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Sanger sequencing is a method of DNA sequencing that involves electrophoresis and is based on the random incorporation of chain-terminating dideoxynucleotides by DNA polymerase during in vitro DNA replication. After first being developed by Frederick Sanger and colleagues in 1977, it became the most widely used sequencing method for approximately 40…
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sequencing dna sanger sequence electrophoresis method automated methods fragments capillary using genome data fluorescent nucleotides four reaction polymerase surveillance used
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Sanger sequencing | is a | method of DNA sequencing that involves electrophoresis and is based on the random incorporation of chain-terminating dideoxynucleotides by DNA polymerase during in vitro DNA rep… | 0.90 | text |
| Sanger sequencing | is a | lab-on-a-chip application for DNA sequencing | 0.90 | text |
| sequencing the spike protein from SARS-CoV-2 as well as for the surveillance of norovirus outbreaks through the United States Center for Disease Control | instance of | Sanger sequencing is still actively being used in efforts for public health initiatives | 0.80 | text |
| Prevention | instance of | Sanger sequencing is still actively being used in efforts for public health initiatives | 0.80 | text |
| the S-gene | instance of | others have opted to sequence very specific genes of the virus | 0.80 | text |
| encoding the information needed to produce the spike protein | instance of | others have opted to sequence very specific genes of the virus | 0.80 | text |
| next generation sequencing | instance of | Laboratories in lower income countries may not have the capabilities to implement expensive applications | 0.80 | text |
| so Sanger methods may prevail in supporting the generation of sequencing data for surveillance of variants.Sanger sequencing is also the | instance of | Laboratories in lower income countries may not have the capabilities to implement expensive applications | 0.80 | text |
| Phred typically provides an estimate of quality to aid in trimming of low-quality regions of sequences.In cases where DNA fragments are cloned before sequencing | instance of | Base calling software | 0.80 | text |
| the resulting sequence may contain parts of the cloning vector | instance of | Base calling software | 0.80 | text |
| Ampliseq | instance of | methods | 0.80 | text |
| SeqSharp have been developed that allow rapid sequencing of target genes without cloning or prior amplification.Current methods can directly sequence only relatively short | instance of | methods | 0.80 | text |
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