I noted the same resource causing the same error for the OSCA books in BIoC
3.20 and Lori said she'll take a look at it tomorrow (only on Slack, sorry:
https://community-bioc.slack.com/archives/CM2CUGBGB/p1719265237989709)
On Tue, 25 Jun 2024 at 12:21, Shian Su via Bioc-devel <
Hi Tiago,
The following will create a similarly sized subset of the PBMC3k
dataset with the counts in-memory as a sparse matrix:
pbmc3k <- TENxPBMCData::TENxPBMCData("pbmc3k")
mini_pbmc3k <- pbmc3k[1:1700, 1:600]
assay(mini_pbmc3k) <- as(assay(mini_pbmc3k), "dgCMatrix")
Cheers,
Pete
On Mon, 16
Great initiative, Mike!
Could these meetings please be recorded?
These will be in the middle of the night in my time zone and I'm sure
others would appreciate being able to view them if they can't make the call.
rOpenSci do something similar with their community calls (
ity between 'matrixStats' and 'Matrix' is basically zero(?).
> I think of 'Matrix' a higher-level package. Do my comments above put
> it in a different light? Or are you saying that what's in
> 'matrixStats' should really have been in 'Matrix'?
>
> All the best,
>
> Henrik
>
> On Fri,
Successful pushed to both devel and release. Thanks, Nitesh!
On Wed., 2 May 2018, 1:35 pm Turaga, Nitesh, <nitesh.tur...@roswellpark.org>
wrote:
> Try one more time please.
>
> I made some changes after seeing your output.
>
> Best,
>
> Nitesh
>
> > On M
SE_3_1
remotes/origin/RELEASE_3_2
remotes/origin/RELEASE_3_3
remotes/origin/RELEASE_3_4
remotes/origin/RELEASE_3_5
remotes/origin/RELEASE_3_6
remotes/origin/RELEASE_3_7
remotes/origin/master
$ git log
commit 5eb4c1ebc03fb1d713e873a77570744b94dc7659
Author: Peter Hickey <peter.hic...@
Tim: As the developer of DelayedMatrixStats (and enthusiastic 'canary down
the coal mine' user-dev of DelayedArray) I'm obviously invested in reducing
the confusion around these packages
I'm going to write some blog posts-cum-vignettes-cum-F1000 around these
issues over the coming weeks, with the
.
> Val
>
>
>
> On 04/29/2018 09:37 AM, Peter Hickey wrote:
>
> I'm still unable to push large files after a fresh clone. I *am* able to
> push smaller changes (I just tweaked the DESCRIPTION to test this). But I
> get the "Error: file larger than 5 Mb" error when
9 Apr 2018 at 11:43 Turaga, Nitesh <nitesh.tur...@roswellpark.org>
wrote:
> Can you try with a fresh clone of the repo?
>
> Best,
>
> Nitesh
>
> > On Apr 29, 2018, at 10:21 AM, Peter Hickey <peter.hic...@gmail.com>
> wrote:
> >
> > Nitesh
ource code on their local machine is using the HTTPS protocol,
> since they will not have access to download it via SSH ( you need
> permissions to do this).
>
> We always advocate developers to only use SSH though. For everyone else,
> HTTPS is the best option.
>
> Best,
>
Nitesh, I am still getting the "Error: file larger than 5 Mb" error.
On Sun, 29 Apr 2018 at 09:59 Turaga, Nitesh <nitesh.tur...@roswellpark.org>
wrote:
> Hi Pete,
>
> This should be resolved now.
>
> Best,
>
> Nitesh
> > On Apr 29, 2018, at 9:50 AM, Pe
The one-liner on the package landing page describing how to check out
a package from the git repo uses HTTPS rather than ssh, e.g.:
# From https://bioconductor.org/packages/bsseq/
git clone https://git.bioconductor.org/packages/bsseq
However, as a developer we should be using the SSH protocol
Thanks, Val. I'm getting an error about "too large files" when I try to
push (see below). Is there a different workflow for pushing an experiment
data package or am I doing something else wrong? bsseqData predates the svn
-> git transition.
Thanks,
Pete
$ git push origin master
Counting objects:
Hi Elizabeth,
Aaron and I were hit by this same error message. As a workaround,
installing DelayedArray and HDF5Array from the git(hub) repo fixed the
issue (https://github.com/Bioconductor/HDF5Array/issues/6). But this
needs to be propagated to the versions made available via BiocLite().
