9-mag-2019 - Esplora la bacheca 'hhhhhhhhhhhhhh' di Fabio Cifarelli su Pinterest. We are pleased to announce Universal Binaries for macOS supporting both Apple's Intel Macs and the all-new Apple Silicon Macs. HandBrake-1.4.0-beta.1.dmg.sig 566.

The bcbioRNASeq constructor function is the main interface connecting bcbio] output data to interactive use in R. It is highly customizable and supports a number of options for advanced use cases. Consult the documentation for additional details.

Upload directory

We have designed the constructor to work as simply as possible by default. The only required argument is uploadDir, the path to the bcbio final upload directory specified with upload: in the YAML configuration. Refer to the bcbio configuration documentation for detailed information on how to set up a bcbio run, which is outside the scope of this vignette.

For example, let’s load up the example bcbio dataset stored internally in the package.

bcbio outputs RNA-seq data in a standardized directory structure, which is described in detail in our workflow paper.

Counts level

By default, bcbioRNASeq imports counts at gene level, which are required for standard differential expression analysis (level = 'genes'). For pseudo-aligned counts (e.g. Salmon, Kallisto, Sailfish) (Bray et al. 2016; Patro, Mount, and Kingsford 2014; Patro et al. 2017), tximport(Soneson, Love, and Robinson 2016) is used internally to aggregate transcript-level counts to gene-level counts, and generates length-scaled transcripts per million (TPM) values. For aligned counts processed with featureCounts(Liao, Smyth, and Shi 2014) (e.g. STAR, HISAT2) (Dobin et al. 2013; Dobin and Gingeras 2016; Kim, Langmead, and Salzberg 2015), these values are already returned at gene level, and therefore not handled by tximport. Once the gene-level counts are imported during the bcbioRNASeq call, the DESeq2 package (Love, Huber, and Anders 2014) is then used to generate an internal DESeqDataSet from which we derive normalized and variance-stabilized counts.

Alternatively, if you want to perform transcript-aware analysis, such as differential exon usage or splicing analysis, transcript-level counts can be obtained using level = 'transcripts'. Note that when counts are loaded at transcript level, TPMs are generated with tximport internally, but no additional normalizations or transformations normally calculated for gene-level counts with DESeq2 are generated.

Expression callers

Since bcbio is flexible and supports a number of expression callers, we have provided advanced options in the bcbioRNASeq constructor to support a variety of workflows using the caller argument. Salmon, Kallisto, and Sailfish counts are supported at either gene or transcript level. Internally, these are loaded using tximport. STAR and HISAT2 aligned counts processed with featureCounts are also supported, but only at gene level.

Sample selection and metadata

If you’d like to load up only a subset of samples, this can be done easily using the samples argument. Note that the character vector declared here must match the description column specified in the sample metadata. Conversely, if you’re working with a large dataset and you simply want to drop a few samples, this can be accomplished with the censorSamples argument.

When working with a bcbio run that has incorrect or outdated metadata, the simplest way to fix this issue is to pass in new metadata from an external spreadsheet (CSV or Excel) using the sampleMetadataFile argument. Note that this can also be used to subset the bcbio dataset, similar to the samples argument (see above), based on the rows that are included in the spreadsheet.

Genome annotations

When analyzing a dataset against a well-annotated genome, we recommend importing the corresponding metadata using AnnotationHub and ensembldb. This functionality is natively supported in the bcbioRNASeq constructor with using the organism, ensemblRelease, and genomeBuild arguments. For example, with our internal bcbio dataset, we’re analyzing counts generated against the EnsemblMus musculus GRCm38 genome build (release 87). These parameters can be defined in the object load call to ensure that the annotations match up exactly with the genome used.

This will return a GRanges object using the GenomicRanges package (Lawrence et al. 2013), which contains coordinates and rich metadata for each gene or transcript. These annotations are accessible with the rowRanges and rowData functions defined in the SummarizedExperiment package (Huber et al. 2015).

Alternatively, transcript-level annotations can also be obtained automatically using this method.

When working with a dataset generated against a poorly-annotated or non-standard genome, we provide a fallback method for loading gene annotations from a general feature format (GFF) file with the gffFile argument. If possible, we recommend providing a general transfer format (GTF) file, which is identical to GFF version 2. GFFv3 is more complicated and non-standard, but Ensembl GFFv3 files are also supported.

