共查询到20条相似文献,搜索用时 0 毫秒
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Tiago Csar Gouvêa Moreira Pricila da Silva Spínola Micheline Campos Rezende Carla Simone Moreira de Freitas Fbio Borges Mury Cibele Rodrigues Bonvicino Luciana de Andrade Agostinho 《Biomédica : revista del Instituto Nacional de Salud》2021,41(4):773
Introduction: Next Generation Sequencing (NGS) is cost-effective and a faster method to study genes, but its protocol is challenging.Objective: To analyze different adjustments to the protocol for screening the BRCA genes using Ion Torrent PGM sequencing and correlate the results with the number of false positive (FP) variants.Material and methods: We conducted a library preparation process and analyzed the number of FP InDels, the library concentration, the number of cycles in the target amplification step, the purity of the nucleic acid, the input, and the number of samples/Ion 314 chips in association with the results obtained by NGS.Results: We carried out 51 reactions and nine adjustments of protocols and observed eight FP InDels in homopolymer regions. No FP Single-Nucleotide Polymorphism variant was observed; 67.5% of protocol variables were jointly associated with the quality of the results obtained (p<0.05). The number of FP InDels decreased when the quality of results increased.Conclusion: The Ion AmpliSeq BRCA1/BRCA2 Community Panel had a better performance using four samples per Ion-314 chip instead of eight and the optimum number of cycles in the amplification step, even when using high-quality DNA, was 23. We observed better results with the manual equalization process and not using the Ion Library Equalizer kit. These adjustments provided a higher coverage of the variants and fewer artifacts (6.7-fold). Laboratories must perform internal validation because FP InDel variants can vary according to the quality of results while the NGS assay should be validated with Sanger. 相似文献
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Aaron M. Elliott Joy Radecki Bellal Moghis Xiang Li Anja Kammesheidt 《Journal of biomolecular techniques》2012,23(1):24-30
Cystic fibrosis (CF) is one of the most frequently diagnosed autosomal-recessive diseases in the Caucasian population. For general-population CF carrier screening, the American College of Medical Genetics (ACMG)/American College of Obstetricians and Gynecologists (ACOG) have recommended a core panel of 23 mutations that will identify 49–98% of carriers, depending on ethnic background. Using a genotyping technology that can rapidly identify disease-causing mutations is important for high-throughput general-population carrier screening, confirming clinical diagnosis, determining treatment options, and prenatal diagnosis. Here, we describe a proof-of-concept study to determine whether the Ion Torrent Personal Genome Machine (PGM) sequencer platform can reliably identify all ACMG/ACOG 23 CF transmembrane conductance regulator (CFTR) mutations. A WT CF specimen along with mutant DNA specimens representing all 23 CFTR mutations were sequenced bidirectionally on the Ion Torrent 314 chip to determine the accuracy of the PGM for CFTR variant detection. We were able to reliably identify all of the targeted mutations except for 2184delA, which lies in a difficult, 7-mer homopolymer tract. Based on our study, we believe PGM sequencing may be a suitable technology for identifying CFTR mutations in the future. However, as a result of the elevated rate of base-calling errors within homopolymer stretches, mutations within such regions currently need to be evaluated carefully using an alternative method. 相似文献
