transcripts were renamed to the gene name plus a number e.g. “BRCA_1”. This change means that TE tracks in this version of the software cannot typically be used together with TE tracks generated using older versions to produce Heat Maps, PCA...
The system requirements for the MLST Scheme tools depend on the size of the MLST schemes (both the number of alleles and the number of sequence types). A laptop with 16GB of memory is normally sufficient for 7-gene schemes or cgMLST schemes based on a moderate number of isolates. Typing o...
Gene ID: 1178 种属 Homo sapiens 基因序列编号: NM_001828.6 基因描述 Homo sapiens Charcot-Leyden crystal galectin (CLC), mRNA DNA编码区: atgtccctgctacccgtgccatacacagaggctgcctctttgtctactggttctactgtg acaatcaaagggcgaccacttgcctgtttcttgaatgaaccatatctgcaggtggatttc cacactgagatgaaggaggaatcagacattgtctt...
2) 通过序列相似性或分类学进行重叠分组(Contig Binning) 3) 使用PFAM、基因本体论(Gene Ontology)、BLAST和DIAMOND进行功能分析。 4) 宏基因组的功能注释需要 MetaGeneMark插件。 3.元数据的可视化和统计分析 1) 堆叠条形图、面积图和可缩放的旭日图(Sunburst Diagram)(下图),用于探索和比较宏基因组样本的分类和...
CLCA2 General Information CLCA2 Gene Information CLCA2 基因概述 CLCA2 cDNA / gene is a gene with protein product which located on 1p22.3. The CLCA2 gene is conserved in chimpanzee, Rhesus monkey, dog, cow, mouse, rat, and chicken. 109 organisms have orthologs with human gene CLCA2. ...
Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012] 基因突变所影响的基因信息 电压依赖性氯离子通道基因...
具体而言,本发明涉及用于检测CLCN1基因的编码区及内含子剪切位点突变的方法,试剂盒及特异性引物. Specifically, the present invention relates to a method for coding regions and intron splice site mutations detected CLCN1, kits and specific primers.魏晓明王金明...
Gene ID:1186CLCN7 UniProt:P51798CLCN7 研究领域 细胞生物学 细胞器标记 GTX55139 ICC/IF Image ICC/IF analysis of formalin-fixed HeLa cells using GTX55139 CLCN7 antibody. Red : Primary antibody Blue : DAPI Permeabilization : 0.1% Triton X-100 in TBS for 5-10 minutes ...
【关键词】先天性肌强直;临床特征;基因突变ClinicalfesturesandCLCN1genemutationscreenonamyotoniacongenitalkindredWANGHai zhen,LIZengfu,ZHENGHong,etal.DepartmentofNeurology,theFirstAffiliatedHospitalofZhengzhouUniversity,Zhengzhou450052,ChinaAbstract:ObjectiveToinvestigatetheclinicalfesturesandCLCN1genemutationscreenona...