a polyadenylated tail, which is consistent with predictions. The expression level was induced by BmCPV infection. The expression tendency was consistent with the CircSeq results.	qRT-PCR, RNA-seq	silkworm midgut												
circRNA_2439	circRNA	bombyx mori						cytoplasmic polyhedrosis virus infection	29268657	Identification and characterization of circular RNAs in the silkworm midgut following Bombyx mori cytoplasmic polyhedrosis virus infection.	Hu X, Zhu M, Zhang X, Liu B, Liang Z, Huang L, Xu J, Yu L, Li K, Zar MS, Xue R, Cao G, Gong C.	RNA Biol.  2018	The expression level was induced by BmCPV infection. The expression tendency was consistent with the CircSeq results.	qRT-PCR, RNA-seq	silkworm midgut