Plant breeding has been beneficial in developing improved varieties using conventional tools, techniques and methodologies. The availability of NGS tools and online resources is leading to a gene revolution of
Next-Gen Sequencing tools from the Horvath Lab. Contribute to HorvathLab/NGS development by creating an account on GitHub.
To perform variant calling, there are numerous tools that usually feature different algorithms, filtering strategies, recommendations and thus, also different output.doi:10.7490/f1000research.1114602.1S. SandmannA. O. GraafM. KarimiB. A. Reijden...
Characterisation of the sewage virome: comparison of NGS tools and occurrence of significant pathogens[J]. Science of the Total Environment, 2020, APR 15. Doi: 10.1016/j.scitotenv.2020.136604. 文中病毒组研究方法: 本研究重点比较了用于检测城市污水中病毒的不同NGS方法(非靶向病毒宏基因组学、目标...
Explore the “Getting Started” and “Troubleshooting” sections for solutions to top inquiries and common problems. Browse through the “Guides and Tools” section to access comprehensive product-related support resources. Getting Started What is the Ion Torrent™...
Characterisation of the sewage virome: comparison of NGS tools and occurrence of significant pathogens[J]. Science of the Total Environment, 2020, APR 15. Doi: 10.1016/j.scitotenv.2020.136604. 文中病毒组研究方法: 本研究重点比较了用于检测城市污水中病毒的不同NGS方法(非靶向病毒宏基因组学、目标...
ClinGen提供了变异的剂量敏感性,有助于辨别突变的显隐性异常模式。更重要的是ClinGen结合临床、遗传模式、人群、功能证据及专家评审,根据ACMG/AMP指南对变异进行致病性分类,结果保存在ClinVar中。实验室和临床医生也可以使用ClinGen的”variant curation tools”来**评估尚未经过专...
I like helping people. Reducing frustration and making people more productive just feels good. A scalable way to help is thorugh tools. That is why I created NGS. It is a programming language with typical Ops tasks in mind. See the use cases below. The next big planned part is the inter...
Code Issues Pull requests Tools for working with genomic and high throughput sequencing data. bioinformatics scala genomics ngs umi analyzing-genomic-data fgbio molecular-indexes Updated May 2, 2025 Scala samtools / htsjdk Star 286 Code Issues Pull requests Discussions A Java API for high-throu...
ClinGen提供了变异的剂量敏感性,有助于辨别突变的显隐性异常模式。更重要的是ClinGen结合临床、遗传模式、人群、功能证据及专家评审,根据ACMG/AMP指南对变异进行致病性分类,结果保存在ClinVar中。实验室和临床医生也可以使用ClinGen的”variant curation tools”来**评估尚未经过专家审查的变异致病性的证据。