On 20-Feb-09, at 6:41 AM, Olivier Grisel wrote:
Alright, thanks for the reply.
Is there a canonical way /sample code to gain low level access to
blas / lapack
atlas routines using ctypes from numpy / scipy code?
I don't mind fixing the dimensions and the ndtype of my array if it
can
On Sun, March 15, 2009 8:57 pm, Sturla Molden wrote:
Regarding ticket #1054. What is the reason for this strange behaviour?
a = np.zeros((10,10),order='F')
a.flags
C_CONTIGUOUS : False
F_CONTIGUOUS : True
OWNDATA : True
WRITEABLE : True
ALIGNED : True
UPDATEIFCOPY : False
On 3/16/2009 9:27 AM, Pearu Peterson wrote:
If a operation produces new array then the new array should have the
storage properties of the lhs operand.
That would not be enough, as 1+a would behave differently from a+1. The
former would change storage order and the latter would not.
Hi,
What's the status on SVN and ticket email notifications? The only messages
I'm seeing since the switch is the occasional spam. Should I try
re-subscribing?
Ryan
--
Ryan May
Graduate Research Assistant
School of Meteorology
University of Oklahoma
Sent from: Norman Oklahoma United States.
On Mon, March 16, 2009 4:05 pm, Sturla Molden wrote:
On 3/16/2009 9:27 AM, Pearu Peterson wrote:
If a operation produces new array then the new array should have the
storage properties of the lhs operand.
That would not be enough, as 1+a would behave differently from a+1. The
former would
2009/3/16 Ryan May rma...@gmail.com
Hi,
What's the status on SVN and ticket email notifications? The only messages
I'm seeing since the switch is the occasional spam. Should I try
re-subscribing?
I get the ticket notifications but I think the svn notifications are still
broken. I needed
Hi,
I have just started the 1.3.x branch - as such, any change done to the
trunk will not end up in the 1.3 release. I will announce the 1.3 beta
release within the day, hopefully,
cheers,
David
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I'm trying to file a set of data points, defined by genome coordinates, into
bins, also based on genome coordinates. Each data point is (chromosome, start,
end, point) and each bin is (chromosome, start, end). I have about 140 million
points to file into around 100,000 bins. Both are (roughly)
2009/3/16 Peter Saffrey p...@dcs.gla.ac.uk:
At the moment, I'm using a fairly naive approach that finds roughly in the
genome (which gene) each point might be and then checking it against the
bins in that gene. If I split the problem into chromosomes, I feel sure
there must be some super-fast
On Mon, Mar 16, 2009 at 5:29 PM, Robert Kern robert.k...@gmail.com wrote:
2009/3/16 Peter Saffrey p...@dcs.gla.ac.uk:
At the moment, I'm using a fairly naive approach that finds roughly in the
genome (which gene) each point might be and then checking it against the
bins in that gene. If I
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