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等位基因频率

等位基因频率的相关文献在1987年到2022年内共计240篇,主要集中在内科学、基础医学、畜牧、动物医学、狩猎、蚕、蜂 等领域,其中期刊论文226篇、会议论文8篇、专利文献120727篇;相关期刊144种,包括中国法医学杂志、遗传、中华医学遗传学杂志等; 相关会议7种,包括第十一届全国中西医结合血液学学术会议暨第二届中西医结合血液学高峰论坛、首都医科大学生物医学工程学科学术年会、中国医师协会输血分会2012年第六届输血学术年会等;等位基因频率的相关文献由925位作者贡献,包括孙宏钰、伍新尧、倪培华等。

等位基因频率—发文量

期刊论文>

论文:226 占比:0.19%

会议论文>

论文:8 占比:0.01%

专利文献>

论文:120727 占比:99.81%

总计:120961篇

等位基因频率—发文趋势图

等位基因频率

-研究学者

  • 孙宏钰
  • 伍新尧
  • 倪培华
  • 储明星
  • 叶欣
  • 李传杰
  • 李军
  • 李桢
  • 李海凤
  • 杨帆
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 潘芹芹; 马骁; 王晓艳; 樊甦; 尤雅洁; 沈捷
    • 摘要: 目的:分析来自中华骨髓库江苏分库8地市汉族造血干细胞志愿者HLA-A位点等位基因频率,了解江苏8地市汉族人群HLA-A位点等位基因分布特征.方法:采用聚合酶链反应-直接测序分型(polymerase chain reaction-sequence based typ-ing,PCR-SBT)技术,对中华骨髓库江苏分库共计27 143例汉族志愿者的HLA-A位点进行高分辨分型,按地市统计HLA-A位点等位基因频率并比较分析.结果:江苏8地市汉族人群共检测出85种HLA-A位点等位基因,其中常州55种,南京55种,镇江38种,扬州37种,淮安41种,宿迁44种,徐州42种,盐城41种.经统计分析,南京与镇江、扬州在A*02:01:01G、11:01、24:02、30:01、33:03等位基因频率上均无显著性差异.南京、镇江非常接近,常见的HLA-A位点等位基因依次为A*11:01、24:02、02:01:01G、33:03、30:01、02:07、02:06、31:01、01:01;常州、扬州非常接近,常见的HLA-A位点等位基因依次为A*11:01、24:02、02:01:01G、33:03、02:07、30:01、02:06、31:01、01:01.盐城、宿迁比较接近,常见的HLA-A位点等位基因大体依次为A*11:01、24:02、02:01:01G、30:01、33:03、02:07、02:06、01:01,仅在A*02:01:01G、30:01的顺序上有所区别.徐州、淮安也比较接近,常见的HLA-A位点等位基因大体依次为A*24:02、11:01、30:01、02:01:01G、33:03,仅在A*30:01、02:01:01G的顺序上有所区别.结论:江苏8地市汉族人群HLA-A位点等位基因频率分布与地域分布基本吻合,徐州、淮安与鲁南地区非常接近,南京、镇江、常州、扬州与上海、浙江有一定相似之处,为研究HLA-A位点等位基因与疾病的相关性以及人类遗传学提供了有意义的基础性资料.
    • 马丽娜; 于洋; 侯鹏霞; 施安; 梁小军
    • 摘要: 为研究FecB基因在滩羊和湖羊杂交后代种群中的多态性及遗传规律,实验以滩羊(或滩湖杂交)公羊为父本,湖羊或滩湖杂交母羊为母本,在饲养条件相同的舍饲条件下进行杂交,统计母羊产羔率,并应用DNA Sanger测序方法对杂交后代羔羊的FecB基因进行检测,分析其基因型与产羔数的相关性.结果表明,滩湖F1代群体中AA、GA、GG基因型频率分别为47%、53% 和0,G、A等位基因频率分别为26%、74%.滩湖F2代群体中AA、GA、GG基因型频率分别为40%、52% 和8%,G、A等位基因频率分别为33%、67%.滩湖G0代群体中AA、GA、GG基因型频率分别为27%、63% 和10%,G、A等位基因频率分别为42%、58%.滩湖G1代群体中GG、AA、GA基因型频率分别为22%、30% 和48%,G、A等位基因频率分别为56% 和54%.对其中具有第1~3胎产羔数记录的200只滩湖母羊的产羔数进行统计分析发现,GG基因型滩羊平均产羔数极显著高于GA、AA基因型(P<0.01).
    • 郑丽平; 王伟; 余正阳
    • 摘要: 目的 探讨脑梗死阿司匹林抵抗(AR)患者C3435T基因多态性的变化.方法 收集2018年10月至2019年10月收治的脑梗死患者180例,所有患者均接受至少1周的阿司匹林治疗(用药规律),按照血栓弹力图(TEG)检查结果对阿司匹林敏感性进行评估,并分成敏感组、抵抗组,其中花生四烯酸(AA)抑制率低于50%纳入抵抗组,AA抑制率超过50%(包含50%)纳入敏感组.经聚合酶链反应-限制性片段长度多态性技术(PCR-RFLP)与直接测序法分析患者C3435T基因频率以及等位基因频率分布情况.经logistic回归模型对脑梗死患者阿司匹林抵抗危险因素进行分析.结果 在180例患者中,阿司匹林抵抗者41例(22.78%),阿司匹林敏感者139例(77.22%).抵抗组C3435T基因CC型占比为19.51%,显著低于敏感组的34.53%;抵抗组TT型占比为39.02%,显著高于敏感组的17.99%,两组比较差异均有统计学意义(均P<0.05).抵抗组C等位基因频率占比为39.02%,显著低于敏感组的58.27%;抵抗组T等位基因频率占比为60.98%,显著高于敏感组的41.73%,两组比较差异均有统计学意义(均P< 0.05).logistic多因素分析显示,体质量指数≥24 kg/m2、高血糖、C3435T基因的TT分型、C3435T的T等位基因频率均是患者阿司匹林抵抗的危险因素(均P<0.05),而C3435T基因的CC分型是预防阿司匹林抵抗的保护性因素(P<0.05).结论 脑梗死AR者的C3435T基因TT分型较敏感者明显增多,其等位基因频率以T等位基因频率为主,且C3435T基因的TT分型、T等位基因频率与患者AR发生密切相关,而CC分型能降低抵抗率.
