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1.
Nucleic Acids Res ; 52(W1): W95-W101, 2024 Jul 05.
Article in English | MEDLINE | ID: mdl-38738626

ABSTRACT

Thousands of long noncoding RNAs (lncRNAs) have been annotated via high-throughput RNA sequencing, yet only a small fraction have been functionally investigated. Genomic knockout is the mainstream strategy for studying the biological function of protein-coding genes and lncRNAs, whereas the complexity of the lncRNA locus, especially the natural antisense lncRNAs (NAT-lncRNAs), presents great challenges. Knocking out lncRNAs often results in unintended disruptions of neighboring protein-coding genes and small RNAs, leading to ambiguity in observing phenotypes and interpreting biological function. To address this issue, we launched LncRNAway, a user-friendly web tool based on the BESST (branchpoint to 3' splicing site targeting) method, to design sgRNAs for lncRNA knockout. LncRNAway not only provides specific and effective lncRNA knockout guidelines but also integrates genotyping primers and quantitative PCR primers designing, thereby streamlining experimental procedures of lncRNA function study. LncRNAway is freely available at https://www.lncrnaway.com.


Subject(s)
Internet , RNA, Guide, CRISPR-Cas Systems , RNA, Long Noncoding , Software , RNA, Long Noncoding/genetics , RNA, Long Noncoding/metabolism , RNA, Guide, CRISPR-Cas Systems/genetics , Humans , Gene Knockout Techniques , CRISPR-Cas Systems
2.
Nucleic Acids Res ; 51(W1): W397-W403, 2023 07 05.
Article in English | MEDLINE | ID: mdl-37114999

ABSTRACT

Advancements in comparative genomics research have led to a growing interest in studying species evolution and genetic diversity. To facilitate this research, OrthoVenn3 has been developed as a powerful, web-based tool that enables users to efficiently identify and annotate orthologous clusters and infer phylogenetic relationships across a range of species. The latest upgrade of OrthoVenn includes several important new features, including enhanced orthologous cluster identification accuracy, improved visualization capabilities for numerous sets of data, and wrapped phylogenetic analysis. Furthermore, OrthoVenn3 now provides gene family contraction and expansion analysis to support researchers better understanding the evolutionary history of gene families, as well as collinearity analysis to detect conserved and variable genomic structures. With its intuitive user interface and robust functionality, OrthoVenn3 is a valuable resource for comparative genomics research. The tool is freely accessible at https://orthovenn3.bioinfotoolkits.net.


Subject(s)
Databases, Genetic , Genomics , Phylogeny , Genome/genetics
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