Description Usage Format Source
A small silly example of transmission isnv comparision data.
1 |
a data frame with 12 rows of 35 variables
Chromosome - genomic segment
position on genomic segment
Specimen id for first sample
Specimen id for second sample
Enroll id for first sample
Enroll id for second sample
Id of the house of the individual
The date of symptom onset for the first sample
The date of symptom onset for the second sample
The infered date of transmission
Logical - was the first sample sequenced
Logical - was the second sample sequenced
Did the first sample qualify for isnv identification
Did the second sample qualify for isnv identification
Is this a valid transmission pair
Does this need to be analyzed in both directions
Did the whole pair get sequenced
Are both samples above the titer cut off (10^3)
Did both samples qualify for isnv detection
Id for the pairing
Does the sample meet the distance criteria for a transmission pair
Date of collection for the first sample
Date of collection for the second sample
mutation as chr_refPosVar
nucleotide in the plasmid control
nucleotide in the sample
qpcr result for the samples-Strain
The frequency of the variant in the first sample
The frequency of the vairant in the second sample
The season of sampling
The genomes/ul in the first sample
The genomes/ul in the second sample
What benchmarking frequency do we consider this to be at
Is the variant found in the second sample
data-raw/small_trans.R
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