    • 李翘
    • 摘要: 以PowerPlex?FuSion 6c荧光标记系统针对无关个体DNA完成PCR扩增处理,并且借助3130XL遗传分析仪完成电泳检测研究.以GeneMapper?ID-X针对基因型展开有效分析及研究,以Power StatS v1.2针对群体遗传学进行研究及评估,并且评估此体系对微量、混合检材的实际检测成效.23个常染色体的STR基因座具备较强的遗传多态性,并且个体识别概率是0.99999999,混合检材Y-STR、微量检材STR基因座的检出率分别是96.67%、93.33%.PowerPlex?FuSion 6c体系具备较强的遗传多态性,因此在亲权鉴定、个体识别与数据库构建等领域中具备较大的实际运用价值.
    • 王勇; 马丽娜; 梁小军
    • 摘要: 试验利用PCR-RFLP的方法对150只绵羊FecB基因型进行检测.结果表明:滩湖F1代群体中基因型频率为++基因型(14%)、B+基因型(28%)、BB基因型(8%),等位基因频率为B(44%)、+(56%);滩羊群体中基因型频率为++基因型(37%)、B+基因型(13%),等位基因频率为B(13%)、+(87%);小尾寒羊群体中基因型频率为++基因型(15%)、B+基因型(25%)、BB基因型(10%),等位基因频率为B(45%)、+(55%).
    • 杨莹; 杨英; 陈晓红; 陈林; 梁翰月; 罗丽; 贾常莎; 陈永艳; 晏文
    • 摘要: Objective To investigate the correlations of the polymorphism of Aiolos gene rs9909593, rs9635726 and rs12150079 with systemic lupus erythematosus (SLE) in Guizhou Han population. Methods The case-control study was conducted on 213 SLE patients and 187 healthy controls. The 3 SNPs (rs9909593, rs9635726 and rs12150079) of Aiolos gene was analyzed by snapshot technology. The susceptibility between gene and SLE was analyzed through the non-conditional logistic-regression model. Results The frequencies of genotype AG, GG and AA in SLE group were 0.437%, 0.080% and 0.483%, respectively; and in control group were 0.412%, 0.064% and 0.524%, respectively. The frequencies of allele A and G of Aiolos rs9909593 were 0.702% and 0.298%, respectively, in SLE group; and 0.730% and 0.270%, respectively, in control group. There was no significant difference in genotype frequency or allele frequency of Aiolos rs9909593 between the two groups (P>0.05). The frequencies of genotype CT, CC and TT in SLE group were 0.437%, 0.094% and 0.469%, respectively; and in control group were 0.422%, 0.064% and 0.513%, respectively. The frequencies of C and T in SLE group were 0.312% and 0.688%, respectively;and in control group were 0.275% and 0.725 %, respectively. There was no significant difference in genotype frequency and allele frequency of Aiolos rs9635726 between the two groups (P>0.05). The frequencies of genotype AG, GG and AA of Aiolos rs12150079 in SLE group were 0.310%, 0.042% and 0.648%, respectively; and in control group were 0.326%, 0.032% and 0.642%, respectively. The frequencies of allele A and G of Aiolos rs12150079 in SLE group were 