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- Publisher Website: 10.3390/ijms18122516
- Scopus: eid_2-s2.0-85035125443
- PMID: 29186809
- WOS: WOS:000418896700020
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Article: Aptamer Bioinformatics
Title | Aptamer Bioinformatics |
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Authors | |
Keywords | HTS aptamer fragment based design in silico selection molecular dynamics simulation |
Issue Date | 2017 |
Publisher | Molecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/ijms |
Citation | International Journal of Molecular Sciences, 2017, v. 18 n. 12, p. E2516 How to Cite? |
Abstract | Aptamers are short nucleic acid sequences capable of specific, high-affinity molecular binding. They are isolated via SELEX (Systematic Evolution of Ligands by Exponential Enrichment), an evolutionary process that involves iterative rounds of selection and amplification before sequencing and aptamer characterization. As aptamers are genetic in nature, bioinformatic approaches have been used to improve both aptamers and their selection. This review will discuss the advancements made in several enclaves of aptamer bioinformatics, including simulation of aptamer selection, fragment-based aptamer design, patterning of libraries, identification of lead aptamers from high-throughput sequencing (HTS) data and in silico aptamer optimization. |
Persistent Identifier | http://hdl.handle.net/10722/259090 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.179 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Kinghorn, AB | - |
dc.contributor.author | Fraser, LA | - |
dc.contributor.author | Liang, S | - |
dc.contributor.author | Shiu, CC | - |
dc.contributor.author | Tanner, JA | - |
dc.date.accessioned | 2018-09-03T04:01:20Z | - |
dc.date.available | 2018-09-03T04:01:20Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | International Journal of Molecular Sciences, 2017, v. 18 n. 12, p. E2516 | - |
dc.identifier.issn | 1422-0067 | - |
dc.identifier.uri | http://hdl.handle.net/10722/259090 | - |
dc.description.abstract | Aptamers are short nucleic acid sequences capable of specific, high-affinity molecular binding. They are isolated via SELEX (Systematic Evolution of Ligands by Exponential Enrichment), an evolutionary process that involves iterative rounds of selection and amplification before sequencing and aptamer characterization. As aptamers are genetic in nature, bioinformatic approaches have been used to improve both aptamers and their selection. This review will discuss the advancements made in several enclaves of aptamer bioinformatics, including simulation of aptamer selection, fragment-based aptamer design, patterning of libraries, identification of lead aptamers from high-throughput sequencing (HTS) data and in silico aptamer optimization. | - |
dc.language | eng | - |
dc.publisher | Molecular Diversity Preservation International. The Journal's web site is located at http://www.mdpi.org/ijms | - |
dc.relation.ispartof | International Journal of Molecular Sciences | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | HTS | - |
dc.subject | aptamer | - |
dc.subject | fragment based design | - |
dc.subject | in silico selection | - |
dc.subject | molecular dynamics | - |
dc.subject | simulation | - |
dc.title | Aptamer Bioinformatics | - |
dc.type | Article | - |
dc.identifier.email | Kinghorn, AB: kinghorn@hku.hk | - |
dc.identifier.email | Tanner, JA: jatanner@hkucc.hku.hk | - |
dc.identifier.authority | Tanner, JA=rp00495 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3390/ijms18122516 | - |
dc.identifier.pmid | 29186809 | - |
dc.identifier.pmcid | PMC5751119 | - |
dc.identifier.scopus | eid_2-s2.0-85035125443 | - |
dc.identifier.hkuros | 289833 | - |
dc.identifier.volume | 18 | - |
dc.identifier.issue | 12 | - |
dc.identifier.spage | E2516 | - |
dc.identifier.epage | E2516 | - |
dc.identifier.isi | WOS:000418896700020 | - |
dc.publisher.place | Switzerland | - |
dc.identifier.issnl | 1422-0067 | - |