Bank Hinrichsen

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]

The cDNA samples derived from the petroleumtreated group and control were designated as T and C, respectively.The RPKM value was calculated as follows: RPKM N, and the exon length was used to determine differentially expressed genes.The false discovery rate was set to determine the threshold of P value in multiple tests.The PCR reactions were…[Read more]