Does `rbind(testhdf, DelayedArray(testdata))` give you what you want?
On Wed, 4 Apr 2018 at 14:58 Elizabeth Purdom
wrote:
> Hello,
>
> I am trying to do a rbind a normal (in memory) matrix with a HDF5Matrix
> object or DelayedArray object and I am hitting problems.
I think that's a good idea, Kylie.
Pete (DelayedMatrixStats developer)
On Thu., 2 Nov. 2017, 6:09 am Kasper Daniel Hansen, <
kasperdanielhan...@gmail.com> wrote:
> I think it makes sense. A lot of sense. Might be useful to involve Henrik
> (matrixStats) as well.
>
> Who are the players, apart
FYI I also began a project to support an additional backend;
https://github.com/PeteHaitch/matterArray. It's incomplete and may not work
with the current version of DelayedArray (it's ~3 months old and I was
naughtily using some internal functions of DelayedArray). I hope to return
to this soon
A partial answer if you are using the 'testthat' framework: you can use
`testthat::skip_on_bioc()` to specify that a test should be skipped if it
is running on the BioC build machines. The test will otherwise be run
(e.g., during local development). There are some other `testthat::skip*()`
Doh, I literally spotted that the second I hit send. Sorry for the noise
and thanks!
On Thu, 21 Sep 2017 at 13:55 Turaga, Nitesh <nitesh.tur...@roswellpark.org>
wrote:
> Hi Peter,
>
> If you notice,
>
> On Sep 21, 2017, at 1:53 PM, Peter Hickey <peter.hic...@gmail.c
Hi Nitesh,
I'm unable to push changes to the GenomicTuples package to the BioC git
host.
$ git push
fatal: remote error: FATAL: W any packages/GenomicTuples nobody DENIED by
fallthru
(or you mis-spelled the reponame)
Following the FAQ (http://bioconductor.org/developers/how-to/git/faq/) I've
Thanks, Martin!
On 22 January 2017 at 13:10, Martin Morgan
<martin.mor...@roswellpark.org> wrote:
> On 01/22/2017 10:18 AM, Peter Hickey wrote:
>>
>> Hi,
>>
>> Recent changes (last few days) that successfully synced from my own GitHub
>> repo to the Bi
Sorry, I forgot to say this is the GenomicTuples package
On 22 January 2017 at 10:18, Peter Hickey <peter.hic...@gmail.com> wrote:
> Hi,
>
> Recent changes (last few days) that successfully synced from my own GitHub
> repo to the BioC SVN and consequent builds don't seem
Hi,
Recent changes (last few days) that successfully synced from my own GitHub
repo to the BioC SVN and consequent builds don't seem to have propagated to
the BioC GitHub mirror. Anything I should/can be doing to address this?
Thanks,
Pete
[[alternative HTML version deleted]]
pothetical FWRanges class in this case?)
>
> -Ryan
>
> On 11/23/16 8:01 PM, Ryan wrote:
> > Is it possible to allow the width slot of IRanges to be either a
> > normal vector or an Rle?
> >
> >
> > On 11/23/16 6:18 PM, Peter Hickey wrote:
> >> I've b
But it
> was fun to remember GPos, which I had forgotten.
>
> On Wed, Nov 23, 2016 at 6:34 PM, Vincent Carey <st...@channing.harvard.edu
> > wrote:
>
> library(GenomicRanges)
> class?GPos
>
> On Wed, Nov 23, 2016 at 6:18 PM, Peter Hickey <peter.hic...@gmail.com&g
I've been toying with the idea of a fixed/constant width Ranges
subclass. The motivation comes from storing DNA methylation data at CH
loci (non-CpG methylation): there are 1.1 billion CH loci in the human
genome, so to store these as a GRanges object requires 2 x 1.1 billion
integer vectors, one
g sequences e.g. ranges [1, 10] and
> [101, 110] represent the same position on a circular sequence of
> length 100 so should be considered equal. However for 'x == y' and
> 'identicalVals(x, y)', they are not. Something we should address at
> some point...
>
> Cheers,
> H.