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In many crop species, DNA fingerprinting is required for the precise identification of cultivars to protect the rights of breeders. Many families of retrotransposons have multiple copies throughout the eukaryotic genome and their integrated copies are inherited genetically. Thus, their insertion polymorphisms among cultivars are useful for DNA fingerprinting. In this study, we conducted a DNA fingerprinting based on the insertion polymorphisms of active retrotransposon families (Rtsp-1 and LIb) in sweet potato. Using 38 cultivars, we identified 2,024 insertion sites in the two families with an Illumina MiSeq sequencing platform. Of these insertion sites, 91.4% appeared to be polymorphic among the cultivars and 376 cultivar-specific insertion sites were identified, which were converted directly into cultivar-specific sequence-characterized amplified region (SCAR) markers. A phylogenetic tree was constructed using these insertion sites, which corresponded well with known pedigree information, thereby indicating their suitability for genetic diversity studies. Thus, the genome-wide comparative analysis of active retrotransposon insertion sites using the bench-top MiSeq sequencing platform is highly effective for DNA fingerprinting without any requirement for whole genome sequence information. This approach may facilitate the development of practical polymerase chain reaction-based cultivar diagnostic system and could also be applied to the determination of genetic relationships. 相似文献
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颜氏大疣蛛Macrothele yani个体大、毒性强、易取毒,是农林生态系统中害虫的重要天敌,也是天然药物研究工作者进行新药挖掘和毒液开发利用的重要选择对象。本研究利用高通量测序平台Illumina Hiseq 2000对颜氏大疣蛛雌雄成体的毒腺进行转录组测序和生物信息学分析,共获得转录组样本数据37.8 G,总计301 024条unigenes,总长度170 512 372 bp,最短201 bp,最长36 105 bp,平均长度566 bp,GC含量平均值为38.17%,N50长度为705 bp。将unigenes序列与NR(非冗余蛋白序列数据库)、String(蛋白质相互作用数据库)、Swiss-prot(蛋白质序列数据库)、Pfam(蛋白质家族数据库)、GO(基因本体论)、KOG(真核生物蛋白质直系同源数据库)、KEGG(京都基因与基因组百科全书)数据库进行比对(e≤10^-10),分别获得31 409、6 549、11 817、8 216、11 480、7 804条unigenes注释。通过生物信息学对雌雄颜氏大疣蛛unigenes进行表达量分析,筛选高表达量且高可信度的差异表达基因,并进行对这些差异基因进行GO和KEGG功能富集分析;与雄蛛相比,雌成体有205条unigenes表达量上调,113条unigenes表达量下调。最后在所有的转录本数据中共比对到68条毒素相关序列。本研究获得的颜氏大疣蛛转录组信息,为颜氏大疣蛛的功能基因挖掘提供了重要的信息资源。 相似文献
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With the gradual maturity of sequencing technology, many microbiome studies have published, driving the emergence and advance of related analysis tools. R language is the widely used platform for microbiome data analysis for powerful functions. However, tens of thousands of R packages and numerous similar analysis tools have brought major challenges for many researchers to explore microbiome data. How to choose suitable, efficient, convenient, and easy-to-learn tools from the numerous R packages has become a problem for many microbiome researchers. We have organized 324 common R packages for microbiome analysis and classified them according to application categories (diversity, difference, biomarker, correlation and network, functional prediction, and others), which could help researchers quickly find relevant R packages for microbiome analysis. Furthermore, we systematically sorted the integrated R packages (phyloseq, microbiome, MicrobiomeAnalystR, Animalcules, microeco, and amplicon) for microbiome analysis, and summarized the advantages and limitations, which will help researchers choose the appropriate tools. Finally, we thoroughly reviewed the R packages for microbiome analysis, summarized most of the common analysis content in the microbiome, and formed the most suitable pipeline for microbiome analysis. This paper is accompanied by hundreds of examples with 10,000 lines codes in GitHub, which can help beginners to learn, also help analysts compare and test different tools. This paper systematically sorts the application of R in microbiome, providing an important theoretical basis and practical reference for the development of better microbiome tools in the future. All the code is available at GitHub github.com/taowenmicro/EasyMicrobiomeR. 相似文献
