片语

High-Speed DNA-sequencing高速测序

automatic dna sequencing equipmentDNA序列自动测定设备

Direct DNA sequencingDNA直接测序

DNA genetic sequencing方法

dna sequencing methodsdna序列分析技术

dna auto-sequencingdna自动测序

DNA methylation sequencing全基因组甲基化测序

dna direct sequencingdna直接测序

英汉例句

• molecular genetic analysis of each proband was performed by direct dna sequencing of the entire coding region of kcnj2.

  通过直接dna测序，对先证者的kcnj2全部编码区进行分子遗传学分析，同时筛查对照受试者。

• screening the mutations and polymorphisms by denaturing high-performance liquid chromatography(dhplc) and dna sequencing results: 1.

  应用变性高效液相色谱（dhplc）分析及直接基因测序筛查突变和多态。

• methods pcrsscp and dna sequencing were used to analyze the ptch gene mutations in 12 okcs, including 10 sporadic and 2 nevoid basal cell carcinoma syndrome(nbccs) associated okc.

  方法采用pcr-sscp筛查与dna直接测序的方法对12例okc进行ptch基因突变的检测，其中2例为痣样基底细胞癌综合征（nbccs）相关okc，10例为散发okc。

• conclusion: dna sequencing is an accurate and reliable method in origin identification of the genuine notoginseng.

  结论：通过序列差异比较分析，dna测序技术可成为三七正品基原鑒定的準确、有效手段。

• the structure principle of dna biosensor, dna chip, dna sequencing technique, pooled dna, laboratory on chip (loc) are introduced in this paper.

  本文简要介绍了其中dna生物传感器、dna芯片、dna测序技术、混合dna样品池、微芯片实验室的结构原理。

• methods the mutations of exon 5, exon 6, and exon 8 of pten gene were detected by pcr, gene clone, and dna sequencing analysis in parotid pleomorphic adenoma and normal gland tissue.

  方法应用聚合酶链反应（pcr）及克隆、基因测序的方法来分析腮腺多形性腺瘤及正常腺体组织中pten基因第5、第6及第8外显子有无突变及缺失。

• methods a randomly primed pcr(rp-pcr) technology were used to amplify the dna of d, f and d. p, three amplified bands were selected for dna sequencing and analysis.

  方法用随机引物pcr对粉尘螨和屋尘螨的dna进行扩增，选择三个扩增条带进行测序和分析。

• on the basis of the obtained results, a simple two-pass dna sequencing scheme is suggested.

  以获得的结果为基础，提出了一个简单的双通道dna测序方案。

• pcr and single strand conformation polymorphism analysis (sscp) were combined with dna sequencing confirmation to screen all 28 exons of scn5a gene.

  采用pcr单链构象多态性技术（sscp）结合dna序列测定证实，对病人scn5a的全部2 8个外显子进行突变检测。

• biochemical reaction, coagglutination test, metabolism inhibition test, polymerase chain reaction (pcr) assay, and dna sequencing were employed to identify the isolated microorganisms.

  阳性培养物用生化反应、协同凝集试验、代谢抑制试验、聚合酶链反应和dna序列测定等方法进行鑒定。

• random dna sequencing result was identical to the results of oligonucleotide array.

  部分样品的随机测序结果与寡核苷酸阵列杂交结果一致。

• dna sequencing and analysis reveal 1 known sequences and 6 known sequences.

  最后分析显示1个为未知基因，另6个为已知基因。

• results dna sequencing analysis proved that the sequence of the radiation-inducible promoter was totallyconsistent with the designing sequence.

  结果合成启动子序列分析与设计序列完全一致；

• direct dna sequencing of the whole coding region of gjb2 revealed that a common homozygous mutation 235delc was responsible for most of the affected members in the nshi family.

  对gjb2基因进行整个编码区域的测序，发现235堿基处发生了堿基c的纯合缺失， 这一突变可能是该家系中绝大多数患者致病的遗传基础。