&g
I hit an error when calling reduce() on a very big GRanges object
(length = 1170402558). The error was:
Error in .Call2("CompressedIRangesList_reduce", x, drop.empty.ranges, :
_get_new_buflength(): MAX_BUFLENGTH reached
I found MAX_BUFLENGTH is defined in S4Vectors in the file src/AEbufs.c
I think this is a recent break. I'm mostly concerned because I need to
use this "broken" functionality in a tutorial for BioC2016 this week
and it would require changes to package internals, not the vignette,
in order to fix this at my end.
library(SummarizedExperiment)
se <-
Typo - github version is 1.5.23
On Mon, 18 Apr 2016 at 09:26 Peter Hickey <peter.hic...@gmail.com> wrote:
> Hi,
>
> The current version of GenomicTuples on the official SVN is 1.5.24
> (
> https://hedgehog.fhcrc.org/bioconductor/trunk/madman/Rpacks/GenomicTuples/DESCR
Hi,
The current version of GenomicTuples on the official SVN is 1.5.24
(https://hedgehog.fhcrc.org/bioconductor/trunk/madman/Rpacks/GenomicTuples/DESCRIPTION),
however, the version available via the GitHub mirror is only 1.5.21
Thanks, Aaron. I implemented a similar workaround, but I think it
would be nice to have in the core Bioconductor implementation. I had a
quick poke around GenomicAlignments::readGAlignmentPairs(), however,
but it looked like I'd have to learn a bit too much about the
underlying
Hi,
GenomicAlignments::readGAlignmentPairs() can take a while to
(correctly) fail if the `which` parameter contains a "bad" seqlevel.
It'd be great if it failed early in the following scenario (just
experienced).
An example BAM is available from
Wonderful. Thanks, Martin
> in svn at 1.23.5, and in Bioc-devel hopefully after tonight's build.
>
> Martin
___
Bioc-devel@r-project.org mailing list
https://stat.ethz.ch/mailman/listinfo/bioc-devel
Hi Pete,
>
> On 03/02/2016 12:42 PM, Peter Hickey wrote:
> > This is mostly directed to Herve and/or Martin, but I'd be interested
> > in other's input too.
> >
> > The SummarizedExperiment package defines rbind,Assays-method and
> > cbind,Assay
This is mostly directed to Herve and/or Martin, but I'd be interested
in other's input too.
The SummarizedExperiment package defines rbind,Assays-method and
cbind,Assays-method that are called when rbind() or cbind() is called
on a SummarizedExperiment object. In the case of two-dimensional assay
The assays slot in a SummarizedExperiment object supports elements
with up to 4 dimensions [*]
library(SummarizedExperiment)
makeSE <- function(n) {
assay <- array(1:2^n,
dim = rep(2, n),
dimnames = split(letters[1:(2 * n)], seq_len(n)))
Thanks, Hervé!
On 26/01/2016, Hervé Pagès <hpa...@fredhutch.org> wrote:
> Hi Pete,
>
> On 01/25/2016 12:32 PM, Peter Hickey wrote:
>> The Matrix virtual class in the Matrix package seems to mostly work as
>> an assays element in a SummarizedExperiment. This is es
While on the topic of SummarizedExperiment colnames, the circumstances in
which these are stripped from the assays and overridden by colData is
confusing to me, particularly case 2 below (a warning in case 3 might be
useful too).
> m1 <- matrix(1:10, ncol = 2)
> m2 <- m1
> colnames(m2) <- c("A",
Hi Leonard,
I'm seeing what I think is a related problem in the devel branch. I
think it derives from some issue with List-based classes. E.g, a
simplified version of your example errors for me (although without
segfault):
> library(IRanges)
# snip - this produces a possibly related warning on
passing S4Vectors:::decodeRle(seqnames(x)),
>> start(x), with(x), and S4Vectors:::decodeRle(strand(x)) to the .Call
>> entry point).
>>
>> I'll take your patch if you want to work on this or I can add this
>> to GenomicRanges, let me know. We should probably take this
al question of whether GenomicRanges
>>> should
>>> have an anyNA method that returns FALSE (and similarly an is.na()
>>> method),
>>> although we have never defined the concept of a "missing range".
>>>
>>> Michael
>&
Hi all,
I sometimes want to test whether a GRanges object (or some object with
a GRanges slot, e.g., a SummarizedExperiment object) is (un)sorted.