0.197% and 0.803%, respectively; and in control group were 0.195% and 0.805%, respectively. There was no significant difference in genotype frequency or allele frequency of Aiolos rs12150079 between the two groups (P>0.05). Logistic regression model analysis suggested that rs9909593, rs9635726 and rs12150079 had no significant correlation with SLE in the additive model, dominant model and implicit model (P>0.05). The rs12150079 were completely unbalant with rs9635726 and rs9909593 (D′≥1, r2≥0.584). The rs9635726 and rs9909593 had strong linkage disequilibrium (D′=0.877, r2=0.733). Joint genotype analysis found that there was no significant difference in the distribution of 5 single haplotype (ACG, GCA, GCG, GTA, GTG) between SLE group and control group (P>0.05). The non-conditional logistic-regression model analysis showed that the haplotype had nothing to do with the incidence of SLE. Conclusion The single nucleotide polymorphism of Aiolos gene rs9909593, rs9635726 and rs12150079 is not associated with the risk of SLE in Guizhou Han population.%目的 探讨贵州汉族人群Aiolos基因rs9909593、rs9635726、rs12150079位点多态性与系统性红斑狼疮(SLE)的相关性.方法 采用病例对照研究,利用SNaPshot技术对贵州汉族213例SLE患者(SLE组)和187例健康对照组的Aiolos基因3个SNP位点rs9909593、rs9635726及rs12150079进行分型,比较两组间基因型频率及等位基因频率的差异,利用非条件logistic回归模型分析基因与疾病易感性的关系.结果 Aiolos rs9909593位点AG、GG、AA基因型频率和等位基因A、G频率在贵州汉族SLE组和健康对照组分别为0.437%、0.080%、0.483%和0.412%、0.064%、0.524%;0.702%、0.298和0.730%、0.270%,两组间基因型频率和等位基因频率分布差异均无统计学意义(P>0.05);Aiolos rs9635726位点CT、CC、TT基因型频率和等位基因C、T频率在贵州汉族SLE组和健康对照组分别为0.437%、0.094%、0.469%和0.422%、0.064%、0.513%;0.312%、0.688%和0.275%、0.725%,两组间基因型频率和等位基因频率分布差异均无统计学意义(P>0.05);Aiolos rs12150079位点AG、GG、AA基因型频率和等位基因A、G频率在贵州汉族SLE组和健康对照组分别为0.310%、0.042%、0.648%和0.326%、0.032%、 0.642%;0.197%、0.803%和0.195%、0.805%,两组间基因型频率和等位基因频率分布差异均无统计学意义(P>0.05).非条件logistic回归模型分析提示rs9909593、rs9635726及rs12150079位点在加性模型、显性模型及隐性模型下均与SLE无相关(P>0.05).这3个SNP间rs12150079与rs9635726、rs9909593存在完全连锁不平衡(D′≥1,r2≥0.584);rs9635726与rs9909593存在强连锁不平衡(D′=0.877,r2=0.733).联合基因型分析发现,5种单体型(ACG、GCA、GCG、GTA、GTG)在SLE组及健康对照组中的分布差异无统计学意义(P>0.05),同时非条件logistic回归分析显示,各单体型与SLE发病均无关.结论 Aiolos基因rs9909593、rs9635726及rs12150079单核苷酸多态性可能与贵州汉族人群SLE的患病风险无相关性.
    • 宋瑞雅; 裴斌; 冉鹏; 宋秀宇
