genome.cn
基因组测序门户|安诺基因 - Powered by Discuz!高通量测序门户，安诺优达基因科技旗下科研服务官方网站。基因组学高通量测序和生物信息分析的领先提供商。
http://www.genome.cn/
高通量测序门户，安诺优达基因科技旗下科研服务官方网站。基因组学高通量测序和生物信息分析的领先提供商。
http://www.genome.cn/
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基因组测序门户|安诺基因 - Powered by Discuz! | genome.cn Reviews
https://genome.cn
高通量测序门户，安诺优达基因科技旗下科研服务官方网站。基因组学高通量测序和生物信息分析的领先提供商。
Annoroad ｜NGS
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing. AnnoCloud blockbuster released, leading Annoroad opening the new era of BT to DT. Annoroad technology successfully developed the first single-cell genome and transcriptome parallel sequencing technology. Current breakthrough of Annoroad’s application of target region sequencing on exploring the Molecular prognostic stratification of MDS was published on Blood. 309th Hospital of the PLA. During the coope...
肿瘤防治与精准医学-知识中心-安诺优达
http://www.annoroad.com/knowledge/health_and_genome
根据全国肿瘤登记中心发布的 2012中国肿瘤登记年报 中的数据，我国肿瘤发病率为285.91/10万，每年新发肿瘤病例约为312万例，平均每天8550人发病，国内平均每分钟就有6人被诊断为恶性肿瘤，癌症已成为我国居民首要死因，同时国内肿瘤发病还呈现逐年上升和年轻化趋势。 世界卫生组织 WHO 指出 早期发现是提高癌症治疗率的关键。 DNA Deoxyribonucleic acid ，即脱氧核糖核酸，是染色体的主要化学成分，同时还是生物体遗传信息的最基本载体。 基因控制着人类生命活动，与人类的 生、老、病、死 息息相关 它决定了人类的相貌、肤色、体质、疾病易感性及药物敏感性等，被誉为人类的 生命之书。 1 报告解读 对检测到的基因变异信息进行解释和说明 这些变异的临床意义及参考依据. 2012 Annoroad.com 安诺优达基因科技 北京 有限公司 版权所有.
Genome-Service-Target-BS-Introduction
http://en.genome.cn/products_and_service/target
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing.
Genome-Service-WGBS-Introduction
http://en.genome.cn/products_and_service/Cardio_Cerebrovascular
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing. Whole Genome Bisulfite Sequencing (WGBS) is based on the next-generation sequencing platform, integrating the whole genome bisulfite treatment and bioinformatics analysis techniques to achieve a sophisticated genome-wide DNA methylation profiling at single-base resolution.
Genome-Service
http://en.genome.cn/products_and_service/index2
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing. Giorgetti L, Lajoie BR, Chen CJ, et al. Structural organization of the inactive X chromosome in the mouse[J]. Gendrel A V, Attia M, Chen C J, et al. Developmental dynamics and disease potential of random monoallelic gene expression[J]. Servant N, Varoquaux N, Lajoie B R, et al. HiC-Pro: an optimized and flexible pipeline for Hi-C data processing[J].
Genome-Service-Plant Hi-C-Introduction
http://en.genome.cn/products_and_service/blood
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing. Hi-C sequencing specialize in exploring the spatial structure of chromatin DNA in the whole genome, namely, a high resolution of 3D structure information can be captured by the model of DNA interaction in chromatins. The unique cell-wall breaking and formaldehyde fixation successfully reduced the self-looping rate and raised the valid data rate.
Genome-Service-RRBS-Introduction
http://en.genome.cn/products_and_service/rrbs
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing.
Genome-Service-Human WGS-Introduction
http://en.genome.cn/products_and_service/mendelianDisease
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing.
Genome-Service-Single Cell Genome Sequencing-Introduction
http://en.genome.cn/products_and_service/prenatal
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing. Single Cell Genome Sequencing. Single Cell Genome Sequencing.
Genome-Service-Animal Hi-C-Introduction
http://en.genome.cn/products_and_service/Breast_Ovarian
Single Cell Genome Sequencing. Single Cell Transcriptome Sequencing. Single Cell Bisulfite Sequencing. Hi-C sequencing, a technique derived from the Chromosome Conformation Capture - 3C, is able to exhibit the 3D structure information about chromatin with high-resolution via high-throughput sequencing technology and bioinformatics methods.
