storing.inds
function and creates an overlapping plot to assess graphically the peaks of several plants in certain channel in order to create a panel for the next functions score.easy
. The function contains several defaults in most of the arguments, please check arguments but in general.Please! once you have found the best parameters for the arguments to match your ladder using the detect.ladder
function, please pass those values to this function since it will use the same function internally and your dna sizes will depend on that, please make sure the 'dev' argument is passed to the new functions.
overview2(my.inds, cols = 1, n.inds = NULL, xlim = NULL,
ylim = NULL, ladder, channel.ladder = NULL, ploidy = 2,
ci.upp = 1.96, ci.low = 1.96, dev = 50, method="cor",
init.thresh=200, ladd.init.thresh=200, lwd=.1, warn=TRUE,
min.panel=100, env = parent.frame())
storing.inds
function outputfind.ladder
functionfind.ladder
functionfind.ladder
functionfind.ladder
functionfind.ladder
function. We recommend not to deal to much with it unless you identified special situations with your ladderCovarrubias-Pazaran G, Diaz-Garcia L, Schlautman B, Salazar W, Zalapa J. (2015) Fragma: An R package for fragment analysis. R package version 1.0. URL https://cran.r-project.org/web/packages/Fragman/.
Robert J. Henry. 2013. Molecular Markers in Plants. Wiley-Blackwell. ISBN 978-0-470-95951-0.
Ben Hui Liu. 1998. Statistical Genomics. CRC Press LLC. ISBN 0-8493-3166-8.
data(my.plants)
my.plants <- my.plants[1]
my.ladder <- c(120, 125, 129, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375)
overview2(my.inds=my.plants, cols = 1, ladder=my.ladder, lwd=1)
# now use:
# my.panel <- locator(type="p", pch=20, col="red")$x
# to click over the peaks and get the sizes in base pairs
# when you are done make sure you press the "Esc" key, do not push the stop button
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