There is no is.unsorted,GRanges-method or, rather, it defers to
is.unsorted,ANY-method. I'm unsure that deferring to the
is.unsorted,ANY-method is
I used to use the git-svn bridge for my GenomicTuples package, which I
develop on GitHub. Several months ago I attempted to switch to the new
method described at
http://bioconductor.org/developers/how-to/git-mirrors/ but made a
complete mess of it. This wasn't so important at the time since I
I often find myself with multiple `SE` objects (I'm using `SE` as a
shorthand for the `SummarizedExperiment0` and `RangedSummarizedExeriment`
classes), each with different samples but possibly non-overlapping
features/ranges. Currently, it is difficult to combine these objects;
`rbind()` can only
Sorry, the URL may have been mangled. It's
https://gist.github.com/PeteHaitch/8993b096cfa7ccd08c13
<https://gist.github.com/PeteHaitch/8993b096cfa7ccd08c13.>
On Thu, 15 Oct 2015 at 12:52 Peter Hickey <peter.hic...@gmail.com> wrote:
> I often find myself with multiple `SE` objects
See
https://github.com/Bioconductor-mirror/SummarizedExperiment/blob/744eea36e9f8ee4daea00baa7a1d9eea68d957ca/R/SummarizedExperiment0-class.R#L210
I think it should be 'i = assayNames(x)[1]'.
I say it is impossible to trigger because I don't think this method is
ever called since if 'i' is
se [[ internally.
>>>
>>> Do you know of any reason why lengths() doesn't do this?
>>>
>>> Thanks,
>>> H.
>>>
>>>
>>> On 09/28/2015 09:51 PM, Michael Lawrence wrote:
>>>
>>> That is the plan. Note that we a
you're seeing. I think that if you just
re-install S4Vectors locally (without making the change you proposed)
the issue will go away. Hopefully...
H.
On 08/10/2015 06:46 PM, Peter Hickey wrote:
Sorry, that should say once I made the proposed change to S4Vectors,
not IRanges.
On Tue
not be necessary (and doing so will
actually trigger a note from R CMD check). Can you provide more
details on why you need this?
Thanks,
H.
On 08/09/2015 09:16 PM, Peter Hickey wrote:
Hi Hervé,
I was having trouble with some devel code of mine and tracked it down to
some recent updates moving
Sorry, that should say once I made the proposed change to S4Vectors, not
IRanges.
On Tue, 11 Aug 2015 8:51 am Peter Hickey peter.hic...@gmail.com wrote:
Hi Hervé,
Hmm, sorry I may have misdiagnosed my problem. I was having problems with
some code in the bsseq vignette.
The following
Hi Marc,
Will a recording be made available? This sounds quite useful, but not quite
staying up until 2am Australian time useful :)
Thanks,
Pete
Message: 5
Date: Tue, 2 Dec 2014 15:08:08 -0800
From: Marc Carlson mcarl...@fredhutch.org
To: bioc-devel bioc-de...@stat.math.ethz.ch
Subject:
with
the behavior of distanceToNearest method for GRanges objects.
The major issue being that it sometimes returns a Hits
object with NAs in it. Val will address this in the next few
days.
Cheers,
H.
On 11/05/2014 06:21 PM, Peter Hickey wrote:
This message may be a bit premature or redundant
Hi Martin,
The last element of 'x' is never accessed in a call to the internal function
GenomicRanges:::.compare when 'GenomicRanges = TRUE'. The attached patch fixes
this.
Cheers,
Pete
===
--- R/SummarizedExperiment-class.R
://stat.ethz.ch/mailman/listinfo/bioc-devel
Peter Hickey,
PhD Student/Research Assistant,
Bioinformatics Division,
Walter and Eliza Hall Institute of Medical Research,
1G Royal Parade, Parkville, Vic 3052, Australia.
Ph: +613 9345 2324
hic...@wehi.edu.au
http://www.wehi.edu.au
/2014 02:28 PM, Peter Hickey wrote:
Just a vote for still allowing for multiple genomes in a Seqinfo object (in
a GRanges object). My use case is in bisulfite-sequencing experiments where
there is often a spike-in of a lambda phage genome along with the genome of
interest (human or mouse
On 29/08/2014, at 1:18 PM, Michael Lawrence lawrence.mich...@gene.com wrote:
Added to S4Vectors. Thanks!
