From: Aparna Kumar <aparnak...@gmail.com>Date: March 15, 2011 7:11:18 PM EDTTo: Murat Can Cobanoglu <mu...@pitt.edu>Subject: Re: QuestionI think you are on the right track... Think about how you could fit a line and make it piecewise continuous. Write down the equation for 1.4 first and force the second line to connect to the first line by considering the largest x value where the first line is defined. Also would you mind posting this to googlegroups? I think others would benefit.
Sent from my iPhoneI would fit a line on the 50 invariant genes in each segment. When you fit a line to 50 points, it automatically has a specified intercept.This is what I understood from mails and the paper. Am I supposed to do something else?On Mar 15, 2011, at 3:28 PM, Aparna Kumar wrote:Well, how did you decide on the intercepts of each line segment?On Tue, Mar 15, 2011 at 3:07 PM, Murat Can Cobanoglu <mu...@pitt.edu> wrote:
Aparna
After calculating line fits to the invariant sets of every segment, the ends of the line segments will not connect. How do we overcone this problem?
-MCC
Sent from my iPhoneMurat Can Cobanoglu, MScPhD StudentCMU-Pitt Computational Biology PhD Program
Lu
I don't think I correctly understood what I should list. For every segment, I created a scatter plot of the genes that I chose for the invariant set. Consequently, I have 66 such plots. Is this correct?
How to construct the curve though, I don't know.
I am still confused. first we get the abs rank difference/65000, then
sort. then get 65 segments of 1000 genes,
if we select 65 PRDs for each segment to select 50 genes. then would they all be different? more
correctly, decreasing?
Then how are the PRDs monotonically nondecreasing?