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Hyunsoo Kang Byeonghyeok Park Nicole R. Bolo Duleepa Pathiraja Shinyoung Park Minseok Cha In‐G. Choi In S. Chang 《Biotechnology journal》2019,14(6)
Syngas fermentation is largely dependent on acetogens that occur in various anaerobic environmental samples including soil, sediment, and feces. Here the authors report the metagenomic isolation of acetogens for C2 chemical production from syngas. Screening acetogens for C2 chemical production typically involves detecting the presence of the Wood‐Ljungdahl Pathway for carbon monoxide conversion. The authors collect samples from river‐bed sediments potentially having conditions suitable for carbon monoxide‐converting anaerobes, and enrich the samples under carbon monoxide selection pressure. Changes in the microbial community during the experimental procedure are investigated using both amplicon and shotgun metagenome sequencing. Combined next‐generation sequencing techniques enabl in situ tracking of the major acetogenic bacterial group and lead to the discovery of a 16 kb of gene cluster for WLP. The authors isolat an acetogenic clostridial strain from the enrichment culture (strain H21‐9). The functional activity of H21‐9 is confirmed by its high level of production of C2 chemicals from carbon monoxide (77.4 mM acetate and 2.5 mM of ethanol). This approach of incorporating experimental enrichment with metagenomic analysis can facilitate the discovery of novel strains from environmental habitats by tracking target strains during the screening process, combined with validation of their functional activity. 相似文献
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Castoe TA Poole AW Gu W Jason de Koning AP Daza JM Smith EN Pollock DD 《Molecular ecology resources》2010,10(2):341-347
Optimal integration of next-generation sequencing into mainstream research requires re-evaluation of how problems can be reasonably overcome and what questions can be asked. One potential application is the rapid acquisition of genomic information to identify microsatellite loci for evolutionary, population genetic and chromosome linkage mapping research on non-model and not previously sequenced organisms. Here, we report on results using high-throughput sequencing to obtain a large number of microsatellite loci from the venomous snake Agkistrodon contortrix, the copperhead. We used the 454 Genome Sequencer FLX next-generation sequencing platform to sample randomly ∼27 Mbp (128 773 reads) of the copperhead genome, thus sampling about 2% of the genome of this species. We identified microsatellite loci in 11.3% of all reads obtained, with 14 612 microsatellite loci identified in total, 4564 of which had flanking sequences suitable for polymerase chain reaction primer design. The random sequencing-based approach to identify microsatellites was rapid, cost-effective and identified thousands of useful microsatellite loci in a previously unstudied species. 相似文献