On Thu, Aug 28, 2014 at 5:04 PM, Peter Hickey hic...@wehi.edu.au wrote:
Thanks, Michael. Do you think there's a general use case for a replaceROWs,
NULL method or shall I just specify
, 2014 at 5:13 PM, Peter Hickey hic...@wehi.edu.au wrote:
Hi Michael,
Thanks for your patience. Here is a self-contained example with comments
https://gist.github.com/PeteHaitch/fdb66d360446ff96ed4b
Thanks,
Pete
On 27/08/2014, at 1:43 AM, Michael Lawrence lawrence.mich...@gene.com wrote
- Original Message -From: Michael Lawrence
lawrence.mich...@gene.comTo: Peter Hickey hic...@wehi.edu.auCc:
bioc-devel@r-project.orgSent: Tue, 26 Aug 2014 13:35:35 +1000 (EST)Subject: Re:
[Bioc-devel] Valid classes for extraColumnSlots
Hi Peter,
Some code would help here. I'm not sure
it to reproduce
the problem and fix things.
Thanks,
Michael
On Tue, Aug 26, 2014 at 4:25 AM, Peter Hickey hic...@wehi.edu.au wrote:
Hi Michael,
Sorry for my misunderstanding. Here is some code describing the class
https://github.com/PeteHaitch/GenomicTuples/blob/master/R/GTuples
Bioconductor data sources.
Thanks,
Pete
Peter Hickey,
PhD Student/Research Assistant,
Bioinformatics Division,
Walter and Eliza Hall Institute of Medical Research,
1G Royal Parade, Parkville, Vic 3052, Australia.
Ph: +613 9345 2324
hic...@wehi.edu.au
http
, but there
is seqnamesStyle infrastructure in GenomeInfoDb that may help.
On Tue, Jun 17, 2014 at 8:17 PM, Peter Hickey hic...@wehi.edu.au wrote:
Is there a reason why the seqnames of SNPlocs.Hsapiens.dbSNP.20120608 (and
possibly the other SNPlocs.*) use the prefix ch instead of chr? E.g.
ch1 instead of chr1
--
On 28/05/2014, at 3:23 AM, Hervé Pagès hpa...@fhcrc.org wrote:
Hi Peter,
On 05/26/2014 04:37 PM, Peter Hickey wrote:
Thanks for the suggested work-around, Martin. In order to define the method
on the group
'=', '!=', '' and '' for free, which is
great!). Unfortunately, as you can see, the MTuples '==' method breaks '==' for
other signatures. Hope that wasn't too tangential.
Cheers,
Pete
On 27/05/2014, at 2:44 AM, Martin Morgan mtmor...@fhcrc.org wrote:
On 05/25/2014 09:39 PM, Peter Hickey wrote
--
Peter Hickey,
PhD Student/Research Assistant,
Bioinformatics Division,
Walter and Eliza Hall Institute of Medical Research,
1G Royal Parade, Parkville, Vic 3052, Australia.
Ph: +613 9345 2324
hic
subject
target Vector SummarizedExperiment
defined Vector SummarizedExperiment
Peter Hickey,
PhD Student/Research Assistant,
Bioinformatics Division,
Walter and Eliza Hall Institute of Medical Research,
1G Royal Parade, Parkville, Vic 3052
Thanks for the explanation and the update, Martin.
Cheers,
Pete
- Original Message -
From: Martin Morgan mtmor...@fhcrc.org
To: Peter Hickey hic...@wehi.edu.au, bioc-devel@r-project.org
Sent: Sat, 12 Apr 2014 06:45:46 +1000 (EST)
Subject: Re: [Bioc-devel] Restrictions on findOverlaps
Apologies for the bump, but is anyone able to help me on this? Or are these
questions more appropriate for the general Bioconductor mailing list rather
than Bioc-Devel?
Many thanks,
Pete
- Original Message -
Date: Mon, 10 Feb 2014 13:20:47 +1100
From: Peter Hickey hic...@wehi.edu.au
of the CoMeth class are appreciated.
Thanks,
Pete
Peter Hickey,
PhD Student/Research Assistant,
Bioinformatics Division,
Walter and Eliza Hall Institute of Medical Research,
1G Royal Parade, Parkville, Vic 3052, Australia.
Ph: +613 9345 2324
hic...@wehi.edu.au
http
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