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Welcome to CBS
CCBR Genome Browser Home
This site hosts genomes sequenced at the CCBR using a local installation of the UCSC Genome Browser. The Cannabis genome project is a collaboration between the Hughes lab. University of Toronto), Page Lab (University of British Columbia) and van Bakel Lab. Icahn School of Medicine at Mount Sinai). November 2011 - finola1 assembly. Public release of the Cannabis sativa. October 2011 - canSat3 assembly. Public release of the Cannabis sativa.
CGRB Bioinformatics Site | Oregon State University
Welcome to the CGRB Genome Resource. Beaver Genome - American Beaver. Brachypodium Genome - American Beaver. Poplar Genome - P. trichocarpa v3.0 (210). 2016 Oregon State University.
BBC Genome
Radio Times 1923 - 2009. Welcome to the BBC Genome Project. This site contains the BBC listings information which the BBC printed in Radio Times between 1923 and 2009. You can search the site for BBC programmes, people, dates and Radio Times editions. We hope it helps you find that long forgotten BBC programme, research a particular person or browse your own involvement with the BBC. Through the listings, you will also be able to find thousands of radio and TV programmes. Browse the issue archive. This i...
CUGI
Storage and Distribution of Clones. High Information Content Fingerprinting. 454 / Illumina Sequencing. Whole BAC Assembly/Gap closure/Finishing. Hybridization Protocol for BAC Colony Filters. Sample Prep for DNA Sequencing. CUGI researchers provide intellectual contribution as PI, Co-PI, Senior Staff or Key Personnel on research grants. Genomic and Bioinformatics services provided through consultation and formal service agreement. Memorial Day: Monday, May 28, 2018. Hrs prior to the closing dates.
基因组测序门户|安诺基因 - Powered by Discuz!
科研工作中经常遇到短期内难以得到大量新鲜组织标本的难题，甲醛固定石蜡包埋 Formalin-Fixed and Parrffin-Embedded，FFPE 样本因其便于运输，可长期保存等特点，是最常用的人类病历档案标本和分子生 阅读全文. 来自:genome 更新时间:2015-08-14 类别: 公司动态. 2015年初，Illumina公司重磅推出HiSeq 4000 测序平台，实现了 工厂级 测序通量的最长读长，以高质量和低成本的显著优势开启了高通量测序又一个辉煌的时代。 来自:genome 更新时间:2015-08-06 类别: 公司动态. 来自:genome 更新时间:2015-07-31 类别: 公司动态. 来自:genome 更新时间:2015-07-30 类别: 公司动态. 来自:genome 更新时间:2015-07-28 类别: 公司动态. 来自:genome 更新时间:2015-07-24 类别: 公司动态. 来自:genome 更新时间:2015-07-22 类别: 公司动态. 来自:genome 更新时间:2015-07-21 类别: 公司动态. 北京时间2015年6月10日...
Genome International Corp.
Hassle free analysis of next-generation sequencing data. Cloud-based analysis of high-throughput data. Powerful data visualization and annotation capabilities. Support for several NGS applications (mRNA-Seq, DNA/Exome Seq, Methylyome-Seq, miRNA-Seq, ChIP-Seq). Largest resource of splicing signals. 3D visualization of domain architecture mapped to exon-intron structures of genes. An integrated database of alternative splicing and transcription events. Dynamic platform to analyze disease causing mutations.
UCSC Genome Browser Home
Reset All User Settings. Interactively visualize genomic data. Rapidly align sequences to the genome. Download data from the Genome Browser database. Get functional effect predictions for variant calls. Combine data sources from the Genome Browser database. Find genes that are similar by expression and other metrics. Genome Browser in a Box (GBiB). Run the Genome Browser on your laptop or server. Rapidly align PCR primer pairs to the genome. Convert genome coordinates between assemblies.
Genome Research
Skip to main page content. Associate Editor Position Available. Top 10 Most Read Articles. Join Us on Facebook. Cold Spring Harbor Molecular Case Studies. Cold Spring Harbor Perspectives in Medicine. Cold Spring Harbor Perspectives in Biology. Cold Spring Harbor Protocols. Cold Spring Harbor Symposia. Books and Other Media. March 27, 2018. GR in the News. E-mail Alerts and RSS Feeds. Enhancer RNA profiling predicts transcription factor activity. Human-specific splicing switch and hepatocellular carcinoma.
Fintech Genome
