| Title: | Real-Time PCR Data Sets by Boggy et al. (2010) |
| Version: | 0.0.1 |
| Description: | Real-time quantitative polymerase chain reaction (qPCR) data sets by Boggy et al. (2008) <doi:10.1371/journal.pone.0012355>. This package provides a dilution series for one PCR target: a random sequence that minimizes secondary structure and off-target primer binding. The data set is a six-point, ten-fold dilution series. For each concentration there are two replicates. Each amplification curve is 40 cycles long. Original raw data file: https://journals.plos.org/plosone/article/file?type=supplementary&id=10.1371/journal.pone.0012355.s004. |
| License: | CC BY 4.0 |
| Encoding: | UTF-8 |
| RoxygenNote: | 7.3.1 |
| Imports: | tibble |
| Depends: | R (≥ 2.10) |
| LazyData: | true |
| URL: | https://rmagno.eu/boggy/, https://github.com/ramiromagno/boggy |
| BugReports: | https://github.com/ramiromagno/boggy/issues |
| NeedsCompilation: | no |
| Packaged: | 2024-04-24 15:41:49 UTC; rmagno |
| Author: | Ramiro Magno |
| Maintainer: | Ramiro Magno <rmagno@pattern.institute> |
| Repository: | CRAN |
| Date/Publication: | 2024-04-25 16:10:02 UTC |
boggy: Real-Time PCR Data Sets by Boggy et al. (2010)
Description
Real-time quantitative polymerase chain reaction (qPCR) data sets by Boggy et al. (2008) doi:10.1371/journal.pone.0012355. This package provides a dilution series for one PCR target: a random sequence that minimizes secondary structure and off-target primer binding. The data set is a six-point, ten-fold dilution series. For each concentration there are two replicates. Each amplification curve is 40 cycles long. Original raw data file: https://journals.plos.org/plosone/article/file?type=supplementary&id=10.1371/journal.pone.0012355.s004.
Author(s)
Maintainer: Ramiro Magno rmagno@pattern.institute (ORCID)
Other contributors:
Pattern Institute [copyright holder, funder]
See Also
Useful links:
Report bugs at https://github.com/ramiromagno/boggy/issues
qPCR data set by Boggy et al. (2010)
Description
The qPCR data set named s1 comprises a six-point, ten-fold dilution series, replicated in duplicates targeting an amplicon designed with a random sequence that minimizes secondary structure and off-target primer binding. Please read the Quantitative PCR data section, qPCR assays subsection of Boggy et al. (2010) for more details.
Format
A tibble with 480 rows and 10 variables:
platePlate identifier. For this data set it is always missing (
NA).wellWell identifier.
dyeThe type of dye used. In this data set the values are always
"SYTO 13", meaning 2 mM of the dsDNA dye SYTO-13 (Invitrogen, Carlsbad, CA).targetTarget identifier: the amplicon used, a random sequence dubbed
"S1"by the original authors.sample_typeSample type (all curves are standards, i.e.
"std").replicateReplicate identifier: either 1 or 2.
copiesStandard copy number.
dilutionDilution factor. Higher number means greater dilution.
cyclePCR cycle.
fluorRaw fluorescence values.
Source
doi:10.1371/journal.pone.0012355
Examples
s1