Conclusion MTC can be diagnosed at gene level by direct gene sequencing analysis. It is possible to diagnose MTC before operation by means of molecular genetic analysis.
结论直接基因测序分析能在基因水平诊断MTC，分子遗传学分析使术前诊断该疾病成为可能。
While the WASP gene sequencing analysis could confirm the diagnosis find carriers and provide the evidences for hematopoietic stem cell transplantation treatment in WAS patients.
WASP基因分析可确诊患者，发现携带者，为干细胞移植治疗患者提供依据。
Additional laboratory analysis, including gene sequencing, is ongoing.
目前正在进行其它实验室分析，包括基因测序。
Gene sequencing and homology analysis show that these novel enzymes share remarkable homology with the amylase family.
基因测序及同源性分析表明这些新酶与淀粉酶家族具有很强的同源性。
After the completion of human genome sequencing, biologists desire for higher processing and analysis power to handle the huge gene data.
人类基因组测序工作完成后，对基因数据的处理和分析能力提出了更高的要求。
After the completion of human genome sequencing, the biologists require higher processing and analysis power to handle the huge gene data.
人类基因组测序工作完成后，对基因数据的处理和分析能力提出了更高的要求。
DNA microarray has been applied to DNA sequencing, pharmaceuticals analysis, gene expression and so on.
DNA微集阵列已广泛用于DNA测序、药物分析、基因表达等研究领域。
MethodsThe corresponding designed primers, RT_PCR, gene cloning, DNA sequencing analysis were used.
方法设计相应的引物，用RT _ PCR，基因克隆，DNA序列分析技术。
Sequencing analysis shows that the CpTI gene has been modified as what was DE - signed.
序列分析表明了基因修饰的准确性。
And identified HEV71 isolates were performed by gene amplification of VP1 coding region, nucleotide sequencing and homology analysis of evolution.
对分离到的HEV71阳性分离株进行VP1编码区基因扩增，核苷酸序列测定和同源进化分析。
Analysis of RT-PCR and sequencing indicated that the ncRNA gene had two different transcripts through alternatively splicing pattern.
PCR和测序结果分析，发现这个非编码RNA基因通过选择性剪接产生两种不同的转录产物。
Methods immunohistochemistry in 52 cases of nasopharyngeal carcinoma PTEN gene expression, the use of PCR SSCP silver staining, DNA sequencing analysis to detect PTEN gene mutation in exon 5, 8.
方法采用免疫组化检测52例鼻咽癌中pten基因的表达，利用PCRSSCP银染、DNA测序分析等方法检测pten基因第5、8外显子突变。
ITS sequences of ten kinds of Iris plants and an outgroup were obtained by primer design, PCR, gene cloning, sequencing and cluster analysis.
通过引物设计、P CR、基因克隆、测序，获得了10种鸢尾属植物和1个外类群种的ITS序列。
Methods:Various analytical techniques including gene sequencing, amino acid composition, analysis of N terminal amino acid analysis, peptide mapping, IEF, molecular weight and UV scanning were used.
方法：用基因测序、氨基酸组成分析、N末端氨基酸测序、胰肽图谱、IEF、分子量、紫外扫描等各种实验手段对重组L 天冬酰胺酶及其天然品进行了全面比较。
Results four positive clones of differential screening were picked out for sequencing. Homology analysis indicated that all of the four clone sequences were the same as that of insulin-I gene.
结果挑选了4个差异筛选的阳性克隆进行测序，序列同源性分析表明它们均与胰岛素- i基因序列高度一致。
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。
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。
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