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【目的】研究水貂远端肠道微生物群落组成及其多样性。【方法】通过高通量测序技术研究水貂远端肠内容物细菌的组成和多样性。【结果】从10只健康水貂远端肠道内容物样品中得到146 287高质量序列代表17个菌门、167个细菌属。水貂肠道细菌以厚壁菌门(59.99%)、拟杆菌门(16.2%)、梭杆菌门(11.5%)、放线菌门(5.9%)和变形菌门(5.3%)为主,其中厚壁菌门最为丰富。厚壁菌门中的梭菌目是最丰富的目,而梭菌目中的链球菌占有50%以上的OTUs,是最大的细菌属。【结论】水貂肠道内存在复杂的微生物区系,这对进一步研究水貂对营养物质吸收利用提供了理论基础。 相似文献
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肠道微生物与人类健康的相关性研究仍然是当前生命科学研究领域的前沿热点之一。不依赖培养的16Sr RNA基因高通量测序是当前的主要研究手段。但随着测序成本的降低和数据分析方法的日渐成熟,宏基因组鸟枪法测序因具有信息量更大、更全等优势,将逐渐成为今后一段时间内研究肠道微生物组的重要手段。美国在人类微生物组计划的资助下,对30 805份样品进行了肠道微生物宏基因测序分析。通过NCBI Pub Med和SRA数据库检索,共发现72项研究收集了约10000份中国人的肠道样品用于宏基因组测序。但到目前为止,仅56项研究进行了公开发表,其中与代谢性疾病相关的文献16篇,与感染和免疫性疾病相关的文献16篇,与心脑血管疾病相关的文献12篇。由于采样地点以北京、广州、上海等大城市为主,测序平台和测序分析方法均存在较大差异,且大部分研究仍以相关性分析为主,相关研究成果在临床疾病诊疗中所发挥的作用仍非常有限。规范采样方法、标准化测序平台和数据分析流程,开展多中心平行研究将有助于数据整合和比较分析。同时,结合使用转录组、蛋白质组和培养组学等多组学方法开展功能验证和分子作用机制研究,将有利于更好地将肠道微生物研究... 相似文献
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南亚热带马尾松-红椎混交林及其纯林土壤细菌群落结构与功能 总被引:1,自引:0,他引:1
营建乡土阔叶树种人工纯林和针阔混交林是我国亚热带地区森林经营的发展趋势,但对人工纯林和针阔混交林土壤细菌群落结构及功能知之甚少。本研究以南亚热带乡土针叶树种马尾松、阔叶树种红椎人工纯林及二者的混交林为对象,运用细菌16S rRNA基因高通量测序技术和PICRUSt基因功能预测,分析了3种人工林不同土层(0~20、20~40和40~60 cm)土壤细菌群落的结构与功能。结果表明: 混交林和马尾松林土壤细菌群落结构相似,但与红椎林差异显著,红椎林土壤细菌群落多样性、生物通路代谢功能和氮循环功能低于马尾松林和混交林;土壤全氮、硝态氮和C/N是导致红椎林与马尾松林和混交林土壤细菌群落结构及功能差异的主要土壤理化因子。就土壤细菌群落结构与功能而言,在该地区营造红椎和马尾松针阔混交林要优于红椎纯林。 相似文献
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DNA sequences can be used for the analysis of genetic variation and gene function. The high-throughput sequencing techniques that have been developed over the past three years can read as many as one billion bases per run, and are far less expensive than the traditional Sanger sequencing method. Therefore, the high-throughput sequencing has been applied extensively to genomic analyses, such as screening for mutations, construction of genomic methylation maps, and the study of DNA-protein interactions. Although they have only been available for a short period, high-throughput sequencing techniques are profoundly affecting many of the life sciences, and are opening out new potential avenues of research. With the highly-developed commercial high-throughput sequencing platforms, each laboratory has the opportunity to explore this research field. Therefore, in this paper, we have focused on commercially-popular high-throughput sequencing techniques and the ways in which they have been applied over the past three years. 相似文献
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中亚热带地区氮沉降对杉木幼林土壤细菌群落多样性及组成的影响 总被引:2,自引:0,他引:2
大气氮沉降量持续增加已经成为当前关注的热点.土壤细菌群落作为土壤环境中大量存在的微生物,在养分循环过程中发挥着不可忽视的作用.在福建三明森林生态系统与全球变化研究站陈大观测点,我们在野外模拟大气氮沉降试验,通过16S rDNA扩增子测序,研究中亚热带地区杉木幼林土壤细菌群落多样性和组成对氮沉降的响应.结果表明:短期施氮对研究区的土壤细菌群落多样性和组成并未产生显著影响,但高氮处理显著改变敏感菌群相对丰度,如富营养型类群丰度增加、贫营养型类群丰度降低.土壤细菌群落的营养策略发生变化,这可能是受到了养分有效性的驱动.因此,了解土壤细菌群落和养分分配格局对氮沉降的响应,有助于提高我们对未来环境的预测能力. 相似文献
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A recent perspective article ably argued that fully sequencing more algal genomes would enable progress in diverse areas of fundamental and applied studies. More algal genomes would add resources needed to build well‐supported phylogenies, improve our understanding of how horizontal gene transfer has influenced the evolution of algal genomes, provide useful ecological insights, and generate information essential to manipulating the genomes of industrially useful algae (J. Phycol. 51:1). We agree that more algal genomes would be quite beneficial, and also propose that more algal metagenomes would enable progress in both predictable and unforeseen directions. 相似文献
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X. X. Zhao X. Q. Zhang J. Wang T. Frazier G. Yin X. Huang D. F. Yan W. J. Zang X. Ma Y. Peng Y. H. Yan W. Liu 《Molecular ecology resources》2015,15(6):1497-1509