transcriptome

DNA Microarray is the best tool to investigate gene expression on transcriptome level .

表达基因芯片分析是在转录组水平研究基因表达情况的最佳工具。

Recent Study of Pollen Transcriptome

花粉发育的转录组研究进展

Genome and transcriptome analyses will complement the proteome and genetic information available today .

基因组和转录组分析无疑将补充现有的蛋白质组和遗传学知识。

Insights into Rubber Biosynthesis from Transcriptome Analysis of Hevea Brasiliensis Latex

通过胶乳转录组分析探析巴西橡胶树橡胶生物合成的研究

Genome Transcriptome Map Construction with cDNA-AFLP Techniques

用cDNA-AFLP技术构建基因组转录图谱

Progress in The Comparison of Transcriptome and Proteome

转录组与蛋白质组比较研究进展

Large-scale transcriptome data for the common carp genome should help reveal the timing of the additional duplication event .

因此，鲤大规模转录组数据有利于我们研究鲤额外的基因组复制事件发生的大致时间。

A-to-I RNA editing act as a central generator of transcriptome diversity regulation in higher eukaryotes .

A-to-ⅠRNA编辑在高等真核生物转录组的多样性及调控性中扮演举足轻重的角色。

Proteome studies aim at the complete set of proteins encoded by the genome and thus complement the transcriptome studies .

蛋白质组研究旨在研究基因组编码的整套蛋白质的结构和功能，从而补充转录组的研究。

Rather than sequence the whole genome of the plant , the team focused on parts of the genetic code called the transcriptome .

这组科学家并没有对这种植物的整个基因组测序，而是把重点放在了称为转录组的遗传编码的部分。

The latest state of the database shows that high registration rate and high page views confirm the human transcriptome annotation system has high practicability .

最新数据库状态表明，短期内的高注册率和高访问量说明人类转录组注释系统具有较高的实用性。

Transcriptome analysis has been used to study the existence and timing of genome duplication in species for which genome sequences are incomplete .

在全基因组还没测序或还没完成的物种中，已经有研究学者利用转录组数据来分析物种基因组复制事件的存在以及复制时间的问题。

Thus , the molecular changes in the transcriptome associated with the transition from normal to intraepithelial neoplasm may influence colorectal cancer progression .

因此，从正常肠上皮转化为上皮内瘤变的阶段中，转录组水平上的分子改变可能会影响结直肠癌的进展。

Rapidly identified the salt-stress induced genes from the massive amount of transcriptome sequencing data by DDRT-PCR combined with local BLAST analysis .

利用DDRT-PCR技术结合本地比对分析快速从海量转录组数据库中筛选耐盐基因。

Transcriptome can be used not only to discover genes that are responsible for particular physiological status , but also to develope new genetic markers .

转录组不仅可以用来获取反映特定生理状态的基因，还可用于开发新的分子标记。

It is clear that in this case quantitative transcriptome data is not indicating directly enzyme activity , therefore more studies are needed to clarify this relation .

很显然，在这种情况下，定量转录组数据并不能直接表明酶的活性，因此需要更多的研究来阐明这种关系。

Transcriptome analyses were carried out on insecticide-treated and control aphids , including the quality of transcriptome data and differentially expressed genes .

将用三种杀虫剂处理的蚜虫及对照组进行转录组测序，运用生物学软件对转录组实验数据进行分析，包括转录组数据库质量的分析和筛选差异性表达基因。

With the usage of transcriptome data , it found that almost all genes are related to the mogrosides V biosynthesis pathway .

利用转录组数据发现了罗汉果甜苷V生物合成通路中几乎所有的基因，涉及到20种基因。

With the rapidly development of New Generation Sequencing technology , it become possible to sequence a species ' transcriptome with low cost , high throughput , faster and precise .

第二，新一代测序技术的发展壮大，使得低成本、高通量、快速、精确且全面地分析基因转录情况成为可能。

We validate these genes differentially expressed by qRT-PCR . The result of qRT-PCR is consistent with the result of transcriptome data .

利用qRT-PCR技术对这些基因的差异表达进行验证，结果显示qRT-PCR数据与转录组数据相一致。

Alternative splicing of pre-messenger RNA is a key feature of transcriptome expansion in eukaryotic cells , yet its regulation is poorly understood .

信使RNA前体可变剪接是真核细胞转录的一个主要特点，但其调控知之甚少。

We elucidate the algorithms , the computing requirements and programs in different transcriptome sequences analysis systems and propose a strategy more suitable for large scale analysis of alternative splicing .

讨论不同转录组分析系统中的数据分析算法及其计算需求，并提出适用于大规模可变剪接分析的策略。

Many different human tissue / cell transcriptome datasets coming from RNA-Seq technology are publicly available at present , which provides the necessary prerequisite and possibility for this study .

目前已有人类许多不同组织或细胞系的RNA-Seq转录组数据，这为本研究提供了必要的前提和可能。

A high quality and complete genome annotation is the basis of transcriptome downstream analysis , such as the analyses of gene expression , epigenetic regulation , and phylogeny .

高质量、完整的基因组注释是转录组下游分析的基础，包括基因表达分析、表观遗传分析、系统发育分析等。

Five DMRT genes were found to be expressed in gonads by transcriptome analysis . They may play important roles in sex determination and differentiation , and gonadal development .

转录组分析发现有5个DMRT基因在性腺中表达，它们可能在尼罗罗非鱼性腺发育、性别决定与分化中起重要作用。

SRAP and TRAP are being applied in germplasm genetic diversity analysis , genetic map including transcriptome map construction , important trait gene tagging and gene cloning in many crops .

目前这两种标记系统已开始在多种作物的种质资源鉴定评价、遗传图谱构建（包括转录图谱）、重要性状标记乃至基因分离克隆等方面成功应用。

The availability of huge transcriptome data produced from various tissues in various organisms , which are based on oligonucleotide microarray technology , makes it possible to study the gene regulation expression .

大量基于基因芯片的不同物种或不同组织基因表达数据的产生为该领域的研究提供了很大便利。

In order to further reveal the mechanism of JA in regulation of strawberry fruit development and ripening , we have a RNA transcriptome analysis using mid-green fruit .

为深入揭示JA调控草莓果实发育和成熟的机理，在草莓果实发育中期，对JA应答基因的表达进行了RNA转录水平分析。

RNA-seq is a powerful tool for comprehensive characterization of whole transcriptome at both gene and exon levels and with a unique ability of identifying novel splicing variants .

在全基因组层面上阐明基因及外显子的表达水平，尤其是鉴定新的剪接异构体，RNA-seq具有独特的优势。

RNA-Sequencing ( RNA-Seq ) provides researchers with a powerful toolbox for characterization and quantification of transcriptome , and is widely used in the study of gene expression regulation .

RNA-Sequencing（RNA-Seq）是当前非常有效的可以定性和定量化分析转录组的技术，被广泛应用于基因表达调控领域的研究。