    • 摘要: 目的 确定福建省泉州地区汉族群体21个常染色体短串联重量复(short tandem repeats,STR)基因座的遗传多态性参数,评估GlobalFiler检测系统在法医学个体识别和亲权鉴定中的应用价值.方法 用GlobalFiler复合扩增体系扩增402名泉州汉族无关个体的DNA样本,计算21个常染色体STR基因座的遗传学参数.结果 21个常染色体STR基因座的基因型分布均符合Hardy-Weinberg平衡,且均具有较高的多态性,其观测杂合度为0.637~0.945,个人识别率为0.801~0.991,多态性信息含量为0.570~0.940,非父排除率为0.337~0.888,匹配概率为0.009~0.199.结论 GlobalFiler检测系统在泉州地区汉族人群法医学个体识别和亲权鉴定有较高的应用价值.%Objective To analyze genetic polymorphisms of 21 autosomal short tandem repeat(STR) loci from Quanzhou Han Chinese groups using a GlobalFiler kit,and to assess its value for forensic practice.Methods For 402 unrelated Han individuals,allelic frequencies of 21 autosomal STR loci were determined by using the GlobalFiler kit.Genetic parameters of the 21 STR loci were calculated.Results No deviation from Hard-Weinberg equilibrium was observed for the 21 loci.Most of the loci were highly polymorphic.Observed heterozygosity has ranged from 0.637 to 0.945,power of discrimination has ranged from 0.801 to 0.991,polymorphism information content has ranged from 0.570 to 0.940,power of exclusion was between 0.337 to 0.888,and match probability was between 0.009 to 0.199.Conclusion GlobalFiler kit has a high value for personal identification and paternity testing for Han Chinese from Quanzhou.
    • 刘广宝; 康冉冉; 管安全; 张起林; 王丽
    • 摘要: 目的:研究济南地区人群ABO血型比例和血型等位基因频率。方法:对山东人类精子库2006年4月至2019年6月7458例捐精志愿者血型情况进行分析,统计A、B、O和AB血型的人数并根据Hardy-Weinberg遗传平衡定律计算等位基因频率。结果:济南地区人群血型比例为:A型,27.06%;B型,33.12%;AB型,10.44%;O型,29.38%;血型等位基因频率为IA,pc = 0.2094;IB,qc = 0.2486;i,rc = 0.5420。结论:济南地区人群中,B型血人数最多,i等位基因占优势。通过研究济南地区人群ABO血型情况,对遗传学研究、输血医学和临床应用等具有重要的意义,并在一定程度上推动人类精子库和血液中心的合作关系,促进献血和捐精公益事业的发展。
    • 农伟伦; 毕英杰; 李宏旭; 张丽
    • 摘要: This study uses bioinformatics method to analyze the function and property of H-FABP gene encoding pro-tein of Gansu black pig. DNA pooling and direct sequencing techniques were used for SNPs rapid screening and the function prediction of H-FABP protein of Gansu black pig. The results showed that the CDS region of H-FABP gene in Gansu black pig was 402 bp,encoding 133 amino residues,4 SNPs in CDS region including C734T-Intron1,T152C-Exon2,G30A-Intron2 and T121G-Intron2. Among them, T152C-Exon2 was a missense mutation, and the amino acids were converted from threonine(Ile)to threonine(Thr). The bioinformatics prediction showed that H-FABP protein of Gansu black pig was a stable hydrophilic protein, and the secondary structure and tertiary structure were mixed protein mainly with β-fold.%采用生物信息学方法从分子水平对甘肃黑猪H-FABP基因编码蛋白质的功能和性质进行分析.采用DNA池和直接测序技术对甘肃黑猪H-FABP基因进行SNPs快速筛查及其编码区蛋白质功能预测.结果表明,甘肃黑猪H-FABP基因编码区全长402 bp,编码133个氨基酸残基,共检测出4个SNPs,分别为C734T-Intron1、T152C-Exon2、G30A-Intron2、T121G-Intron2,其中 T152C-Exon2为错义突变,氨基酸由原来的异亮氨酸(Ile)转变为苏氨酸(Thr).生物信息学预测发现,甘肃黑猪H-FABP蛋白是一种稳定的亲水蛋白,蛋白质二三级结构均以β-折叠为主的混合型蛋白.
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