GeneCovPancreas: Data from the Jones et al. 2008 study: Total number of...
In CancerMutationAnalysis: Cancer mutation analysis
Description
Usage
Format
References
See Also
Description
Total numbers of nucleotides "at risk" that were
successfully sequenced in RefSeq genes in the Jones et al. 2008
pancreatic cancer study.
Usage
1
data(JonesPancreas08)
Format
Total number of nucleotides available for mutations ("coverage")
in the pancreatic cancer study from Jones et al.,
broken down by gene, screen (Discovery or Prevalence),
and mutation type, composed of the wild type nucleotide
and its context. The object is a data frame, with the
variables: Gene, Screen, WTNuc (wild type nucleotide),
Context, and Coverage. The two possible values
for Screen are Disc ("Discovery") and Prev ("Prevalence").
For this study, only the Discovery screen is considered.
The nucleotides availables for indels are all the successfully
sequenced nucleotides in a gene; the corresponding rows
have a "" entry for WTNuc and an "All" entry for "Context."
The nucleotides availables for other
mutations are excluding nucleotides which can only give rise to
synonymous mutations.
References
Jones S, Zhang X, Parsons DW, Lin JC, Leary RJ, Angenendt P, Mankoo P,
Carter H, Kamiyama H, Jimeno A, et al.
Core signaling pathways in human pancreatic cancers revealed by global
genomic analyses.
Science. DOI: 10.1126/science.1164368
Parmigiani G, Lin J, Boca S, Sjoeblom T, Kinzler KW,
Velculescu VE, Vogelstein B. Statistical methods for the analysis of
cancer genome sequencing data.
http://www.bepress.com/jhubiostat/paper126/
See Also
cma.scores, cma.fdr,
cma.set.stat, cma.set.sim,
SimMethodsSims-class,
GeneAlterPancreas,
GeneSampPancreas
CancerMutationAnalysis documentation built on Nov. 8, 2020, 6:47 p.m.
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Description Usage Format References See Also
Description
Total numbers of nucleotides "at risk" that were successfully sequenced in RefSeq genes in the Jones et al. 2008 pancreatic cancer study.
Usage
1 | data(JonesPancreas08)
|
Format
Total number of nucleotides available for mutations ("coverage") in the pancreatic cancer study from Jones et al., broken down by gene, screen (Discovery or Prevalence), and mutation type, composed of the wild type nucleotide and its context. The object is a data frame, with the variables: Gene, Screen, WTNuc (wild type nucleotide), Context, and Coverage. The two possible values for Screen are Disc ("Discovery") and Prev ("Prevalence"). For this study, only the Discovery screen is considered. The nucleotides availables for indels are all the successfully sequenced nucleotides in a gene; the corresponding rows have a "" entry for WTNuc and an "All" entry for "Context." The nucleotides availables for other mutations are excluding nucleotides which can only give rise to synonymous mutations.
References
Jones S, Zhang X, Parsons DW, Lin JC, Leary RJ, Angenendt P, Mankoo P, Carter H, Kamiyama H, Jimeno A, et al. Core signaling pathways in human pancreatic cancers revealed by global genomic analyses. Science. DOI: 10.1126/science.1164368
Parmigiani G, Lin J, Boca S, Sjoeblom T, Kinzler KW, Velculescu VE, Vogelstein B. Statistical methods for the analysis of cancer genome sequencing data. http://www.bepress.com/jhubiostat/paper126/
See Also
cma.scores, cma.fdr,
cma.set.stat, cma.set.sim,
SimMethodsSims-class,
GeneAlterPancreas,
GeneSampPancreas
R Package Documentation
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We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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