If your dataset contains transgenes (e.g. EGFP, TDTOMATO), these features can be defined with the transgeneNames argument, which will automatically populate the rowRanges slot with placeholder metadata.

We recommend loading up data per genome in its own bcbioRNASeq object when possible, so that rich metadata can be imported easily. In the edge case where you need to look at multiple genomes simultaneously, set organism = NULL, and bcbioRNASeq will skip the gene annotation acquisition step.

Refer to the the GenomicRanges and SummarizedExperiment package documentation for more details on working with the genome annotations defined in the rowRanges slot of the object. Here are some useful examples:

Variance stabilization

During the bcbioRNASeq constructor call, log2 variance stabilizaton of gene-level counts can be calculated automatically, and is recommended. This is performed internally by the DESeq2 package, using the varianceStabilizingTransformation and/or rlog functions. These transformations will be slotted into assays.

Dear Laurent,
Late reply... See the copied message below. Note that you need to create symbolic links in the shell, not MacOS aliases. E.g.,
ln -s Aquamacs.app 'Aquamacs Emacs.app'
Best,
Torsten
From: David Reye <***@codeworks.com.au>
Subject: RE: Mozart 1.4.0 for Mac OS X not finding Aquamacs
Date: 6 November 2010 22:42:36 GMT
Robert,
MacOS port of oz requires Aquamacs Emacs.
/Applications/Aquamacs Emacs.app/Contents/… to /Applications/Aquamacs.app/Contents/…
Similarly, the name of the binary has changed from 'Aquamacs Emacs' to 'Aquamacs'
/Applications/Aquamacs Emacs.app -> /Applications/Aquamacs.app
and
/Applications/Aquamacs.app/Contents/MacOS/'Aquamacs Emacs' -> (samedir)/Aquamacs
Cheers,
David
Hi

Base Jump 1.4.0 For Macos Version

I have the same problem but all of the solutions to this problem don't work (or I am to much of a noob to understand them)
macpro:~ laurentlutgen$ ln -s /Applications/Aquamacs Emacs.app /Applications/Aquamacs.app
macpro:~ laurentlutgen$ ln -s /Applications/Aquamacs.app/Contents/MacOS/'Aquamacs Emacs' /Applications/Aquamacs.app/Contents/MacOS/'Aquamacs'
But the Ozapp still asks for Aquamacs
#!/bin/bash
OZHOME=$1/Contents/Resources
CD='$1/Contents/Resources/CocoaDialog.app/Contents/MacOS/CocoaDialog'
#CD='Mozart.app/Contents/Resources/CocoaDialog.app/Contents/MacOS/CocoaDialog'
detectAquamacs()
{
if [ ! -e '/Applications/Aquamacs.app' ]; then
`$CD ok-msgbox --no-cancel --icon info --timeout 20 --title 'Aquamacs not found' --text 'This application is needed to run Mozart' --informative-text 'Yo$

Base Jump 1.4.0 For Macos Windows 10

exit 2
fi
}
detectAquamacs
######################################################################
# you should not edit below this line
No more popup but the app bounces 2 times and then nothing? I am a terminal noob so I am sure I missed something but no idea what.
There were also some scripts posted to change the path but I tried them and I got some syntax and command not found errors.

Base Jump 1.4.0 For Macos Download

https://github.com/steshaw/shelly/blob/master/bin/sync-env-to-plist
http://olabini.com/blog/2009/12/path-problem-with-emacs-on-mac-os-x/
I know that the terminal exits and I am able to copy paste some commands together but I don't want to use it all the time to learn Oz.
Any ideas how to solve my problem?
Thanks
Laurent Lutgen
_________________________________________________________________________________
http://www.mozart-oz.org/mailman/listinfo/mozart-users
Best wishes,
Torsten
--
Dr Torsten Anders
Course Leader, Music Technology
University of Bedfordshire
Park Square, Room A315
http://strasheela.sourceforge.net
http://www.torsten-anders.de
_________________________________________________________________________________

Base Jump 1.4.0 For Macos 2

mozart-users mailing list mozart-***@mozart-oz.org

Base Jump 1 4 0 For Macos 7

Base Jump 1.4.0 For Macos Mac

http://www.mozart-oz.org/mailman/listinfo/mozart-users

Base Jump 1 4 0 For Macos High Sierra