国产青榴社区91精品,久久成人精品免费播放,久久精品人人做人人试看

Home>(Research) Service>Transcriptome & Epigenome Sequencing>Transcriptome>Eukaryotic mRNA Sequencing with Reference Genome

Eukaryotic mRNA Sequencing with Reference Genome

FAQ

  •  A brief introduction of the construction of eukaryotic transcriptome library


    1) mRNA was separated by magnetic beads for polyA structure of mRNA

    2) mRNA fragmentation

    3) The base T is replaced by U during the second strand of cDNA synthetization to achieve the purpose of strand specific library.

    4) 5 'end repair, 3' end add “A”

    5) Add adapters

    6) Collect fragments with specific length, generally 300bp

    7) PCR

    8) Sequencing


  • How to select appropriate genes for qRT-PCR verification?


     Firstly, according to the enrichment results of GO/KEGG, the genes concerned shall be selected. Then, according to the results of differential expression analysis, the genes with higher fold change value, smaller P value and higher FPKM value shall be verified by qRT-PCR.


主站蜘蛛池模板: 滨州市| 宾川县| 盐山县| 鹰潭市| 连云港市| 海晏县| 台东市| 张家港市| 天门市| 萨迦县| 凤凰县| 旺苍县| 郎溪县| 土默特左旗| 平塘县| 湘潭县| 大渡口区| 岳池县| 崇明县| 玛多县| 富阳市| 平利县| 新乐市| 赤峰市| 宁国市| 陆丰市| 隆德县| 黑龙江省| 上杭县| 鹤壁市| 芦溪县| 三门县| 康平县| 仲巴县| 渝北区| 平潭县| 喀什市| 资源县| 蒙自县| 三穗县| 贵溪市|